| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:88913042-88913475 | Common:8; Rare:112 | ||||
| chr15:89243833-89244030 | Common:1; Rare:62; Clinvar:2 | ||||
| chr15:89328740-89328978 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:89334772-89335069 | Common:3; Rare:115 | ||||
| chr15:89690681-89690816 | Common:2; Rare:41 | ||||
| chr15:89803443-89803739 | Common:2; Rare:107 | ||||
| chr15:89814793-89814961 | Common:2; Rare:33 | ||||
| chr15:89889049-89889314 | Common:2; Rare:59 | ||||
| chr15:90001222-90001505 | Common:1; Rare:71 | ||||
| chr15:90233828-90234280 | Common:6; Rare:130 | ||||
| chr15:90265653-90265729 | Rare:40 | ||||
| chr15:90265908-90266263 | Common:7; Rare:98 | ||||
| chr15:90388167-90388395 | Common:3; Rare:102 | ||||
| chr15:90473714-90473962 | Rare:78 | ||||
| chr15:90529789-90530129 | Common:4; Rare:113 |