Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6602850-6603107 | Common:4; Rare:98 | ||||
chr1:6603305-6603504 | Common:1; Rare:46 | ||||
chr1:7954209-7954293 | Rare:17 | ||||
chr1:7961455-7961758 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026163-8026459 | Common:2; Rare:134 | ||||
chr1:8318015-8318151 | Rare:44 | ||||
chr1:8422986-8423019 | Rare:5 | ||||
chr1:8423667-8423913 | Common:1; Rare:112 | ||||
chr1:8424064-8424220 | Common:2; Rare:41 | ||||
chr1:8525889-8526041 | Rare:32 | ||||
chr1:8878583-8878885 | Rare:161 | ||||
chr1:9942783-9942922 | Common:1; Rare:23 | ||||
chr1:9943279-9943492 | Common:2; Rare:54 | ||||
chr1:10033463-10033527 | Rare:8 | ||||
chr1:10398736-10399103 | Common:2; Rare:132 |