chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222677480222677481AG6GENIChomozygous108547005
1222677529222677530AT6GENIChomozygous120476010
1222679150222679151TC10GENIChomozygous108547007
1222682608222682609GT6GENIChomozygous108547009
1222684559222684560GA8GENIChomozygous108547011
1222685614222685615AG7GENIChomozygous108547013
1222685901222685902GA4GENIChomozygous108547015
1222687721222687722TC13GENIChomozygous108547017
1222689564222689565CG8GENIChomozygous108547019
1222690836222690837TG10GENIChomozygous108547021
1222690922222690923GA16GENIChomozygous108547023
1222691719222691720GA13GENIChomozygous108547025
1222692444222692445TG7GENIChomozygous108547027
1222692514222692515AG7GENIChomozygous108547029
1222693970222693971TC10GENIChomozygous108547033
1222694851222694852CT12GENIChomozygous108547035
1222694866222694867CT11GENIChomozygous108547037
1222695611222695612AG14GENIChomozygous108547039
1222698337222698338CT8GENIChomozygous108547047
1222698687222698688GA10GENIChomozygous108547049
1222699773222699774TC11GENIChomozygous108547053
1222702043222702044GA15GENIChomozygous108547055
1222702925222702926AC6GENIChomozygous108547058
1222705915222705916TC15GENIChomozygous108547066
1222706230222706231GA6GENIChomozygous108547068
1222709359222709360TC10GENIChomozygous108547070
1222713607222713608CG3GENIChomozygous108547076
1222715631222715632TA5GENIChomozygous108547078
1222720409222720410TA13GENIChomozygous108547080
1222722834222722835TC8GENIChomozygous108547082
1222722983222722984CT9GENIChomozygous108547084
1222724133222724134CT6GENIChomozygous108547086
1222727682222727683CT12GENICpossibly homozygous108547088
1222728237222728238GA11GENIChomozygous108547090
1222728915222728916CT9GENICpossibly homozygous108547092
1222733522222733523AT4GENIChomozygous108547096