chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1542099494209950TC19GENIChomozygous112785736
1542139844213985CT13GENIChomozygous112785738
1542142324214233AG20GENIChomozygous112785740
1542145004214501CA7GENICheterozygous125793762
1542177114217712CT16GENIChomozygous112785742
1542179224217923TC17GENIChomozygous112785744
1542192374219238AG17GENIChomozygous112785746
1542211584221159TC18GENIChomozygous112785748
1542225834222584TA20GENIChomozygous112785750
1542226634222664CT15GENIChomozygous112785752
1542230984223099CT16GENIChomozygous112785754
1542232914223292TG14GENIChomozygous112785758
1542240314224032GC21GENIChomozygous112785760
1542249124224913TC6GENIChomozygous112785762
1542249394224940TC4GENIChomozygous112785764
1542271904227191AG17GENIChomozygous112785766
1542294254229426GC21GENIChomozygous112785768
1542295384229539TA16GENIChomozygous112785770
1542313094231310AG11GENIChomozygous112785772
1542327374232738TG20GENIChomozygous112785775
1542329774232978GA7GENIChomozygous112785777
1542353574235358AG14GENIChomozygous112785779
1542366094236610TC21GENIChomozygous118860341