| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74391795-74392143 | Common:2; Rare:163 | ||||
| chr2:74421639-74421753 | Rare:38 | ||||
| chr2:74458113-74458509 | Common:1; Rare:122 | ||||
| chr2:74465323-74465587 | Common:2; Rare:65; Clinvar:1 | ||||
| chr2:74482887-74483106 | Common:1; Rare:73 | ||||
| chr2:74502482-74502670 | Rare:50 | ||||
| chr2:74505621-74505725 | Rare:30 | ||||
| chr2:74507639-74507823 | Rare:45 | ||||
| chr2:74529653-74530009 | Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74554656-74554755 | Common:1; Rare:41 | ||||
| chr2:74958488-74958697 | Common:3; Rare:76 | ||||
| chr2:74958872-74959071 | Rare:72 | ||||
| chr2:75518610-75519052 | Common:2; Rare:81 | ||||
| chr2:75710627-75710755 | Common:1; Rare:52 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |