Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183549140-183549261 | Rare:23 | ||||
chr1:183563432-183563758 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):1 | ||||
chr1:183590283-183590625 | Common:3; Rare:90; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:183590801-183591065 | Common:3; Rare:50 | ||||
chr1:183635552-183636114 | Common:5; Rare:155 | ||||
chr1:183636336-183636479 | Rare:23 | ||||
chr1:183805004-183805282 | Rare:79 | ||||
chr1:184051681-184051774 | Common:2; Rare:38 | ||||
chr1:184386714-184387150 | Common:3; Rare:129 | ||||
chr1:184387249-184387368 | Rare:19 | ||||
chr1:184754779-184755111 | Common:1; Rare:76 | ||||
chr1:184974302-184974666 | Rare:101 | ||||
chr1:184974713-184974749 | Rare:1 | ||||
chr1:185156699-185157303 | Common:3; Rare:180 | ||||
chr1:185157372-185157540 | Common:1; Rare:52 |