chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35360355153603552TC17INTERGENIChomozygous58355514
35360407253604073CCAA7INTERGENIChomozygous58355516
35360512853605129TTA2INTERGENICheterozygous58582961
35360775553607757AT--6INTERGENIChomozygous58132551
35361213753612138CCA4GENIChomozygous58582962
35361331153613312AT7GENIChomozygous58132567
35361513553615136TTC4GENICheterozygous58420490
35361981453619815CCTG2GENIChomozygous58685397
35361981853619820AG--2GENIChomozygous58685398
35362227453622275CCAAT11GENIChomozygous58355518
35362295453622955CT11GENIChomozygous58132597
35362499853624999G-14GENIChomozygous57376293
35362500953625010G-13GENIChomozygous57376294
35362505253625053G-17GENIChomozygous57376295
35362505753625058G-19GENIChomozygous57376296
35363064653630650ACAC----3GENICheterozygous58582963
35363069853630702GCAA----9GENICheterozygous58582964
35363099553630996CT18GENIChomozygous58132605
35363480553634806AAT11GENIChomozygous57376297
35363482753634828AAT9GENIChomozygous57376298
35363483253634833GGT9GENIChomozygous57376299
35363483853634839TA9GENIChomozygous58582965
35363484253634843AT9GENIChomozygous58582966
35363496353634964C-15GENIChomozygous57376300
35363623653636237AAC1GENIChomozygous59372770
35363679753636798TC5GENIChomozygous58132620
35363713553637136CA8GENICpossibly homozygous58132622
35363823553638236GA13GENIChomozygous58132624
35363913753639138GGAT1GENIChomozygous59420096
35364536553645366TA7GENIChomozygous58132628
35364662153646622TC18GENIChomozygous58132634
35364919753649198T-12GENIChomozygous58355524
35365405353654054GGA11GENIChomozygous57376303
35365417353654174GGA19GENIChomozygous57376304