Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:90001023-90001170 | Rare:38 | ||||
chr15:90233906-90234246 | Common:6; Rare:94 | ||||
chr15:90915848-90916050 | Rare:42 | ||||
chr15:92997062-92997304 | Rare:48; Clinvar (benign):2 | ||||
chr15:99251204-99251460 | Common:3; Rare:79 | ||||
chr15:101295194-101295396 | Common:1; Rare:63 | ||||
chr15:101652272-101652522 | Common:5; Rare:124 | ||||
chr16:53538-53882 | Common:7; Rare:116 | ||||
chr16:138661-138869 | Common:6; Rare:77 | ||||
chr16:234703-234886 | Rare:87 | ||||
chr16:636207-636439 | Common:4; Rare:74 | ||||
chr16:680339-680494 | Common:2; Rare:56 | ||||
chr16:684172-684485 | Common:3; Rare:153 | ||||
chr16:1420730-1420944 | Common:1; Rare:85 | ||||
chr16:1488768-1488886 | Rare:39 |