Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:37099012-37099074 | Rare:19 | ||||
chr15:37100445-37100801 | Common:1; Rare:124 | ||||
chr15:37101708-37101843 | Rare:45 | ||||
chr15:38454072-38454191 | Rare:51 | ||||
chr15:39782787-39782877 | Rare:25 | ||||
chr15:40039091-40039329 | Rare:99 | ||||
chr15:40405624-40405839 | Common:2; Rare:66; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr15:40593902-40594334 | Common:2; Rare:136 | ||||
chr15:40695050-40695210 | Rare:45 | ||||
chr15:40755220-40755425 | Common:2; Rare:66 | ||||
chr15:40763935-40764125 | Rare:47 | ||||
chr15:40807057-40807111 | Rare:14 | ||||
chr15:40807450-40807754 | Common:4; Rare:101 | ||||
chr15:40844380-40844477 | Rare:34 | ||||
chr15:40894354-40894477 | Rare:45 |