chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136976519269765193TC44GENIChomozygous776997214
136976635369766354GA43GENIChomozygous776997215
136976637269766373CT36GENIChomozygous776997216
136976708969767090AG27GENIChomozygous776997217
136976725569767256TC36GENIChomozygous776997218
136976769169767692TC44GENICpossibly homozygous776997219
136976905969769060GA40GENIChomozygous776997220
136977083469770835TC42GENIChomozygous776997221
136977095969770960CT41GENIChomozygous776997222
136977098669770987AG54GENIChomozygous776997223
136977149369771494AG25GENIChomozygous776997224
136977246169772462AT36GENIChomozygous776997225
136977270069772701AG22GENIChomozygous776997226
136977297569772976CA54GENIChomozygous776997227
136977319369773194TA52GENIChomozygous776997228
136977337269773373CT59GENIChomozygous776997229
136977413269774133CG37GENIChomozygous776997230
136977422769774228AG36GENIChomozygous776997231
136977432669774327AG37GENICpossibly homozygous776997232
136977440469774405TC40GENIChomozygous776997233
136977584269775843GT26GENIChomozygous776997234
136977602969776030CT14GENICpossibly homozygous776997235
136977739769777398GT51GENIChomozygous776997236
136977793169777932GA35GENIChomozygous776997237
136977895569778956TC27GENIChomozygous776997238
136977963469779635CT37GENIChomozygous776997239
136978009569780096TG26GENIChomozygous776997240