Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824817-173824982 | Rare:40 | ||||
chr1:174999648-175000114 | Common:1; Rare:136 | ||||
chr1:178725105-178725320 | Common:10; Rare:81 | ||||
chr1:181088498-181088702 | Rare:66 | ||||
chr1:183186182-183186348 | Common:3; Rare:40; Clinvar:2; Clinvar (benign):3 | ||||
chr1:183472310-183472515 | Common:2; Rare:74 | ||||
chr1:183635670-183636079 | Common:3; Rare:115 | ||||
chr1:185156941-185157225 | Common:1; Rare:72 | ||||
chr1:185317231-185317449 | Common:1; Rare:66 | ||||
chr1:186375209-186375589 | Rare:87 | ||||
chr1:186375685-186375912 | Common:1; Rare:59 | ||||
chr1:192808813-192809061 | Common:4; Rare:101 | ||||
chr1:193059330-193059653 | Rare:147 | ||||
chr1:197146623-197146808 | Rare:45; Clinvar:2 | ||||
chr1:197902529-197902656 | Common:1; Rare:44 |