| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75051204-75051340 | Rare:23 | ||||
| chr14:75051349-75051596 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75063566-75063727 | Common:1; Rare:32 | ||||
| chr14:75063770-75063803 | Rare:5 | ||||
| chr14:75063849-75064224 | Common:1; Rare:96 | ||||
| chr14:75068892-75069148 | Common:2; Rare:38 | ||||
| chr14:75069152-75069424 | Common:3; Rare:87 | ||||
| chr14:75069431-75069774 | Common:2; Rare:91 | ||||
| chr14:75126578-75126653 | Rare:17 | ||||
| chr14:75126659-75126878 | Common:2; Rare:60 | ||||
| chr14:75126900-75127281 | Common:3; Rare:120 | ||||
| chr14:75127625-75127715 | Common:1; Rare:13 | ||||
| chr14:75147593-75148001 | Common:3; Rare:81 | ||||
| chr14:75176031-75176468 | Common:1; Rare:94 | ||||
| chr14:75176526-75177132 | Common:1; Rare:153 |