| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73714177-73714416 | Common:1; Rare:73 | ||||
| chr14:73740751-73741180 | Common:1; Rare:70 | ||||
| chr14:73759818-73759954 | Rare:15 | ||||
| chr14:73759971-73760637 | Common:4; Rare:127 | ||||
| chr14:73787129-73787389 | Common:2; Rare:91 | ||||
| chr14:73851515-73852095 | Common:9; Rare:146 | ||||
| chr14:73852251-73852923 | Common:7; Rare:131 | ||||
| chr14:73886392-73886427 | Rare:6 | ||||
| chr14:73886495-73886999 | Common:5; Rare:147 | ||||
| chr14:73887016-73887061 | Rare:13 | ||||
| chr14:73887324-73887376 | Rare:16 | ||||
| chr14:73949820-73949973 | Common:4; Rare:50 | ||||
| chr14:73950017-73950133 | Common:2; Rare:42; Clinvar (benign):3 | ||||
| chr14:73950141-73950459 | Common:3; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:73950476-73950699 | Common:1; Rare:54; Clinvar (benign):1 |