| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45201031-45201154 | Common:2; Rare:44 | ||||
| chr15:45378176-45378576 | Common:2; Rare:148; Clinvar:4; Clinvar (benign):12 | ||||
| chr15:45402149-45402525 | Common:17; Rare:274; Clinvar:1 | ||||
| chr15:45402577-45403073 | Common:3; Rare:329 | ||||
| chr15:45522660-45523040 | Common:3; Rare:194 | ||||
| chr15:45587013-45587617 | Common:4; Rare:327; Clinvar:19; Clinvar (benign):5 | ||||
| chr15:45588085-45588693 | Common:3; Rare:136 | ||||
| chr15:45634596-45635115 | Common:3; Rare:332 | ||||
| chr15:47716950-47717650 | Common:3; Rare:141 | ||||
| chr15:48177272-48178032 | Rare:261 | ||||
| chr15:48178219-48178431 | Rare:127 | ||||
| chr15:48330955-48331161 | Common:6; Rare:77 | ||||
| chr15:48331285-48331529 | Common:7; Rare:212 | ||||
| chr15:48331779-48332288 | Common:27; Rare:440; Clinvar:1 | ||||
| chr15:48645667-48645818 | Common:1; Rare:44; Clinvar (benign):1 |