| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34338035-34338212 | Common:1; Rare:54 | ||||
| chr15:34343026-34343297 | Common:5; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
| chr15:34366340-34366630 | Common:1; Rare:60 | ||||
| chr15:34367132-34367365 | Common:2; Rare:101 | ||||
| chr15:34367600-34368030 | Rare:81 | ||||
| chr15:34437730-34437873 | Common:5; Rare:44 | ||||
| chr15:34582863-34583087 | Common:4; Rare:74 | ||||
| chr15:34969677-34969887 | Common:4; Rare:62 | ||||
| chr15:34988232-34988472 | Common:1; Rare:97 | ||||
| chr15:34988570-34988730 | Rare:29 | ||||
| chr15:35545554-35545717 | Rare:46 | ||||
| chr15:35545909-35546071 | Common:1; Rare:50 | ||||
| chr15:35546108-35546462 | Common:1; Rare:113 | ||||
| chr15:36579466-36579676 | Common:3; Rare:50 | ||||
| chr15:37095019-37095428 | Rare:123 |