| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710663-75710779 | Common:2; Rare:46 | ||||
| chr2:84459226-84459606 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85327916-85328081 | Common:2; Rare:74 | ||||
| chr2:85354496-85354786 | Common:1; Rare:97 | ||||
| chr2:85539057-85539168 | Common:1; Rare:43 | ||||
| chr2:85561431-85561571 | Rare:51; Clinvar:4 | ||||
| chr2:85577522-85577623 | Common:1; Rare:31 | ||||
| chr2:85595549-85595786 | Common:2; Rare:77 | ||||
| chr2:85602384-85602483 | Common:1; Rare:17 | ||||
| chr2:85602657-85602892 | Rare:59 | ||||
| chr2:85611974-85612113 | Rare:60 | ||||
| chr2:86105843-86106250 | Common:2; Rare:112 | ||||
| chr2:86195387-86195674 | Common:6; Rare:91 | ||||
| chr2:86441071-86441419 | Common:1; Rare:121 | ||||
| chr2:86623826-86623972 | Common:1; Rare:66 |