| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736404-33736586 | Common:1; Rare:61 | ||||
| chr11:34438797-34439016 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr11:34916311-34916653 | Common:10; Rare:139; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138979-35139221 | Common:1; Rare:52 | ||||
| chr11:36510222-36510372 | Rare:45 | ||||
| chr11:43358883-43359006 | Rare:67 | ||||
| chr11:44066100-44066349 | Common:3; Rare:65 | ||||
| chr11:46617213-46617580 | Common:5; Rare:102 | ||||
| chr11:46700561-46700818 | Common:1; Rare:65 | ||||
| chr11:46846204-46846412 | Common:1; Rare:59 | ||||
| chr11:47183033-47183327 | Common:1; Rare:58 | ||||
| chr11:47185366-47185652 | Common:2; Rare:57 | ||||
| chr11:47186347-47186542 | Rare:56 | ||||
| chr11:47214832-47215003 | Common:1; Rare:42 | ||||
| chr11:47269972-47270184 | Common:1; Rare:71 |