chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7135048571350486TG18GENICpossibly homozygous45893633
X7135227371352274GT19GENIChomozygous45260073
X7135630871356316TCTTTCTT--------1GENIChomozygous45511836
X7136108371361087GTGT----2GENIChomozygous45511838
X7137202671372027AG20GENIChomozygous45260118
X7137739071377392AC--3GENICheterozygous45588199
X7137202771372028GT20GENIChomozygous45478617
X7137203971372040A-19GENIChomozygous45146764
X7137204471372045AAG18GENIChomozygous45146765
X7137277171372772TC14GENIChomozygous45146766
X7138797671387978GT--9GENICheterozygous45633476
X7139640771396409CA--8GENICheterozygous45511844
X7139645971396461AC--8GENICheterozygous45260145
X7139706571397066AAG13GENIChomozygous45146773
X7139794471397945G-3GENICheterozygous45478621
X7140190071401901GT19GENIChomozygous45146774
X7140580371405804CCA14GENICheterozygous45613106
X7140696571406966CCGT1GENIChomozygous45547638
X7140851171408512T-6GENICheterozygous45569734
X7141817771418207TGGAAGCAACCCCCAGTGTTGCTGATTATG------------------------------8GENIChomozygous45511848
X7142454871424555GTTGATG-------8GENICheterozygous45588201
X7142459171424600ATGAAGCCT---------18GENICheterozygous45146777
X7142943271429433AATG7GENICheterozygous45260191