| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:24909081-24909148 | Rare:10 | ||||
| chr15:24978202-24978439 | Rare:63; Clinvar (benign):1 | ||||
| chr15:24983917-24984277 | Common:2; Rare:50 | ||||
| chr15:24986695-24986810 | Rare:23 | ||||
| chr15:24987107-24987165 | Rare:8 | ||||
| chr15:24989519-24989579 | Rare:8 | ||||
| chr15:24990397-24990587 | Common:1; Rare:41 | ||||
| chr15:24991829-24991969 | Rare:25 | ||||
| chr15:24993145-24993255 | Rare:17 | ||||
| chr15:25028753-25028864 | Common:1; Rare:23 | ||||
| chr15:25115602-25115657 | Rare:10 | ||||
| chr15:25121762-25122096 | Rare:41 | ||||
| chr15:25320845-25321146 | Common:1; Rare:63 | ||||
| chr15:25345938-25345945 | Rare:1 | ||||
| chr15:25542205-25542368 | Rare:22 |