Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:72108181-72108364 | Rare:40 | ||||
chr5:72183491-72183792 | Rare:62 | ||||
chr5:75510616-75510776 | Rare:33 | ||||
chr5:76543235-76543478 | Common:5; Rare:45 | ||||
chr5:77143831-77144107 | Common:4; Rare:35 | ||||
chr5:77419713-77419837 | Rare:38; Clinvar (benign):2 | ||||
chr5:78510318-78510503 | Common:1; Rare:42 | ||||
chr5:78527118-78527486 | Common:2; Rare:63 | ||||
chr5:78543606-78543888 | Common:3; Rare:41 | ||||
chr5:79513298-79513342 | Rare:11 | ||||
chr5:82424969-82425120 | Common:2; Rare:26 | ||||
chr5:87369581-87369847 | Rare:39; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr5:87383846-87384073 | Rare:40 | ||||
chr5:87393084-87393337 | Common:2; Rare:62 | ||||
chr5:93621490-93621717 | Common:2; Rare:55 |