| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103385257-103385459 | Common:1; Rare:74 | ||||
| chr14:103498087-103498429 | Common:1; Rare:53 | ||||
| chr14:103529008-103529260 | Common:1; Rare:74 | ||||
| chr14:103562586-103563222 | Common:11; Rare:263; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103629341-103629490 | Common:4; Rare:50 | ||||
| chr14:103675562-103675829 | Common:1; Rare:62 | ||||
| chr14:103715409-103715856 | Common:1; Rare:154 | ||||
| chr14:104689313-104689674 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr14:104752976-104753319 | Common:2; Rare:123 | ||||
| chr14:104970465-104970818 | Common:4; Rare:67 | ||||
| chr14:104985628-104985829 | Common:3; Rare:82 | ||||
| chr14:105021029-105021518 | Common:3; Rare:176 | ||||
| chr14:105248416-105248602 | Common:6; Rare:85 | ||||
| chr14:105301002-105301112 | Rare:22 | ||||
| chr14:105419737-105420036 | Rare:94 |