| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562570-103563013 | Common:6; Rare:165; Clinvar (benign):2 | ||||
| chr14:103628685-103628792 | Rare:25 | ||||
| chr14:103628870-103629296 | Common:2; Rare:139 | ||||
| chr14:103629385-103629460 | Common:2; Rare:30 | ||||
| chr14:103629758-103629867 | Common:1; Rare:33 | ||||
| chr14:103714952-103715061 | Common:1; Rare:24 | ||||
| chr14:103715348-103715875 | Common:1; Rare:184 | ||||
| chr14:103847494-103847847 | Common:5; Rare:148 | ||||
| chr14:103921464-103921756 | Common:3; Rare:86 | ||||
| chr14:104138225-104138646 | Common:3; Rare:139 | ||||
| chr14:104689442-104689654 | Rare:46 | ||||
| chr14:104690062-104690102 | Common:1; Rare:5 | ||||
| chr14:104724173-104724242 | Common:2; Rare:32 | ||||
| chr14:104752542-104752794 | Common:2; Rare:71 | ||||
| chr14:104752949-104753286 | Common:3; Rare:129 |