| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:29927809-29928154 | Common:1; Rare:110 | ||||
| chr14:30559049-30559235 | Common:2; Rare:71 | ||||
| chr14:30577611-30577796 | Common:1; Rare:31 | ||||
| chr14:30622203-30622384 | Common:1; Rare:89 | ||||
| chr14:30874743-30874846 | Common:1; Rare:23 | ||||
| chr14:30964495-30964670 | Rare:33 | ||||
| chr14:31025322-31025524 | Rare:45 | ||||
| chr14:31025618-31025709 | Common:1; Rare:33 | ||||
| chr14:31207456-31207847 | Common:2; Rare:130 | ||||
| chr14:31208137-31208204 | Rare:14 | ||||
| chr14:31420511-31420768 | Common:3; Rare:80 | ||||
| chr14:31561322-31561486 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075977-32076330 | Common:2; Rare:91 | ||||
| chr14:32076563-32077349 | Common:4; Rare:196 | ||||
| chr14:32616829-32616990 | Common:1; Rare:19 |