chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1589855098985510AAGC36GENIChomozygous48224217
1589984558998456CG30GENIChomozygous48224219
1589984718998472TA29GENIChomozygous48224220
1589984818998482CG29GENIChomozygous48224221
1589987488998749TA27GENIChomozygous48224222
1589987788998779CG32GENIChomozygous48224223
1589987988998799GA38GENIChomozygous48224224
1589988138998814TA39GENIChomozygous48224225
1590032229003223A-19GENICheterozygous49028104
1590118429011844TG--15GENICheterozygous49219998
1590149649014965TTC35GENIChomozygous48224226
1590149689014969C-37GENIChomozygous48224227
1590212689021269GGCA15GENICheterozygous48452121
1590219729021973C-83GENICheterozygous49028186
1590235239023524T-13GENICheterozygous48927521
1590240859024086AACT68GENICheterozygous49028190
1590241859024187TT--34GENICheterozygous49028192
1590241879024188CCAA33GENICheterozygous49028194
1590243759024376AATACATCAG29GENICheterozygous49028196
1590248859024886G-42GENICheterozygous49184947
1590262529026262CCCTCTCCTC----------66GENICheterozygous49117118
1590262669026267AAG65GENICheterozygous48224240
1590265879026604ACTTAGCAGGGAAAGCC-----------------81GENICheterozygous49028200
1590272709027271A-54GENICheterozygous49028202
1590327199032720TTG1GENIChomozygous48224307
1590354479035449TC--58GENICheterozygous49028208
1590383009038301G-104GENICheterozygous48944685
1590383029038303C-101GENICheterozygous48944687
1590388969038897A-102GENICheterozygous49079511
1590389639038964G-160GENICheterozygous48224329
1590390849039086AC--9GENICheterozygous49079513