chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1107229586107229587CA28GENIChomozygous108168360
1107229874107229875GA29GENIChomozygous108168361
1107230193107230194CT17GENIChomozygous108168362
1107230473107230474CT21GENICpossibly homozygous108168363
1107230499107230500AG19GENIChomozygous108168364
1107230584107230585CT18GENIChomozygous108168365
1107230638107230639AT13GENIChomozygous108168366
1107230680107230681TA17GENIChomozygous108168367
1107230745107230746CG22GENIChomozygous108168368
1107230999107231000TC6GENIChomozygous108735853
1107231140107231141CT5GENIChomozygous108168369
1107231181107231182GA6GENIChomozygous108168370
1107231970107231971TC6GENIChomozygous108168371
1107231996107231997CT4GENIChomozygous108168372
1107232115107232116AG5GENIChomozygous108168373
1107232223107232224GT7GENIChomozygous108168374
1107232224107232225CA7GENIChomozygous108168375
1107232225107232226GA7GENIChomozygous108168376