| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55196273-55197479 | Common:47; Rare:1193 | ||||
| chr15:55289128-55289528 | Common:5; Rare:83 | ||||
| chr15:55289524-55290011 | Common:8; Rare:361 | ||||
| chr15:55290204-55290450 | Common:7; Rare:135 | ||||
| chr15:55318700-55319690 | Common:35; Rare:1129 | ||||
| chr15:55348577-55348977 | Common:4; Rare:71 | ||||
| chr15:55398234-55398634 | Common:3; Rare:103 | ||||
| chr15:55407970-55408690 | Common:42; Rare:1019 | ||||
| chr15:55498180-55498580 | Common:13; Rare:299; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr15:55588310-55588720 | Common:1; Rare:129 | ||||
| chr15:55992928-55994016 | Common:16; Rare:1081 | ||||
| chr15:56242841-56243241 | Common:4; Rare:172 | ||||
| chr15:56243230-56244734 | Common:20; Rare:1501 | ||||
| chr15:56365211-56365611 | Common:6; Rare:453 | ||||
| chr15:56464970-56465360 | Common:18; Rare:478 |