Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816230-42816630 | Common:4; Rare:130 | ||||
chr1:42816932-42817171 | Common:1; Rare:72 | ||||
chr1:42817180-42817610 | Rare:129 | ||||
chr1:42846362-42846643 | Common:1; Rare:82 | ||||
chr1:42958826-42959111 | Common:4; Rare:74; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43147688-43147926 | Common:5; Rare:57 | ||||
chr1:43152722-43153143 | Common:5; Rare:116 | ||||
chr1:43172230-43172352 | Common:1; Rare:64 | ||||
chr1:43172523-43172740 | Common:6; Rare:56 | ||||
chr1:43184986-43185386 | Common:1; Rare:178 | ||||
chr1:43358634-43359018 | Common:7; Rare:123 | ||||
chr1:43367967-43368301 | Rare:90 | ||||
chr1:43389751-43390065 | Common:4; Rare:130; Clinvar:1 | ||||
chr1:43453820-43454080 | Common:4; Rare:71 | ||||
chr1:43530773-43530886 | Common:2; Rare:31 |