chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117724263117724264TTAAC16GENICpossibly homozygous60813115
1117724274117724275C-12GENICheterozygous62153119
1117724276117724279GGC---12GENICheterozygous62153121
1117724279117724280CCTGATAACAAAA12GENICheterozygous62153123
1117724283117724284TTA16GENICheterozygous60813119
1117724302117724304TT--16GENICheterozygous60813120
1117724354117724355TTGTACAACA39GENICheterozygous60813121
1117724449117724450GGTCACCAT26GENICheterozygous62153125
1117724450117724451GGCTTATCA27GENICheterozygous62153127
1117724470117724482CAGACTATGGCT------------37GENICheterozygous62153129
1117724767117724768TTC29GENICheterozygous60813129