chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2057336945733695GC11GENIChomozygous109234357
2057342945734295GT13GENIChomozygous109079037
2057343295734330GT6GENIChomozygous109297228
2057355045735505GA7GENIChomozygous109079039
2057394575739458TC15GENIChomozygous109234363
2057399105739911AG10GENIChomozygous109234364
2057404615740462AG9GENIChomozygous109079065
2057407615740762GA5GENIChomozygous109234367
2057413555741356AG10GENIChomozygous109234369
2057414775741478AG13GENIChomozygous109079069
2057414915741492TC11GENIChomozygous109079071
2057415685741569TC17GENIChomozygous109079075
2057417175741718TC7GENIChomozygous109079077
2057417335741734TC8GENIChomozygous109079079
2057425135742514AG8GENIChomozygous109079083
2057427795742780CT7GENIChomozygous109079085
2057428985742899TC20GENIChomozygous109079087
2057430085743009TC10GENIChomozygous109079089
2057434015743402CT10GENIChomozygous109079091
2057436345743635CT9GENIChomozygous109234370
2057439405743941CT7GENIChomozygous109079093
2057447445744745CA12GENIChomozygous109079097
2057448325744833TC7GENIChomozygous109079099
2057448515744852AG4GENIChomozygous109079101
2057456835745684AG19GENIChomozygous109079105
2057457305745731GA6GENIChomozygous109079107
2057457415745742CT4GENIChomozygous109234371
2057457705745771GT7GENIChomozygous109079109
2057462055746206GA12GENIChomozygous109079117
2057466825746683AG8GENIChomozygous109234372
2057470125747013CT14GENIChomozygous109234373
2057476055747606AG6GENIChomozygous109079132
2057477375747738AG9GENIChomozygous109079134
2057479815747982AC11GENIChomozygous109079136
2057487345748735AC13GENIChomozygous109079140
2057506165750617CT19GENIChomozygous109234375
2057522855752286CT16GENIChomozygous109234376
2057520595752060TG8GENIChomozygous125200509
2057529475752948CT8GENIChomozygous109234377
2057534745753475CT10GENIChomozygous109297236
2057544505754451GC13GENICheterozygous109234378
2057545155754516CT11GENIChomozygous109234379
2057546155754616GA6GENIChomozygous109234380