| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103629126-103629484 | Common:4; Rare:135 | ||||
| chr14:105419737-105420027 | Rare:87 | ||||
| chr15:23565496-23565693 | Common:1; Rare:55 | ||||
| chr15:30903779-30903936 | Rare:40 | ||||
| chr15:32615127-32615603 | Common:7; Rare:118 | ||||
| chr15:34101841-34102087 | Common:1; Rare:49 | ||||
| chr15:34343081-34343258 | Common:4; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34988228-34988354 | Rare:53 | ||||
| chr15:35546137-35546220 | Rare:34 | ||||
| chr15:37100389-37100827 | Common:1; Rare:137 | ||||
| chr15:37101295-37101411 | Common:23; Rare:53 | ||||
| chr15:37101706-37101851 | Rare:47 | ||||
| chr15:39580853-39581086 | Common:1; Rare:61 | ||||
| chr15:39782766-39782877 | Rare:29 | ||||
| chr15:39920921-39920998 | Common:1; Rare:24 |