chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122089430720894308GA20GENIChomozygous139108157
122089440320894403TGC20GENIChomozygous139046385
122089554620895547CG19GENIChomozygous139108158
122089576520895766CT28GENIChomozygous139108159
122089736820897369TA20GENIChomozygous139108161
122089741320897414AG17GENIChomozygous139108162
122089745820897459TC13GENIChomozygous139108163
122089765420897655TG28GENIChomozygous139108167
122089789620897897TC28GENIChomozygous139108168
122089843320898434TC20GENIChomozygous139108170
122089902720899033AAAAAG20GENIChomozygous139046386
122089937920899380CT23GENIChomozygous139108174
122089873320898734CT21GENIChomozygous139108171
122089908520899086AG24GENIChomozygous139108172
122089792020897921GT26GENICpossibly homozygous145774245
122089939320899394TA21GENIChomozygous139108175
122089942020899421CA20GENIChomozygous139108176
122089942420899425TC20GENIChomozygous139108177
122090045320900454G24GENIChomozygous139046387
122090060920900610AC16GENIChomozygous139108179
122090064820900649CG18GENIChomozygous145774246
122090067020900671CT17GENIChomozygous145774247
122090073520900736CA20GENIChomozygous139108180
122090089220900893CT24GENICpossibly homozygous145774248
122090100520901006TA21GENIChomozygous139108181
122090175920901759CAGCTCCGCCCAGGCCGC18GENIChomozygous139046388
122090464220904643CT19GENIChomozygous139108191
122089951520899516AG23GENICheterozygous154734866
122090165120901652TC18GENIChomozygous139108183
122090188320901884AC22GENIChomozygous139108184
122090211420902115TA24GENIChomozygous139108185
122090304120903042TC21GENIChomozygous139108187
122090402320904024AG20GENIChomozygous139108189
122090430020904301CT29GENIChomozygous142322866
122090462220904623CT19GENIChomozygous145774249
122089946720899469CT18GENIChomozygous143520366
122089951520899516A23GENIChomozygous403903367
122090003420900036CA31GENIChomozygous145770869