Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156741071-156741417 | Common:1; Rare:91 | ||||
chr1:156767380-156767542 | Common:1; Rare:53 | ||||
chr1:159780606-159781000 | Common:5; Rare:95 | ||||
chr1:159924540-159924804 | Rare:60 | ||||
chr1:159925465-159925617 | Common:1; Rare:42 | ||||
chr1:160205206-160205459 | Common:2; Rare:71 | ||||
chr1:160262411-160262624 | Rare:65 | ||||
chr1:160285110-160285302 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr1:160343181-160343391 | Rare:86 | ||||
chr1:161045888-161046052 | Common:1; Rare:43 | ||||
chr1:161117995-161118141 | Rare:77 | ||||
chr1:161132583-161132674 | Common:1; Rare:35 | ||||
chr1:161159410-161159507 | Common:1; Rare:23 | ||||
chr1:161314265-161314401 | Common:3; Rare:47; Clinvar (benign):2 | ||||
chr1:162497761-162497859 | Common:1; Rare:33 |