| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103519911-103520314 | Common:1; Rare:121 | ||||
| chr14:103521465-103521790 | Common:2; Rare:92 | ||||
| chr14:103529035-103529243 | Common:1; Rare:64 | ||||
| chr14:103562265-103562372 | Rare:39 | ||||
| chr14:103562442-103562567 | Common:1; Rare:40 | ||||
| chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:103629117-103629428 | Common:2; Rare:128 | ||||
| chr14:103715466-103715877 | Common:1; Rare:134 | ||||
| chr14:104970465-104970584 | Common:3; Rare:23 | ||||
| chr14:104970634-104970799 | Common:1; Rare:37 | ||||
| chr14:104985626-104985795 | Common:3; Rare:61 | ||||
| chr14:105301009-105301115 | Rare:19 | ||||
| chr14:105419735-105420027 | Rare:88 | ||||
| chr14:105487015-105487242 | Common:1; Rare:64 | ||||
| chr15:22838356-22838800 | Common:3; Rare:156 |