| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76826229-76826532 | Common:2; Rare:54 | ||||
| chr14:77028458-77028672 | Common:1; Rare:60 | ||||
| chr14:77028706-77028919 | Rare:72 | ||||
| chr14:77097842-77098368 | Common:1; Rare:166 | ||||
| chr14:77175758-77175879 | Common:1; Rare:24 | ||||
| chr14:77181497-77181845 | Common:2; Rare:76 | ||||
| chr14:77296162-77296460 | Common:3; Rare:90; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr14:77320609-77321137 | Common:5; Rare:166; Clinvar:8; Clinvar (benign):5 | ||||
| chr14:77321171-77321398 | Common:3; Rare:114 | ||||
| chr14:77376936-77377425 | Common:5; Rare:140 | ||||
| chr14:77423035-77423093 | Rare:9 | ||||
| chr14:77457493-77458263 | Common:2; Rare:209 | ||||
| chr14:77616569-77617084 | Common:3; Rare:138; Clinvar:3; Clinvar (benign):5 | ||||
| chr14:77707970-77708208 | Common:2; Rare:122 | ||||
| chr14:77761097-77761222 | Rare:51 |