| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:62165248-62165441 | Common:1; Rare:47 | ||||
| chr15:62390367-62390613 | Rare:130 | ||||
| chr15:62561100-62561425 | Common:2; Rare:78 | ||||
| chr15:63041979-63042269 | Rare:57 | ||||
| chr15:63042377-63042917 | Common:8; Rare:168; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63043628-63043665 | Rare:9 | ||||
| chr15:63043931-63044018 | Rare:27 | ||||
| chr15:63048234-63048632 | Common:5; Rare:156; Clinvar:3; Clinvar (benign):3 | ||||
| chr15:63121745-63121957 | Common:4; Rare:66; Clinvar (benign):1 | ||||
| chr15:63122392-63122576 | Common:3; Rare:56 | ||||
| chr15:63156847-63156886 | Rare:6 | ||||
| chr15:63157141-63157326 | Rare:37 | ||||
| chr15:63157415-63157660 | Common:4; Rare:100 | ||||
| chr15:63157955-63158133 | Common:2; Rare:42 | ||||
| chr15:63189268-63189665 | Common:3; Rare:125 |