chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147803989147803991CC62GENIChomozygous128253962
5147805155147805156TC56GENIChomozygous114047380
5147805333147805334AC48GENIChomozygous114047382
5147805352147805352A48GENIChomozygous128253963
5147805356147805357A49GENIChomozygous128253964
5147805500147805501G58GENIChomozygous128253965
5147805883147805884GA37GENIChomozygous114047384
5147806880147806880A41GENICpossibly homozygous128253966
5147807611147807612TC57GENIChomozygous114047386
5147809187147809188AG42GENIChomozygous114047388
5147809230147809231TC28GENIChomozygous122415376
5147809318147809319AC4GENIChomozygous132636917
5147809316147809316CC6GENIChomozygous132628375
5147809321147809330AGAACTTAT3GENIChomozygous132628376
5147809815147809816CG30GENIChomozygous114047390
5147810036147810037AT48GENIChomozygous114047392
5147810064147810067CTC41GENIChomozygous128253968
5147810187147810188TG40GENIChomozygous114047394
5147810259147810260TG38GENIChomozygous114047396
5147810358147810359GA36GENIChomozygous114047398
5147810632147810633A39GENICheterozygous128253969
5147811709147811710TC53GENIChomozygous114047408
5147811735147811736TC56GENIChomozygous114047410
5147809755147809756TC12GENIChomozygous133154496
5147811930147811931CT53GENIChomozygous114153116
5147811962147811963GA62GENIChomozygous114153117
5147812098147812099CG70GENICpossibly homozygous114153118