chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100131579100131580AG7GENIChomozygous108898305
1100131616100131617CG6GENIChomozygous108898306
1100131640100131641CG11GENIChomozygous108898307
1100131729100131730AC22GENIChomozygous108898308
1100131833100131834TC22GENIChomozygous108898309
1100131874100131875CT20GENIChomozygous108898310
1100131901100131902CT30GENIChomozygous108898311
1100131973100131974AC5GENIChomozygous108898312
1100132507100132508AG27GENIChomozygous108898313
1100132612100132613AG20GENIChomozygous108898314
1100132970100132971TA18GENICheterozygous109046505
1100133078100133079TC20GENIChomozygous108898316
1100133110100133111TG21GENIChomozygous108898317
1100133263100133264TC16GENIChomozygous109562823
1100133300100133301TG5GENIChomozygous108898318
1100133385100133386TC16GENIChomozygous108898319
1100133496100133497AG12GENIChomozygous109562824
1100133545100133546AG22GENIChomozygous108898320
1100133653100133654GA19GENIChomozygous108898321
1100133913100133914GA7GENIChomozygous108898322
1100133971100133972AG19GENIChomozygous108898323
1100134348100134349CT4GENICheterozygous125456540
1100134397100134398GA8GENIChomozygous108898326
1100134454100134455TC5GENIChomozygous108898327
1100134593100134594TC11GENIChomozygous108898328
1100134775100134776CT13GENIChomozygous108898329
1100135335100135336TC29GENIChomozygous108898330