chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1106982670106982670G3GENIChomozygous127410901
1106982680106982680A3GENIChomozygous127410902
1106982681106982682AC3GENIChomozygous121041876
1106982682106982683CA3GENIChomozygous121041877
1106982687106982688C4GENIChomozygous127410903
1106989491106989492TC25GENICheterozygous108167671
1106989615106989616TG23GENIChomozygous108167672
1106991136106991136G6GENIChomozygous127410911
1106991149106991150A7GENIChomozygous127410912
1106991155106991156G7GENIChomozygous127410913
1106991158106991158C7GENIChomozygous127410914
1106991165106991166G6GENIChomozygous127410915
1106991175106991176G6GENIChomozygous127410916
1106991182106991182CC4GENIChomozygous127410917
1106991132106991133CT6GENIChomozygous109120839
1106991198106991199GC5GENIChomozygous109120841
1106991168106991169GT5GENIChomozygous127546546
1106991171106991172TC6GENIChomozygous127546547
1106991187106991188AC4GENIChomozygous127546548
1106991188106991189GC4GENIChomozygous127546549
1107032271107032272AT9GENICheterozygous127546552
1107032461107032461GAATATCCACTTATAAGCAAACAAACACACCCACATTATTCTTTCCTA22GENIChomozygous127410943
1107032501107032502AG20GENIChomozygous108167848
1107032502107032503CT20GENIChomozygous108167849
1107032853107032855TT6GENIChomozygous130211118