| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37527827-37528196 | Common:5; Rare:133 | ||||
| chr20:38033416-38033757 | Common:2; Rare:99 | ||||
| chr20:38962148-38962374 | Common:1; Rare:94 | ||||
| chr20:41618350-41618742 | Common:2; Rare:116 | ||||
| chr20:43590904-43591000 | Rare:26 | ||||
| chr20:44210685-44210990 | Common:4; Rare:114 | ||||
| chr20:44475817-44475888 | Rare:25 | ||||
| chr20:44522014-44522175 | Common:2; Rare:55 | ||||
| chr20:44531779-44531953 | Rare:60 | ||||
| chr20:44960354-44960535 | Common:1; Rare:68 | ||||
| chr20:44966396-44966549 | Rare:56 | ||||
| chr20:45415982-45416153 | Rare:44 | ||||
| chr20:45834076-45834145 | Rare:21 | ||||
| chr20:45857350-45857639 | Common:3; Rare:77 | ||||
| chr20:45891043-45891353 | Common:3; Rare:90; Clinvar:6; Clinvar (benign):3 |