| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68157477-68157949 | Common:2; Rare:244 | ||||
| chr2:68467269-68467675 | Common:1; Rare:108 | ||||
| chr2:69387172-69387384 | Rare:54; Clinvar:2 | ||||
| chr2:69643616-69643829 | Rare:76 | ||||
| chr2:69829508-69829741 | Common:1; Rare:95 | ||||
| chr2:70086931-70087116 | Common:1; Rare:93 | ||||
| chr2:70087307-70088012 | Common:2; Rare:239 | ||||
| chr2:70258007-70258167 | Common:1; Rare:57 | ||||
| chr2:71068534-71068672 | Rare:64 | ||||
| chr2:71129771-71129891 | Rare:21 | ||||
| chr2:71130225-71130677 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73828785-73829037 | Common:1; Rare:58 | ||||
| chr2:73926801-73926926 | Common:1; Rare:80; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:74147836-74148052 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178756-74179053 | Common:3; Rare:79 |