chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5132029582132029586ATAA----12GENIChomozygous693996657
5132030095132030099AATG----4GENICheterozygous693996659
5132031604132031605CT7GENIChomozygous528717640
5132031771132031772TTC7GENIChomozygous693996660
5132032200132032201AG19GENIChomozygous528717641
5132032501132032502TC26GENIChomozygous528717642
5132034504132034509TAAAA-----16GENIChomozygous693996661
5132034760132034761T-12GENICpossibly homozygous693996662
5132034773132034774GA13GENIChomozygous528717643
5132034797132034798CG8GENIChomozygous528717644
5132034806132034807G-8GENIChomozygous693996663
5132034812132034813G-8GENIChomozygous693996664
5132034819132034820C-9GENIChomozygous693996665
5132034840132034841T-8GENIChomozygous693996666
5132034849132034850C-7GENIChomozygous693996667
5132034912132034913G-9GENIChomozygous693996668
5132036607132036608G-9GENIChomozygous693996669
5132037954132037955AAC15GENIChomozygous693996670
5132038358132038359AT11GENIChomozygous530747526
5132040493132040494AC16GENIChomozygous528717645
5132041371132041372AAT5GENICheterozygous693996671
5132041727132041728TTGAA7GENIChomozygous693996672
5132041729132041730TTAC7GENIChomozygous693996673
5132043567132043568AG21GENIChomozygous530747527
5132045607132045608AT36GENIChomozygous528717646
5132046386132046387AG14GENIChomozygous528717647
5132047559132047560CT19GENIChomozygous530747528
5132049865132049866GGT17GENIChomozygous693996674
5132052134132052135AC26GENIChomozygous528717648