chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23018006630180066T55GENIChomozygous127607275
23018007330180074C52GENIChomozygous127607276
23018007630180077GA50GENIChomozygous120122962
23018008130180082CT52GENIChomozygous109672753
23018008430180084C51GENIChomozygous127607277
23018010030180101CT47GENIChomozygous109672755
23018200130182001G49GENIChomozygous127607278
23018329330183294T37GENIChomozygous127607279
23018352230183523A28GENICheterozygous127607280
23018837030188371AG7GENIChomozygous109672775
23018839930188400CT9GENIChomozygous109672777
23018873630188737TG32GENICheterozygous109672787
23018874030188741CT29GENICheterozygous109672789
23018875130188753AT29GENICheterozygous130739487
23018978030189781TC46GENIChomozygous111098066
23019855030198551GA50GENICheterozygous127785860
23019855530198556AG47GENICheterozygous127785861
23020155130201552CT33GENIChomozygous109672829
23020165830201662CCCC42GENIChomozygous127607283
23020166330201663AAT42GENIChomozygous127607284
23020783130207832T2GENIChomozygous129863666
23020784730207848C4GENIChomozygous129863667
23020785530207855C4GENIChomozygous129863668
23020785730207864CCATAGA5GENIChomozygous129863669
23024157430241574G38GENIChomozygous127607339
23024157630241577A40GENIChomozygous127607340
23024159230241593C43GENIChomozygous127607341
23024160730241607T45GENIChomozygous127607342
23024162130241622G53GENIChomozygous127607343
23024165430241655C49GENIChomozygous127607344
23024166730241668CT47GENIChomozygous109673333
23024167230241673A45GENIChomozygous127607345
23024168030241682TA45GENIChomozygous127607346
23024169230241692C41GENIChomozygous127607347
23024171930241719GTCTAACTCCATTTC31GENIChomozygous127607348
23023451630234516GTG21GENICpossibly homozygous130860654
23020784330207844AC4GENIChomozygous120165314
23023663630236637CT58GENIChomozygous120165315
23023378630233854ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA12GENIChomozygous130244041