Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61742893-61742985 | Rare:26 | ||||
chr1:61951782-61951829 | Rare:9 | ||||
chr1:62436140-62436451 | Common:3; Rare:98 | ||||
chr1:62436555-62436900 | Rare:75 | ||||
chr1:62436978-62437287 | Common:2; Rare:86 | ||||
chr1:62687746-62688003 | Rare:75 | ||||
chr1:62688086-62688621 | Common:2; Rare:187; Clinvar:1 | ||||
chr1:62688799-62688819 | Rare:3 | ||||
chr1:62783671-62783906 | Rare:49 | ||||
chr1:62784032-62784272 | Rare:79 | ||||
chr1:63322387-63322826 | Common:2; Rare:131 | ||||
chr1:63323511-63323850 | Rare:85 | ||||
chr1:63367395-63367751 | Rare:111; Clinvar (benign):1 | ||||
chr1:63368045-63368121 | Rare:16 | ||||
chr1:63523131-63523676 | Common:4; Rare:150 |