| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58297641-58298041 | Common:5; Rare:331 | ||||
| chr14:58298043-58298604 | Rare:868 | ||||
| chr14:58298931-58299537 | Common:24; Rare:654 | ||||
| chr14:58299530-58299840 | Common:1; Rare:92 | ||||
| chr14:58299902-58300029 | Rare:22 | ||||
| chr14:58331163-58331344 | Common:2; Rare:48 | ||||
| chr14:58395706-58396130 | Rare:284 | ||||
| chr14:58426980-58427440 | Common:9; Rare:520 | ||||
| chr14:58427392-58428037 | Common:1; Rare:691 | ||||
| chr14:58428027-58428427 | Common:1; Rare:109; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr14:59187977-59188377 | Common:1; Rare:75 | ||||
| chr14:59188328-59188803 | Common:13; Rare:577 | ||||
| chr14:59483592-59484270 | Common:25; Rare:655 | ||||
| chr14:59484290-59484990 | Common:26; Rare:762 | ||||
| chr14:60091170-60091570 | Common:3; Rare:136 |