chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124062013240620132C37GENIChomozygous131914644
124062061440620615TC35GENIChomozygous115328424
124062064340620644CT36GENIChomozygous115515376
124062129640621306TTTTTTTTAA43GENICheterozygous131914645
124062323240623233TA45GENIChomozygous115328428
124062342340623424AG32GENIChomozygous115328430
124062346340623463GC18GENIChomozygous131914646
124062347040623473CGC19GENIChomozygous131914647
124062149140621492CT49GENICpossibly homozygous115477589
124062179440621795AT48GENIChomozygous115477591
124062192140621922CT54GENIChomozygous115477593
124062279940622800CT45GENIChomozygous115477595
124062354240623543CT30GENIChomozygous115383897
124062360040623601CT41GENIChomozygous115515378
124062376140623762AC59GENIChomozygous115477597
124062528740625288GA51GENIChomozygous115515380
124062427840624279CT26GENIChomozygous118270577