chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124053799840537999CT14GENIChomozygous115328362
124053866640538667CT8GENIChomozygous115328364
124053976140539762GA6GENIChomozygous115328366
124054012940540130GT6GENIChomozygous115328368
124054190040541901GT13GENIChomozygous115328370
124054419540544196AT7GENIChomozygous115383871
124054805440548055AG3GENIChomozygous115328378
124055641240556413CT10GENIChomozygous115383873
124055851940558520GC13GENIChomozygous115383875
124056103740561038TC7GENIChomozygous115328386
124056225540562256TC9GENIChomozygous115328388
124056324540563246GA13GENIChomozygous115383877
124056451940564520TC13GENIChomozygous115328392
124057623240576233CT8GENIChomozygous115383879
124057822240578223AT6GENIChomozygous115383881
124057882840578829AG6GENIChomozygous115328394
124057897740578978TC6GENIChomozygous115383883
124058060440580605AG9GENIChomozygous115328396
124058288740582888AG9GENIChomozygous115328400
124058289840582899TC8GENIChomozygous115328402
124058514740585148CT7GENIChomozygous115383885
124058678740586788GA14GENIChomozygous115328406
124060720740607208TC14GENIChomozygous115328412
124060899240608993TA11GENIChomozygous115328414
124060899740608998TC10GENIChomozygous115328416
124061051140610512CT9GENIChomozygous115383887
124061605240616053AG8GENICheterozygous115383889