chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123445431334454314AG36GENIChomozygous145776036
123445447934454480AT46GENIChomozygous145776037
123445474834454749AG41GENIChomozygous145776038
123445498934454990TC47GENIChomozygous139134727
123445502134455022TG46GENICpossibly homozygous145776039
123445529234455292T29GENIChomozygous145771504
123445529434455295AT29GENIChomozygous145776040
123445534134455342AG35GENIChomozygous139134728
123445551534455516TA27GENIChomozygous139134729
123445565534455655TGGGTGATATGCACCTGGGTTAACAGCTGGTTCTCAT28GENIChomozygous145771505
123445566734455667A32GENIChomozygous145771506
123445566834455668CTGGGTTAACAGCTGGTTCTCACTGGGTGATATGCA32GENIChomozygous145771507
123445618134456182TC44GENICpossibly homozygous145776041
123445636834456369C28GENIChomozygous145771508
123445637134456375AGCA28GENIChomozygous145771509
123445660534456606TC40GENIChomozygous145776042
123445661134456612TC41GENIChomozygous145776043
123445675134456752G35GENIChomozygous145771510
123445694634456947CA39GENIChomozygous145776044
123445716834457169AG34GENIChomozygous139134732
123445726134457262GA39GENIChomozygous145776045
123445820234458216ACTGTAATCCCAGC28GENIChomozygous145771511
123445529434455295A29GENICheterozygous404569345
123445858834458589AG30GENIChomozygous145776046
123445889434459009GTAATTTGAGTTTTCTTTTTTTTTTTGGTTCTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGTTCTACCACTGAGCTAAATCCCCAACCCCC29GENIChomozygous139053466
123445955234459553CA31GENIChomozygous139134734
123445962534459626AG36GENIChomozygous145776047
123445995734459958TC39GENIChomozygous145776048
123446012234460123CT38GENIChomozygous145776049
123446018334460183ATACA42GENIChomozygous145771512
123446042734460428CT41GENIChomozygous145776050
123446076934460778AAAAAAAAA7GENIChomozygous145771513
123446078134460783CC7GENIChomozygous145771514
123446080334460805AG3GENIChomozygous145771515
123446090734460908CT33GENIChomozygous145776051
123446096534460965T25GENIChomozygous145771516
123446098734460988GA22GENIChomozygous145776052
123446101334461013GGTCCTTG20GENIChomozygous145771517
123446102834461028AGGGCTAGGGTCTCTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGTTTGGTTCTTTTTTTCGGAGGGCCTTGCGCTTCCTAGGTAAG9GENIChomozygous145771518
123446144234461443TC26GENIChomozygous145776053
123446150434461505GA21GENIChomozygous139134735
123446153234461533GA18GENIChomozygous145776054
123446217734462178AT33GENICpossibly homozygous145776055
123446223734462238CT34GENICpossibly homozygous145776056
123446247534462475C37GENIChomozygous145771519
123446263734462638GA30GENIChomozygous145776060
123446224334462244TA32GENICpossibly homozygous145776057
123446229334462294CT32GENICpossibly homozygous145776058
123446235234462353TC36GENICpossibly homozygous145776059
123446272134462722CT28GENIChomozygous145776061
123446285234462853GC27GENIChomozygous145776062
123446297734462978GA27GENIChomozygous145776063
123446326234463262G37GENIChomozygous139053469
123446343534463436TA35GENIChomozygous139134737
123446357434463575AG33GENIChomozygous145776064
123446373234463733GA23GENIChomozygous145776065
123446441934464420TC27GENIChomozygous139134739
123446442734464428TC24GENIChomozygous139134741
123446454234464543CA27GENICpossibly homozygous145776066
123446496134464962GA42GENIChomozygous139134742
123446635834466359GT29GENIChomozygous145776067
123446651434466514CAAA22GENIChomozygous139053472
123446667334466674AC34GENIChomozygous139134743
123446812034468121AG31GENIChomozygous145776068