| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5112845-5113171 | Common:1; Rare:119 | ||||
| chr20:5119953-5120174 | Common:1; Rare:66 | ||||
| chr20:5126517-5126863 | Common:3; Rare:99 | ||||
| chr20:5610904-5611202 | Common:2; Rare:108 | ||||
| chr20:5911160-5911642 | Common:5; Rare:133 | ||||
| chr20:5950410-5950656 | Common:8; Rare:75 | ||||
| chr20:13784878-13785080 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr20:16573297-16573547 | Common:1; Rare:72 | ||||
| chr20:17569180-17569244 | Rare:14 | ||||
| chr20:17569949-17570222 | Common:3; Rare:119 | ||||
| chr20:17968442-17968613 | Common:4; Rare:78 | ||||
| chr20:17968783-17969127 | Common:3; Rare:121 | ||||
| chr20:18467136-18467439 | Common:1; Rare:64 | ||||
| chr20:20017215-20017399 | Rare:65 | ||||
| chr20:21303204-21303464 | Rare:89 |