Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:159789545-159789966 | Common:4; Rare:141 | ||||
chr6:159790244-159790514 | Common:7; Rare:86 | ||||
chr6:162727766-162727985 | Rare:57; Clinvar:1 | ||||
chr6:166342508-166342665 | Common:3; Rare:61 | ||||
chr6:166627961-166628032 | Rare:12 | ||||
chr6:166999095-166999405 | Common:1; Rare:106 | ||||
chr6:169702043-169702317 | Common:5; Rare:116 | ||||
chr6:169751526-169751644 | Rare:41; Clinvar (benign):1 | ||||
chr6:170554211-170554411 | Common:1; Rare:64 | ||||
chr7:727233-727308 | Rare:26; Clinvar:1 | ||||
chr7:975498-975671 | Common:1; Rare:77 | ||||
chr7:1570007-1570142 | Common:1; Rare:43 | ||||
chr7:2242168-2242261 | Common:2; Rare:56 | ||||
chr7:2354041-2354123 | Rare:39 | ||||
chr7:2403293-2403637 | Common:1; Rare:135 |