| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67359739-67360011 | Common:1; Rare:86 | ||||
| chr14:67360265-67360371 | Common:1; Rare:33 | ||||
| chr14:68978236-68978402 | Common:2; Rare:49 | ||||
| chr14:69398324-69398386 | Rare:18 | ||||
| chr14:69398576-69398723 | Rare:36 | ||||
| chr14:69611478-69611781 | Common:1; Rare:103 | ||||
| chr14:70417025-70417146 | Rare:31 | ||||
| chr14:71320830-71321136 | Common:3; Rare:96 | ||||
| chr14:73886751-73886889 | Common:2; Rare:47 | ||||
| chr14:73950113-73950330 | Common:5; Rare:85; Clinvar (benign):3 | ||||
| chr14:74019263-74019427 | Common:1; Rare:64 | ||||
| chr14:74493252-74493770 | Common:4; Rare:166; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713078-74713192 | Rare:56 | ||||
| chr14:75069399-75069680 | Common:2; Rare:72 | ||||
| chr14:75660867-75661319 | Common:4; Rare:103 |