chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2196237380196237381TC21GENIChomozygous110195917
2196239216196239216ACA14GENIChomozygous127722567
2196239713196239714AG21GENIChomozygous110195918
2196239797196239798TC19GENIChomozygous110195919
2196239839196239853GAGATACTGTCTCA21GENIChomozygous134184459
2196240950196240951AC4GENIChomozygous110195920
2196241038196241039AG16GENIChomozygous110195921
2196241136196241136A13GENICpossibly homozygous127722568
2196247310196247311AG18GENIChomozygous110195925
2196247609196247609A17GENIChomozygous127722569
2196251394196251395TC18GENIChomozygous110195927
2196251990196251994AAAC14GENIChomozygous131298986
2196252106196252107TG24GENIChomozygous110195928
2196253047196253047ATTTA12GENIChomozygous127722571
2196257290196257291CT8GENIChomozygous110195933
2196257657196257658AG17GENIChomozygous110195934
2196259419196259420GA18GENIChomozygous110195936
2196262435196262435AAGAAG11GENIChomozygous127722572
2196266494196266502AAACAAAC18GENIChomozygous131298989
2196244312196244313TC16GENIChomozygous111354800
2196257113196257114CT23GENIChomozygous111354806
2196261337196261338AG20GENIChomozygous111354808
2196263463196263464TC11GENICheterozygous120156476
2196263464196263465TC12GENICheterozygous134189423
2196270839196270839C21GENIChomozygous134184460