| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93333022-93333250 | Common:1; Rare:85 | ||||
| chr14:93955690-93955888 | Common:2; Rare:51 | ||||
| chr14:93956857-93957265 | Common:4; Rare:112 | ||||
| chr14:93976559-93976688 | Rare:29 | ||||
| chr14:93976703-93976908 | Rare:39 | ||||
| chr14:94081128-94081406 | Common:5; Rare:84 | ||||
| chr14:94129325-94129408 | Common:1; Rare:14 | ||||
| chr14:94129565-94129756 | Common:3; Rare:64 | ||||
| chr14:95157434-95157753 | Common:4; Rare:120 | ||||
| chr14:95534559-95534701 | Rare:58 | ||||
| chr14:95534781-95535019 | Common:3; Rare:64 | ||||
| chr14:95535368-95535389 | Rare:9; Clinvar (pathogenic):1 | ||||
| chr14:96363286-96363567 | Common:1; Rare:96 | ||||
| chr14:96391808-96392119 | Common:2; Rare:83 | ||||
| chr14:96502256-96502580 | Common:2; Rare:141 |