| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:32972629-32972855 | Rare:49 | ||||
| chr15:33066793-33066908 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:33098235-33098418 | Common:2; Rare:48 | ||||
| chr15:33114088-33114265 | Common:4; Rare:44 | ||||
| chr15:33126604-33126746 | Common:1; Rare:60 | ||||
| chr15:34101122-34101221 | Rare:25 | ||||
| chr15:36832919-36833038 | Common:1; Rare:21 | ||||
| chr15:37000902-37000962 | Rare:14 | ||||
| chr15:37021928-37022150 | Common:2; Rare:40 | ||||
| chr15:37022249-37022540 | Common:1; Rare:45 | ||||
| chr15:37026280-37026378 | Common:1; Rare:18 | ||||
| chr15:37027466-37027664 | Rare:31 | ||||
| chr15:37028453-37028508 | Rare:9 | ||||
| chr15:37031695-37031706 | Rare:2 | ||||
| chr15:37081812-37082129 | Common:1; Rare:67 |