| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70203161-70203343 | Common:2; Rare:69 | ||||
| chr11:70398421-70398596 | Common:2; Rare:63 | ||||
| chr11:71448352-71448673 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:72041007-72041220 | Common:1; Rare:39 | ||||
| chr11:72080231-72080335 | Common:6; Rare:15 | ||||
| chr11:72080400-72080786 | Common:2; Rare:94; Clinvar:7 | ||||
| chr11:72103193-72103518 | Rare:94 | ||||
| chr11:72814054-72814440 | Common:4; Rare:115 | ||||
| chr11:73876756-73877036 | Common:5; Rare:81 | ||||
| chr11:74170838-74171377 | Common:3; Rare:170 | ||||
| chr11:74398378-74398558 | Common:3; Rare:40 | ||||
| chr11:74949055-74949294 | Common:6; Rare:64 | ||||
| chr11:75150932-75151120 | Common:1; Rare:33 | ||||
| chr11:75351610-75351878 | Common:3; Rare:80 | ||||
| chr11:75525885-75526021 | Common:2; Rare:39 |