chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123599663123599664TA70INTERGENICheterozygous54090423
7123599721123599722AG90INTERGENICheterozygous54090424
7123599808123599809AG94INTERGENICheterozygous54090426
7123599813123599814GGT89INTERGENICheterozygous54090427
7123599827123599828GA100INTERGENICheterozygous54090428
7123599844123599845GA100INTERGENICheterozygous54090430
7123599847123599848TC101INTERGENICheterozygous54090431
7123599976123599977CG102INTERGENICheterozygous54090432
7123600041123600042CA98INTERGENICheterozygous54090433
7123600985123600986GA50INTERGENIChomozygous54090436
7123601612123601613GA27GENICheterozygous54090437
7123601633123601634CG26GENICheterozygous54090439
7123601643123601644GA24GENICheterozygous54090440
7123601654123601655CT24GENICheterozygous54090442
7123601925123601926GA72GENICheterozygous54090443
7123601970123601971CT83GENICheterozygous54090445
7123602532123602533TG55GENIChomozygous54090446
7123602969123602970TC42GENICpossibly homozygous54090448
7123603020123603021GT52GENICpossibly homozygous54090449
7123603052123603053GT51GENIChomozygous54090451
7123603099123603100AG43GENIChomozygous54090452
7123603119123603120CA29GENICpossibly homozygous54090454
7123603124123603125CA27GENICpossibly homozygous54090456
7123603190123603191CT36GENICpossibly homozygous54090457
7123603198123603199TC40GENICpossibly homozygous54090459
7123603270123603271TG31GENIChomozygous54090460
7123603570123603571AG8GENIChomozygous54090462
7123603578123603579TC9GENIChomozygous54090463
7123604102123604103GA50GENICheterozygous54090465
7123604465123604466GGTC21GENICheterozygous54090467
7123604497123604498GC54GENIChomozygous54090468
7123605258123605259TG33GENIChomozygous54090470
7123606581123606582AG41INTERGENIChomozygous54090471