chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7105480629105480630TC51GENIChomozygous138172456
7105480778105480779AG46GENIChomozygous138172457
7105482143105482144AT65GENICpossibly homozygous143365003
7105483483105483484TC56GENIChomozygous138172459
7105485127105485128CA50GENIChomozygous138172460
7105487274105487275AG73GENIChomozygous138172462
7105492982105492983AG43GENIChomozygous138172464
7105494632105494633AG57GENIChomozygous138172467
7105499479105499480AT38GENIChomozygous143365004
7105500073105500074TC63GENIChomozygous138172475
7105501139105501140AC74GENIChomozygous138172478
7105505769105505770AG60GENIChomozygous138172481
7105506670105506671CA58GENIChomozygous143365005
7105506694105506695TC50GENIChomozygous143365006
7105512143105512144TC36GENIChomozygous143365007
7105516462105516463GA66GENIChomozygous138172483
7105520596105520597CT71GENIChomozygous143365008
7105522070105522071TC58GENIChomozygous138172486
7105523061105523062AG55GENIChomozygous138172488
7105527950105527951CT64GENIChomozygous143365009
7105501372105501373A43GENIChomozygous137972187
7105515254105515254A44GENICpossibly homozygous143350469
7105529689105529689CCT46GENICpossibly homozygous143350470
7105531024105531025CT39GENIChomozygous143365010
7105531924105531925TA78GENIChomozygous143365011
7105533410105533411AC57GENIChomozygous143365012
7105533903105533904GA55GENIChomozygous143365013
7105537918105537919TC54GENIChomozygous138172490
7105540017105540018TG50GENIChomozygous143365014
7105540781105540782T33GENICpossibly homozygous137972190
7105541016105541017TA58GENIChomozygous138172491
7105542394105542395TC52GENIChomozygous138172494
7105544402105544406TAAA39GENIChomozygous137972191
7105547275105547276GA43GENIChomozygous143365015
7105544830105544843TCACACACACACT27GENIChomozygous140892727
7105533410105533411A57GENICheterozygous403221167
7105530385105530386TC10GENIChomozygous403221165
7105530385105530386T10GENICheterozygous403221166