Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23825416-23825579 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23868298-23868525 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23959608-23959992 | Common:2; Rare:93 | ||||
chr1:23961244-23961465 | Common:5; Rare:45 | ||||
chr1:23980269-23980525 | Rare:80 | ||||
chr1:24642959-24643335 | Common:2; Rare:117 | ||||
chr1:25232460-25232589 | Rare:47 | ||||
chr1:25338100-25338383 | Common:1; Rare:86 | ||||
chr1:25819887-25820013 | Common:2; Rare:38 | ||||
chr1:26278904-26279143 | Common:5; Rare:40 | ||||
chr1:26279844-26280204 | Rare:192 | ||||
chr1:26306932-26307263 | Rare:45 | ||||
chr1:26317856-26318146 | Common:3; Rare:59 | ||||
chr1:26432218-26432418 | Common:4; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472242-26472526 | Common:4; Rare:91 |