| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61538496-61539048 | Common:3; Rare:328 | ||||
| chr2:61853975-61854109 | Common:4; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61854446-61854785 | Rare:165 | ||||
| chr2:61888352-61888971 | Common:6; Rare:555 | ||||
| chr2:61905480-61905767 | Rare:101 | ||||
| chr2:62195896-62196230 | Common:8; Rare:286 | ||||
| chr2:62196432-62196644 | Rare:43 | ||||
| chr2:62215280-62215720 | Common:3; Rare:98 | ||||
| chr2:62505660-62506110 | Common:15; Rare:387 | ||||
| chr2:62506120-62506740 | Common:3; Rare:257 | ||||
| chr2:62705115-62705910 | Common:4; Rare:447 | ||||
| chr2:62705838-62706580 | Common:1; Rare:199 | ||||
| chr2:63050536-63050885 | Common:3; Rare:211 | ||||
| chr2:63588158-63589080 | Common:3; Rare:661; Clinvar:15; Clinvar (benign):1 | ||||
| chr2:63840732-63841154 | Common:5; Rare:312 |