| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75280474-75280663 | Common:1; Rare:49 | ||||
| chr14:75427913-75428250 | Common:1; Rare:81 | ||||
| chr14:75578824-75578969 | Common:3; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:75660789-75661361 | Common:5; Rare:143 | ||||
| chr14:75982986-75983066 | Rare:18 | ||||
| chr14:75985717-75985802 | Rare:41; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:77028684-77028708 | Rare:5 | ||||
| chr14:77098174-77098389 | Rare:67 | ||||
| chr14:77320731-77321064 | Common:4; Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
| chr14:77377045-77377441 | Common:2; Rare:125 | ||||
| chr14:77457536-77457877 | Common:1; Rare:103 | ||||
| chr14:77707991-77708131 | Common:1; Rare:71 | ||||
| chr14:77736971-77737300 | Common:2; Rare:56 | ||||
| chr14:77761114-77761196 | Rare:39 | ||||
| chr14:79279244-79279390 | Common:3; Rare:29 |