chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104501580745015808CT22GENIChomozygous51441582
104501679045016791TTG5GENIChomozygous51441583
104501714645017147TG28GENIChomozygous51441584
104501795245017953GA19GENIChomozygous51635851
104501889345018894AG21GENIChomozygous51635852
104501959745019603GTGTGT------3GENIChomozygous52438980
104501984545019846AG14GENIChomozygous51635854
104501991545019916AG22GENIChomozygous51635855
104501991745019918GGC22GENIChomozygous51635856
104502002845020029CA23GENIChomozygous51635857
104502052445020525TG25GENIChomozygous51635858
104502056745020568TC28GENIChomozygous51635859
104502062545020626TA36GENIChomozygous51635860
104502078345020784TC22GENIChomozygous51441587
104502146645021467CT18GENIChomozygous51635861
104502179845021799TC28GENIChomozygous51635862
104502192745021928TC29GENIChomozygous51635867
104502196545021966TC29GENIChomozygous51635868
104502219745022198TC18GENIChomozygous51441590
104502232845022329GA28GENIChomozygous51635869
104502242545022426AG35GENIChomozygous51635870
104502258445022585GA17GENIChomozygous51635871
104502270845022711TCT---14GENIChomozygous51635874
104502271245022721TCTGTCTGT---------14GENIChomozygous51635875
104502272845022729TG16GENIChomozygous51635877
104502286845022869CG22GENIChomozygous51635878
104502293545022936TA12GENIChomozygous51635879
104502327245023273GGA14GENIChomozygous51635880
104502334645023347AAC13GENIChomozygous51441594
104502346445023465GA27GENIChomozygous51635881
104502356445023566TT--14GENIChomozygous51635882
104502366345023664T-23GENIChomozygous51441595