| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74465354-74465432 | Rare:22 | ||||
| chr2:74482908-74483098 | Common:1; Rare:61 | ||||
| chr2:74503307-74503445 | Rare:35 | ||||
| chr2:74507351-74507541 | Rare:57 | ||||
| chr2:74529649-74529948 | Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74554646-74554761 | Common:1; Rare:49 | ||||
| chr2:74835141-74835300 | Rare:44 | ||||
| chr2:74958572-74958673 | Common:1; Rare:37 | ||||
| chr2:75710675-75711028 | Common:2; Rare:147 | ||||
| chr2:84459228-84459585 | Common:3; Rare:90; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84905484-84905953 | Common:2; Rare:142 | ||||
| chr2:85354517-85354786 | Common:1; Rare:88 | ||||
| chr2:85539019-85539168 | Common:1; Rare:60 | ||||
| chr2:85561432-85561556 | Rare:47; Clinvar:4 | ||||
| chr2:85584312-85584478 | Common:2; Rare:47 |