| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:52568761-52569048 | Common:2; Rare:127 | ||||
| chr15:52569111-52569343 | Common:2; Rare:71 | ||||
| chr15:52651947-52652197 | Common:2; Rare:54 | ||||
| chr15:52678197-52678245 | Rare:7 | ||||
| chr15:52679267-52679584 | Common:2; Rare:92 | ||||
| chr15:52679637-52679681 | Rare:6 | ||||
| chr15:55196562-55196760 | Rare:56 | ||||
| chr15:55196790-55197158 | Common:6; Rare:131 | ||||
| chr15:55197178-55197328 | Common:2; Rare:36 | ||||
| chr15:55290165-55290243 | Common:1; Rare:13 | ||||
| chr15:55318849-55319318 | Common:5; Rare:140 | ||||
| chr15:55319343-55319505 | Rare:47 | ||||
| chr15:55407713-55407904 | Common:1; Rare:37 | ||||
| chr15:55408128-55408697 | Common:6; Rare:138 | ||||
| chr15:55498158-55498253 | Common:2; Rare:43; Clinvar (benign):2 |