chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139653888139653889TC6GENIChomozygous126541142
7139654904139654918GTGGTAGAGCACTT12GENIChomozygous128528641
7139656585139656585ATTCTTTT8GENIChomozygous128528642
7139657618139657619AG16GENIChomozygous115937137
7139656157139656158GA15GENIChomozygous115937134
7139656331139656332CT19GENIChomozygous115937135
7139657403139657404TG19GENIChomozygous115937136
7139657893139657893C22GENIChomozygous128528643
7139657908139657908GCT19GENIChomozygous128528644
7139657913139657917TCAC20GENIChomozygous128528645
7139657923139657923T18GENIChomozygous128528646
7139657926139657926GGT18GENIChomozygous128528647
7139658125139658126TG20GENIChomozygous115937138
7139658343139658344TG10GENIChomozygous115937139
7139658412139658413AG11GENIChomozygous115937140
7139660396139660397GT18GENIChomozygous115937141
7139662596139662597AC14GENIChomozygous115937142
7139662690139662691AC17GENIChomozygous115937143
7139663291139663292A9GENIChomozygous128528648
7139664006139664006AAAC11GENIChomozygous128528649
7139664443139664444GA19GENIChomozygous115937145
7139665621139665622AG11GENIChomozygous115937146
7139666825139666826AG17GENIChomozygous115937147
7139666944139666945A18GENIChomozygous128528650
7139667301139667303TA9GENIChomozygous128528651
7139668011139668012GA10GENIChomozygous115937148
7139669037139669038AG21GENIChomozygous115937150
7139669539139669540TC17GENIChomozygous115937151
7139669606139669607TC22GENIChomozygous115937152
7139670351139670352GT16GENIChomozygous115937153
7139671307139671308TG16GENIChomozygous115937154
7139676071139676072CA20GENIChomozygous115937155
7139677293139677294A14GENIChomozygous128528653
7139681863139681879CTCTCTCTCTCTCTCT8GENIChomozygous128528654
7139682053139682054TG12GENIChomozygous115937156
7139682928139682939ACCTGTATGCA14GENIChomozygous128528655
7139682941139682942TA15GENIChomozygous115937157
7139683976139683977CT14GENIChomozygous115937158
7139684260139684261TA14GENIChomozygous115937159