chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103378247103378248TC18GENIChomozygous108903280
1103378257103378258AC16GENIChomozygous108903281
1103378280103378280AT9GENIChomozygous132264060
1103378344103378345GA16GENIChomozygous108903282
1103378356103378357AG20GENIChomozygous108903283
1103378471103378472TC24GENIChomozygous108903284
1103378481103378482CT25GENIChomozygous108903285
1103378487103378488TC26GENIChomozygous108903286
1103378502103378503AG25GENIChomozygous108903287
1103378519103378520CT26GENIChomozygous108903288
1103378596103378597TC19GENIChomozygous108903290
1103378620103378621TC23GENIChomozygous108903291
1103378638103378639GA21GENIChomozygous108903292
1103379285103379286GA25GENIChomozygous108903293
1103379978103379979TA21GENIChomozygous108903294
1103379983103379984GA21GENIChomozygous108903295
1103382657103382658AC23GENIChomozygous108903297
1103383877103383878AC14GENIChomozygous108903298
1103384227103384228AG22GENIChomozygous108903299
1103381207103381207CTGGAGAGA14GENIChomozygous127409108
1103381235103381236A14GENIChomozygous127409109
1103381240103381241T13GENIChomozygous127409110
1103381263103381265CG8GENIChomozygous127409111
1103381216103381217CT13GENIChomozygous109116895
1103385562103385563CT26GENIChomozygous108903300
1103385572103385573GA24GENIChomozygous108903301
1103385614103385615GA18GENIChomozygous108903302
1103385615103385616GA18GENIChomozygous109116899
1103385677103385678GA17GENIChomozygous108903303
1103387169103387170TC21GENIChomozygous108903305
1103387515103387516AC19GENIChomozygous108903306
1103387711103387712CT13GENIChomozygous109116901
1103388064103388065GA15GENIChomozygous108903307
1103388081103388082TC17GENIChomozygous108903308
1103388101103388102GA18GENIChomozygous108903309
1103382467103382467A24GENIChomozygous130818696