| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195400-24195732 | Common:2; Rare:73 | ||||
| chr14:24232256-24232714 | Common:8; Rare:116 | ||||
| chr14:24232763-24232934 | Common:1; Rare:39 | ||||
| chr14:24242276-24242420 | Rare:48; Clinvar (benign):1 | ||||
| chr14:24242562-24242741 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271453-24271630 | Common:1; Rare:51 | ||||
| chr14:24299738-24299890 | Common:4; Rare:48 | ||||
| chr14:24335062-24335190 | Common:1; Rare:28 | ||||
| chr14:24429855-24429949 | Rare:24 | ||||
| chr14:24442681-24443096 | Common:5; Rare:119 | ||||
| chr14:30559071-30559191 | Common:1; Rare:38 | ||||
| chr14:31420524-31420752 | Common:3; Rare:69 | ||||
| chr14:32076687-32077051 | Common:3; Rare:110 | ||||
| chr14:34462203-34462577 | Common:1; Rare:133 | ||||
| chr14:34629905-34630246 | Common:5; Rare:132 |