| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213393-24213539 | Rare:54 | ||||
| chr14:24213542-24213621 | Common:1; Rare:21 | ||||
| chr14:24215937-24216016 | Common:1; Rare:34 | ||||
| chr14:24232249-24232721 | Common:8; Rare:119 | ||||
| chr14:24232805-24232980 | Common:1; Rare:43 | ||||
| chr14:24242254-24242408 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242593-24242669 | Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24271439-24271747 | Common:2; Rare:91 | ||||
| chr14:24299712-24299917 | Common:5; Rare:69 | ||||
| chr14:24368079-24368439 | Common:1; Rare:78 | ||||
| chr14:24429526-24430106 | Common:6; Rare:129 | ||||
| chr14:24430422-24430583 | Rare:32 | ||||
| chr14:24435643-24435880 | Rare:39 | ||||
| chr14:24442641-24443046 | Common:6; Rare:125 | ||||
| chr14:25049997-25050344 | Common:3; Rare:104 |