Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169485688-169486206 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794868-169795094 | Common:3; Rare:58 | ||||
chr1:170532057-170532192 | Rare:65; Clinvar:1 | ||||
chr1:170663024-170663174 | Rare:36 | ||||
chr1:171485219-171485598 | Rare:112 | ||||
chr1:171781371-171781745 | Common:4; Rare:99 | ||||
chr1:173477163-173477492 | Common:3; Rare:117 | ||||
chr1:173714861-173715026 | Common:1; Rare:38 | ||||
chr1:173824390-173824714 | Rare:59; Clinvar:2 | ||||
chr1:173824827-173824962 | Rare:35 | ||||
chr1:173867981-173868169 | Common:1; Rare:69 | ||||
chr1:173868291-173868398 | Rare:30 | ||||
chr1:174022370-174022501 | Rare:35 | ||||
chr1:174999644-175000152 | Common:3; Rare:163 | ||||
chr1:178871003-178871295 | Rare:55 |