chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155294274155294275CT12GENIChomozygous946985301
5155294360155294361TC7GENIChomozygous946985302
5155295748155295749TC22GENIChomozygous946985303
5155300981155300982TG21GENIChomozygous946985304
5155302190155302191GA26GENIChomozygous946985305
5155307760155307761AG18GENIChomozygous946985306
5155308199155308200AC15GENIChomozygous946985307
5155308271155308272CT17GENIChomozygous946985308
5155308396155308397TC26GENIChomozygous946985309
5155308975155308976TC31GENIChomozygous946985310
5155309320155309321TG25GENIChomozygous946985311
5155309712155309713CT32GENIChomozygous946985312
5155311340155311341TC18GENIChomozygous946985313
5155311536155311537GC25GENIChomozygous946985314
5155311877155311878AG25GENIChomozygous946985315
5155311999155312000AG21GENIChomozygous946985316
5155312352155312353AT44GENIChomozygous946985317
5155316409155316410AG21GENIChomozygous946985318
5155316472155316473TA21GENIChomozygous946985319
5155316675155316676TG18GENIChomozygous946985320
5155317165155317166TC13GENIChomozygous946985321
5155318171155318172CT17GENIChomozygous946985322
5155318392155318393CT19GENIChomozygous946985323
5155318688155318689AG19GENIChomozygous946985324
5155319466155319467GA13GENIChomozygous946985325