chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14106450161106450162CA24GENIChomozygous48885301
14106453031106453032GC5GENIChomozygous48885303
14106453175106453176TTA14GENIChomozygous48885305
14106453531106453532CT24GENIChomozygous48885307
14106454105106454106CT15GENIChomozygous48885309
14106455139106455140CT21GENIChomozygous48885311
14106455182106455183CT13GENICheterozygous49218939
14106455190106455191T-2GENIChomozygous48885313
14106455230106455231CT17GENICheterozygous49059195
14106455265106455266CG17GENICheterozygous49059197
14106455297106455298CCCT11GENICheterozygous48885315
14106455437106455438AT9GENICpossibly homozygous48885317
14106455445106455446AC8GENIChomozygous48885319
14106455448106455449TC10GENIChomozygous48885321
14106455450106455451GA9GENIChomozygous48885322
14106455504106455506TT--1GENIChomozygous48885324
14106455670106455671TA24GENIChomozygous48885326
14106455781106455782CT17GENIChomozygous48885328
14106456112106456113TC18GENIChomozygous48885330
14106456160106456161AC21GENIChomozygous48885332
14106456208106456209CT31GENIChomozygous48885334
14106456544106456545AAACAC4GENICheterozygous48885336
14106456544106456545AAAC4GENICheterozygous49059205
14106457443106457444TC24GENIChomozygous48885338
14106457516106457517TC17GENIChomozygous48885340
14106457915106457916AAT15GENIChomozygous48885342
14106461136106461137GA14GENIChomozygous48885344
14106461323106461324CT29GENIChomozygous48885346
14106462222106462224AA--5GENICheterozygous48885348
14106462223106462224A-5GENICheterozygous48885350
14106462243106462246AAA---11GENICpossibly homozygous48885354
14106462269106462270CT8GENICheterozygous48885356
14106462372106462373TC16GENIChomozygous48885358
14106463105106463106AG23GENIChomozygous48885360
14106463508106463509CT28GENIChomozygous48885362