| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34112102-34112427 | Rare:107 | ||||
| chr20:34302966-34303127 | Rare:50 | ||||
| chr20:34303266-34303315 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr20:34303345-34303481 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:34516283-34516451 | Common:3; Rare:68 | ||||
| chr20:34677076-34677318 | Rare:63 | ||||
| chr20:34955733-34955868 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35092785-35092950 | Common:1; Rare:74 | ||||
| chr20:35279673-35279890 | Rare:51 | ||||
| chr20:35284545-35284882 | Common:2; Rare:90 | ||||
| chr20:35455051-35455215 | Common:1; Rare:59 | ||||
| chr20:35664880-35665029 | Common:1; Rare:37 | ||||
| chr20:35699181-35699264 | Rare:12 | ||||
| chr20:35699298-35699475 | Rare:61; Clinvar (benign):3 | ||||
| chr20:35742133-35742657 | Common:5; Rare:165 |