| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89087738-89088731 | Common:40; Rare:907 | ||||
| chr15:89088956-89089605 | Common:2; Rare:100 | ||||
| chr15:89243679-89244216 | Common:10; Rare:611; Clinvar:18 | ||||
| chr15:89244205-89244600 | Common:17; Rare:189 | ||||
| chr15:89334718-89335158 | Common:19; Rare:953; Clinvar:1 | ||||
| chr15:89335200-89335886 | Common:8; Rare:216 | ||||
| chr15:89575062-89575950 | Common:27; Rare:1198 | ||||
| chr15:89655338-89655870 | Common:9; Rare:307; Clinvar (benign):4 | ||||
| chr15:89691090-89691490 | Common:4; Rare:102 | ||||
| chr15:89750723-89751130 | Common:35; Rare:715 | ||||
| chr15:89760251-89761094 | Common:27; Rare:339 | ||||
| chr15:89776439-89776839 | Common:13; Rare:605; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):30 | ||||
| chr15:89802447-89802847 | Common:5; Rare:104 | ||||
| chr15:89814840-89815362 | Common:2; Rare:239 | ||||
| chr15:89893146-89893747 | Common:2; Rare:196 |