| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10034876-10035097 | Common:5; Rare:84 | ||||
| chr20:10218716-10218939 | Rare:48 | ||||
| chr20:11890620-11890904 | Common:2; Rare:103 | ||||
| chr20:13784865-13785080 | Common:2; Rare:94; Clinvar (benign):3 | ||||
| chr20:13995265-13995617 | Rare:97 | ||||
| chr20:16573288-16573543 | Common:1; Rare:74 | ||||
| chr20:17226780-17227053 | Common:1; Rare:78 | ||||
| chr20:17569982-17570202 | Common:3; Rare:96 | ||||
| chr20:17968411-17968590 | Common:4; Rare:73 | ||||
| chr20:17968788-17969118 | Common:3; Rare:118 | ||||
| chr20:18288178-18288583 | Common:1; Rare:103 | ||||
| chr20:18466751-18466837 | Rare:19 | ||||
| chr20:18467007-18467448 | Common:1; Rare:98 | ||||
| chr20:18497165-18497308 | Common:1; Rare:54 | ||||
| chr20:18507816-18507961 | Common:1; Rare:44; Clinvar:4; Clinvar (benign):1 |