chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4197768084197768085AT10GENIChomozygous57872152
4197768485197768486AG10GENIChomozygous57036320
4197768680197768681GGT4GENIChomozygous59169816
4197768699197768700TG6GENIChomozygous57036321
4197768935197768936AG14GENIChomozygous57036323
4197769673197769674GA2GENIChomozygous59169818
4197770227197770228AG9GENICpossibly homozygous57036329
4197770890197770891GA5GENIChomozygous57872158
4197771623197771624TC7GENIChomozygous59169820
4197772222197772226ACCT----4GENIChomozygous57872164
4197772334197772338CTTT----1GENIChomozygous59169822
4197772864197772865TC6GENIChomozygous59169824
4197772949197772950AAT9GENIChomozygous57036335
4197773170197773171GGAA8GENIChomozygous57872166
4197774093197774094AT2GENIChomozygous59169826
4197774897197774898CT7GENIChomozygous57872172
4197775023197775024CCT3GENICheterozygous57872174
4197775255197775257TT--1GENIChomozygous58598626
4197775993197775994CT6GENIChomozygous59169828
4197776192197776193A-7GENIChomozygous59169830
4197776384197776385CT1GENIChomozygous57872176
4197777219197777220GA4GENIChomozygous57036348
4197798054197798055AAT4GENICheterozygous57036355
4197798319197798320GA6GENIChomozygous58000171
4197798464197798465CCACTGACAT3GENIChomozygous57036360
4197798637197798638GC4GENIChomozygous57036361
4197799089197799090T-10GENICpossibly homozygous58530818
4197802161197802162T-8GENIChomozygous57036370