| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50794854-50795075 | Common:1; Rare:82 | ||||
| chr20:50958519-50958840 | Common:1; Rare:95; Clinvar (benign):1 | ||||
| chr20:51562816-51563052 | Common:2; Rare:39 | ||||
| chr20:53593787-53593894 | Common:1; Rare:39 | ||||
| chr20:56392187-56392697 | Common:6; Rare:135 | ||||
| chr20:58515317-58515528 | Common:3; Rare:43 | ||||
| chr20:58651138-58651305 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:59042726-59043128 | Common:2; Rare:145 | ||||
| chr20:59835734-59836066 | Common:1; Rare:68 | ||||
| chr20:59940230-59940435 | Rare:83 | ||||
| chr20:62143291-62143725 | Common:6; Rare:178 | ||||
| chr20:62386948-62387331 | Common:3; Rare:143 | ||||
| chr20:62937883-62938185 | Common:2; Rare:110 | ||||
| chr20:63521094-63521219 | Common:5; Rare:26 | ||||
| chr20:63707875-63708085 | Rare:61 |