| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401774-67402075 | Common:3; Rare:113 | ||||
| chr11:67428341-67428543 | Rare:73 | ||||
| chr11:67443435-67443626 | Common:1; Rare:73 | ||||
| chr11:67482913-67483154 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67508115-67508454 | Common:1; Rare:73 | ||||
| chr11:67508615-67508774 | Common:3; Rare:55 | ||||
| chr11:68030393-68030744 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271891-68272139 | Common:2; Rare:105 | ||||
| chr11:68460223-68460312 | Common:2; Rare:48 | ||||
| chr11:68903773-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
| chr11:69048701-69048953 | Common:5; Rare:86 | ||||
| chr11:69640945-69641255 | Common:1; Rare:63 | ||||
| chr11:69675289-69675519 | Rare:64 | ||||
| chr11:70398369-70398596 | Common:2; Rare:80 | ||||
| chr11:71448334-71448677 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 |