Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47848325-47848406 | Rare:40 | ||||
chr11:57530703-57531061 | Common:1; Rare:88 | ||||
chr11:57567612-57567767 | Rare:49 | ||||
chr11:57567829-57567887 | Rare:14 | ||||
chr11:57567920-57567975 | Rare:11 | ||||
chr11:57597595-57597712 | Rare:26; Clinvar:3; Clinvar (benign):1 | ||||
chr11:57712184-57712621 | Common:9; Rare:144 | ||||
chr11:57741290-57741596 | Common:1; Rare:116 | ||||
chr11:58578199-58578498 | Common:4; Rare:96 | ||||
chr11:59106905-59107243 | Common:2; Rare:112 | ||||
chr11:59142646-59142860 | Rare:34 | ||||
chr11:59142990-59143190 | Common:1; Rare:38 | ||||
chr11:59810734-59810869 | Common:3; Rare:40 | ||||
chr11:60906537-60906882 | Rare:81 | ||||
chr11:60914057-60914193 | Common:1; Rare:37 |