chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108683934986839350GA15INTERGENIChomozygous51528966
108684105086841051CA7INTERGENICpossibly homozygous51528967
108684106186841062AT6INTERGENIChomozygous51528968
108684124986841250TA9INTERGENICheterozygous51528970
108684254586842546CT9INTERGENICheterozygous51528974
108684277686842777TA5INTERGENIChomozygous51528975
108684292386842924CG6INTERGENIChomozygous51528976
108684852086848521CT3INTERGENIChomozygous51528982
108685076286850763TC14INTERGENICpossibly homozygous51528983
108685105786851058GA11INTERGENIChomozygous51528984
108685117986851180AG1INTERGENIChomozygous51528985
108685161586851616TC11INTERGENICpossibly homozygous51528988
108685174386851744TC13INTERGENIChomozygous51528989
108685257386852574CT10GENIChomozygous51528990
108685394486853945GT7GENIChomozygous51528991
108685436186854363GA--1GENIChomozygous51528992
108685490086854901AT18GENICpossibly homozygous51528993
108685517286855173CT19GENICpossibly homozygous51528994
108685567186855672GA11GENICpossibly homozygous51528995
108685621286856213TG7GENICpossibly homozygous51528996
108685678686856787C-4GENIChomozygous51528997
108685783686857837CT9GENICheterozygous51528998
108685824786858248AC12GENIChomozygous51528999
108685833986858340GT5GENICheterozygous51529000
108686415986864160T-2INTERGENICheterozygous52392567