Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:159789545-159789990 | Common:4; Rare:151 | ||||
chr6:162727736-162727954 | Rare:60; Clinvar:1 | ||||
chr6:166342508-166342665 | Common:3; Rare:61 | ||||
chr6:166999081-166999402 | Common:1; Rare:109 | ||||
chr6:169702021-169702138 | Common:1; Rare:46 | ||||
chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
chr6:170554221-170554409 | Common:1; Rare:63 | ||||
chr7:727236-727291 | Rare:18; Clinvar:1 | ||||
chr7:1570018-1570142 | Common:1; Rare:41 | ||||
chr7:1816560-1816822 | Common:2; Rare:67 | ||||
chr7:2242168-2242255 | Common:2; Rare:53 | ||||
chr7:2403304-2403622 | Common:1; Rare:124 | ||||
chr7:4775502-4775652 | Common:5; Rare:60; Clinvar:1 | ||||
chr7:5513772-5513886 | Common:1; Rare:48 | ||||
chr7:5592676-5592839 | Common:1; Rare:59 |