Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159923714-159923941 | Common:1; Rare:41 | ||||
chr1:159924574-159924805 | Rare:47 | ||||
chr1:159925428-159925621 | Common:1; Rare:48 | ||||
chr1:160031852-160032149 | Common:3; Rare:77 | ||||
chr1:160262152-160262292 | Rare:39 | ||||
chr1:160343143-160343389 | Rare:92 | ||||
chr1:161021110-161021495 | Common:2; Rare:99 | ||||
chr1:161045880-161046057 | Common:1; Rare:45 | ||||
chr1:161098330-161098383 | Rare:10 | ||||
chr1:161117955-161118137 | Rare:87 | ||||
chr1:161132411-161132705 | Common:1; Rare:95 | ||||
chr1:161153732-161153792 | Rare:16 | ||||
chr1:161159404-161159529 | Common:1; Rare:35 | ||||
chr1:161166263-161166480 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161197167-161197428 | Common:3; Rare:42 |