chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91508911115089112CT18GENIChomozygous117267254
91509260915092610GA21GENIChomozygous117267258
91509267715092678AG19GENIChomozygous117267259
91509541115095412TG17GENIChomozygous117267261
91509610215096103TA14GENIChomozygous117267262
91509636315096364CT29GENIChomozygous117267263
91509642215096423CT18GENIChomozygous117267264
91509784115097842AG21GENIChomozygous117267265
91510040115100402GA27GENIChomozygous117267270
91510054215100543AC28GENIChomozygous117267271
91510055415100555GA27GENIChomozygous117267272
91510070615100707TC11GENIChomozygous117267273
91510088115100882GA17GENIChomozygous117267274
91510103715101038CG18GENIChomozygous117267276
91510321615103217AG10GENIChomozygous117267277
91510420515104206AG12GENIChomozygous117267278
91510615215106153AC17GENIChomozygous117267279
91510632715106328GT21GENIChomozygous117267280
91510974915109750TC18GENIChomozygous117267281
91511119015111191CT21GENIChomozygous117267282
91511124015111241AG12GENIChomozygous117267283
91511208215112083AG17GENIChomozygous117267285
91511211615112117TC20GENIChomozygous117267286
91511521115115212CT23GENIChomozygous117267289
91511566615115667GC19GENICheterozygous117460673
91511799015117991CT12GENIChomozygous117267291
91511863015118631TG18GENIChomozygous117267292
91511962815119629CT4GENIChomozygous117267293
91512034915120350GA27GENIChomozygous117267294
91512153215121533GA25GENIChomozygous117267295
91512243515122436AG17GENIChomozygous117267296
91511677115116772CT17GENIChomozygous120460748