chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122394148923941490GA4GENIChomozygous115286191
122394272823942729CG3GENIChomozygous115286193
122394294723942948CT6GENIChomozygous115286195
122394326923943270GA8GENIChomozygous115469773
122394368323943684TG8GENIChomozygous115286197
122394455023944551TA5GENIChomozygous115422062
122394483523944836TG4GENIChomozygous115286199
122394507723945078TC6GENIChomozygous115286201
122394561423945615TC2GENIChomozygous115286205
122394591423945915CT5GENIChomozygous115286207
122394626623946267AG7GENIChomozygous115286209
122394656023946561CT4GENIChomozygous115286213
122394657423946575TA5GENIChomozygous115438578
122394660123946602CA7GENIChomozygous115438579
122394660523946606TC6GENIChomozygous115438580
122394680223946803GA5GENIChomozygous115422064
122394779023947791AC2GENIChomozygous115286215
122394791623947917CA4GENIChomozygous115286217
122394818623948187TA7GENIChomozygous115286219
122394872823948729CA3GENIChomozygous115286221
122394883223948833TC4GENIChomozygous115286223
122394906423949065AC8GENIChomozygous115286225
122394929523949296TA4GENIChomozygous115286227
122394983323949834AT4GENIChomozygous115286229
122395022223950223TC3GENIChomozygous115286231
122395033923950340CT10GENIChomozygous115286233
122395120423951205AG4GENIChomozygous115286235
122395131823951319GA8GENIChomozygous115286237
122395148123951482CT6GENIChomozygous115438584
122395182323951824CT11GENIChomozygous115286239
122395251723952518GA5GENIChomozygous115286243