chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261754511261754512GA22GENIChomozygous108630023
1261755324261755325GA9GENIChomozygous109216235
1261758224261758225AG23GENIChomozygous108630027
1261759678261759679TC30GENIChomozygous108630028
1261760339261760340AG30GENIChomozygous108630029
1261764771261764772GA34GENIChomozygous109216237
1261765535261765536CT18GENIChomozygous109216239
1261773024261773025GA25GENIChomozygous109216241
1261779812261779813CT21GENIChomozygous109216243
1261784234261784235CT24GENIChomozygous109216245
1261784303261784304CG21GENIChomozygous108630039
1261785288261785289TG21GENIChomozygous108630040
1261785382261785383GT30GENIChomozygous108630041
1261788421261788422TC24GENIChomozygous108630044
1261801062261801063TC34GENIChomozygous108630047
1261801063261801064TC34GENIChomozygous108630048
1261803990261803991CT32GENIChomozygous109216247
1261807134261807135AT36GENIChomozygous109216249
1261807504261807505TA27GENIChomozygous108630051
1261813071261813072TC36GENIChomozygous108630055
1261815681261815682AC33GENIChomozygous108630057
1261817735261817736CT21GENIChomozygous120605623
1261817736261817737TC22GENIChomozygous120694536
1261817788261817789TA23GENIChomozygous108630065
1261817916261817917CA21GENIChomozygous108630066
1261818003261818004GT10GENIChomozygous120762692
1261818004261818005TC10GENIChomozygous120605625
1261820788261820789AG24GENIChomozygous109216255
1261822778261822779AT17GENIChomozygous108630079
1261823918261823919CA22GENIChomozygous120494248
1261823920261823921AG22GENIChomozygous120494249
1261823921261823922TG22GENIChomozygous120494250
1261824126261824127GT19GENIChomozygous120494251
1261825066261825067GT24GENIChomozygous108782652
1261825067261825068TC24GENIChomozygous108782653
1261825103261825104GT29GENIChomozygous108782654
1261825105261825106GT29GENIChomozygous120477215
1261827490261827491GT24GENICpossibly homozygous108630086
1261830463261830464GA33GENIChomozygous108630087
1261831341261831342TC21GENIChomozygous109216257
1261832175261832176GA34GENIChomozygous108630091