Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168225712-168226082 | Common:4; Rare:122 | ||||
chr1:169367767-169368279 | Common:4; Rare:96 | ||||
chr1:171485339-171485599 | Rare:94 | ||||
chr1:171781346-171781732 | Common:4; Rare:102 | ||||
chr1:173477141-173477492 | Common:4; Rare:128 | ||||
chr1:173824397-173824708 | Rare:56; Clinvar:1 | ||||
chr1:173867981-173868270 | Common:2; Rare:97 | ||||
chr1:174022306-174022547 | Rare:66 | ||||
chr1:174999838-175000156 | Common:3; Rare:112 | ||||
chr1:179081895-179082086 | Common:1; Rare:59 | ||||
chr1:179882162-179882297 | Common:1; Rare:25 | ||||
chr1:179882488-179882957 | Common:1; Rare:235; Clinvar:10; Clinvar (benign):4 | ||||
chr1:180154661-180154898 | Common:3; Rare:78 | ||||
chr1:182391295-182391480 | Rare:39 | ||||
chr1:182789622-182789891 | Common:2; Rare:92 |