Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160579454-160579630 | Rare:34 | ||||
chr1:160646993-160647096 | Rare:23 | ||||
chr1:160739157-160739281 | Rare:37 | ||||
chr1:161021012-161021291 | Common:5; Rare:90 | ||||
chr1:161038550-161039003 | Common:3; Rare:159 | ||||
chr1:161045860-161046057 | Common:1; Rare:51 | ||||
chr1:161098304-161098395 | Common:1; Rare:15 | ||||
chr1:161117965-161118141 | Rare:91 | ||||
chr1:161131690-161131792 | Rare:18 | ||||
chr1:161132417-161132862 | Common:2; Rare:139 | ||||
chr1:161153733-161153803 | Rare:20 | ||||
chr1:161159238-161159520 | Common:2; Rare:73 | ||||
chr1:161166279-161166529 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197150-161197424 | Common:3; Rare:45 | ||||
chr1:161198972-161199326 | Rare:55 |