| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102087556-102087661 | Common:1; Rare:29 | ||||
| chr14:102139148-102139371 | Rare:93 | ||||
| chr14:102139667-102139947 | Rare:97 | ||||
| chr14:102235415-102235505 | Rare:16 | ||||
| chr14:102305096-102305333 | Common:1; Rare:74 | ||||
| chr14:102362836-102363092 | Rare:118 | ||||
| chr14:102928383-102928679 | Rare:107; Clinvar (pathogenic):1 | ||||
| chr14:103123206-103123464 | Rare:47 | ||||
| chr14:103333924-103334258 | Common:3; Rare:143 | ||||
| chr14:103335445-103335493 | Rare:12 | ||||
| chr14:103521465-103521805 | Common:2; Rare:96 | ||||
| chr14:103529029-103529235 | Common:1; Rare:62 | ||||
| chr14:103562223-103562475 | Common:1; Rare:106 | ||||
| chr14:103562624-103563085 | Common:8; Rare:182; Clinvar (benign):5 | ||||
| chr14:103629082-103629436 | Common:3; Rare:143 |