| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:81189759-81189936 | Rare:27 | ||||
| chr15:81313147-81313320 | Rare:54 | ||||
| chr15:81419384-81419591 | Common:1; Rare:37 | ||||
| chr15:82045068-82045291 | Rare:96 | ||||
| chr15:82046656-82046847 | Common:4; Rare:71 | ||||
| chr15:82046930-82047506 | Common:3; Rare:216 | ||||
| chr15:82445511-82445527 | Rare:1 | ||||
| chr15:82538970-82539094 | Common:3; Rare:26; Clinvar (pathogenic):1 | ||||
| chr15:82738047-82738148 | Common:1; Rare:14 | ||||
| chr15:82750120-82750191 | Rare:10 | ||||
| chr15:82750302-82750657 | Common:3; Rare:95 | ||||
| chr15:82810214-82810366 | Rare:48 | ||||
| chr15:82810374-82810716 | Common:1; Rare:90 | ||||
| chr15:83061714-83062027 | Rare:51 | ||||
| chr15:83108657-83108768 | Rare:21 |