chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142202712142202713AG9GENICheterozygous115941536
7142204642142204643AG10GENIChomozygous115941537
7142204974142204975TC18GENIChomozygous115941538
7142205990142205991TC28GENIChomozygous115941539
7142208176142208177GC31GENIChomozygous116097636
7142208312142208313GT7GENIChomozygous118407185
7142209559142209560TC12GENIChomozygous116350252
7142211327142211328GT10GENIChomozygous116097640
7142215212142215213TA21GENIChomozygous116097642
7142215393142215394GA28GENIChomozygous118323330
7142217149142217150AG25GENICheterozygous115941543
7142217265142217266GT10GENICheterozygous115941545
7142217293142217294TG6GENICheterozygous126603037
7142217406142217407CT5GENICheterozygous126603038
7142217439142217440TG10GENICheterozygous126547021
7142217582142217583TC19GENICheterozygous115941549
7142217641142217642AG4GENICheterozygous115941551
7142218160142218161AG13GENIChomozygous115941553
7142220473142220474TC16GENIChomozygous116097648
7142221392142221393AG20GENIChomozygous115941555
7142221697142221698AC16GENIChomozygous115941556
7142221796142221797GA14GENIChomozygous116097650
7142222008142222009TC10GENIChomozygous115941557
7142223300142223301TA18GENIChomozygous115941563