| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68820733-68820816 | Rare:27 | ||||
| chr15:68820845-68821044 | Rare:57 | ||||
| chr15:69160343-69160670 | Common:4; Rare:97 | ||||
| chr15:69298596-69298924 | Common:6; Rare:67 | ||||
| chr15:69452701-69453020 | Common:5; Rare:132 | ||||
| chr15:72118167-72118432 | Common:2; Rare:87 | ||||
| chr15:72231142-72231520 | Common:3; Rare:120 | ||||
| chr15:72272514-72272720 | Rare:57 | ||||
| chr15:72375509-72375761 | Common:1; Rare:50; Clinvar (pathogenic):3 | ||||
| chr15:72375922-72376129 | Common:2; Rare:82; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474195-72474630 | Rare:157 | ||||
| chr15:72783494-72783794 | Common:1; Rare:118 | ||||
| chr15:73633172-73633595 | Common:2; Rare:168 | ||||
| chr15:73926312-73926466 | Rare:43 | ||||
| chr15:73994587-73994801 | Rare:46 |