Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42658089-42658480 | Common:3; Rare:98 | ||||
chr1:42682038-42682500 | Common:2; Rare:145 | ||||
chr1:42766927-42767354 | Common:6; Rare:153; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42816907-42817196 | Common:1; Rare:84 | ||||
chr1:42846340-42846766 | Common:1; Rare:115 | ||||
chr1:42931356-42931532 | Rare:35 | ||||
chr1:42957980-42958598 | Common:7; Rare:184 | ||||
chr1:42958740-42959111 | Common:4; Rare:90; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172180-43172374 | Common:2; Rare:82 | ||||
chr1:43172557-43172748 | Common:6; Rare:48 | ||||
chr1:43358497-43359014 | Common:7; Rare:162 | ||||
chr1:43366892-43367145 | Rare:47 | ||||
chr1:43367665-43367771 | Common:2; Rare:18 | ||||
chr1:43367927-43368275 | Rare:92 | ||||
chr1:43368380-43368476 | Common:1; Rare:23 |