| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33774477-33774685 | Common:2; Rare:74 | ||||
| chr11:34051437-34051763 | Rare:113 | ||||
| chr11:34052119-34052630 | Common:4; Rare:225 | ||||
| chr11:34053309-34053519 | Rare:51 | ||||
| chr11:34105469-34105724 | Common:2; Rare:88 | ||||
| chr11:34357986-34358298 | Common:2; Rare:84 | ||||
| chr11:34438776-34439009 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr11:34916242-34916746 | Common:14; Rare:203; Clinvar:8; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr11:35138997-35139221 | Common:1; Rare:50 | ||||
| chr11:35943927-35944101 | Common:3; Rare:60 | ||||
| chr11:36289373-36289510 | Common:1; Rare:55 | ||||
| chr11:36510229-36510377 | Rare:45 | ||||
| chr11:43358874-43358988 | Rare:58 | ||||
| chr11:43644128-43644256 | Common:1; Rare:21 | ||||
| chr11:43680461-43680837 | Common:1; Rare:104 |