| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74421582-74421768 | Rare:65 | ||||
| chr2:74440528-74440694 | Rare:46 | ||||
| chr2:74441863-74442053 | Common:2; Rare:38 | ||||
| chr2:74465350-74465491 | Common:1; Rare:41; Clinvar:1 | ||||
| chr2:74482916-74483129 | Common:1; Rare:80 | ||||
| chr2:74507669-74507790 | Rare:25 | ||||
| chr2:74529668-74530009 | Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74654078-74654280 | Common:1; Rare:53 | ||||
| chr2:74833843-74834127 | Rare:85 | ||||
| chr2:74958877-74959031 | Rare:57 | ||||
| chr2:84459222-84459598 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905461-84905858 | Common:2; Rare:123 | ||||
| chr2:85327902-85328095 | Common:3; Rare:89 | ||||
| chr2:85354517-85354792 | Common:1; Rare:90 | ||||
| chr2:85539072-85539177 | Common:1; Rare:41 |