chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210881635210881636AG36GENICpossibly homozygous806592068
2210882761210882762GA39GENIChomozygous806592069
2210883146210883147GA51GENICpossibly homozygous806592070
2210883147210883148CT53GENICpossibly homozygous806592071
2210883210210883211TC69GENIChomozygous806592072
2210883782210883783CT69GENIChomozygous806592073
2210884805210884806GT53GENICpossibly homozygous806592074
2210885012210885013AC49GENIChomozygous806592075
2210886860210886861TC30GENICheterozygous806592076
2210887501210887502AC44GENICheterozygous806592077
2210887535210887536CT101GENICheterozygous806592078
2210887998210887999GT62GENICpossibly homozygous806592079
2210889226210889227CT56GENIChomozygous806592080
2210890256210890257GA52GENIChomozygous806592081