chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135209311752093118TG25GENIChomozygous962007597
135209358352093584GA21GENIChomozygous962007598
135209401952094020CT18GENIChomozygous962007599
135209457352094574CT20GENIChomozygous962007600
135209478952094790TC32GENIChomozygous962007601
135209546852095469CT22GENIChomozygous962007602
135209575552095756CT18GENIChomozygous962007603
135209591152095912AC17GENIChomozygous962007604
135209591252095913GA17GENIChomozygous962007605
135209750152097502CT22GENIChomozygous962007606
135209885352098854TC12GENIChomozygous962007607
135209892652098927TG14GENIChomozygous962007608
135210154452101545GT36GENICpossibly homozygous962007609
135210237252102373AT15GENICpossibly homozygous962007610
135210270752102708TC18GENIChomozygous962007611
135210476652104767GA32GENIChomozygous962007612
135210508952105090TA20GENIChomozygous962007613
135210583452105835TC22GENIChomozygous962007614
135210597752105978TC21GENIChomozygous962007615
135210604052106041TC29GENIChomozygous962007616
135210633352106334GT24GENIChomozygous962007617
135210634452106345CT25GENICpossibly homozygous962007618
135210716152107162AT34GENIChomozygous962007619
135210756652107567GA25GENIChomozygous962007620
135210780152107802TG27GENICpossibly homozygous962007621
135210825352108254AC18GENIChomozygous962007622
135210861652108617TC28GENIChomozygous962007623
135210910752109108AT28GENIChomozygous962007624
135210912952109130TA24GENIChomozygous962007625
135210918252109183CT23GENIChomozygous962007626
135210927752109278AG20GENIChomozygous962007627
135210985352109854TC20GENIChomozygous962007628
135211076752110768GA8GENIChomozygous962007629
135211139952111400AC14GENIChomozygous962007630
135211150052111501GA19GENIChomozygous962007631