| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34794104-34794363 | Common:5; Rare:46 | ||||
| chr15:34794620-34794658 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr15:34794668-34794951 | Rare:71; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:34796897-34797148 | Common:1; Rare:52 | ||||
| chr15:35362217-35362433 | Rare:39 | ||||
| chr15:36773605-36773913 | Common:2; Rare:36 | ||||
| chr15:36882409-36882548 | Common:1; Rare:38 | ||||
| chr15:36888709-36888887 | Common:1; Rare:30 | ||||
| chr15:37102003-37102241 | Common:1; Rare:59 | ||||
| chr15:38454879-38455199 | Common:1; Rare:68 | ||||
| chr15:39420939-39421134 | Common:6; Rare:68 | ||||
| chr15:39579707-39579986 | Common:3; Rare:63 | ||||
| chr15:39580305-39580441 | Common:1; Rare:35 | ||||
| chr15:40301765-40301978 | Rare:36 | ||||
| chr15:41914484-41914709 | Common:4; Rare:48 |