chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155526136655261367TC16GENIChomozygous48314020
155526140855261412AAAA----17GENIChomozygous49054476
155526141155261412AACTGT17GENIChomozygous49054478
155526141455261415AT18GENIChomozygous48602483
155526143355261434TC14GENIChomozygous48314021
155526144855261449AT14GENIChomozygous48314022
155526170555261706TTATGTC28GENIChomozygous48314024
155526170755261708TTGCTATGGAGGAACCTCA28GENIChomozygous48314026
155526811355268114AAGAATGAAAGCTGCAAAGACCAGGGGTTCAGGAAAGTATTCTCTGCCCGGGTGAAACTGGCTGGGAGTGGGAAGGAGAGGTAGGAAGGGATGTGGAGAGTCAGGT27GENIChomozygous49054480
155526817655268177CG15GENIChomozygous48314033
155526817855268179C-16GENIChomozygous48314034
155526152555261526GGCA7GENICpossibly homozygous49121878
155526443655264438TG--14GENICheterozygous49086217