| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958872-74959024 | Rare:58 | ||||
| chr2:75199513-75199629 | Rare:23 | ||||
| chr2:75710669-75710779 | Common:2; Rare:42 | ||||
| chr2:75710857-75711212 | Common:2; Rare:99 | ||||
| chr2:84459204-84459606 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84516277-84516503 | Common:1; Rare:59 | ||||
| chr2:84880984-84881293 | Common:2; Rare:85 | ||||
| chr2:84905537-84905953 | Common:1; Rare:121 | ||||
| chr2:84970663-84970966 | Common:2; Rare:100 | ||||
| chr2:84971201-84971454 | Rare:60 | ||||
| chr2:85327915-85328084 | Common:2; Rare:76 | ||||
| chr2:85354336-85354386 | Rare:21 | ||||
| chr2:85354407-85354826 | Common:2; Rare:140 | ||||
| chr2:85539024-85539353 | Common:3; Rare:165; Clinvar (benign):7 | ||||
| chr2:85561432-85561599 | Rare:61; Clinvar:4 |