Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:188043596-188043701 | Common:2; Rare:15 | ||||
chr1:188069456-188069465 | Rare:1 | ||||
chr1:188190908-188191062 | Common:2; Rare:30 | ||||
chr1:190530885-190531114 | Common:1; Rare:52 | ||||
chr1:192716485-192716674 | Common:1; Rare:29 | ||||
chr1:192812191-192812420 | Common:1; Rare:36 | ||||
chr1:193021161-193021221 | Rare:9 | ||||
chr1:193042913-193043144 | Common:2; Rare:25 | ||||
chr1:193058367-193058678 | Common:1; Rare:54 | ||||
chr1:193324798-193325030 | Common:2; Rare:35 | ||||
chr1:194978474-194978654 | Common:1; Rare:33 | ||||
chr1:195919149-195919294 | Common:4; Rare:33 | ||||
chr1:197086801-197087085 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:197089008-197089144 | Rare:27 | ||||
chr1:197122035-197122251 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 |