chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123599663123599664TA21INTERGENICheterozygous54090423
7123599721123599722AG25INTERGENICheterozygous54090424
7123599808123599809AG36INTERGENICheterozygous54090426
7123599813123599814GGT38INTERGENICheterozygous54090427
7123599827123599828GA35INTERGENICheterozygous54090428
7123599844123599845GA34INTERGENICheterozygous54090430
7123599847123599848TC34INTERGENICheterozygous54090431
7123599976123599977CG32INTERGENICheterozygous54090432
7123600041123600042CA37INTERGENICheterozygous54090433
7123600118123600119CT20INTERGENICheterozygous54090434
7123600139123600140CA18INTERGENICheterozygous56439171
7123600671123600672TG15INTERGENICheterozygous54236856
7123600985123600986GA10INTERGENICheterozygous54090436
7123601612123601613GA17GENICheterozygous54090437
7123601643123601644GA20GENICheterozygous54090440
7123601907123601908GC7GENICheterozygous54236858
7123601925123601926GA7GENICheterozygous54090443
7123601970123601971CT9GENICheterozygous54090445
7123603119123603120CA14GENICheterozygous54090454
7123603124123603125CA14GENICheterozygous54090456
7123603190123603191CT13GENICheterozygous54090457
7123603198123603199TC15GENIChomozygous54090459
7123603270123603271TG12GENICheterozygous54090460
7123604327123604328AT21GENICheterozygous56439173
7123604465123604466GGTC17GENICheterozygous54090467
7123604497123604498GC22GENICheterozygous54090468
7123604570123604571AATG7GENICheterozygous54236862
7123605258123605259TG16GENICheterozygous54090470
7123606265123606266CT12INTERGENICheterozygous54236864
7123606581123606582AG20INTERGENICheterozygous54090471
7123607896123607897GA22INTERGENICheterozygous54236866