chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122344831823448319AC46GENIChomozygous818670375
122344948923449490CT56GENIChomozygous818670376
122345129423451295CT8GENIChomozygous818670377
122345273923452740TG53GENIChomozygous818670378
122345301523453016GA48GENICheterozygous818670379
122345337723453378CT64GENICheterozygous818670380
122345338523453386CT63GENICheterozygous818670381
122345340623453407AC67GENICheterozygous818670382
122345371623453717GA63GENIChomozygous818670383
122345393023453931TG34GENIChomozygous818670384
122345401223454013TC23GENIChomozygous818670385
122345479723454798AT28GENICheterozygous818670386
122345482323454824TA29GENICheterozygous818670387
122345501223455013TC66GENICheterozygous818670388
122345502823455029TG59GENICheterozygous818670389
122345508723455088TC63GENICheterozygous818670390
122345538923455390A-45GENIChomozygous818670391
122345549223455493AT40GENICheterozygous818670392
122345549323455494CG39GENICheterozygous818670393
122345551923455520AG40GENICheterozygous818670394
122345552023455521CA40GENICheterozygous818670395
122345552523455526TC41GENICheterozygous818670396
122345557323455574AT34GENICheterozygous818670397
122345559223455593AG36GENICheterozygous818670398
122345561323455614GA33GENICheterozygous818670399
122345563723455638GA29GENICheterozygous818670400
122345564523455646TC22GENICheterozygous818670401
122345564623455647AT22GENICheterozygous818670402
122345565823455659CT23GENICheterozygous818670403
122345568823455689CT17GENICheterozygous818670404
122345572723455728GT16GENICheterozygous818670405
122345579323455794TC17GENICheterozygous818670406
122345579623455797AG16GENICheterozygous818670407
122345581723455818GA17GENICheterozygous818670408
122345582623455827TC13GENICheterozygous818670409
122345584123455842AG13GENICheterozygous818670410
122345584823455849GC10GENICheterozygous818670411
122345584923455850TC10GENICheterozygous818670412
122345585123455852GT10GENICheterozygous818670413