Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824402-173824694 | Rare:53 | ||||
chr1:174999679-175000119 | Common:1; Rare:129 | ||||
chr1:178725123-178725291 | Common:9; Rare:69 | ||||
chr1:180502538-180502940 | Common:1; Rare:158 | ||||
chr1:182839041-182839371 | Common:1; Rare:106 | ||||
chr1:183186002-183186366 | Common:6; Rare:94; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:183472261-183472515 | Common:2; Rare:91 | ||||
chr1:184051676-184051753 | Common:2; Rare:27 | ||||
chr1:185156941-185157198 | Rare:67 | ||||
chr1:186375194-186375430 | Rare:55 | ||||
chr1:186375685-186375892 | Common:1; Rare:55 | ||||
chr1:186680421-186680688 | Common:2; Rare:57 | ||||
chr1:193059306-193059665 | Rare:167 | ||||
chr1:201399302-201399633 | Common:1; Rare:130 | ||||
chr1:203007282-203007401 | Rare:41 |