chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176534736176534737TC24GENIChomozygous57810882
3176535459176535460GA30GENICpossibly homozygous58443896
3176536620176536621TTG28GENIChomozygous57810884
3176537910176537911GGGGGCA30GENIChomozygous57810888
3176538130176538131AG33GENIChomozygous57810890
3176538294176538295AG30GENIChomozygous57810892
3176538549176538550TA35GENICpossibly homozygous57810894
3176538918176538919CA32GENIChomozygous57810896
3176539035176539036AG32GENICpossibly homozygous57810898
3176539610176539626TGTGTGTGTGTGTGTG----------------14GENICheterozygous58699829
3176539612176539626TGTGTGTGTGTGTG--------------14GENICpossibly homozygous58955363
3176542037176542038GT34GENICpossibly homozygous57810908
3176542975176542976AG31GENIChomozygous57810910
3176543022176543023GT28GENIChomozygous58443898
3176543380176543381TC20GENIChomozygous58253909
3176543400176543401T-23GENIChomozygous57810912
3176545259176545260GT28GENIChomozygous57810914
3176545266176545267GC32GENIChomozygous57810916
3176545824176545825T-18GENICheterozygous58443900
3176545801176545803TT--16GENICheterozygous58634049
3176545799176545800C-20GENICheterozygous58634047
3176545800176545803TTT---16GENICheterozygous58634048