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. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Mol Cancer Res. 2014 Aug 4;12(12):1818–1828. doi: 10.1158/1541-7786.MCR-14-0167

Table 1.

Analysis of RRP1B-binding regions detected through ChIP-seq. Regions bound by endogenous RRP1B in MDA-MB-231 and HeLa cells were defined with MACS. Genomic sequences were partitioned into four bins relative to RefSeq genes; distal promoter, proximal promoter, downstream, and genic. The genic bin was further divided by 5′ UTR, exons, introns, and 3′ UTR. The number of peaks for each bin is shown here

Peak Position Relative to Gene HeLa MDA-MB-231
Distal promoter 150 64
Proximal promoter 156 54
Downstream 263 102
Genic 205 90

Genic 5′ UTR 61 21
Exons 60 13
Introns 129 74
3′ UTR 33 19