| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196799454-196799831 | Common:2; Rare:126 | ||||
| chr2:196926647-196926851 | Common:3; Rare:90 | ||||
| chr2:197310413-197310650 | Common:3; Rare:71 | ||||
| chr2:197310752-197310853 | Rare:18 | ||||
| chr2:197434564-197434625 | Rare:10 | ||||
| chr2:197434959-197435372 | Common:1; Rare:123 | ||||
| chr2:197452950-197453599 | Common:1; Rare:207 | ||||
| chr2:197453830-197454072 | Rare:65 | ||||
| chr2:197499302-197499325 | Rare:11 | ||||
| chr2:197499748-197500149 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:197500172-197500493 | Common:1; Rare:134 | ||||
| chr2:197515736-197516132 | Common:2; Rare:133 | ||||
| chr2:197516594-197516608 | Rare:2 | ||||
| chr2:197704999-197705583 | Common:3; Rare:248; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr2:197804407-197804593 | Rare:50 |