Encode`s chromHMM and Segway data is available on ucsc genome browser.

you might want to look at the recent paper published in nature Mapping and analysis of chromatin state dynamics in nine human cell types

Here is the UCSC genome browser link to Chromatin State Segmentation by HMM from ENCODE/Broad

I hope this helps.

May be not, as chromatin states are specific to regulatory elements that are tissue/cell specific.

Also I would like to add, there are so many regions in the human genome that are not covered by any of these 15 chromatin states predicted by using 8 histone and 1 ctcf marks may lower your predictive power.

If you are really serious about your question, I would suggest you to start with 50 chromatin states (covers more histone modifications and human genome) for your prediction and then 15 chromatin states.

You can train your datasets by using chromHMM (This software is used in predicting the above chromatin states by Jason in his 2 Nature papers)

Good luck!

I would be very surprised if there was an existing tool for answering your question in a straightforward way. Why not try yourself and see?

You could select a certain number of regions from the genome, and represent each by a vector containing a segmentation value for each of the assayed cell lines or tissued (I don't know whether it will be a binary or a continuous value, I guess either would be OK). So each region would have a kind of "tissue specificity profile." Then you could do leave-one-out cross-validation, leaving out one tissue/cell line in turn, train some statistical learning model on the profiles for the rest of the tissues/cell lines, and try to predict the value of the left-out tissue/cell-line, finally averaging the accuracy of the predictions across the tissues and regions.

Actually I would consider taking a shot at this when I get the time, the question is just whn this mythical day will come ... :-)

Comming initially from molecular biology....don't forget that many many cell lines have adapted significantly to in vitro conditions and many many chromosome reshuffling, duplication events are to be considered (as my professor used to say on cell culture work: make sure the cells are happy and fresh; dead cells in culture are like "french fries" to the happy cells, the happy (meals) take up everything until they got fed up and burst...or develop some genome reshuffling to deal with it)....

So depending on the question WHY you want to do this using cell lines...BE CAREFUL! Tissue sections might be a different piece of cookie though.

My 2ct (or did I misunderstand your question?).