chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130227861130227862TC11GENICpossibly homozygous54521239
7130228472130228473AG23GENIChomozygous54110633
7130229049130229050C-9GENICheterozygous54110634
7130229049130229050CT10GENICheterozygous54922374
7130230110130230111AG18GENICpossibly homozygous54110636
7130230762130230763GGCGGGGGGGAAGGGGCCTTACCCTCCCTA5GENIChomozygous55408813
7130231955130231956CT13GENICpossibly homozygous54521243
7130232372130232373CT10GENIChomozygous54754837
7130232647130232648T-3GENICheterozygous54754839
7130233261130233262AG10GENICpossibly homozygous54110642