chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119144577119144578AG24GENIChomozygous115851174
7119150645119150646AG25GENIChomozygous115851176
7119150999119151000CT35GENIChomozygous115851178
7119151113119151114AT34GENIChomozygous115851180
7119151266119151267TC33GENIChomozygous115851182
7119151512119151513TA25GENIChomozygous115851184
7119151622119151623CT23GENIChomozygous115851186
7119151904119151980TCTGAGAAGGCAGCCCTCTGACGGACGTGATGCCGGTGCATGCTTACAAGCACTGCACTTGGAGGGTGGCAGGGGA10GENIChomozygous128511279
7119148191119148195TGGG26GENIChomozygous128511275
7119149940119149941T12GENICpossibly homozygous128511277
7119151130119151130C29GENIChomozygous128511278
7119149170119149171AC9GENIChomozygous129947080
7119149170119149170C9GENIChomozygous129939139
7119149944119149945TG11GENICpossibly homozygous118259005
7119149946119149947TG12GENICpossibly homozygous118259007
7119149948119149949TG11GENICpossibly homozygous118259009
7119152381119152382CT27GENIChomozygous115851188
7119152882119152883T23GENIChomozygous128511280
7119153213119153213C30GENIChomozygous128511281
7119153214119153215GA31GENIChomozygous118259011
7119153931119153932CG27GENIChomozygous115851190
7119153943119153944GA26GENIChomozygous115851192
7119154619119154620CT22GENIChomozygous115851194
7119154789119154790TC26GENIChomozygous115851196
7119154819119154820CG22GENIChomozygous115851198
7119155758119155759GT17GENIChomozygous115851200
7119156267119156268CA23GENIChomozygous115851202
7119156776119156777CT28GENIChomozygous115851204
7119156800119156801GA28GENIChomozygous115851206
7119156862119156862GA35GENIChomozygous128511282
7119157193119157194TC29GENIChomozygous115851208
7119157837119157838AG23GENIChomozygous115851210