chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204722551547225516CG7GENIChomozygous109212330
204722605747226058GT5GENICheterozygous109460410
204722627347226274TC4GENIChomozygous109212334
204722627447226275CT4GENIChomozygous109276466
204723127247231273GT2GENIChomozygous109276468
204723130847231309TC11GENIChomozygous109276470
204723130947231310CT11GENIChomozygous109276472
204723586347235864AC22GENIChomozygous109212336
204723586447235865CA22GENIChomozygous109212338
204723964747239648AT17GENIChomozygous109212340
204723966947239670AT15GENIChomozygous109212342
204723967447239675GC17GENIChomozygous109212344
204723968647239687GC17GENIChomozygous109212346
204723970947239710TA14GENIChomozygous109212348
204723974947239750TA17GENIChomozygous109212350
204723975147239752TA18GENIChomozygous109212352
204723985847239859TA12GENIChomozygous109212354
204726078347260784CT27GENICheterozygous109212360
204726079647260797GA24GENICheterozygous109212362
204726273447262735GA32GENICheterozygous109212364
204726277147262772AC47GENICheterozygous109212366
204726281047262811AG53GENICheterozygous109212368
204726283247262833TC59GENICheterozygous109212370
204726287747262878CG66GENICheterozygous109212374
204726288247262883AC65GENICheterozygous109212376
204726288847262889GA67GENICheterozygous109212378
204726297647262977AG52GENICheterozygous109276476
204726300047263001CT53GENICheterozygous109276478
204726300747263008AG49GENICheterozygous109276480
204726300947263010CT48GENICheterozygous109276482
204726302147263022TC54GENICheterozygous109212380
204726309947263100TG49GENICheterozygous109212382