| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40807439-40807760 | Common:4; Rare:107 | ||||
| chr15:40894220-40894508 | Rare:84 | ||||
| chr15:41972535-41972788 | Common:2; Rare:67 | ||||
| chr15:42273097-42273224 | Common:1; Rare:51 | ||||
| chr15:42273416-42273523 | Rare:39 | ||||
| chr15:42548733-42548956 | Common:1; Rare:111 | ||||
| chr15:43106032-43106175 | Rare:41 | ||||
| chr15:43746251-43746459 | Common:2; Rare:79 | ||||
| chr15:44288628-44288925 | Common:1; Rare:83 | ||||
| chr15:44427533-44427642 | Rare:32 | ||||
| chr15:44536874-44537236 | Common:3; Rare:136 | ||||
| chr15:44711304-44712018 | Rare:177; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44712856-44712969 | Common:1; Rare:20 | ||||
| chr15:44729414-44729533 | Common:1; Rare:26 | ||||
| chr15:45587233-45587521 | Common:1; Rare:90; Clinvar:6; Clinvar (benign):2 |