| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67508627-67508778 | Common:3; Rare:54 | ||||
| chr11:68030423-68030744 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039078 | Rare:50; Clinvar:1 | ||||
| chr11:68271891-68272148 | Common:2; Rare:110 | ||||
| chr11:68460223-68460399 | Common:3; Rare:64 | ||||
| chr11:68460505-68460782 | Common:3; Rare:101 | ||||
| chr11:68903764-68903955 | Common:5; Rare:88; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69640945-69641294 | Common:1; Rare:80 | ||||
| chr11:69675303-69675519 | Rare:57 | ||||
| chr11:70203133-70203358 | Common:3; Rare:86 | ||||
| chr11:70398421-70398596 | Common:2; Rare:63 | ||||
| chr11:71448334-71448702 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787303-71787537 | Common:14; Rare:84 | ||||
| chr11:71928887-71929064 | Common:1; Rare:59 | ||||
| chr11:72041015-72041175 | Common:1; Rare:32 |