Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:59296508-59297103 | Common:14; Rare:166 | ||||
chr1:61724952-61725228 | Common:1; Rare:119 | ||||
chr1:62688266-62688510 | Common:1; Rare:99 | ||||
chr1:63523165-63523592 | Common:3; Rare:113 | ||||
chr1:63593643-63593818 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
chr1:64841311-64841529 | Rare:49; Clinvar:1 | ||||
chr1:65147547-65147653 | Rare:30 | ||||
chr1:66924810-66925050 | Rare:98 | ||||
chr1:66925233-66925525 | Common:2; Rare:94 | ||||
chr1:67429991-67430129 | Rare:49 | ||||
chr1:68232476-68232633 | Rare:37 | ||||
chr1:70205542-70205751 | Rare:65 | ||||
chr1:70221303-70221537 | Rare:103 | ||||
chr1:70354687-70354848 | Rare:60 | ||||
chr1:70411059-70411291 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1 |