| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75982477-75982635 | Common:1; Rare:30 | ||||
| chr14:75982755-75982926 | Common:1; Rare:34 | ||||
| chr14:75982973-75983011 | Rare:8 | ||||
| chr14:75985669-75985814 | Rare:63; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr14:76151716-76152055 | Common:1; Rare:109 | ||||
| chr14:76812775-76813056 | Common:2; Rare:108 | ||||
| chr14:77028391-77028528 | Common:2; Rare:37 | ||||
| chr14:77028579-77028956 | Rare:123 | ||||
| chr14:77097536-77098388 | Common:1; Rare:256 | ||||
| chr14:77320259-77320525 | Common:5; Rare:83; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr14:77320773-77321172 | Common:2; Rare:122; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77321221-77321537 | Common:7; Rare:156 | ||||
| chr14:77321717-77321926 | Common:4; Rare:45 | ||||
| chr14:77376143-77376568 | Common:1; Rare:80 | ||||
| chr14:77376575-77376854 | Common:1; Rare:58 |