chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1106982670106982670G3GENIChomozygous127410901
1106982680106982680A4GENIChomozygous127410902
1106982681106982682AC4GENIChomozygous121041876
1106982682106982683CA4GENIChomozygous121041877
1106982687106982688C4GENIChomozygous127410903
1106989615106989616TG34GENIChomozygous108167672
1106991136106991136G15GENIChomozygous127410911
1106991149106991150A12GENIChomozygous127410912
1106991155106991156G11GENIChomozygous127410913
1106991158106991158C11GENIChomozygous127410914
1106991165106991166G10GENIChomozygous127410915
1106991175106991176G5GENIChomozygous127410916
1106991182106991182CC4GENIChomozygous127410917
1106991132106991133CT17GENIChomozygous109120839
1106991198106991199GC4GENIChomozygous109120841
1106991168106991169GT7GENIChomozygous127546546
1106991171106991172TC6GENIChomozygous127546547
1106991187106991188AC4GENIChomozygous127546548
1106991188106991189GC4GENIChomozygous127546549
1107032461107032461GAATATCCACTTATAAGCAAACAAACACACCCACATTATTCTTTCCTA38GENIChomozygous127410943
1107032501107032502AG32GENIChomozygous108167848
1107032502107032503CT32GENIChomozygous108167849
1107032849107032850T17GENICheterozygous131985569
1107032853107032855TT16GENICpossibly homozygous130211118
1107001958107001959TC19GENICheterozygous133992904
1107001958107001958GGGGCCC17GENICheterozygous133990292