| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33257115-33257442 | Common:3; Rare:108 | ||||
| chr11:33257585-33257727 | Rare:35 | ||||
| chr11:33774475-33774696 | Common:2; Rare:80 | ||||
| chr11:34051463-34051741 | Rare:101 | ||||
| chr11:34105481-34105673 | Common:2; Rare:62 | ||||
| chr11:34438773-34439034 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr11:34916282-34916709 | Common:10; Rare:175; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35619472-35619567 | Rare:28 | ||||
| chr11:35662567-35663092 | Common:3; Rare:163 | ||||
| chr11:35943984-35944131 | Common:1; Rare:46 | ||||
| chr11:36289369-36289539 | Common:2; Rare:62 | ||||
| chr11:36510229-36510350 | Rare:36 | ||||
| chr11:41459561-41459688 | Rare:21 | ||||
| chr11:41459755-41459879 | Rare:20 | ||||
| chr11:41459910-41460270 | Common:2; Rare:69 |