chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37136799171367992GA16GENIChomozygous57441028
37136867971368680GC20GENIChomozygous57441030
37136904671369047GA20GENIChomozygous58154647
37136920371369204AG21GENIChomozygous58371713
37136972071369721TC30GENIChomozygous57441032
37137067771370678GA26GENIChomozygous58371715
37137094471370945T-16GENIChomozygous57441040
37137114571371146AG23GENIChomozygous57441042
37137117771371178TA21GENIChomozygous57441044
37137143071371431TA15GENIChomozygous57441046
37137169071371691CT14GENIChomozygous58154651
37137171071371711GA18GENIChomozygous57441058
37137194671371947AG15GENIChomozygous57441060
37137195971371960AG14GENIChomozygous57441062
37137222771372228TC29GENIChomozygous57441066
37137226271372263GGC30GENIChomozygous57441068
37137249071372512AGGCACAGGACAGGGATATATT----------------------19GENIChomozygous57441070
37137280271372803TC17GENIChomozygous57441072
37137283971372840TC25GENIChomozygous57441074
37137284771372848AT29GENIChomozygous57441076
37137292771372928CT23GENIChomozygous58371717
37137314671373147CT23GENIChomozygous57441078
37137314871373149AATCTGTG22GENIChomozygous57441080
37137369971373700TA29GENIChomozygous57441082
37137375571373756GT31GENIChomozygous57441084
37137380871373809CT31GENIChomozygous58371719
37137460971374610TC20GENIChomozygous57441086
37137463771374638GC28GENIChomozygous58371721
37137464071374641CT29GENIChomozygous57441088
37137518171375182GA16GENICpossibly homozygous58371723
37137519171375192GT17GENIChomozygous57441090
37137523871375239GA16GENIChomozygous57441092
37137536071375361TC18GENIChomozygous57441096
37137543371375436GTT---8GENIChomozygous58687954
37137550871375509CT17GENIChomozygous58371725
37137551271375513CT19GENIChomozygous58371727
37137571171375712AG21GENIChomozygous57441106
37137577071375771AC32GENIChomozygous57441108
37137623671376237CT22GENIChomozygous57441116
37137642371376424TC25GENIChomozygous57441119