chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185506178955061790AC52GENIChomozygous46607660
185506228755062288GGA64GENIChomozygous46607661
185506252155062522AG64GENIChomozygous46607662
185506264455062645CG49GENIChomozygous46607663
185506266555062666TC52GENIChomozygous46607664
185506286455062865AAT27GENICpossibly homozygous46607665
185506289555062896AAAAAAAC29GENIChomozygous46607666
185506350855063509TC40GENIChomozygous46607667
185506405155064052GA59GENIChomozygous46607668
185506484655064847GA66GENIChomozygous46607669
185506528855065292TGTT----32GENIChomozygous46607670
185506543555065436CT54GENIChomozygous46607671
185506549555065496G-44GENIChomozygous46607672
185506557855065579AG73GENIChomozygous46607673
185506591955065920CCTAGA59GENIChomozygous46607674
185506650355066504AG55GENIChomozygous46463915
185506674255066743CT50GENIChomozygous46607675
185506706055067061TC57GENIChomozygous46607676
185506707155067072TC55GENIChomozygous46607677
185506729255067293GA62GENIChomozygous46607678
185506754355067544TC68GENIChomozygous46607679
185506824555068246TG32GENICpossibly homozygous46607680
185506844155068442GA45GENIChomozygous46607681
185506847755068478GA43GENIChomozygous46607682
185506949555069496GA50GENIChomozygous46607683
185506963555069636GA56GENIChomozygous46607684
185506967755069678AG61GENICpossibly homozygous46607685
185506982055069821AG54GENIChomozygous46607686
185506988855069889TA48GENICpossibly homozygous46607687
185507035355070357TTCT----28GENICheterozygous46607688
185507035555070356C-31GENIChomozygous46607689
185507036955070370AAG23GENIChomozygous46607690
185507051355070514AG46GENIChomozygous46607691
185507101255071013CA60GENIChomozygous46607692
185507113955071140AG38GENIChomozygous46463921
185507119355071194CT38GENIChomozygous46607693
185507168055071681TC40GENIChomozygous46607694