Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824390-173824702 | Rare:57; Clinvar:1 | ||||
chr1:173867962-173868396 | Common:2; Rare:151 | ||||
chr1:174159336-174159590 | Common:2; Rare:96 | ||||
chr1:174999679-175000183 | Common:3; Rare:168 | ||||
chr1:178725131-178725316 | Common:10; Rare:71 | ||||
chr1:178870977-178871114 | Rare:25 | ||||
chr1:179882195-179882318 | Rare:23 | ||||
chr1:179882352-179882841 | Rare:199; Clinvar:7; Clinvar (benign):2 | ||||
chr1:180502493-180502683 | Common:1; Rare:74 | ||||
chr1:182391821-182392144 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
chr1:182789664-182789778 | Common:2; Rare:36 | ||||
chr1:182839298-182839391 | Rare:45 | ||||
chr1:183635655-183636040 | Common:2; Rare:106 | ||||
chr1:183805013-183805243 | Rare:61 | ||||
chr1:185156900-185157297 | Common:2; Rare:109 |