| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017171-61017770 | Common:5; Rare:181; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61018122-61018204 | Rare:29 | ||||
| chr2:61144907-61145176 | Common:3; Rare:87 | ||||
| chr2:61177279-61177472 | Common:3; Rare:83 | ||||
| chr2:61177922-61178162 | Common:1; Rare:71 | ||||
| chr2:61184561-61184800 | Rare:68 | ||||
| chr2:61185374-61185534 | Common:1; Rare:52 | ||||
| chr2:61190297-61190880 | Common:1; Rare:178 | ||||
| chr2:61191514-61191632 | Rare:25 | ||||
| chr2:61221718-61221806 | Rare:19 | ||||
| chr2:61223536-61223613 | Rare:18 | ||||
| chr2:61470651-61470991 | Rare:112 | ||||
| chr2:61471230-61471393 | Common:4; Rare:58 | ||||
| chr2:61536448-61536767 | Common:2; Rare:91 | ||||
| chr2:61537976-61538118 | Common:2; Rare:25 |