chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7105480629105480630TC15GENIChomozygous138172456
7105480778105480779AG18GENIChomozygous138172457
7105482143105482144AT16GENIChomozygous143365003
7105483483105483484TC18GENIChomozygous138172459
7105484655105484656T11GENIChomozygous404872576
7105484655105484656TC11GENICheterozygous404872577
7105485127105485128CA20GENIChomozygous138172460
7105487274105487275AG11GENIChomozygous138172462
7105492982105492983AG19GENIChomozygous138172464
7105494632105494633AG16GENIChomozygous138172467
7105499479105499480AT11GENIChomozygous143365004
7105500073105500074TC33GENIChomozygous138172475
7105501139105501140AC28GENIChomozygous138172478
7105505769105505770AG17GENIChomozygous138172481
7105506670105506671CA18GENICpossibly homozygous143365005
7105506694105506695TC17GENIChomozygous143365006
7105512143105512144TC15GENIChomozygous143365007
7105516462105516463GA20GENIChomozygous138172483
7105520596105520597CT16GENIChomozygous143365008
7105523061105523062AG18GENIChomozygous138172488
7105501372105501373A14GENIChomozygous137972187
7105500327105500353CATCCCAACCTACTATGTATGCTGCG23GENICheterozygous143350468
7105515254105515254A12GENIChomozygous143350469
7105522070105522071TC20GENIChomozygous138172486
7105527950105527951CT22GENIChomozygous143365009
7105529689105529689CCT22GENIChomozygous143350470
7105531024105531025CT11GENIChomozygous143365010
7105531924105531925TA14GENIChomozygous143365011
7105533410105533411AC19GENIChomozygous143365012
7105533903105533904GA14GENIChomozygous143365013
7105537918105537919TC21GENIChomozygous138172490
7105540017105540018TG24GENIChomozygous143365014
7105540781105540782T15GENICpossibly homozygous137972190
7105541016105541017TA16GENIChomozygous138172491
7105542394105542395TC18GENIChomozygous138172494
7105544402105544406TAAA15GENIChomozygous137972191
7105544830105544843TCACACACACACT15GENIChomozygous140892727
7105547275105547276GA12GENIChomozygous143365015
7105533410105533411A19GENICheterozygous403221167