chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2367064923670650GC11GENIChomozygous108373364
X2367072323670724TC12GENIChomozygous108373366
X2367764423677645TC9GENIChomozygous108240494
X2367839723678398TG9GENIChomozygous108240496
X2368067823680679CT8GENIChomozygous108240498
X2368099323680994GA15GENIChomozygous108240500
X2368292523682926AG10GENIChomozygous108240502
X2368371723683718TC8GENIChomozygous108240504
X2367851723678518A6GENIChomozygous129728242
X2368156523681565T10GENIChomozygous129728243
X2368425123684252T11GENIChomozygous129728244
X2368463223684633A9GENIChomozygous129728245
X2368801423688015AC13GENIChomozygous108240507
X2368838223688382A5GENICheterozygous129728246
X2368884123688842AG3GENIChomozygous108240509
X2368960123689602TA11GENIChomozygous108240511
X2369035323690354CA15GENIChomozygous108240513
X2369119123691197TCCCTC4GENIChomozygous129728247
X2369120323691227TCCTTCTCCCTCTCCCTCTCCCTC5GENIChomozygous129728248
X2369146223691463GA12GENIChomozygous108240515
X2369154423691545AG6GENIChomozygous108240517
X2369216323692164GA6GENIChomozygous108240519