| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:9068467-9069521 | Common:7; Rare:507 | ||||
| chr20:10034742-10035196 | Common:12; Rare:266 | ||||
| chr20:10218638-10218949 | Rare:133 | ||||
| chr20:10433570-10434000 | Common:7; Rare:225 | ||||
| chr20:10434066-10434275 | Common:6; Rare:184; Clinvar (benign):3 | ||||
| chr20:10434415-10434922 | Common:7; Rare:282 | ||||
| chr20:10434993-10435479 | Rare:257 | ||||
| chr20:10435751-10435876 | Common:1; Rare:12 | ||||
| chr20:10673930-10674226 | Common:8; Rare:251; Clinvar:9; Clinvar (benign):9 | ||||
| chr20:10674330-10674543 | Rare:80 | ||||
| chr20:11890646-11890949 | Common:2; Rare:115 | ||||
| chr20:11890920-11891190 | Common:2; Rare:96 | ||||
| chr20:11891210-11891840 | Common:2; Rare:243 | ||||
| chr20:13009047-13009365 | Common:2; Rare:99 | ||||
| chr20:13221570-13221929 | Common:8; Rare:170 |