| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:30621951-30622035 | Rare:12 | ||||
| chr14:30622108-30622608 | Common:2; Rare:168 | ||||
| chr14:30622714-30622763 | Rare:7 | ||||
| chr14:30874500-30874570 | Rare:19 | ||||
| chr14:31025581-31025784 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr14:31025817-31025932 | Rare:34 | ||||
| chr14:31025946-31026730 | Common:7; Rare:226 | ||||
| chr14:31026821-31027101 | Common:3; Rare:59 | ||||
| chr14:31205734-31205903 | Rare:37 | ||||
| chr14:31205945-31206262 | Rare:61 | ||||
| chr14:31206785-31207161 | Common:2; Rare:93 | ||||
| chr14:31207174-31208011 | Common:2; Rare:256 | ||||
| chr14:31208029-31208471 | Common:2; Rare:105 | ||||
| chr14:31419584-31419910 | Common:1; Rare:66 | ||||
| chr14:31419916-31420213 | Common:2; Rare:71 |