| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:57268821-57269115 | Common:2; Rare:90 | ||||
| chr14:57390402-57390594 | Common:1; Rare:47 | ||||
| chr14:58244685-58244940 | Rare:81 | ||||
| chr14:58298078-58298442 | Rare:96 | ||||
| chr14:58427498-58427747 | Rare:81 | ||||
| chr14:59188448-59188741 | Common:1; Rare:71 | ||||
| chr14:59484021-59484182 | Common:1; Rare:74 | ||||
| chr14:59484321-59484565 | Common:3; Rare:98 | ||||
| chr14:60091824-60092227 | Common:5; Rare:143 | ||||
| chr14:60248981-60249251 | Common:3; Rare:102 | ||||
| chr14:60724312-60724483 | Common:1; Rare:38 | ||||
| chr14:60981011-60981260 | Rare:100 | ||||
| chr14:61695299-61695601 | Common:2; Rare:88 | ||||
| chr14:63543305-63543609 | Common:3; Rare:81 | ||||
| chr14:63852913-63852993 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 |