| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20461767-20462016 | Common:4; Rare:98 | ||||
| chr14:20684389-20684636 | Common:4; Rare:74; Clinvar (benign):5 | ||||
| chr14:20989653-20990078 | Common:14; Rare:204 | ||||
| chr14:21069870-21070501 | Common:6; Rare:213 | ||||
| chr14:21098590-21098960 | Rare:126 | ||||
| chr14:21103520-21103890 | Common:3; Rare:123 | ||||
| chr14:21104004-21104112 | Common:1; Rare:47 | ||||
| chr14:21269410-21269980 | Common:8; Rare:309 | ||||
| chr14:21383873-21384312 | Common:16; Rare:253 | ||||
| chr14:21437188-21437406 | Common:7; Rare:174 | ||||
| chr14:21455996-21456486 | Common:8; Rare:244 | ||||
| chr14:21476584-21476781 | Rare:157 | ||||
| chr14:21476855-21477278 | Common:4; Rare:275 | ||||
| chr14:21511210-21511565 | Rare:208 | ||||
| chr14:22589028-22589485 | Common:8; Rare:249 |