| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213431-24213602 | Common:1; Rare:56 | ||||
| chr14:24232312-24232728 | Common:8; Rare:97 | ||||
| chr14:24242272-24242409 | Rare:47; Clinvar (benign):1 | ||||
| chr14:24242562-24242774 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271461-24271636 | Common:1; Rare:50 | ||||
| chr14:24299726-24299854 | Common:4; Rare:37 | ||||
| chr14:24367878-24368196 | Common:2; Rare:55 | ||||
| chr14:24429852-24429970 | Rare:26 | ||||
| chr14:24442666-24443028 | Common:5; Rare:114 | ||||
| chr14:30559048-30559185 | Common:2; Rare:48 | ||||
| chr14:30622190-30622344 | Rare:55 | ||||
| chr14:31025538-31025673 | Common:1; Rare:32 | ||||
| chr14:31420524-31420756 | Common:3; Rare:69 | ||||
| chr14:31561089-31561456 | Common:4; Rare:99; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076636-32077043 | Common:3; Rare:119 |