Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183590402-183590725 | Common:4; Rare:62; Clinvar (benign):2 | ||||
chr1:183590766-183591065 | Common:3; Rare:56 | ||||
chr1:183635561-183635626 | Rare:15 | ||||
chr1:183635630-183636053 | Common:2; Rare:116 | ||||
chr1:184386740-184387158 | Common:3; Rare:124 | ||||
chr1:184974303-184974642 | Rare:97 | ||||
chr1:185156690-185156748 | Rare:31 | ||||
chr1:185156922-185157297 | Common:1; Rare:102 | ||||
chr1:185157439-185157540 | Common:1; Rare:35 | ||||
chr1:185316794-185317315 | Common:2; Rare:139 | ||||
chr1:185317321-185317439 | Rare:26 | ||||
chr1:186375104-186375441 | Rare:95 | ||||
chr1:186375660-186375928 | Common:1; Rare:72 | ||||
chr1:186680417-186680688 | Common:2; Rare:58 | ||||
chr1:192808889-192809119 | Common:3; Rare:108 |