Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178869202-178869331 | Common:1; Rare:22 | ||||
chr1:178871037-178871258 | Rare:45 | ||||
chr1:179882067-179882313 | Common:1; Rare:57 | ||||
chr1:179882441-179882816 | Rare:168; Clinvar:7; Clinvar (benign):2 | ||||
chr1:181088494-181088704 | Rare:67 | ||||
chr1:182391325-182391444 | Rare:24 | ||||
chr1:182789659-182789778 | Common:2; Rare:38 | ||||
chr1:183023065-183023256 | Common:4; Rare:51 | ||||
chr1:183635660-183635971 | Common:2; Rare:93 | ||||
chr1:185156934-185157297 | Common:1; Rare:96 | ||||
chr1:185317197-185317555 | Common:2; Rare:106 | ||||
chr1:186375123-186375557 | Rare:111 | ||||
chr1:186375667-186375899 | Common:1; Rare:61 | ||||
chr1:186680403-186680670 | Common:3; Rare:60 | ||||
chr1:192575667-192575814 | Rare:41 |