chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2108517100108517101GT17GENIChomozygous518422654
2108518874108518875GGA14GENIChomozygous688680301
2108520262108520263AATATT7GENIChomozygous688680302
2108520700108520701A-11GENIChomozygous688680303
2108522014108522015CT7GENIChomozygous518422655
2108522751108522752AG12GENIChomozygous518422656
2108522800108522801AT8GENIChomozygous516803333
2108523270108523278ACACACAC--------3GENIChomozygous688680304
2108523728108523729C-10GENIChomozygous688680306
2108526362108526363TC18GENIChomozygous518422657
2108526503108526504TC15GENIChomozygous518422658
2108527508108527509TC21GENIChomozygous518422659
2108527770108527771CT17GENIChomozygous518422660
2108528742108528743AG11GENIChomozygous518422661
2108529310108529311CA22GENIChomozygous518422662
2108529484108529485CT19GENIChomozygous518422663
2108530578108530579TC23GENIChomozygous518422664
2108530793108530794AG26GENICpossibly homozygous516803334
2108531162108531163GT15GENIChomozygous518422665
2108531342108531343CCTTTT4GENIChomozygous688680307
2108531955108531956TC30GENICheterozygous518422666
2108532037108532038CG25GENICheterozygous518422667
2108532255108532256TTA1GENIChomozygous688680308
2108532270108532271GGA5GENIChomozygous688680309
2108532300108532301A-6GENIChomozygous688680311
2108532753108532754CT26GENIChomozygous518422668
2108533194108533195CT7GENIChomozygous518422669
2108534345108534346AG10GENIChomozygous516803335
2108535579108535580TC12GENIChomozygous516803336