| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100832916-100833034 | Rare:29 | ||||
| chr14:101731294-101731428 | Common:3; Rare:33 | ||||
| chr14:104780090-104780375 | Common:4; Rare:81; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:106269132-106269235 | Common:8; Rare:24 | ||||
| chr15:22880013-22880209 | Common:2; Rare:50 | ||||
| chr15:23303524-23303786 | Common:1; Rare:29 | ||||
| chr15:23403621-23403879 | Common:2; Rare:44 | ||||
| chr15:25056470-25056588 | Common:1; Rare:27 | ||||
| chr15:25062104-25062334 | Common:1; Rare:73 | ||||
| chr15:25718285-25718486 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr15:25739268-25739496 | Common:2; Rare:44 | ||||
| chr15:25776966-25777283 | Common:6; Rare:87 | ||||
| chr15:28589305-28589521 | Common:1; Rare:8 | ||||
| chr15:39580402-39580407 | Rare:2 | ||||
| chr15:39581864-39582275 | Common:4; Rare:96 |