| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69048703-69048944 | Common:5; Rare:83 | ||||
| chr11:69640972-69641242 | Common:1; Rare:55 | ||||
| chr11:69675297-69675503 | Rare:57 | ||||
| chr11:70398407-70398596 | Common:2; Rare:69 | ||||
| chr11:71448352-71448673 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71928940-71929058 | Common:1; Rare:42 | ||||
| chr11:72041098-72041295 | Common:1; Rare:36 | ||||
| chr11:72080471-72080809 | Common:1; Rare:75; Clinvar:5 | ||||
| chr11:73598033-73598255 | Common:3; Rare:55 | ||||
| chr11:73876794-73877019 | Common:4; Rare:58 | ||||
| chr11:74170958-74171370 | Common:3; Rare:134 | ||||
| chr11:74949089-74949294 | Common:6; Rare:51 | ||||
| chr11:75562063-75562303 | Common:1; Rare:61; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:76381101-76381348 | Common:3; Rare:75 | ||||
| chr11:76444654-76444923 | Rare:60 |