| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104581125-104581309 | Rare:32 | ||||
| chr14:104689506-104689674 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr14:104985635-104985800 | Common:3; Rare:63 | ||||
| chr14:105021053-105021394 | Common:1; Rare:120 | ||||
| chr14:105301009-105301121 | Rare:19 | ||||
| chr14:105419737-105420032 | Rare:93 | ||||
| chr14:105487118-105487226 | Common:1; Rare:36 | ||||
| chr15:22838356-22838804 | Common:3; Rare:156 | ||||
| chr15:22947069-22947192 | Rare:31 | ||||
| chr15:23039529-23039710 | Common:1; Rare:77 | ||||
| chr15:24954909-24955095 | Rare:92 | ||||
| chr15:25438984-25439253 | Common:2; Rare:106 | ||||
| chr15:29269785-29269902 | Common:1; Rare:49 | ||||
| chr15:29822217-29822627 | Common:2; Rare:156 | ||||
| chr15:30903786-30903946 | Rare:37 |