Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805686-11806363 | Common:12; Rare:472; Clinvar:6 | ||||
chr1:11926371-11926705 | Common:18; Rare:206 | ||||
chr1:11934459-11934969 | Common:15; Rare:334; Clinvar:19; Clinvar (benign):4 | ||||
chr1:11980033-11980374 | Common:6; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
chr1:11980371-11980512 | Common:4; Rare:80; Clinvar (benign):8 | ||||
chr1:12019176-12019617 | Common:15; Rare:386 | ||||
chr1:12229767-12230119 | Common:4; Rare:163 | ||||
chr1:12595957-12596131 | Rare:29 | ||||
chr1:12618070-12618780 | Common:8; Rare:231 | ||||
chr1:13700106-13700318 | Rare:137 | ||||
chr1:13700540-13700940 | Rare:169 | ||||
chr1:13749106-13749506 | Common:6; Rare:360 | ||||
chr1:13749800-13750340 | Common:3; Rare:127 | ||||
chr1:14923977-14924236 | Common:4; Rare:155 | ||||
chr1:14924519-14924693 | Common:3; Rare:48 |