| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69398595-69398731 | Rare:33 | ||||
| chr14:69611480-69611759 | Common:1; Rare:93 | ||||
| chr14:69767687-69767786 | Common:1; Rare:58 | ||||
| chr14:71320296-71320491 | Rare:62 | ||||
| chr14:72926221-72926535 | Common:3; Rare:74 | ||||
| chr14:73058330-73058622 | Common:3; Rare:92 | ||||
| chr14:73297232-73297434 | Common:2; Rare:44 | ||||
| chr14:73569053-73569292 | Rare:57 | ||||
| chr14:73592048-73592176 | Common:2; Rare:47 | ||||
| chr14:73644885-73645034 | Common:2; Rare:41; Clinvar:2 | ||||
| chr14:73787109-73787365 | Common:3; Rare:89 | ||||
| chr14:73790084-73790396 | Common:2; Rare:51 | ||||
| chr14:73950107-73950350 | Common:5; Rare:106; Clinvar (benign):3 | ||||
| chr14:74019248-74019467 | Common:1; Rare:82 | ||||
| chr14:74493240-74493781 | Common:4; Rare:172; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 |