Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178725129-178725316 | Common:10; Rare:72 | ||||
chr1:179081931-179082102 | Common:1; Rare:52 | ||||
chr1:179143016-179143255 | Rare:51 | ||||
chr1:179293674-179293922 | Common:3; Rare:73 | ||||
chr1:179877747-179877896 | Rare:34 | ||||
chr1:179882008-179882860 | Common:4; Rare:288; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954675-179954814 | Common:1; Rare:33 | ||||
chr1:180502281-180502658 | Common:1; Rare:133 | ||||
chr1:183185961-183186335 | Common:5; Rare:83; Clinvar:4; Clinvar (benign):4 | ||||
chr1:183635601-183636114 | Common:5; Rare:139 | ||||
chr1:183805011-183805240 | Rare:61 | ||||
chr1:184754805-184755177 | Common:1; Rare:93 | ||||
chr1:185156895-185157164 | Common:1; Rare:66 | ||||
chr1:185317178-185317452 | Common:1; Rare:80 | ||||
chr1:186375079-186375510 | Rare:122 |