chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------3GENIChomozygous717790574
85378107053781071CT15GENICheterozygous579793365
85378121053781211AG5GENIChomozygous579793366
85378133353781334AG10GENICheterozygous579793367
85378146653781467AG14GENIChomozygous579793368
85378180553781806AG9GENIChomozygous579793369
85378193153781932TTTA2GENICheterozygous717790575
85378200853782013GTTTG-----6GENICheterozygous717790578
85378241353782414CT16GENIChomozygous579793370
85378277053782771GA8GENIChomozygous579793371
85378331953783320AG16GENIChomozygous579793372
85378373853783739GT13GENIChomozygous579793373
85378379353783794TC9GENIChomozygous579793374
85378438353784384A-4GENICheterozygous717790579
85378450953784517CGCGCGCA--------3GENIChomozygous717790580
85378454153784542CCTAATTAA1GENIChomozygous717790581
85378454453784545AG1GENIChomozygous581346763
85378457253784573AT9GENIChomozygous581346764
85378477253784773AG9GENIChomozygous581346765
85378500253785003CT13GENIChomozygous581346766
85378539453785395AG11GENIChomozygous581346767
85378544653785447CT9GENIChomozygous581346768
85378563753785638A-14GENICpossibly homozygous717790582
85378589753785898AC14GENICpossibly homozygous581346769
85378598653785987AC9GENIChomozygous581346770
85378644453786445TC1GENIChomozygous581346771
85378677453786775GA14GENICheterozygous581346772
85378689053786891AG22GENIChomozygous581346773
85378691253786913GA22GENIChomozygous581346774
85378713253787133CG3GENIChomozygous581346775
85378718953787190AG7GENIChomozygous581346776