| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23094566-23094795 | Common:1; Rare:76 | ||||
| chr14:23094853-23094929 | Rare:24 | ||||
| chr14:23095035-23095622 | Common:3; Rare:243 | ||||
| chr14:23095684-23095889 | Common:4; Rare:51 | ||||
| chr14:23285930-23286684 | Common:3; Rare:177 | ||||
| chr14:23301176-23302086 | Common:4; Rare:270 | ||||
| chr14:23302339-23302570 | Common:1; Rare:68 | ||||
| chr14:23302739-23303022 | Rare:54 | ||||
| chr14:23306596-23306882 | Common:1; Rare:62 | ||||
| chr14:23320866-23320997 | Common:1; Rare:34 | ||||
| chr14:23321022-23321516 | Common:2; Rare:137; Clinvar (pathogenic):1 | ||||
| chr14:23321814-23321979 | Common:1; Rare:42 | ||||
| chr14:23322049-23322131 | Rare:27 | ||||
| chr14:23322283-23322367 | Rare:24 | ||||
| chr14:23469176-23469482 | Common:3; Rare:97 |