chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134170002141700022T25GENIChomozygous129046393
134170003341700034GA24GENIChomozygous118449092
134170006441700065A19GENIChomozygous129046394
134170008841700090CC18GENIChomozygous129046395
134170015041700152AG11GENIChomozygous130416948
134170018341700184G11GENIChomozygous130416949
134170069441700695A7GENIChomozygous129046396
134170070941700710CA10GENIChomozygous118449093
134170071241700712C10GENIChomozygous129046397
134170072441700725C11GENIChomozygous129046398
134170072841700729G12GENIChomozygous129046399
134170073541700736A12GENIChomozygous129046400
134170074541700746C12GENIChomozygous129046401
134170075841700759C17GENIChomozygous129046402
134170076241700763A17GENIChomozygous129046403
134170077641700777C20GENIChomozygous129046404
134170078641700787A23GENIChomozygous129046405
134170078841700789A23GENIChomozygous129046406
134170151441701514A19GENIChomozygous129046407
134170075341700754TC16GENIChomozygous114719433
134170143241701433TC26GENIChomozygous114719435
134170075441700755GT16GENIChomozygous114857334
134170078241700783TA22GENIChomozygous114857336
134171242241712423GT16GENIChomozygous130422184
134171317441713175C59GENIChomozygous129046412
134171319341713194C63GENIChomozygous129046413
134171320741713208G63GENIChomozygous129046414