Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11012554-11012742 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11055845-11056089 | Rare:71 | ||||
chr1:11099794-11099922 | Common:1; Rare:55 | ||||
chr1:11189311-11189375 | Rare:12 | ||||
chr1:11262493-11262836 | Common:2; Rare:101 | ||||
chr1:11654396-11654501 | Rare:29 | ||||
chr1:11654710-11654938 | Common:4; Rare:60 | ||||
chr1:11805900-11806265 | Common:2; Rare:100; Clinvar:1 | ||||
chr1:11934551-11934754 | Common:3; Rare:66; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980104-11980478 | Common:6; Rare:121; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12616634-12616793 | Common:1; Rare:31 | ||||
chr1:12617202-12617612 | Rare:99 | ||||
chr1:12617658-12618012 | Common:5; Rare:38 | ||||
chr1:12618034-12618482 | Common:4; Rare:99 | ||||
chr1:15152685-15152815 | Common:6; Rare:27 |