Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110424741-110424993 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110870249-110870566 | Common:3; Rare:49 | ||||
chr14:49633938-49634047 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862713-49863036 | Rare:147 | ||||
chr14:61570562-61570682 | Common:1; Rare:27 | ||||
chr14:61618689-61618802 | Rare:24 | ||||
chr14:73246004-73246082 | Rare:24 | ||||
chr14:100825954-100826139 | Rare:32 | ||||
chr15:28589195-28589495 | Common:1; Rare:10 | ||||
chr15:44726773-44727072 | Common:1; Rare:41 | ||||
chr15:73927762-73927875 | Rare:29 | ||||
chr15:82750445-82750583 | Common:2; Rare:35 | ||||
chr15:96327329-96327426 | Common:3; Rare:14 | ||||
chr16:74368127-74368370 | Common:1; Rare:69 | ||||
chr17:15786897-15787017 | Common:4; Rare:35 |