Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:55215354-55215407 | Rare:26 | ||||
chr1:58784058-58784373 | Common:1; Rare:81 | ||||
chr1:59296512-59297114 | Common:14; Rare:169 | ||||
chr1:61724918-61725228 | Common:1; Rare:134 | ||||
chr1:61742357-61742552 | Rare:58 | ||||
chr1:62436256-62436364 | Common:2; Rare:36 | ||||
chr1:62436962-62437165 | Common:1; Rare:58 | ||||
chr1:62688260-62688535 | Common:1; Rare:105; Clinvar:1 | ||||
chr1:62784069-62784185 | Rare:48 | ||||
chr1:63523204-63523576 | Common:3; Rare:96 | ||||
chr1:63592887-63593198 | Rare:50 | ||||
chr1:63593214-63593447 | Rare:84; Clinvar (benign):1 | ||||
chr1:63593486-63593687 | Rare:96; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:66924824-66925023 | Rare:85 | ||||
chr1:66925196-66925514 | Common:2; Rare:99 |