chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161070513010705131AG18GENIChomozygous632843009
161070820810708209T-12GENICpossibly homozygous746456223
161071168810711689AG32GENIChomozygous632843010
161071211010712112GT--7GENICheterozygous746456226
161071365410713655CT25GENIChomozygous632843011
161071616010716161CT26GENIChomozygous632843012
161071898410718985C-21GENIChomozygous746456228
161071902010719021AT19GENIChomozygous632843013
161071905610719058CC--13GENIChomozygous746456229
161072195710721958AG19GENIChomozygous632843014
161072413510724136GGCCCC4GENIChomozygous746456230
161072553210725533AG28GENIChomozygous632843015
161073131710731332TTCTTTTCTTTTCTT---------------7GENIChomozygous746456232
161073280110732802GT32GENIChomozygous632843016
161073280210732803CA34GENIChomozygous632843017
161073310110733102CA37GENIChomozygous632843018
161073338010733381TC32GENIChomozygous632843019
161073567510735676TTCAGGGGC7GENIChomozygous746456235
161073582310735824AG10GENIChomozygous632843020
161074541310745414AG34GENIChomozygous632843021
161074650810746509TTTGCCAGGCAAGCG5GENIChomozygous746456236
161074651210746513TTACCACTGAGCTAAA5GENIChomozygous746456237
161074651410746515CCCCCAA4GENIChomozygous746456238
161075243610752437TC16GENIChomozygous632843022
161075301710753018TC22GENIChomozygous632843023
161075466610754667GGACAC9GENICheterozygous746456239
161075466610754667GGACACAC9GENICheterozygous746456240
161075975210759753TC15GENIChomozygous632843024
161076253410762535TA29GENIChomozygous632843025
161076324510763246A-6GENICheterozygous746456242
161076901210769013CT30GENIChomozygous632843026