chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154189889141898893AC19GENIChomozygous139631130
154189915441899157ATC20GENIChomozygous139631131
154190069641900697CT13GENIChomozygous139722057
154190390041903901TC22GENIChomozygous139722058
154190448441904485GA22GENIChomozygous139722059
154190462541904625A17GENIChomozygous139631132
154190484841904849CT25GENIChomozygous139722060
154191139241911393CT16GENIChomozygous139722061
154191159441911595CT25GENIChomozygous139722062
154191447841914478A15GENIChomozygous139631135
154191508841915089AG20GENIChomozygous139722063
154191516141915162GA20GENIChomozygous139722064
154191516241915163CT20GENIChomozygous139722065
154191716341917164GC21GENIChomozygous139722066
154191888041918881GA23GENIChomozygous139722067
154191969441919695CT16GENIChomozygous139722068
154192670641926719CCCTATAATTATA10GENIChomozygous139631136
154192781741927818AG16GENIChomozygous139722072
154192350941923510TC17GENIChomozygous139722069
154192598341925984CT27GENIChomozygous139722070
154192662941926630AG24GENIChomozygous139722071
154192827141928275AGGG5GENIChomozygous139631137
154193438341934384TC27GENIChomozygous139722073
154193635041936351TC25GENIChomozygous139722074
154193686541936866CG34GENIChomozygous139722075
154193720141937202C24GENIChomozygous139631138
154193915441939155AC28GENIChomozygous139722076
154194195141941951TGGC13GENIChomozygous139631139