chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3105204157105204158TC39GENICpossibly homozygous111993345
3105204281105204282CT18GENIChomozygous111993347
3105204325105204326GA34GENIChomozygous111993349
3105204466105204467GA27GENICpossibly homozygous111993351
3105205088105205089GA23GENIChomozygous111993353
3105205258105205259CT23GENIChomozygous111993355
3105205269105205270CG27GENIChomozygous111993357
3105205377105205378AG32GENIChomozygous111993359
3105205482105205483TA22GENIChomozygous111993361
3105205841105205842AG32GENIChomozygous111993363
3105206138105206139AT35GENIChomozygous111993365
3105210968105210969CT33GENIChomozygous111993369
3105214606105214607TA26GENIChomozygous111993371