chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178645395486453955GA45GENIChomozygous142627009
178645504786455048AG42GENIChomozygous140204788
178645812586458126GA56GENIChomozygous142627010
178645852086458521AG53GENIChomozygous142627011
178646301586463016GC49GENIChomozygous142627012
178646385086463851GA42GENIChomozygous142627013
178646433586464336TC59GENIChomozygous140204795
178646433686464337TC59GENIChomozygous140204796
178646511586465116GA29GENIChomozygous142627014
178646785086467851T61GENIChomozygous140042485
178646894386468944GA54GENIChomozygous142627015
178647056486470565GA62GENIChomozygous142627016
178647079186470792GA54GENIChomozygous142627017
178647148886471489GA50GENIChomozygous142627018
178647618986476190GC52GENIChomozygous142627019
178647656886476569GC38GENICpossibly homozygous142627020
178647674286476743CG44GENIChomozygous140204801
178647977086479771CT28GENICpossibly homozygous142627021
178648245786482458TC20GENIChomozygous142627022
178648337586483376CG38GENIChomozygous142627023
178648398986483989A17GENIChomozygous140042487
178648409786484098TC56GENIChomozygous142627024
178648440186484402TA49GENIChomozygous140204804
178648443686484437CT47GENIChomozygous142627025
178648492686484927CT46GENIChomozygous140204805
178648719486487195GA72GENIChomozygous142627026
178648865786488658A49GENICpossibly homozygous140042488
178649005186490052CT54GENIChomozygous142627027
178649425986494260TA46GENIChomozygous140204806
178649670886496709CT44GENIChomozygous142627028
178646966986469675TCTGTG37GENIChomozygous142589297
178649736386497363GCAAGG45GENIChomozygous142589298
178648022086480221AG33GENIChomozygous403426164