chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6112463253112463254T-21GENIChomozygous54644430
6112464992112464993AAAC12GENICpossibly homozygous54644432
6112466894112466908ACACACACACACAC--------------14GENICheterozygous54948162
6112466898112466908ACACACACAC----------14GENICpossibly homozygous54644434
6112466963112466964TG31GENIChomozygous54644436
6112467132112467133CG25GENIChomozygous54644438
6112471262112471263CCT8GENICpossibly homozygous54644440
6112473838112473839TTA19GENIChomozygous54644442
6112474667112474668CT33GENIChomozygous54644444
6112474697112474698AG29GENIChomozygous54644446
6112475234112475235GGA13GENIChomozygous54644448
6112476691112476692CA14GENIChomozygous54644450
6112477250112477251CT13GENIChomozygous54644452
6112477255112477258TCC---13GENIChomozygous54644454
6112480210112480211CCATGCGTGTGTGT23GENICheterozygous55612392
6112480210112480211CCATGCGTGTGTGTGT23GENICheterozygous55529988
6112472999112473003AAAA----2GENICheterozygous55725701
6112477954112477956GA--8GENIChomozygous55725703
6112480210112480211CCATGCGT23GENICheterozygous55725706
6112480214112480215CT30GENICpossibly homozygous54644458
6112482041112482042CCGTGTGTGTGTGTGTGTGTGTGTGTGTGT2GENIChomozygous55725709
6112482834112482836TT--5GENICheterozygous55529992
6112482835112482836T-5GENICheterozygous55529994
6112484553112484554CCCTCCCCTCATGG7GENIChomozygous54644462
6112489821112489822T-7GENIChomozygous54644464
6112490069112490070GGTGTGTA18GENIChomozygous54644466
6112492092112492093TA20GENIChomozygous54644470
6112492323112492324TC26GENIChomozygous54644472
6112493017112493018TC12GENIChomozygous54644474
6112494001112494007TTTTTT------6GENIChomozygous55529996
6112494180112494181CT27GENIChomozygous54644478
6112494773112494774AAT18GENIChomozygous54644480
6112495121112495122GA20GENIChomozygous54644482
6112497383112497384AG37GENIChomozygous54644484