chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1797500119750012CT65GENIChomozygous110953011
1797514549751455TG49GENIChomozygous110953013
1797528029752803TC59GENIChomozygous110953015
1797532159753216TA65GENIChomozygous110953017
1797507979750798TC45GENIChomozygous119263822
1797539609753961GA45GENIChomozygous111479515
1797563649756365TC51GENIChomozygous110953019
1797569959756996TC64GENIChomozygous110953021
1797584399758440CA59GENIChomozygous110953023
1797588779758878TC55GENIChomozygous110953025
1797597019759702CT61GENIChomozygous110953027
1797602539760254AG59GENIChomozygous110953029
1797610519761052GA66GENIChomozygous110953031
1797621779762178TC61GENIChomozygous110953033
1797624149762415TA43GENIChomozygous110953035
1797625009762501CA60GENIChomozygous110953037
1797625579762558TC58GENIChomozygous110953039
1797626809762681AG52GENIChomozygous110953041
1797626919762692CT51GENIChomozygous110953043
1797627219762722TC43GENIChomozygous110953045
1797547409754742TG39GENIChomozygous129421280
1797514519751454ATC49GENIChomozygous129421278
1797517099751710T37GENICpossibly homozygous129421279
1797605249760524T45GENICpossibly homozygous129421281
1797607309760730A56GENIChomozygous129421282
1797609819760982T61GENIChomozygous129421283