| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102086986-102087330 | Common:4; Rare:140 | ||||
| chr14:102087546-102087589 | Common:1; Rare:7 | ||||
| chr14:102139650-102139932 | Rare:99 | ||||
| chr14:102362847-102363103 | Rare:114 | ||||
| chr14:103123147-103123482 | Rare:63 | ||||
| chr14:103333969-103334258 | Common:1; Rare:121 | ||||
| chr14:103385260-103385452 | Common:1; Rare:68 | ||||
| chr14:103520478-103520742 | Common:1; Rare:65 | ||||
| chr14:103521071-103521325 | Common:1; Rare:87 | ||||
| chr14:103521363-103521805 | Common:2; Rare:134 | ||||
| chr14:103529008-103529250 | Common:1; Rare:70 | ||||
| chr14:103562224-103562475 | Common:1; Rare:106 | ||||
| chr14:103562624-103563062 | Common:8; Rare:175; Clinvar (benign):5 | ||||
| chr14:103629126-103629440 | Common:3; Rare:128 | ||||
| chr14:103715442-103715883 | Common:1; Rare:146 |