| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73886758-73886905 | Common:2; Rare:52 | ||||
| chr14:73950035-73950333 | Common:6; Rare:125; Clinvar (benign):5 | ||||
| chr14:74019263-74019432 | Common:1; Rare:66 | ||||
| chr14:74084397-74084628 | Common:2; Rare:60 | ||||
| chr14:74302922-74303150 | Common:3; Rare:85; Clinvar (benign):1 | ||||
| chr14:74493371-74493777 | Common:4; Rare:123; Clinvar (benign):4 | ||||
| chr14:74713035-74713206 | Rare:97 | ||||
| chr14:74763087-74763425 | Rare:101 | ||||
| chr14:74881816-74881982 | Rare:75 | ||||
| chr14:74923196-74923494 | Common:5; Rare:71 | ||||
| chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
| chr14:75069443-75069680 | Common:2; Rare:62 | ||||
| chr14:75127001-75127110 | Rare:33 | ||||
| chr14:75278590-75278860 | Common:2; Rare:64 | ||||
| chr14:75660813-75660962 | Rare:38 |