chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17849065178490652GT6GENICheterozygous127542329
17856461178564612CT6GENIChomozygous121012269
17856461278564613TA6GENIChomozygous121012270
17856461778564617GCACA5GENIChomozygous127397238
17856462178564622CA4GENIChomozygous121012273
17856462178564621A4GENIChomozygous127397239
17856462378564624CA4GENIChomozygous121012274
17856462778564627GGG4GENIChomozygous127397240
17856463378564634AC3GENIChomozygous121012276
17856463578564635CTTTT3GENIChomozygous127397241
17856463978564644ACATA3GENIChomozygous127397242
17856464678564647C3GENIChomozygous127397243
17856465078564657AAGAAAT3GENIChomozygous127397244
17856493378564933GA3GENIChomozygous127397245
17856493678564936A3GENIChomozygous127397246
17856493978564939C4GENIChomozygous127397247
17856494978564950C4GENIChomozygous127397248
17856496378564964A5GENIChomozygous127397249
17856497078564972AT5GENIChomozygous127397250
17856497478564975T5GENIChomozygous127397251
17856497778564978G5GENIChomozygous127397252
17856498078564981CA5GENIChomozygous109295063
17856669478566694T9GENICheterozygous129840397
17856495878564959CA4GENIChomozygous120522132
17856257578562576A17GENICheterozygous130210026