chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3105203612105203613GT14GENIChomozygous125831015
3105203630105203631CG10GENIChomozygous125831017
3105204157105204158TC15GENIChomozygous111993345
3105204281105204282CT18GENIChomozygous111993347
3105204325105204326GA19GENIChomozygous111993349
3105204466105204467GA16GENIChomozygous111993351
3105205088105205089GA21GENIChomozygous111993353
3105205258105205259CT23GENICpossibly homozygous111993355
3105205269105205270CG16GENICheterozygous111993357
3105205377105205378AG32GENIChomozygous111993359
3105205482105205483TA23GENIChomozygous111993361
3105205841105205842AG10GENIChomozygous111993363
3105206138105206139AT23GENIChomozygous111993365
3105210968105210969CT24GENIChomozygous111993369
3105214606105214607TA14GENIChomozygous111993371