Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:222644146-222644386 | Common:1; Rare:71 | ||||
chr1:222712447-222712602 | Rare:56 | ||||
chr1:223143240-223143327 | Common:2; Rare:21 | ||||
chr1:223701354-223701597 | Common:2; Rare:33 | ||||
chr1:224183149-224183289 | Common:2; Rare:70 | ||||
chr1:224616189-224616317 | Common:1; Rare:39 | ||||
chr1:225427991-225428324 | Common:3; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
chr1:225777698-225777890 | Common:3; Rare:54 | ||||
chr1:225924236-225924536 | Common:8; Rare:88 | ||||
chr1:225999316-225999616 | Common:2; Rare:100 | ||||
chr1:226062024-226062094 | Common:1; Rare:22 | ||||
chr1:226309135-226309461 | Common:1; Rare:145 | ||||
chr1:226870520-226870635 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr1:227735237-227735471 | Common:3; Rare:136 | ||||
chr1:228103317-228103494 | Common:1; Rare:58 |