| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68030367-68030744 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68213584-68213819 | Rare:135 | ||||
| chr11:68271895-68272134 | Common:2; Rare:100 | ||||
| chr11:68460592-68460793 | Common:3; Rare:73 | ||||
| chr11:68903788-68903931 | Common:4; Rare:66; Clinvar (benign):6 | ||||
| chr11:69048735-69048949 | Common:5; Rare:74 | ||||
| chr11:69640972-69641185 | Rare:44 | ||||
| chr11:69675309-69675478 | Rare:47 | ||||
| chr11:70398355-70398596 | Common:2; Rare:84 | ||||
| chr11:71448328-71448690 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928940-71929076 | Common:1; Rare:47 | ||||
| chr11:72041097-72041190 | Common:1; Rare:17 | ||||
| chr11:72041936-72042059 | Rare:28 | ||||
| chr11:72080449-72080872 | Common:2; Rare:96; Clinvar:8 | ||||
| chr11:72103219-72103518 | Rare:88 |