chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6126282869126282870AT24GENIChomozygous114981281
6126283775126283776AG26GENIChomozygous114981282
6126284967126284968TC17GENIChomozygous114981283
6126285743126285744TA11GENIChomozygous114981284
6126286353126286354AG15GENIChomozygous114981285
6126291907126291908AG28GENIChomozygous114981286
6126289972126289976TTGT15GENIChomozygous128393535
6126290580126290580TGG10GENIChomozygous128393536
6126298003126298004AG23GENIChomozygous114981287
6126300319126300320AT22GENIChomozygous114981288
6126300373126300374GA31GENIChomozygous114981289
6126301302126301312ACGGCAGGTT20GENIChomozygous128393537
6126305715126305715TGTGTGTGTGTA7GENICheterozygous128393538
6126305745126305746AT6GENIChomozygous122636186
6126305747126305748AT6GENIChomozygous122636187
6126305749126305750AT6GENIChomozygous122636188
6126303956126303957AT18GENIChomozygous118575559
6126305751126305752AT10GENICheterozygous129933967
6126305786126305787GA17GENIChomozygous115080548
6126307195126307196CG19GENIChomozygous114981291
6126307291126307292GA25GENIChomozygous114981292
6126307350126307351TC30GENIChomozygous114981293
6126307838126307839GC26GENIChomozygous114981294
6126308031126308032TC14GENIChomozygous114981295