chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142293282322932824GA10GENIChomozygous881298039
142293304222933043CT6GENIChomozygous881298040
142293466522934666AG21GENIChomozygous881298041
142293636622936367GA17GENIChomozygous881298042
142293700922937010CG3GENICheterozygous881298043
142293709522937096CG7GENICheterozygous881298044
142293715222937153CG4GENICheterozygous881298045
142293739722937398GA13GENIChomozygous881298046
142293764622937647TA23GENIChomozygous881298047
142293768322937684TC14GENIChomozygous881298048
142293849422938495TC10GENIChomozygous881298049
142293978322939784CT5GENICheterozygous881298051
142294094922940950AG17GENIChomozygous881298052
142294134322941344CA26GENIChomozygous881298053
142294277722942778CA14GENIChomozygous881298054
142294389522943896AG17GENIChomozygous881298055
142294402922944030TA8GENIChomozygous881298056
142294751922947520CA5GENIChomozygous881298057
142294752122947522AC5GENIChomozygous881298058
142294826322948264CA11GENIChomozygous881298059
142295235922952360CG19GENIChomozygous881298060
142295552222955523CT15GENIChomozygous881298061
142295557922955580GT17GENIChomozygous881298062