chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65647125056471251AC48GENIChomozygous114808607
65647304556473046TC34GENIChomozygous114808608
65647310056473101TA37GENIChomozygous114808609
65647533456475335AC10GENIChomozygous114808610
65647534956475350GA10GENIChomozygous114808611
65647535156475352TC11GENIChomozygous114808612
65647535856475359TC13GENIChomozygous114808613
65647537156475372TC17GENIChomozygous114808614
65647537556475376CT17GENIChomozygous114808615
65647566956475670CT73GENICpossibly homozygous114808616
65647583556475836TA42GENICpossibly homozygous114808617
65647600756476008AG122GENICheterozygous114808618
65647618756476188CT70GENICheterozygous114808619
65647651556476516GA43GENICheterozygous114808620
65647693356476934AC46GENICheterozygous114808621
65647697356476974CA28GENICheterozygous114808622
65647834556478346GA39GENICheterozygous114808623
65647949556479496GA26GENICheterozygous114808624
65648192656481927AG40GENIChomozygous114808625
65648613756486138CT40GENIChomozygous114808626
65648909556489096CT51GENICheterozygous114808627
65649394056493941AG16GENIChomozygous114808628
65649805956498060AG57GENIChomozygous114808629
65649937756499378CT31GENICheterozygous114808630
65649987756499878AG21GENIChomozygous114808631
65650028956500290CT30GENIChomozygous114808632