| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70641590-70642045 | Common:3; Rare:123 | ||||
| chr14:70809504-70809929 | Common:4; Rare:124 | ||||
| chr14:70907300-70907586 | Common:2; Rare:111 | ||||
| chr14:71320172-71320518 | Rare:108 | ||||
| chr14:71320797-71321146 | Common:3; Rare:105 | ||||
| chr14:72926166-72926538 | Common:6; Rare:97 | ||||
| chr14:73027019-73027351 | Common:2; Rare:89 | ||||
| chr14:73058288-73058684 | Common:3; Rare:119 | ||||
| chr14:73105800-73106285 | Common:2; Rare:125 | ||||
| chr14:73237212-73237562 | Common:1; Rare:68 | ||||
| chr14:73458492-73458870 | Common:5; Rare:102 | ||||
| chr14:73537094-73537369 | Rare:21 | ||||
| chr14:73591568-73591873 | Common:3; Rare:62 | ||||
| chr14:73644835-73645042 | Common:3; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73787125-73787376 | Common:2; Rare:87 |