chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176534736176534737TC21GENIChomozygous57810882
3176535459176535460GA40GENICpossibly homozygous58443896
3176536620176536621TTG20GENIChomozygous57810884
3176537910176537911GGGGGCA10GENIChomozygous57810888
3176538130176538131AG25GENIChomozygous57810890
3176538294176538295AG21GENIChomozygous57810892
3176538549176538550TA30GENIChomozygous57810894
3176538918176538919CA21GENIChomozygous57810896
3176539035176539036AG30GENIChomozygous57810898
3176539610176539626TGTGTGTGTGTGTGTG----------------11GENICheterozygous58699829
3176539612176539626TGTGTGTGTGTGTG--------------11GENICheterozygous58955363
3176542037176542038GT33GENIChomozygous57810908
3176542975176542976AG17GENIChomozygous57810910
3176543022176543023GT22GENICpossibly homozygous58443898
3176543380176543381TC22GENIChomozygous58253909
3176543400176543401T-21GENIChomozygous57810912
3176545259176545260GT17GENIChomozygous57810914
3176545266176545267GC16GENIChomozygous57810916
3176545824176545825T-8GENICpossibly homozygous58443900
3176546829176546835ATAGAA------6GENICheterozygous58661003
3176545801176545803TT--7GENICheterozygous58634049
3176545799176545800C-9GENICheterozygous58634047
3176545800176545803TTT---7GENICheterozygous58634048