Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:59296508-59297103 | Common:14; Rare:166 | ||||
chr1:61076954-61077308 | Common:3; Rare:86 | ||||
chr1:61077338-61077358 | Rare:6 | ||||
chr1:61403939-61404213 | Common:3; Rare:62 | ||||
chr1:61725050-61725195 | Rare:80 | ||||
chr1:61742369-61742505 | Rare:39 | ||||
chr1:62436248-62436364 | Common:2; Rare:37 | ||||
chr1:62436800-62437110 | Common:1; Rare:83 | ||||
chr1:62688256-62688553 | Common:1; Rare:113; Clinvar:1 | ||||
chr1:62784041-62784193 | Rare:62 | ||||
chr1:63367495-63367696 | Rare:63; Clinvar (benign):1 | ||||
chr1:63523152-63523602 | Common:3; Rare:123 | ||||
chr1:63593074-63593699 | Rare:229; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:66257362-66257440 | Rare:16 | ||||
chr1:66354288-66354427 | Rare:16 |