Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6680891-6681150 | Rare:64 | ||||
chr1:6701770-6701976 | Rare:63 | ||||
chr1:7771146-7771375 | Common:4; Rare:98 | ||||
chr1:7783998-7784391 | Common:3; Rare:160 | ||||
chr1:7954176-7954358 | Rare:57 | ||||
chr1:7961449-7961923 | Common:6; Rare:155; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:8026176-8026531 | Common:3; Rare:158 | ||||
chr1:8423643-8423889 | Common:1; Rare:100 | ||||
chr1:8424080-8424164 | Common:1; Rare:24 | ||||
chr1:8424168-8424320 | Rare:37 | ||||
chr1:8424489-8424644 | Rare:36 | ||||
chr1:8703064-8703505 | Common:2; Rare:143 | ||||
chr1:8817153-8817346 | Rare:52 | ||||
chr1:8817614-8818041 | Common:4; Rare:137 | ||||
chr1:8878041-8878118 | Rare:28 |