| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736380-33736541 | Common:2; Rare:52 | ||||
| chr11:33774484-33774625 | Common:2; Rare:50 | ||||
| chr11:34051555-34051762 | Rare:84 | ||||
| chr11:34052126-34052630 | Common:4; Rare:222 | ||||
| chr11:34105491-34105764 | Common:2; Rare:88 | ||||
| chr11:34438784-34439038 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr11:34620865-34621272 | Common:3; Rare:74 | ||||
| chr11:34624158-34624290 | Common:1; Rare:27 | ||||
| chr11:34915837-34915888 | Common:1; Rare:17 | ||||
| chr11:34916064-34916813 | Common:17; Rare:283; Clinvar:8; Clinvar (benign):18; Clinvar (pathogenic):1 | ||||
| chr11:35138810-35139360 | Common:2; Rare:144 | ||||
| chr11:35525590-35525821 | Rare:54 | ||||
| chr11:35943958-35944140 | Common:3; Rare:62 | ||||
| chr11:36289363-36289505 | Common:1; Rare:56 | ||||
| chr11:36510236-36510377 | Rare:40 |