| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72117862-72117949 | Rare:26 | ||||
| chr15:72117977-72118468 | Common:5; Rare:169 | ||||
| chr15:72118501-72118672 | Common:1; Rare:41 | ||||
| chr15:72168566-72168748 | Common:2; Rare:44 | ||||
| chr15:72228170-72228290 | Rare:18 | ||||
| chr15:72228464-72228698 | Common:3; Rare:65 | ||||
| chr15:72228847-72229273 | Common:4; Rare:64 | ||||
| chr15:72229550-72229709 | Rare:35 | ||||
| chr15:72230300-72230748 | Common:4; Rare:130 | ||||
| chr15:72231086-72231560 | Common:4; Rare:154 | ||||
| chr15:72231644-72231773 | Common:2; Rare:29 | ||||
| chr15:72272622-72273012 | Common:3; Rare:98 | ||||
| chr15:72320136-72320397 | Common:1; Rare:83 | ||||
| chr15:72375917-72376291 | Common:4; Rare:137; Clinvar:11; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72376418-72376515 | Rare:24 |