chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176477651176477652TG18GENIChomozygous112218952
3176478083176478084AG22GENIChomozygous112218953
3176479436176479437AT15GENIChomozygous112218955
3176479522176479523CT11GENIChomozygous112218956
3176479741176479742CT14GENIChomozygous112218957
3176481310176481311CT8GENIChomozygous112218958
3176481701176481702CT14GENIChomozygous112218959
3176482102176482103AT15GENIChomozygous112218960
3176482144176482145CT13GENICpossibly homozygous112218961
3176482173176482174AG16GENIChomozygous112218962
3176482773176482774GA10GENIChomozygous112218963
3176483753176483754TC20GENIChomozygous111841402
3176485091176485092TG18GENICheterozygous119831106
3176485220176485221CG15GENICheterozygous119831107
3176485221176485222TG15GENICheterozygous119831108
3176485235176485236TC16GENIChomozygous112218965
3176485663176485664AC24GENIChomozygous119686719
3176485664176485665CA23GENIChomozygous112319245
3176485991176485992TG10GENIChomozygous112218966
3176486757176486758GA16GENIChomozygous112218967
3176487969176487970TC17GENIChomozygous112218968
3176488663176488664TC16GENIChomozygous111841406