chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153774644153774645GT28GENICpossibly homozygous112890371
4153776733153776734TC58GENIChomozygous112890372
4153777091153777092CT42GENIChomozygous112890373
4153777965153777966CT51GENIChomozygous112890374
4153778240153778241GT52GENIChomozygous112890375
4153778328153778329AT50GENIChomozygous112890376
4153780804153780805TC37GENIChomozygous112890377
4153782359153782360TG10GENIChomozygous112890378
4153782360153782361TG10GENIChomozygous112890379
4153783531153783532TC51GENIChomozygous112890380
4153784338153784339TC53GENIChomozygous112890381
4153785894153785895CT23GENICpossibly homozygous112890382
4153786361153786362GT24GENICpossibly homozygous112890383
4153787656153787657CG53GENICheterozygous112890384
4153789676153789677GA51GENIChomozygous112890385
4153790568153790569CT56GENIChomozygous112890386
4153790870153790871GA63GENIChomozygous112890387
4153790952153790953AG47GENIChomozygous112890388
4153790976153790977AC54GENICpossibly homozygous112890389