| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:48178110-48178423 | Common:1; Rare:97 | ||||
| chr15:48645646-48646115 | Common:2; Rare:147; Clinvar (benign):1 | ||||
| chr15:48878006-48878304 | Rare:111 | ||||
| chr15:49046346-49046625 | Common:2; Rare:99 | ||||
| chr15:49155552-49155865 | Common:2; Rare:103 | ||||
| chr15:49170371-49170503 | Common:1; Rare:25 | ||||
| chr15:49423093-49423415 | Common:1; Rare:53 | ||||
| chr15:49620764-49621127 | Common:6; Rare:137 | ||||
| chr15:50354734-50354772 | Rare:12 | ||||
| chr15:50354882-50355010 | Rare:21 | ||||
| chr15:50355103-50355513 | Common:3; Rare:165 | ||||
| chr15:50424156-50424511 | Common:2; Rare:128 | ||||
| chr15:50686535-50686581 | Rare:13 | ||||
| chr15:50686723-50686937 | Common:5; Rare:91 | ||||
| chr15:50765498-50765520 | Rare:8 |