Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23778250-23778540 | Common:9; Rare:139 | ||||
chr1:23800730-23800929 | Common:1; Rare:65 | ||||
chr1:23825421-23825537 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23959641-23959908 | Common:2; Rare:72 | ||||
chr1:24112088-24112347 | Rare:69 | ||||
chr1:25232448-25232667 | Rare:88 | ||||
chr1:25338242-25338440 | Common:1; Rare:71 | ||||
chr1:25819913-25820013 | Common:1; Rare:28 | ||||
chr1:25859406-25859556 | Rare:51 | ||||
chr1:25906397-25906707 | Rare:100 | ||||
chr1:26279953-26280169 | Rare:126 | ||||
chr1:26432073-26432403 | Common:5; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472264-26472539 | Common:4; Rare:94 | ||||
chr1:26473042-26473251 | Rare:109 | ||||
chr1:26787870-26787978 | Common:1; Rare:38; Clinvar (benign):1 |