| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293663-70293852 | Common:3; Rare:62 | ||||
| chr2:71068538-71068654 | Rare:53 | ||||
| chr2:71130220-71130321 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276450-71276616 | Rare:55 | ||||
| chr2:71466551-71466707 | Common:3; Rare:41 | ||||
| chr2:73233200-73233468 | Common:1; Rare:72 | ||||
| chr2:73385694-73386023 | Common:4; Rare:155; Clinvar:16; Clinvar (benign):8 | ||||
| chr2:74441886-74442048 | Common:2; Rare:28 | ||||
| chr2:74454885-74455128 | Rare:70 | ||||
| chr2:74465383-74465455 | Common:1; Rare:15 | ||||
| chr2:74483015-74483098 | Rare:33 | ||||
| chr2:74529665-74529838 | Rare:61; Clinvar:1 | ||||
| chr2:85327945-85328066 | Common:1; Rare:57 | ||||
| chr2:85354526-85354790 | Common:1; Rare:85 | ||||
| chr2:85561432-85561623 | Common:1; Rare:65; Clinvar:4 |