Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:314790-315083 | Common:3; Rare:84 | ||||
chr11:320633-321021 | Common:11; Rare:137; Clinvar:1 | ||||
chr11:506722-507001 | Common:3; Rare:93 | ||||
chr11:537267-537539 | Common:5; Rare:80 | ||||
chr11:560710-561016 | Common:5; Rare:142 | ||||
chr11:576418-576531 | Rare:45 | ||||
chr11:615946-616093 | Common:1; Rare:45 | ||||
chr11:695724-695818 | Rare:31 | ||||
chr11:747292-747520 | Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777460-777623 | Common:1; Rare:71 | ||||
chr11:809516-809603 | Rare:24 | ||||
chr11:809799-810038 | Common:2; Rare:110 | ||||
chr11:832872-833018 | Common:7; Rare:53 | ||||
chr11:842465-842895 | Common:7; Rare:179 | ||||
chr11:843965-844153 | Common:1; Rare:46 |