| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74843053-74843636 | Common:7; Rare:470 | ||||
| chr15:74872873-74873273 | Common:5; Rare:259 | ||||
| chr15:74873280-74873520 | Common:32; Rare:307 | ||||
| chr15:74889475-74889910 | Rare:139 | ||||
| chr15:74889881-74890161 | Rare:418; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:74890062-74890796 | Common:5; Rare:313; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:74900284-74900684 | Common:1; Rare:67 | ||||
| chr15:74905692-74907056 | Common:9; Rare:1151 | ||||
| chr15:74907311-74907493 | Rare:40 | ||||
| chr15:74937283-74938348 | Common:16; Rare:910 | ||||
| chr15:74956640-74957040 | Common:5; Rare:340 | ||||
| chr15:74957021-74957444 | Common:2; Rare:197 | ||||
| chr15:74995300-74995600 | Common:6; Rare:102 | ||||
| chr15:75023250-75023734 | Common:16; Rare:292 | ||||
| chr15:75023753-75024233 | Common:4; Rare:137 |