chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1107229586107229587CA23GENIChomozygous108168360
1107229874107229875GA19GENIChomozygous108168361
1107230193107230194CT19GENIChomozygous108168362
1107230473107230474CT31GENIChomozygous108168363
1107230499107230500AG29GENIChomozygous108168364
1107230584107230585CT34GENICpossibly homozygous108168365
1107230638107230639AT30GENIChomozygous108168366
1107230680107230681TA23GENIChomozygous108168367
1107230745107230746CG22GENICpossibly homozygous108168368
1107230999107231000TC6GENICheterozygous108735853
1107231140107231141CT10GENIChomozygous108168369
1107231181107231182GA13GENIChomozygous108168370
1107231970107231971TC12GENIChomozygous108168371
1107231996107231997CT9GENIChomozygous108168372
1107232115107232116AG15GENIChomozygous108168373
1107232223107232224GT19GENIChomozygous108168374
1107232224107232225CA20GENIChomozygous108168375
1107232225107232226GA19GENIChomozygous108168376