| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73886685-73886925 | Common:3; Rare:74 | ||||
| chr14:73950027-73950350 | Common:6; Rare:142; Clinvar (benign):5 | ||||
| chr14:74019233-74019442 | Common:1; Rare:82 | ||||
| chr14:74084399-74084745 | Common:7; Rare:89 | ||||
| chr14:74302899-74303078 | Common:1; Rare:79; Clinvar (benign):3 | ||||
| chr14:74493193-74493783 | Common:4; Rare:190; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74713052-74713213 | Rare:90 | ||||
| chr14:74881840-74882016 | Rare:80 | ||||
| chr14:75002741-75002982 | Common:1; Rare:79; Clinvar:2 | ||||
| chr14:75051416-75051518 | Common:1; Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:75069465-75069732 | Common:2; Rare:67 | ||||
| chr14:75126908-75127128 | Rare:80 | ||||
| chr14:75176377-75176430 | Rare:13 | ||||
| chr14:75176435-75176657 | Rare:74 | ||||
| chr14:75279506-75279675 | Rare:34 |