| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67482910-67483154 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030367-68030744 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271895-68272217 | Common:2; Rare:137 | ||||
| chr11:68903770-68903943 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:69640983-69641250 | Common:1; Rare:55 | ||||
| chr11:69675301-69675515 | Rare:58 | ||||
| chr11:70398342-70398596 | Common:2; Rare:86 | ||||
| chr11:71448338-71448713 | Common:4; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787303-71787539 | Common:14; Rare:86 | ||||
| chr11:71928915-71929082 | Common:1; Rare:53 | ||||
| chr11:72080449-72080858 | Common:2; Rare:91; Clinvar:7 | ||||
| chr11:72103195-72103518 | Rare:94 | ||||
| chr11:72434478-72434748 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr11:72752380-72752591 | Common:3; Rare:58 | ||||
| chr11:73598049-73598296 | Common:3; Rare:64 |