Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213015380-213015628 | Rare:66 | ||||
chr1:213015677-213015923 | Rare:80 | ||||
chr1:213051183-213051370 | Rare:65 | ||||
chr1:214280970-214281273 | Common:2; Rare:129 | ||||
chr1:214551554-214551939 | Common:2; Rare:123 | ||||
chr1:214602934-214603328 | Common:4; Rare:111 | ||||
chr1:217089606-217089918 | Common:1; Rare:70 | ||||
chr1:217630963-217631391 | Common:4; Rare:128 | ||||
chr1:218285178-218285479 | Common:4; Rare:119 | ||||
chr1:218345736-218346165 | Common:5; Rare:118; Clinvar:10; Clinvar (benign):4 | ||||
chr1:218346244-218346363 | Rare:14 | ||||
chr1:218346740-218346963 | Rare:58; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:218347354-218347528 | Common:2; Rare:29 | ||||
chr1:219173734-219173975 | Common:2; Rare:134 | ||||
chr1:219174119-219174285 | Rare:35 |