chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905051449050515TTC11GENIChomozygous50230908
124905051549050516TTTTC5GENIChomozygous50230910
124905051949050520AC11GENIChomozygous50575612
124905052349050524AC11GENIChomozygous50230912
124905052749050528AC11GENIChomozygous50230914
124905053149050532AC14GENIChomozygous50230916
124905053549050536AC13GENIChomozygous50230918
124905053949050540AC10GENIChomozygous50230920
124905054349050544AC10GENIChomozygous50230922
124905139449051395CA6GENIChomozygous50230926
124905175549051756GGT3GENICheterozygous50546601
124905230049052301AAGT13GENIChomozygous50230930
124905236449052365AT19GENIChomozygous50230932
124905276849052769TC19GENIChomozygous50230934
124905539549055396AC7GENIChomozygous50230936
124905566749055668GGA6GENIChomozygous50230938
124905572249055723TG1GENIChomozygous50513695
124905593049055933AAG---4GENIChomozygous50513697
124905607749056078CCA10GENIChomozygous50230940
124905614649056147CA5GENIChomozygous50230942
124905616249056163AAGCTATTTCTTACTCCCAACTTCCCCGATGGGCACCCATTACCTGTTCCCTGCTGC11GENIChomozygous50513699