Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42658309-42658466 | Common:1; Rare:46 | ||||
chr1:42682140-42682730 | Common:3; Rare:186 | ||||
chr1:42683293-42683465 | Common:3; Rare:66 | ||||
chr1:42766983-42767309 | Common:4; Rare:109; Clinvar (benign):1 | ||||
chr1:42816932-42817149 | Common:1; Rare:63 | ||||
chr1:42817213-42817260 | Rare:16 | ||||
chr1:42817263-42817504 | Rare:80 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958726-42959108 | Common:4; Rare:93; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172207-43172377 | Common:1; Rare:77 | ||||
chr1:43358684-43359025 | Common:7; Rare:111 | ||||
chr1:43367367-43367496 | Rare:32 | ||||
chr1:43367946-43368226 | Rare:71 | ||||
chr1:43389741-43389966 | Common:4; Rare:102; Clinvar:1 | ||||
chr1:43524970-43525110 | Rare:23 |