chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104501580745015808CT13GENIChomozygous51441582
104501679045016791TTG3GENIChomozygous51441583
104501714645017147TG25GENIChomozygous51441584
104501795245017953GA25GENIChomozygous51635851
104501889345018894AG21GENIChomozygous51635852
104501959745019603GTGTGT------3GENIChomozygous52438980
104501984545019846AG19GENIChomozygous51635854
104501991545019916AG25GENIChomozygous51635855
104501991745019918GGC25GENIChomozygous51635856
104502002845020029CA15GENIChomozygous51635857
104502052445020525TG24GENIChomozygous51635858
104502056745020568TC23GENIChomozygous51635859
104502062545020626TA24GENIChomozygous51635860
104502078345020784TC14GENIChomozygous51441587
104502146645021467CT17GENIChomozygous51635861
104502179845021799TC7GENIChomozygous51635862
104502192745021928TC27GENIChomozygous51635867
104502196545021966TC31GENIChomozygous51635868
104502219745022198TC23GENIChomozygous51441590
104502232845022329GA18GENIChomozygous51635869
104502242545022426AG14GENIChomozygous51635870
104502258445022585GA15GENICpossibly homozygous51635871
104502270845022711TCT---20GENIChomozygous51635874
104502271245022721TCTGTCTGT---------23GENIChomozygous51635875
104502272845022729TG21GENIChomozygous51635877
104502286845022869CG23GENIChomozygous51635878
104502293545022936TA22GENIChomozygous51635879
104502327245023273GGA14GENIChomozygous51635880
104502334645023347AAC7GENIChomozygous51441594
104502346445023465GA21GENIChomozygous51635881
104502356445023566TT--16GENIChomozygous51635882
104502366345023664T-22GENIChomozygous51441595