chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125744277125744278AC13GENICpossibly homozygous580501382
7125744898125744899GA19GENICpossibly homozygous580501383
7125745046125745047TA10GENIChomozygous580501384
7125745150125745151AT6GENIChomozygous580501385
7125745717125745718GT8GENIChomozygous580501386
7125745937125745938GA22GENIChomozygous580501387
7125746484125746485AG22GENICpossibly homozygous580501388
7125746618125746619GA30GENIChomozygous580501389
7125747534125747535CT30GENIChomozygous579950186
7125747571125747572GA8GENICpossibly homozygous579950187
7125748329125748330AG24GENICpossibly homozygous579950188
7125748927125748928GA34GENICpossibly homozygous579950189
7125749012125749013GA19GENIChomozygous579950190
7125749414125749415AG16GENIChomozygous579950191
7125749466125749467TTG15GENIChomozygous717767105
7125751521125751522AATT2GENIChomozygous717767107
7125752000125752001TC26GENICpossibly homozygous579950192
7125752756125752757GA14GENIChomozygous579950193
7125753877125753878CCTG10GENICheterozygous717767108
7125753897125753898CT6GENICheterozygous579950194
7125753949125753950GA12GENICpossibly homozygous579950195
7125754274125754275AG13GENIChomozygous579950196
7125754320125754321CT11GENIChomozygous579950197
7125754367125754368CT16GENIChomozygous579950198
7125754379125754380GC14GENICpossibly homozygous579950199
7125755157125755158GA11GENICheterozygous579950200
7125755666125755667CT22GENICpossibly homozygous579950201
7125755703125755704CT25GENICpossibly homozygous579950202
7125756500125756501TC20GENICpossibly homozygous579950203
7125756849125756850AG9GENICpossibly homozygous579950204
7125757153125757154TTA4GENICheterozygous717767109