chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172354779823547799AG4GENIChomozygous140081590
172354787523547875T11GENIChomozygous140015626
172354820023548200A12GENIChomozygous140015627
172355000223550003AG20GENIChomozygous140081591
172355119823551199AG17GENIChomozygous140081592
172355221923552220GA28GENIChomozygous140081593
172355234123552342CT14GENIChomozygous140081594
172355279123552792CA20GENIChomozygous140081595
172355317023553171TC19GENIChomozygous140081596
172355370523553706TA24GENIChomozygous140081597
172355575623555757GA18GENIChomozygous140081598
172355686923556870GT20GENIChomozygous140081599
172355946823559469CG16GENIChomozygous140081600
172355991223559924GAGTTGAAAACC12GENIChomozygous140015630
172356197223561973CT12GENIChomozygous140081601
172356209923562100GA21GENIChomozygous140081602
172356388423563885GC24GENIChomozygous140081603
172356570823565708G19GENIChomozygous140015631
172356715923567160GA18GENIChomozygous140081604
172356762023567621GC18GENIChomozygous140081605
172356933723569338TG18GENIChomozygous140081606
172357099523570995TG8GENIChomozygous140015632
172357142323571424TG27GENIChomozygous140081607
172357293723572938AG17GENIChomozygous140081608
172357604823576049CT27GENIChomozygous140081609
172358207423582075CT20GENIChomozygous140081610
172358236223582363AG22GENIChomozygous140081611
172358253223582533GC22GENIChomozygous140081612
172358269523582696TC27GENIChomozygous140081613
172358271423582715CT19GENIChomozygous140081614
172358332323583324TA16GENIChomozygous140081615
172358411723584118TC18GENIChomozygous140081616
172358445123584452AT16GENIChomozygous140081617
172358458623584587T22GENIChomozygous140015633
172356879823568799TG12GENIChomozygous155023182
172356303123563032TC14GENIChomozygous403410326
172356879823568799TA12GENICheterozygous155023181