Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:74988641-74988963 | Rare:71 | ||||
chr11:75351646-75351945 | Common:3; Rare:88 | ||||
chr11:75399356-75399601 | Common:4; Rare:101 | ||||
chr11:75561727-75562002 | Rare:48 | ||||
chr11:75562071-75562367 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
chr11:75562733-75562875 | Common:1; Rare:28 | ||||
chr11:75768676-75768811 | Rare:57 | ||||
chr11:76380987-76381369 | Common:4; Rare:125 | ||||
chr11:76444570-76445108 | Common:1; Rare:135 | ||||
chr11:76783022-76783388 | Common:10; Rare:120 | ||||
chr11:76783980-76784193 | Common:4; Rare:53 | ||||
chr11:77349409-77349664 | Common:1; Rare:40 | ||||
chr11:77411790-77412083 | Common:1; Rare:74 | ||||
chr11:77473528-77473811 | Common:1; Rare:99 | ||||
chr11:77589524-77589959 | Common:6; Rare:172 |