| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73569195-73569292 | Rare:32 | ||||
| chr14:73644891-73645031 | Common:2; Rare:41; Clinvar:2 | ||||
| chr14:73760288-73760475 | Common:2; Rare:36 | ||||
| chr14:73787175-73787387 | Common:2; Rare:77 | ||||
| chr14:73851750-73852028 | Common:6; Rare:90 | ||||
| chr14:73950066-73950328 | Common:6; Rare:108; Clinvar (benign):4 | ||||
| chr14:74019233-74019436 | Common:1; Rare:81 | ||||
| chr14:74084459-74085008 | Common:9; Rare:150 | ||||
| chr14:74302908-74303079 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr14:74493268-74493777 | Common:4; Rare:161; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713026-74713213 | Common:1; Rare:104 | ||||
| chr14:74763086-74763429 | Rare:101 | ||||
| chr14:74881769-74881964 | Common:1; Rare:85 | ||||
| chr14:74923208-74923463 | Common:3; Rare:65 | ||||
| chr14:74955594-74955752 | Common:1; Rare:35 |