| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22766511-22766749 | Common:1; Rare:133 | ||||
| chr14:22836337-22836675 | Common:4; Rare:73 | ||||
| chr14:22982521-22982675 | Rare:51 | ||||
| chr14:23094551-23094690 | Common:2; Rare:44 | ||||
| chr14:23095090-23095592 | Common:3; Rare:223 | ||||
| chr14:23556226-23556361 | Common:1; Rare:24 | ||||
| chr14:23953644-23953868 | Common:8; Rare:89 | ||||
| chr14:23988837-23988935 | Common:4; Rare:39 | ||||
| chr14:24114986-24115292 | Common:2; Rare:86 | ||||
| chr14:24146573-24146875 | Common:1; Rare:96 | ||||
| chr14:24147228-24147510 | Common:2; Rare:73 | ||||
| chr14:24195414-24195806 | Common:2; Rare:98 | ||||
| chr14:24232317-24232687 | Common:8; Rare:87 | ||||
| chr14:24232847-24232949 | Rare:23 | ||||
| chr14:24242264-24242436 | Rare:55; Clinvar:1; Clinvar (benign):2 |