| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74472390-74472712 | Common:4; Rare:145 | ||||
| chr2:74482982-74483098 | Rare:42 | ||||
| chr2:74503307-74503438 | Rare:33 | ||||
| chr2:74529668-74529918 | Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74958874-74959060 | Rare:67 | ||||
| chr2:75710872-75711148 | Common:2; Rare:80 | ||||
| chr2:84459219-84459585 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85327916-85328054 | Common:1; Rare:63 | ||||
| chr2:85354501-85354798 | Common:1; Rare:100 | ||||
| chr2:85539057-85539182 | Common:2; Rare:50 | ||||
| chr2:85561432-85561571 | Rare:51; Clinvar:4 | ||||
| chr2:85595464-85595798 | Common:3; Rare:110 | ||||
| chr2:85602657-85602904 | Rare:61 | ||||
| chr2:85612024-85612103 | Rare:23 | ||||
| chr2:86105843-86106266 | Common:3; Rare:123 |