Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116392760-116392930 | Rare:34 | ||||
chr1:116393297-116393609 | Common:1; Rare:63 | ||||
chr1:116404706-116404934 | Rare:37 | ||||
chr1:116418566-116418663 | Common:1; Rare:32 | ||||
chr1:119605760-119605908 | Common:1; Rare:40 | ||||
chr1:119740265-119740494 | Rare:62; Clinvar (pathogenic):1 | ||||
chr1:119930580-119930704 | Rare:17 | ||||
chr1:119975398-119975699 | Rare:52 | ||||
chr1:120464387-120464444 | Rare:7 | ||||
chr1:121288054-121288231 | Rare:22 | ||||
chr1:144412281-144412576 | Common:4; Rare:85 | ||||
chr1:144551931-144552215 | Rare:92 | ||||
chr1:145280815-145281122 | Common:7; Rare:106 | ||||
chr1:145998227-145998432 | Rare:30 | ||||
chr1:146007310-146007533 | Common:1; Rare:33 |