| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69398230-69398403 | Rare:72 | ||||
| chr14:69398576-69398747 | Rare:41 | ||||
| chr14:69611462-69611778 | Common:1; Rare:105 | ||||
| chr14:70417005-70417140 | Rare:35 | ||||
| chr14:71320164-71320491 | Rare:103 | ||||
| chr14:72894077-72894260 | Common:4; Rare:63 | ||||
| chr14:73058314-73058603 | Common:3; Rare:90 | ||||
| chr14:73569240-73569292 | Rare:19 | ||||
| chr14:73644891-73645034 | Common:2; Rare:41; Clinvar:2 | ||||
| chr14:73787125-73787379 | Common:2; Rare:88 | ||||
| chr14:73851592-73852001 | Common:5; Rare:116 | ||||
| chr14:73950107-73950348 | Common:5; Rare:105; Clinvar (benign):3 | ||||
| chr14:74019254-74019436 | Common:1; Rare:72 | ||||
| chr14:74493261-74493833 | Common:4; Rare:191; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74612647-74612856 | Common:1; Rare:58 |