| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102591813-102592238 | Common:6; Rare:139 | ||||
| chr14:102592288-102592747 | Common:1; Rare:188 | ||||
| chr14:102593008-102593277 | Rare:125 | ||||
| chr14:102777091-102777496 | Common:5; Rare:85 | ||||
| chr14:102777499-102777619 | Common:2; Rare:34 | ||||
| chr14:102922473-102922753 | Common:5; Rare:96; Clinvar (pathogenic):1 | ||||
| chr14:102922765-102923121 | Common:3; Rare:127 | ||||
| chr14:102928413-102928735 | Common:1; Rare:120; Clinvar (pathogenic):1 | ||||
| chr14:102928946-102929104 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr14:103057302-103057614 | Common:2; Rare:101 | ||||
| chr14:103057710-103057907 | Common:6; Rare:92 | ||||
| chr14:103103990-103104270 | Common:2; Rare:79 | ||||
| chr14:103126905-103127269 | Common:2; Rare:97 | ||||
| chr14:103333290-103333361 | Common:4; Rare:20 | ||||
| chr14:103333452-103333644 | Rare:47 |