chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112999200629992007GA25GENIChomozygous145764336
112999201129992012AG26GENIChomozygous138951518
112999249129992492GA22GENIChomozygous145764337
112999288129992882T26GENIChomozygous145753167
112999293529992936AG21GENIChomozygous145764338
112999408629994087CA36GENIChomozygous145764339
112999412829994129TC35GENIChomozygous138951520
112999474129994742GA29GENIChomozygous145764340
112999479129994792GT24GENIChomozygous138951523
112999559129995592AG32GENIChomozygous145764341
112999584329995844AG31GENIChomozygous145764342
112999617829996179GA22GENIChomozygous144093708
112999663229996633TC22GENIChomozygous145764343
112999675629996757TC28GENIChomozygous145764344
112999685229996852T29GENIChomozygous145753168
112999691729996918TC25GENIChomozygous145764345
112999731829997319TC11GENIChomozygous145764346
112999741529997416CG27GENIChomozygous145764347
112999794929997950CT29GENIChomozygous145764348
112999830729998308CT26GENIChomozygous145764349
112999848829998489GT26GENIChomozygous145764350
112999871829998719TC11GENIChomozygous145764351
112999875429998755AG6GENIChomozygous145764352
112999888929998890TG11GENIChomozygous145764353
112999891329998914GA13GENICheterozygous145764354
112999893929998940AG14GENIChomozygous145764355
112999964329999644T25GENIChomozygous145753169
112999973629999736G19GENIChomozygous145753170
113000001130000012GA30GENIChomozygous145764356
113000061030000611AG21GENIChomozygous138951526
113000082230000823CT27GENIChomozygous145764357
113000165230001653TG20GENIChomozygous145764358
113000251330002514GA21GENIChomozygous145764359
112999891129998912GA13GENICheterozygous403640432
112999320429993205T11GENICheterozygous403302587
112999320429993205TA11GENICheterozygous403302588
112999320429993205TC11GENICheterozygous403302589
112999891529998916GA13GENICheterozygous403640433