Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183186019-183186370 | Common:6; Rare:91; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:183472263-183472538 | Common:2; Rare:94 | ||||
chr1:183590744-183591063 | Common:3; Rare:57 | ||||
chr1:183635579-183635626 | Rare:9 | ||||
chr1:183635666-183636054 | Common:2; Rare:107 | ||||
chr1:184051617-184051758 | Common:3; Rare:51 | ||||
chr1:185156699-185156748 | Rare:28 | ||||
chr1:185156927-185157318 | Common:1; Rare:107 | ||||
chr1:185317149-185317262 | Rare:36 | ||||
chr1:185317264-185317406 | Common:1; Rare:36 | ||||
chr1:186374977-186375488 | Common:1; Rare:152 | ||||
chr1:186375656-186375920 | Common:1; Rare:69 | ||||
chr1:186680417-186680670 | Common:2; Rare:55 | ||||
chr1:192808813-192809056 | Common:4; Rare:97 | ||||
chr1:193059298-193059762 | Common:1; Rare:220 |