Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:182391330-182391479 | Rare:31 | ||||
chr1:182839194-182839367 | Common:1; Rare:72 | ||||
chr1:183635643-183636114 | Common:5; Rare:130 | ||||
chr1:184386905-184387119 | Rare:63 | ||||
chr1:185156923-185157159 | Rare:57 | ||||
chr1:186375209-186375473 | Rare:63 | ||||
chr1:186375685-186375928 | Common:1; Rare:65 | ||||
chr1:186680414-186680715 | Common:2; Rare:65 | ||||
chr1:193059275-193059659 | Rare:184 | ||||
chr1:193122102-193122196 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
chr1:193186578-193186626 | Rare:3 | ||||
chr1:201955288-201955535 | Common:1; Rare:70 | ||||
chr1:202010417-202010598 | Common:1; Rare:41 | ||||
chr1:202927170-202927493 | Common:6; Rare:126 | ||||
chr1:205813148-205813347 | Common:2; Rare:79 |