| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40103594-40103770 | Rare:38 | ||||
| chr15:40104916-40105068 | Common:1; Rare:45 | ||||
| chr15:40107451-40107642 | Common:3; Rare:30 | ||||
| chr15:40107667-40107935 | Common:1; Rare:39 | ||||
| chr15:40245329-40245506 | Rare:34 | ||||
| chr15:40286609-40286931 | Common:1; Rare:57 | ||||
| chr15:40323246-40323521 | Common:2; Rare:68 | ||||
| chr15:40323567-40323733 | Common:2; Rare:59 | ||||
| chr15:40324208-40324344 | Common:1; Rare:37 | ||||
| chr15:40346292-40346498 | Common:1; Rare:47 | ||||
| chr15:40346902-40347111 | Common:1; Rare:45 | ||||
| chr15:40349241-40349581 | Common:3; Rare:58 | ||||
| chr15:40436259-40436347 | Common:1; Rare:21 | ||||
| chr15:40442183-40442347 | Rare:34 | ||||
| chr15:40471633-40472017 | Rare:119; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 |