| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20343161-20343661 | Common:13; Rare:293 | ||||
| chr14:20413409-20413517 | Common:2; Rare:29 | ||||
| chr14:20454793-20455564 | Common:7; Rare:194 | ||||
| chr14:20684438-20684595 | Common:2; Rare:25; Clinvar (benign):2 | ||||
| chr14:21024886-21025350 | Common:1; Rare:147 | ||||
| chr14:21025392-21025585 | Common:1; Rare:45 | ||||
| chr14:21025675-21026067 | Common:2; Rare:68 | ||||
| chr14:21383884-21384083 | Common:1; Rare:69 | ||||
| chr14:21437187-21437408 | Common:4; Rare:89 | ||||
| chr14:21456042-21456458 | Common:4; Rare:105 | ||||
| chr14:21476643-21476738 | Rare:44 | ||||
| chr14:21476825-21477275 | Common:2; Rare:146 | ||||
| chr14:21511238-21511553 | Rare:94 | ||||
| chr14:21526199-21526459 | Rare:53 | ||||
| chr14:22589138-22589479 | Common:4; Rare:111 |