chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124634122246341223CCTG29INTERGENIChomozygous50218452
124634564246345652ACAGCAGCTG----------27INTERGENICheterozygous50340062
124637410146374102AG19GENIChomozygous50218456
124637615746376158AAG29GENIChomozygous50218457
124638215546382156CT22GENICheterozygous50340328
124638577646385777CCT18GENIChomozygous50218463
124639441446394415CCA8GENICheterozygous50615825
124636304446363045CCCTAT20GENICpossibly homozygous50886449
124638681546386816CT28GENIChomozygous50886451
124639628246396284AC--9GENICheterozygous50806124
124642828146428282GGAT23GENIChomozygous50218482
124642828646428287AAG19GENIChomozygous50218485
124642843446428435CCAGAT4GENIChomozygous50886453
124644172446441725G-1GENIChomozygous50340785
124644173346441734GT1GENIChomozygous50387293
124644174146441742GT2GENIChomozygous50218488
124644605146446052TC21GENIChomozygous50611853
124644608146446082CCCACCATCATCACCACCATCATCACCACCATCATCATCACCATCACCACCATCATCATCACCATCATCATCACCGTCACTGTCACCATCATCACCACCATCATCACCATCATCATCACCATCACCACCATCATCAT7GENIChomozygous50615829
124646191646461917CCA16GENICheterozygous50806133
124646340146463405TCTC----4GENICheterozygous50615831
124647035046470352GT--9GENICheterozygous50218495
124647134046471343AAG---23GENICheterozygous50341150
124647301046473012TC--19GENIChomozygous50218499
124648203846482040GT--7GENICheterozygous50218501
124648328146483282AAGT42GENIChomozygous50218502
124648331146483312C-47GENIChomozygous50218504
124648510846485109CT31GENIChomozygous50218506
124648513446485135CG28GENIChomozygous50218507
124648523746485240GTG---31GENIChomozygous50218509