Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212791756-212791930 | Common:3; Rare:70 | ||||
chr1:212858057-212858308 | Common:5; Rare:68; Clinvar:2 | ||||
chr1:213000882-213001048 | Rare:39 | ||||
chr1:213015734-213015923 | Rare:55 | ||||
chr1:214551552-214551977 | Common:2; Rare:133 | ||||
chr1:215005094-215005423 | Common:2; Rare:55 | ||||
chr1:215567301-215567763 | Common:1; Rare:145 | ||||
chr1:217089608-217089950 | Common:1; Rare:76 | ||||
chr1:217630939-217631406 | Common:4; Rare:144 | ||||
chr1:218285268-218285449 | Common:2; Rare:78 | ||||
chr1:218345687-218346143 | Common:5; Rare:119; Clinvar:10; Clinvar (benign):4 | ||||
chr1:218346145-218346274 | Rare:21 | ||||
chr1:218346343-218346503 | Rare:32; Clinvar (benign):2 | ||||
chr1:219173734-219173975 | Common:2; Rare:134 | ||||
chr1:219174818-219175023 | Rare:32 |