| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72398275-72398386 | Rare:39 | ||||
| chr15:72474154-72474580 | Rare:150 | ||||
| chr15:72686129-72686251 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:72731204-72731230 | Rare:5 | ||||
| chr15:72783600-72783864 | Common:2; Rare:115 | ||||
| chr15:73443014-73443247 | Common:3; Rare:92 | ||||
| chr15:73633123-73633346 | Rare:94 | ||||
| chr15:73633354-73633712 | Common:4; Rare:110 | ||||
| chr15:73684096-73684414 | Rare:88 | ||||
| chr15:73873502-73873639 | Rare:19 | ||||
| chr15:73992221-73992451 | Common:1; Rare:84 | ||||
| chr15:73994587-73994783 | Rare:41 | ||||
| chr15:74100181-74100323 | Rare:19 | ||||
| chr15:74173729-74173846 | Common:2; Rare:30 | ||||
| chr15:74202438-74202546 | Rare:19 |