| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74458113-74458509 | Common:1; Rare:122 | ||||
| chr2:74465367-74465439 | Rare:16 | ||||
| chr2:74482921-74483124 | Common:1; Rare:77 | ||||
| chr2:74507669-74507781 | Rare:24 | ||||
| chr2:74527484-74527743 | Common:1; Rare:89 | ||||
| chr2:74529668-74529848 | Rare:60; Clinvar:1 | ||||
| chr2:74555624-74555784 | Common:1; Rare:48 | ||||
| chr2:74958498-74958677 | Common:3; Rare:64 | ||||
| chr2:74958872-74959024 | Rare:58 | ||||
| chr2:75199513-75199654 | Rare:25 | ||||
| chr2:75710669-75710774 | Common:2; Rare:41 | ||||
| chr2:80304174-80304466 | Rare:68 | ||||
| chr2:84459231-84459587 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84905484-84905905 | Common:2; Rare:128 | ||||
| chr2:85327916-85328084 | Common:2; Rare:76 |