| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34337937-34338204 | Common:1; Rare:84 | ||||
| chr15:34343019-34343207 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):2 | ||||
| chr15:34366934-34367052 | Rare:36 | ||||
| chr15:34367126-34367291 | Rare:60 | ||||
| chr15:34367518-34367706 | Rare:51 | ||||
| chr15:34437720-34437976 | Common:12; Rare:68 | ||||
| chr15:34583524-34583713 | Common:3; Rare:58 | ||||
| chr15:34588443-34588575 | Rare:36 | ||||
| chr15:34969644-34969898 | Common:4; Rare:73 | ||||
| chr15:35546114-35546242 | Common:1; Rare:50 | ||||
| chr15:37098194-37098327 | Common:2; Rare:37 | ||||
| chr15:37099405-37099648 | Rare:63 | ||||
| chr15:37099856-37100002 | Rare:25 | ||||
| chr15:37100520-37100681 | Common:1; Rare:47 | ||||
| chr15:38252032-38252923 | Common:3; Rare:329; Clinvar:1; Clinvar (benign):1 |