chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199093432199093433TC12GENICheterozygous668369526
1199093873199093874GA17GENICpossibly homozygous668369527
1199094029199094030A-4GENIChomozygous768121793
1199094082199094085CTG---11GENIChomozygous768121794
1199094981199094982AG24GENIChomozygous668369528
1199095171199095172GT26GENIChomozygous668369529
1199095810199095811AG19GENIChomozygous668369530
1199095971199095972AAT8GENIChomozygous768121795
1199095979199095980CT7GENIChomozygous668369531
1199097199199097200CCA14GENICheterozygous768121796
1199097532199097533GC19GENIChomozygous668369532
1199098345199098346T-4GENIChomozygous768121797
1199099660199099661T-6GENICheterozygous768121798