| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55196828-55197323 | Common:8; Rare:167 | ||||
| chr15:55289800-55289992 | Common:1; Rare:46 | ||||
| chr15:55290109-55290226 | Rare:20 | ||||
| chr15:55290232-55290272 | Common:2; Rare:10 | ||||
| chr15:55318919-55319491 | Common:4; Rare:164 | ||||
| chr15:55407692-55407905 | Common:1; Rare:42 | ||||
| chr15:55408010-55408531 | Common:6; Rare:138 | ||||
| chr15:55498173-55498527 | Common:7; Rare:152; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:55993128-55993176 | Rare:12 | ||||
| chr15:55993321-55993443 | Common:2; Rare:35 | ||||
| chr15:56243373-56243503 | Rare:34 | ||||
| chr15:56243703-56244042 | Common:3; Rare:148 | ||||
| chr15:56244319-56244550 | Common:1; Rare:57 | ||||
| chr15:56365273-56365595 | Common:2; Rare:160 | ||||
| chr15:56464952-56465308 | Common:5; Rare:118 |