| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50931229-50931373 | Common:2; Rare:45 | ||||
| chr20:50958472-50958897 | Common:1; Rare:164; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593775-53593937 | Common:1; Rare:61 | ||||
| chr20:53609771-53609827 | Rare:12 | ||||
| chr20:54173982-54174120 | Rare:45 | ||||
| chr20:56392086-56392704 | Common:6; Rare:165 | ||||
| chr20:56468536-56468719 | Rare:77 | ||||
| chr20:58388989-58389289 | Common:3; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651131-58651360 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58652345-58652619 | Common:2; Rare:89 | ||||
| chr20:58888781-58888999 | Common:1; Rare:67 | ||||
| chr20:58981098-58981328 | Common:2; Rare:109 | ||||
| chr20:59032217-59032625 | Common:5; Rare:182; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042698-59043057 | Common:1; Rare:130 | ||||
| chr20:59940214-59940481 | Rare:106 |