chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123239320932393210GA8GENICheterozygous50443169
123239426732394271AAAC----6GENIChomozygous50932602
123239604132396042A-1GENIChomozygous50827418
123239625232396253GA4GENIChomozygous50443206
123239632632396327AAAG3GENICheterozygous50443208
123239641032396411TC2GENIChomozygous50443210
123239641632396417AT5GENIChomozygous50443212
123239662432396625GC9GENIChomozygous50932608
123239662532396626AG10GENIChomozygous50443214
123239736432397365TTG10GENIChomozygous50932611
123239785732397858A-5GENICheterozygous50443227
123239786332397864AT5GENICheterozygous50932617
123239807132398072AT2GENIChomozygous50443229
123239943032399431TG14GENIChomozygous50443241
123239959532399596GT5GENICheterozygous50443243
123239988232399883AC21GENICpossibly homozygous50443245
123240045132400452AT11GENIChomozygous50932626
123240094432400945TC17GENIChomozygous50443251
123240102332401024TC20GENIChomozygous50443253
123240143732401438TC17GENIChomozygous50443257
123240155732401558CT15GENICpossibly homozygous50443259
123240155932401560CT13GENIChomozygous50443261
123240159732401598AT9GENICpossibly homozygous50443263
123240168932401690AG12GENICpossibly homozygous50443265
123240172332401724CG18GENICheterozygous50443268
123240188132401882AG19GENIChomozygous50443270
123240201232402013TG6GENICheterozygous50443274
123240304532403046TC4GENIChomozygous50443278
123240307132403072CCAAAAT2GENICheterozygous50827420
123240307332403074CA2GENICheterozygous50443280
123240351632403517TC16GENICheterozygous50443282
123240378932403790AG24GENIChomozygous50443284
123240382232403823CT12GENIChomozygous50932632
123240383932403840AG6GENIChomozygous50443286
123240607232406073TA7GENICpossibly homozygous50443296
123240609532406096G-3GENIChomozygous50443298
123240668332406684AT12GENICheterozygous50443300
123240670532406706AG11GENICheterozygous50443302