| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74787873-74788178 | Common:1; Rare:64 | ||||
| chr15:74788385-74788553 | Common:1; Rare:28 | ||||
| chr15:74788665-74789029 | Common:1; Rare:75 | ||||
| chr15:74842899-74842972 | Rare:17 | ||||
| chr15:74843082-74843339 | Common:2; Rare:77 | ||||
| chr15:74872935-74873146 | Common:1; Rare:53 | ||||
| chr15:74873278-74873550 | Common:6; Rare:75 | ||||
| chr15:74873819-74873855 | Rare:5 | ||||
| chr15:74889903-74890172 | Rare:106; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74906012-74906375 | Rare:96 | ||||
| chr15:74906710-74906943 | Common:1; Rare:92 | ||||
| chr15:74937495-74937588 | Rare:18 | ||||
| chr15:74937644-74937824 | Rare:51 | ||||
| chr15:74937931-74938327 | Common:3; Rare:120 | ||||
| chr15:74956667-74956842 | Common:1; Rare:68 |