chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116086080116086081AAAAAC21GENICheterozygous52827368
8116086581116086582AG13GENIChomozygous52827369
8116088536116088537AG19GENIChomozygous52827376
8116090188116090189AG10GENICheterozygous52827383
8116090195116090196TTAAATCCCC11GENICheterozygous52827384
8116091185116091186AG19GENIChomozygous52827385
8116091358116091359GA13GENICheterozygous52827386
8116091830116091831TC18GENICheterozygous52827387
8116091940116091941TG14GENICheterozygous52827388
8116092163116092164CT14GENICheterozygous53305570
8116092224116092225CT12GENICheterozygous52827390
8116092698116092699TTG10GENIChomozygous52827391
8116092970116092972CT--10GENICheterozygous52827392
8116093018116093019GA17GENICheterozygous52827393
8116093266116093268GC--15GENICheterozygous52827394
8116094636116094637AG13GENIChomozygous52827396
8116095057116095058CT10GENICheterozygous52827397
8116095694116095695GA11GENICheterozygous52827398
8116096390116096391TC17GENICheterozygous52827399
8116096763116096764TC9GENICheterozygous52827400
8116097145116097146CT12GENICheterozygous52827403
8116097893116097894CT9GENICheterozygous52827405
8116098206116098207TC7GENICheterozygous52827407
8116099170116099171CT22GENICheterozygous52827408
8116099289116099290AT14GENICheterozygous52827409
8116099784116099785AG10GENICheterozygous52827410
8116099833116099834GA9GENICheterozygous52827411
8116100358116100359CT11GENICheterozygous52827412
8116100785116100786GA19GENICheterozygous52827413
8116101091116101092CT20GENIChomozygous52827414
8116101289116101290GA14GENICheterozygous52827415
8116102209116102210GA9GENIChomozygous52827417
8116102467116102468CG15GENICheterozygous53305573
8116102621116102622GA15GENICheterozygous52827418
8116102988116102989GC14GENICheterozygous53305574
8116103538116103539AG18GENICheterozygous53305575
8116103976116103977CT14GENICheterozygous52827422
8116104318116104319AG13GENIChomozygous52827423
8116104662116104663AT13GENIChomozygous52827424