| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43106009-43106231 | Rare:69 | ||||
| chr15:43185208-43185492 | Common:1; Rare:87 | ||||
| chr15:43220843-43221312 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:43330223-43330373 | Common:1; Rare:101 | ||||
| chr15:43330588-43330737 | Common:1; Rare:51 | ||||
| chr15:43371030-43371216 | Common:1; Rare:40 | ||||
| chr15:43648753-43649030 | Common:3; Rare:120 | ||||
| chr15:43746257-43746704 | Common:3; Rare:175 | ||||
| chr15:43777116-43777410 | Rare:65 | ||||
| chr15:43792734-43793030 | Rare:87 | ||||
| chr15:43824552-43824840 | Common:2; Rare:91 | ||||
| chr15:44288406-44288749 | Common:38; Rare:217 | ||||
| chr15:44536663-44537449 | Common:3; Rare:255 | ||||
| chr15:44711331-44711635 | Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711989 | Rare:26 |