| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5950900-5950999 | Common:2; Rare:18 | ||||
| chr20:6005869-6006173 | Common:2; Rare:91 | ||||
| chr20:6006363-6006539 | Common:2; Rare:39 | ||||
| chr20:6123020-6123183 | Common:2; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:8019625-8019906 | Common:3; Rare:88 | ||||
| chr20:9068612-9068780 | Rare:37 | ||||
| chr20:10035039-10035104 | Common:1; Rare:25 | ||||
| chr20:10673552-10674138 | Common:4; Rare:165; Clinvar:8; Clinvar (benign):6 | ||||
| chr20:11890660-11890959 | Common:2; Rare:111 | ||||
| chr20:13638888-13639098 | Common:2; Rare:70 | ||||
| chr20:13784851-13785145 | Common:3; Rare:134; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13785335-13785390 | Rare:15 | ||||
| chr20:13995287-13995516 | Rare:54 | ||||
| chr20:16573277-16573590 | Common:2; Rare:93 | ||||
| chr20:17531290-17531343 | Rare:11 |