Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161069815-161070124 | Rare:41 | ||||
chr1:161117956-161118141 | Rare:92 | ||||
chr1:161132592-161132831 | Common:2; Rare:65 | ||||
chr1:161159341-161159511 | Common:2; Rare:47 | ||||
chr1:161215117-161215368 | Common:2; Rare:80 | ||||
chr1:161306076-161306243 | Common:1; Rare:53; Clinvar:4; Clinvar (benign):3 | ||||
chr1:161314315-161314403 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
chr1:161505641-161505871 | Rare:37 | ||||
chr1:161524183-161524246 | Rare:12 | ||||
chr1:161549669-161549901 | Common:1; Rare:90 | ||||
chr1:161766149-161766411 | Common:3; Rare:86 | ||||
chr1:165768778-165768897 | Common:1; Rare:55 | ||||
chr1:167630111-167630410 | Common:4; Rare:61 | ||||
chr1:167935931-167936333 | Common:2; Rare:118 | ||||
chr1:167936561-167936921 | Common:1; Rare:130 |