Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212608448-212608761 | Common:1; Rare:80 | ||||
chr1:212791721-212791926 | Common:5; Rare:91 | ||||
chr1:212858081-212858273 | Common:3; Rare:49; Clinvar:1 | ||||
chr1:213015761-213015899 | Rare:37 | ||||
chr1:213051218-213051345 | Rare:43 | ||||
chr1:214280977-214281266 | Common:2; Rare:123 | ||||
chr1:214551554-214551922 | Common:2; Rare:118 | ||||
chr1:214602903-214603333 | Common:4; Rare:121 | ||||
chr1:217631020-217631385 | Common:3; Rare:104 | ||||
chr1:218285133-218285382 | Common:5; Rare:106 | ||||
chr1:218345774-218346098 | Common:5; Rare:101; Clinvar:9; Clinvar (benign):4 | ||||
chr1:218346145-218346192 | Rare:8 | ||||
chr1:218346338-218346393 | Rare:9; Clinvar (benign):1 | ||||
chr1:219173757-219173938 | Common:1; Rare:104 | ||||
chr1:220046398-220046742 | Common:1; Rare:108 |