| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20333251-20333440 | Common:1; Rare:36 | ||||
| chr14:20343014-20343769 | Common:41; Rare:932 | ||||
| chr14:20412860-20413398 | Common:9; Rare:136 | ||||
| chr14:20413371-20413633 | Common:10; Rare:169 | ||||
| chr14:20413780-20414080 | Rare:86 | ||||
| chr14:20454430-20454710 | Rare:125 | ||||
| chr14:20454639-20455631 | Common:21; Rare:657 | ||||
| chr14:20455962-20456810 | Common:11; Rare:465; Clinvar:1 | ||||
| chr14:20460882-20461318 | Common:2; Rare:167 | ||||
| chr14:20461333-20462056 | Common:12; Rare:438 | ||||
| chr14:20469273-20469552 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:20469997-20470397 | Common:3; Rare:76 | ||||
| chr14:20684032-20684235 | Common:10; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:20684340-20684650 | Common:7; Rare:129; Clinvar (benign):9 | ||||
| chr14:20989626-20990095 | Common:23; Rare:333 |