| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:29730495-29730611 | Rare:30 | ||||
| chr15:34790092-34790336 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:34794100-34794319 | Common:3; Rare:39 | ||||
| chr15:34794678-34794950 | Rare:68; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:82750429-82750621 | Common:2; Rare:59 | ||||
| chr15:84631314-84631485 | Common:3; Rare:50 | ||||
| chr15:84785609-84785727 | Common:1; Rare:16 | ||||
| chr15:86079704-86079925 | Common:4; Rare:52 | ||||
| chr15:96327346-96327471 | Common:3; Rare:16 | ||||
| chr16:2673372-2673685 | Common:8; Rare:107 | ||||
| chr16:3021407-3021615 | Common:1; Rare:63 | ||||
| chr16:3022983-3023265 | Common:1; Rare:77 | ||||
| chr16:29139471-29139668 | Common:2; Rare:40 | ||||
| chr16:30634276-30634559 | Common:1; Rare:71 | ||||
| chr16:31085835-31086134 | Rare:93 |