| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:64205552-64206145 | Common:2; Rare:152 | ||||
| chr14:64215980-64216270 | Common:2; Rare:97; Clinvar (benign):3 | ||||
| chr14:64216239-64216868 | Common:2; Rare:226; Clinvar (benign):7 | ||||
| chr14:64220456-64220856 | Common:1; Rare:130; Clinvar:5; Clinvar (benign):3 | ||||
| chr14:64233138-64233819 | Common:7; Rare:235 | ||||
| chr14:64235702-64235810 | Rare:22 | ||||
| chr14:64235770-64236285 | Common:3; Rare:175 | ||||
| chr14:64236340-64236740 | Common:1; Rare:107 | ||||
| chr14:64387048-64387448 | Rare:120 | ||||
| chr14:64409605-64409818 | Common:2; Rare:30 | ||||
| chr14:64422958-64423151 | Common:4; Rare:37 | ||||
| chr14:64445570-64445770 | Rare:64 | ||||
| chr14:64448272-64448672 | Common:2; Rare:124 | ||||
| chr14:64458778-64459930 | Common:9; Rare:229 | ||||
| chr14:64501528-64501692 | Rare:36 |