| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43746271-43746701 | Common:1; Rare:171 | ||||
| chr15:43746906-43747183 | Common:2; Rare:57 | ||||
| chr15:43776955-43777094 | Common:1; Rare:39 | ||||
| chr15:43777114-43777405 | Rare:65 | ||||
| chr15:43792756-43793083 | Rare:95 | ||||
| chr15:44288386-44288771 | Common:39; Rare:225 | ||||
| chr15:44427269-44427653 | Common:1; Rare:96 | ||||
| chr15:44536659-44537401 | Common:3; Rare:243 | ||||
| chr15:44663532-44663883 | Rare:160; Clinvar:13; Clinvar (benign):6 | ||||
| chr15:44711252-44711627 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711850-44712104 | Rare:51 | ||||
| chr15:44712630-44712940 | Rare:75 | ||||
| chr15:44728848-44729232 | Common:1; Rare:80 | ||||
| chr15:45023026-45023237 | Common:3; Rare:56 | ||||
| chr15:45200482-45200656 | Common:1; Rare:51 |