chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826811862681187GT16GENIChomozygous579769519
826812072681208AT11GENICpossibly homozygous579769520
826814902681491AC18GENICpossibly homozygous579769521
826819802681981TG9GENICpossibly homozygous579769522
826837072683708CT3GENIChomozygous579769523
826838642683865CT13GENIChomozygous579769524
826839712683972TC8GENICpossibly homozygous579769525
826840892684090TG15GENIChomozygous579769526
826850182685019CT16GENIChomozygous579769527
826855252685526AG19GENICpossibly homozygous579769528
826863492686350T-4GENIChomozygous717777697
826864892686490CG4GENIChomozygous579769529
826893082689309TC12GENIChomozygous579769530
826902662690267CT13GENIChomozygous579769531
826905612690562CT3GENIChomozygous579769532
826914072691408GA1GENIChomozygous579769533
826916292691630TG8GENICheterozygous581333611
826917282691729TA4GENICheterozygous581333612
826924892692490CA8GENICheterozygous581333613
826932602693261GT7GENICheterozygous579769534
826941252694126C-2GENICheterozygous717777700
826944932694494CT7GENIChomozygous581333614
826946482694649AAT1GENIChomozygous717777701
826956792695680GA11GENIChomozygous581333615
826970242697025CA13GENIChomozygous581333616
826979702697971TA2GENIChomozygous579769535
826980292698030GT8GENICpossibly homozygous579769536
827015502701551AG20GENICpossibly homozygous579769537
827026552702656GGT4GENIChomozygous717777702
827055122705513GA7GENIChomozygous579769538
827080192708020A-8GENIChomozygous717777703
827083562708357AG11GENIChomozygous579769539
827108742710875AG18GENIChomozygous579769540