Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160646993-160647096 | Rare:23 | ||||
chr1:160711757-160711935 | Common:2; Rare:43 | ||||
chr1:161021078-161021280 | Common:5; Rare:65 | ||||
chr1:161021381-161021690 | Common:1; Rare:70 | ||||
chr1:161038885-161039010 | Rare:45 | ||||
chr1:161044974-161045264 | Common:1; Rare:55 | ||||
chr1:161045884-161046052 | Common:1; Rare:44 | ||||
chr1:161069786-161070120 | Rare:46 | ||||
chr1:161098080-161098383 | Common:1; Rare:45 | ||||
chr1:161117982-161118165 | Rare:97 | ||||
chr1:161118276-161118575 | Common:1; Rare:73 | ||||
chr1:161131690-161131792 | Rare:18 | ||||
chr1:161132223-161132707 | Common:1; Rare:133 | ||||
chr1:161133054-161133308 | Rare:47 | ||||
chr1:161153738-161154093 | Common:1; Rare:108; Clinvar (pathogenic):1 |