| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71453469-71453686 | Common:1; Rare:44 | ||||
| chr2:73284287-73284516 | Common:1; Rare:58 | ||||
| chr2:73828905-73829028 | Rare:34 | ||||
| chr2:73926696-73926945 | Common:2; Rare:121; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74178807-74179091 | Common:4; Rare:93 | ||||
| chr2:74198440-74198620 | Rare:68 | ||||
| chr2:74503356-74503475 | Rare:27 | ||||
| chr2:74529680-74530007 | Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74555677-74555735 | Common:1; Rare:21 | ||||
| chr2:74833869-74834147 | Rare:81 | ||||
| chr2:74835182-74835324 | Rare:37 | ||||
| chr2:74958618-74959091 | Common:3; Rare:193 | ||||
| chr2:84459180-84459581 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905517-84905696 | Common:1; Rare:59 | ||||
| chr2:85327945-85328308 | Common:7; Rare:122 |