| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44288374-44289189 | Common:40; Rare:349 | ||||
| chr15:44427552-44427653 | Rare:29 | ||||
| chr15:44536855-44537401 | Common:3; Rare:200 | ||||
| chr15:44663532-44663692 | Rare:90; Clinvar:13; Clinvar (benign):6 | ||||
| chr15:44711307-44711611 | Rare:90; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711829-44711977 | Rare:30 | ||||
| chr15:45114170-45114332 | Common:2; Rare:29 | ||||
| chr15:45201095-45201163 | Common:1; Rare:35 | ||||
| chr15:45378471-45378717 | Common:4; Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
| chr15:45522557-45522682 | Rare:30 | ||||
| chr15:45586873-45587281 | Common:1; Rare:81 | ||||
| chr15:45587300-45587598 | Rare:105; Clinvar:7; Clinvar (benign):2 | ||||
| chr15:45587703-45587822 | Common:1; Rare:28 | ||||
| chr15:47718389-47718532 | Rare:32 | ||||
| chr15:48330893-48331470 | Common:7; Rare:170 |