| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49688192-49688346 | Common:2; Rare:94 | ||||
| chr14:49693180-49693420 | Rare:95 | ||||
| chr14:49767280-49767714 | Common:5; Rare:184 | ||||
| chr14:49768004-49768223 | Common:4; Rare:157 | ||||
| chr14:49768770-49769120 | Rare:112 | ||||
| chr14:49852741-49853240 | Common:7; Rare:211 | ||||
| chr14:49892783-49893145 | Common:1; Rare:250 | ||||
| chr14:50116560-50116699 | Rare:61 | ||||
| chr14:50231855-50232029 | Common:1; Rare:66 | ||||
| chr14:50312067-50312399 | Common:2; Rare:250; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:50396830-50397043 | Common:5; Rare:116 | ||||
| chr14:50532493-50532767 | Common:6; Rare:175 | ||||
| chr14:50668263-50668560 | Common:7; Rare:215 | ||||
| chr14:50831117-50831256 | Common:1; Rare:79 | ||||
| chr14:50944317-50944583 | Common:8; Rare:178; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 |