Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155978129-155978288 | Common:1; Rare:36 | ||||
chr1:155978442-155978612 | Rare:43 | ||||
chr1:155979085-155979262 | Common:1; Rare:30 | ||||
chr1:156054614-156054871 | Common:3; Rare:71 | ||||
chr1:156135934-156136312 | Common:3; Rare:124; Clinvar:26; Clinvar (benign):16; Clinvar (pathogenic):10 | ||||
chr1:156193819-156194121 | Common:3; Rare:76 | ||||
chr1:156282799-156282950 | Common:2; Rare:42 | ||||
chr1:156338177-156338551 | Common:2; Rare:135 | ||||
chr1:156728392-156728511 | Common:1; Rare:25 | ||||
chr1:156751662-156751903 | Common:1; Rare:53 | ||||
chr1:156767393-156767588 | Rare:64 | ||||
chr1:157138342-157138468 | Common:2; Rare:34 | ||||
chr1:158999705-159000010 | Common:2; Rare:68 | ||||
chr1:159925442-159925618 | Common:1; Rare:45 | ||||
chr1:160205354-160205478 | Common:1; Rare:43 |