chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2309316623093167GC16GENIChomozygous108239622
X2309318823093189CT18GENIChomozygous108239624
X2309899623098997TG6GENIChomozygous108239626
X2310342123103422GC2GENIChomozygous108439824
X2310342223103423AT2GENIChomozygous108439826
X2310384923103850CG3GENIChomozygous108476285
X2311234923112350AG7GENIChomozygous108239628
X2311762123117622CT7GENIChomozygous108239630
X2311817423118175TC13GENIChomozygous108239632
X2311952623119527GC11GENIChomozygous108239636
X2311961623119617TG8GENIChomozygous108239638
X2311996923119970CT14GENIChomozygous108239640
X2312159723121598GC14GENIChomozygous108373190
X2312322723123228CT22GENIChomozygous108373192
X2312352823123529TC11GENIChomozygous108373194
X2312411323124114CT13GENIChomozygous108239642
X2312782223127823AT10GENIChomozygous108239644
X2312864523128646TC5GENIChomozygous108239646
X2313098023130981CG9GENIChomozygous108239648
X2313146423131465CA20GENIChomozygous108239650
X2313278023132781TC10GENIChomozygous108373200
X2313528323135284CA8GENIChomozygous108239652
X2313876323138764TC12GENIChomozygous108239654
X2314172723141728GA8GENIChomozygous108373202
X2314486023144861AT9GENIChomozygous108239656
X2314569323145694CT20GENIChomozygous108239658