chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2309316423093165CG10GENIChomozygous125102073
X2309318623093187GA12GENIChomozygous125102074
X2309522223095223TC8GENIChomozygous125102075
X2309605623096057TA16GENIChomozygous125148262
X2310022223100223CT5GENICheterozygous125128983
X2311126423111265TC5GENIChomozygous125128984
X2311817223118173AG9GENICheterozygous125102077
X2311830523118306TC4GENICheterozygous125148263
X2311846123118462GT12GENIChomozygous125102078
X2311952423119525CG13GENIChomozygous125102079
X2311961423119615AC7GENIChomozygous125102080
X2311996723119968GA10GENICheterozygous125102081
X2312159523121596CG7GENIChomozygous125102082
X2312352623123527AG8GENIChomozygous125102083
X2312411123124112GA12GENIChomozygous125102084
X2312782023127821TA8GENIChomozygous125102085
X2312864323128644AG18GENIChomozygous125102086
X2313097823130979GC10GENIChomozygous125102087
X2313146223131463GT11GENIChomozygous125102088
X2313277823132779AG8GENIChomozygous125102089
X2313528123135282GT11GENIChomozygous125102090
X2313876123138762AG8GENIChomozygous125102091
X2314485823144859TA8GENIChomozygous125128987
X2314569123145692GA7GENIChomozygous125102092