chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134590364445903645AG57GENIChomozygous139287260
134590404345904044GA52GENIChomozygous142368017
134590563245905633TG58GENIChomozygous147025247
134590567045905671CT54GENIChomozygous142368018
134590629745906298GA41GENIChomozygous147025248
134590745745907458TC51GENIChomozygous147025249
134590858445908585AG57GENIChomozygous147025250
134590870045908701TC59GENIChomozygous142368019
134590870145908702TC59GENIChomozygous142368020
134590957745909578TC70GENIChomozygous139287261
134590961745909618GA67GENIChomozygous147025251
134591297045912971T49GENIChomozygous147008995
134591495745914958GA60GENIChomozygous142368024
134591533945915340CT60GENICpossibly homozygous147025252
134591600345916004GA44GENIChomozygous147025253
134591622345916224TC23GENICpossibly homozygous147025254
134591363745913637TT45GENIChomozygous142343771
134591771045917711GC60GENIChomozygous142368027
134591771145917712GA58GENIChomozygous142368028
134591868845918722ATACACAACTTTCTGCTTTATATGCGCCATTGTT52GENICpossibly homozygous147008996
134591998345919984AT10GENIChomozygous142368031
134592196745921968CT46GENIChomozygous147025255
134592213745922138GT68GENIChomozygous147025256
134592271245922713TC49GENIChomozygous142368032
134592274045922741AG52GENIChomozygous147025257
134592312645923126A33GENICheterozygous147008997
134592313545923136GA40GENIChomozygous142368033
134592556145925562CT50GENIChomozygous147025258
134592636845926369T9GENIChomozygous140910420
134592665545926656GA45GENIChomozygous147025259
134592699945927000AG55GENIChomozygous147025260
134593042345930424AG30GENIChomozygous147025261
134593059345930594CT61GENIChomozygous147025262
134593075445930754G48GENIChomozygous147008998
134593206745932068CA47GENIChomozygous147025263
134593255545932556AG21GENIChomozygous147025264