Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155563088-155563260 | Rare:74 | ||||
chr1:155688559-155689150 | Common:3; Rare:181 | ||||
chr1:155859330-155859572 | Common:3; Rare:60 | ||||
chr1:155911234-155911588 | Common:2; Rare:111; Clinvar (benign):1 | ||||
chr1:155934349-155934468 | Common:1; Rare:57 | ||||
chr1:155978140-155978234 | Rare:25 | ||||
chr1:155978468-155978635 | Rare:42 | ||||
chr1:155979110-155979291 | Common:1; Rare:31 | ||||
chr1:156054616-156054904 | Common:3; Rare:81 | ||||
chr1:156061023-156061443 | Common:1; Rare:102 | ||||
chr1:156154365-156154558 | Rare:44 | ||||
chr1:156193832-156194138 | Common:3; Rare:79 | ||||
chr1:156212875-156213049 | Common:1; Rare:49 | ||||
chr1:156282780-156282947 | Common:2; Rare:50 | ||||
chr1:156284202-156284363 | Rare:38 |