chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95277829752778298TC13GENIChomozygous645561475
95277884852778849AC15GENICpossibly homozygous645561476
95277885952778860GA12GENICpossibly homozygous645561477
95277892152778922A-6GENIChomozygous754414119
95277898852778989GC16GENIChomozygous645561478
95277928552779286GA20GENICpossibly homozygous645561479
95278047652780477TC21GENIChomozygous645561480
95278064552780646AG18GENICpossibly homozygous645561481
95278092652780927AG18GENIChomozygous645561482
95278094052780941AG20GENIChomozygous645561483
95278107352781074TC12GENIChomozygous645561484
95278130652781307AAGATAGAG5GENIChomozygous754414120
95278188052781881TTA17GENIChomozygous754414121
95278294652782947GT26GENIChomozygous645561485
95278338352783384TTGG9GENICpossibly homozygous754414123
95278360252783603TC15GENIChomozygous645561486
95278385852783859CCGGGGG1GENIChomozygous754414124
95278388552783886TC10GENIChomozygous645561487
95278409952784100AG15GENIChomozygous645561488