chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1097584599758460AG16GENICpossibly homozygous51323371
1097593239759324TC5GENIChomozygous52110712
1097593299759331AT--5GENICheterozygous51323374
1097603079760308TC16GENICheterozygous51323376
1097609349760935AG13GENICpossibly homozygous51323377
1097611849761185CG12GENIChomozygous51323379
1097635459763546GA29GENIChomozygous51616013
1097638499763850CG9GENIChomozygous51323383
1097644139764414CT24GENICpossibly homozygous51616015
1097644539764454CCTG18GENICheterozygous51323384
1097649249764925GA26GENICpossibly homozygous52110714
1097652379765238CA11GENICpossibly homozygous51616017
1097662189766219TC11GENICpossibly homozygous51323396
1097667739766774AG14GENICpossibly homozygous51323398
1097692809769281G-19GENICpossibly homozygous51323401
1097711439771145AA--2GENICheterozygous51616020
1097721099772110AT15GENICpossibly homozygous52110716
1097724139772414AG20GENIChomozygous51323406
1097727989772799TC17GENICpossibly homozygous51323407
1097755589775559TG7GENICpossibly homozygous51323411
1097755729775573TG14GENIChomozygous51323412
1097900589790059GA7GENIChomozygous51323417
1097904729790473AATGTTCTC5GENIChomozygous51616031
1097913919791392GA19GENICpossibly homozygous52110720
1097922459792246AT16GENIChomozygous51323418
1097928399792840A-16GENIChomozygous51323419
1097941619794162GA19GENIChomozygous52110722
1097945689794569TC19GENICpossibly homozygous51616034
1097953839795384TTCCTTC4GENIChomozygous51616036
1097977489797749AG18GENIChomozygous51616037
1097979479797948GA14GENICpossibly homozygous52110724
1097983369798337TC11GENIChomozygous51323425
1097985149798515AC20GENIChomozygous51323426
1097990889799089GA13GENICpossibly homozygous51323427
1097991309799131AG12GENICpossibly homozygous51323428
1097991859799186TG19GENIChomozygous51323429
1097992109799211GGA2GENICheterozygous51616038
1097996159799616CCAA1GENIChomozygous51616039