Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16352424-16352702 | Common:4; Rare:124 | ||||
chr1:16978529-16978921 | Common:1; Rare:78 | ||||
chr1:17439662-17439901 | Rare:80 | ||||
chr1:19210243-19210395 | Rare:56 | ||||
chr1:19251510-19251848 | Common:6; Rare:110 | ||||
chr1:19312067-19312350 | Common:7; Rare:137 | ||||
chr1:19485439-19485780 | Common:1; Rare:126 | ||||
chr1:20661352-20661730 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21345463-21345640 | Common:2; Rare:70 | ||||
chr1:23019259-23019570 | Rare:102 | ||||
chr1:23344219-23344378 | Common:2; Rare:73 | ||||
chr1:23778316-23778431 | Common:6; Rare:69 | ||||
chr1:23825375-23825539 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:24415633-24415827 | Common:1; Rare:55 | ||||
chr1:24745359-24745611 | Common:2; Rare:86 |