chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41491328214913283CCT9GENICheterozygous56761940
41491367114913672GA27GENICpossibly homozygous56761941
41491382714913831TTTT----7GENICheterozygous56761942
41491383014913831T-7GENICheterozygous56761943
41491562114915622TTACACACACACACACAC4GENIChomozygous58452922
41491571814915726AGAAAGAA--------6GENIChomozygous58404286
41491823714918238AG31GENIChomozygous56761951
41491851514918516TA18GENIChomozygous56761952
41491874714918751TTTG----7GENIChomozygous56761953
41491878914918790TTTTTTTG13GENIChomozygous56761955
41491974914919750CT22GENIChomozygous56761956
41492017614920177GT31GENIChomozygous56761957