chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2309316623093167GC10GENIChomozygous108239622
X2309318823093189CT10GENIChomozygous108239624
X2309899623098997TG14GENIChomozygous108239626
X2311234923112350AG3GENIChomozygous108239628
X2311762123117622CT10GENIChomozygous108239630
X2311817423118175TC6GENIChomozygous108239632
X2311846323118464CA13GENIChomozygous108239634
X2311952623119527GC10GENIChomozygous108239636
X2311961623119617TG14GENIChomozygous108239638
X2311996923119970CT15GENIChomozygous108239640
X2312352823123529TC13GENIChomozygous108373194
X2312159723121598GC13GENIChomozygous108373190
X2312411323124114CT8GENIChomozygous108239642
X2312782223127823AT12GENIChomozygous108239644
X2312864523128646TC14GENIChomozygous108239646
X2313098023130981CG10GENIChomozygous108239648
X2313146423131465CA12GENIChomozygous108239650
X2313278023132781TC5GENIChomozygous108373200
X2313528323135284CA5GENIChomozygous108239652
X2313876323138764TC11GENIChomozygous108239654
X2314172723141728GA10GENIChomozygous108373202
X2314486023144861AT15GENIChomozygous108239656
X2314569323145694CT15GENIChomozygous108239658