chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85890990458909905CG34GENIChomozygous52982698
85890997358909974CT38GENIChomozygous52982699
85891001558910016CT31GENIChomozygous52982700
85891100658911007GA36GENIChomozygous53122370
85891138658911387TC28GENIChomozygous52982702
85891148458911485GA28GENIChomozygous52982703
85891149158911492A-22GENIChomozygous53122371
85891169758911698TC33GENIChomozygous53699714
85891187958911880TC19GENIChomozygous52982707
85891193158911932A-18GENIChomozygous52982708
85891201058912011CCTAT10GENIChomozygous52982710
85891221658912217AC24GENIChomozygous52982711
85891302858913029TA25GENIChomozygous53122373
85891323858913239AG30GENIChomozygous52982713
85891690558916906TTTGTGTGTGTGTG3GENIChomozygous53388561
85891751958917523TCCT----5GENIChomozygous53699715
85892483158924839TGTGTGTG--------6GENICheterozygous53433145
85892483358924839TGTGTG------6GENICheterozygous53433147
85892488258924883GA16GENICpossibly homozygous53699716
85892519158925192TC17GENIChomozygous53318980
85892642858926429TA29GENIChomozygous53318981
85892709458927095GA31GENIChomozygous53318982
85892722058927221AC20GENIChomozygous53318983
85892765058927651CA30GENIChomozygous53699717
85893270058932701GT29GENIChomozygous52982728
85892791358927914AATGTG34GENIChomozygous53318984
85893149958931500GA24GENIChomozygous52982726
85893212158932122AC25GENIChomozygous52982727
85893282558932829CTCT----23GENIChomozygous52982729
85893285158932852GGTGTGTGTA12GENIChomozygous53699718
85893370758933708TTC14GENIChomozygous53122383
85893411958934120AG24GENIChomozygous53122384
85893457258934573GA28GENIChomozygous53699719
85893550458935505CT27GENIChomozygous53699720
85893577558935776AAT11GENIChomozygous53122385