| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102139654-102139926 | Rare:94 | ||||
| chr14:102362853-102363092 | Rare:107 | ||||
| chr14:103123331-103123464 | Rare:22 | ||||
| chr14:103333909-103334253 | Common:3; Rare:143 | ||||
| chr14:103385247-103385433 | Rare:71 | ||||
| chr14:103529015-103529235 | Common:1; Rare:64 | ||||
| chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:103715479-103715853 | Common:1; Rare:121 | ||||
| chr14:105419733-105420050 | Rare:98 | ||||
| chr15:22838356-22838753 | Common:3; Rare:143 | ||||
| chr15:23039546-23039746 | Common:1; Rare:80 | ||||
| chr15:23687269-23687467 | Common:1; Rare:68 | ||||
| chr15:24856426-24856589 | Common:3; Rare:47 | ||||
| chr15:24954822-24955056 | Common:1; Rare:107 | ||||
| chr15:25438982-25439229 | Common:2; Rare:94 |