Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8878578-8878880 | Rare:161 | ||||
chr1:9069685-9069991 | Common:3; Rare:47 | ||||
chr1:9943280-9943489 | Common:2; Rare:53 | ||||
chr1:10398817-10399117 | Common:2; Rare:118 | ||||
chr1:11099833-11099911 | Rare:33 | ||||
chr1:11189236-11189359 | Rare:29 | ||||
chr1:11262493-11262711 | Common:2; Rare:69 | ||||
chr1:11654709-11654914 | Common:4; Rare:58 | ||||
chr1:11736104-11736224 | Common:2; Rare:41 | ||||
chr1:11805905-11806255 | Common:2; Rare:97; Clinvar:1 | ||||
chr1:11980112-11980469 | Common:6; Rare:116; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12617673-12617882 | Common:5; Rare:18 | ||||
chr1:12618202-12618439 | Rare:51 | ||||
chr1:15526572-15526918 | Common:2; Rare:112 | ||||
chr1:16017324-16017736 | Common:2; Rare:91 |