Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:118591667-118591795 | Rare:49 | ||||
chr4:119501203-119501429 | Common:1; Rare:56 | ||||
chr4:122877764-122877977 | Common:2; Rare:36 | ||||
chr4:128970389-128970650 | Rare:61 | ||||
chr4:147637371-147637473 | Rare:18 | ||||
chr4:150002028-150002378 | Common:5; Rare:54 | ||||
chr4:168925993-168926328 | Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
chr4:183350817-183350920 | Rare:17 | ||||
chr4:186727285-186727394 | Rare:23 | ||||
chr5:8457559-8457741 | Common:2; Rare:62 | ||||
chr5:14145258-14145568 | Common:3; Rare:86 | ||||
chr5:32173300-32173416 | Common:1; Rare:24 | ||||
chr5:43041454-43041593 | Common:2; Rare:26 | ||||
chr5:53484839-53485089 | Rare:56 | ||||
chr5:54519495-54519539 | Rare:18 |