chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	181655513	181655514	C	A	33	GENIC	homozygous	110157051
2	181655655	181655656	G	A	34	GENIC	homozygous	110157052
2	181655696	181655697	C	T	25	GENIC	homozygous	110157053
2	181655783	181655784	G	A	24	GENIC	homozygous	110157054
2	181655992	181655993	A	C	19	GENIC	homozygous	110157055
2	181656116	181656117	C	T	16	GENIC	homozygous	110157056
2	181656191	181656192	C	T	15	GENIC	heterozygous	110157058
2	181656207	181656208	T	C	13	GENIC	homozygous	110157059
2	181656379	181656380	T	C	19	GENIC	homozygous	110157060
2	181656519	181656520	A	G	13	GENIC	homozygous	110157061
2	181656658	181656659	T	A	14	GENIC	homozygous	110157062
2	181656677	181656678	C	T	11	GENIC	homozygous	110157063
2	181657530	181657531	C	T	25	GENIC	homozygous	110157064
2	181658029	181658030	A	G	14	GENIC	homozygous	110157065
2	181658120	181658121	A	C	14	GENIC	homozygous	110157066
2	181658352	181658353	A	C	16	GENIC	homozygous	110157067
2	181658841	181658842	C	T	17	GENIC	homozygous	110157068
2	181659803	181659804	C	T	35	GENIC	homozygous	110157069
2	181659917	181659918	C	T	35	GENIC	homozygous	110157070
2	181660288	181660289	G	A	35	GENIC	possibly homozygous	110157071
2	181660322	181660323	A	T	43	GENIC	homozygous	110157072
2	181660331	181660332	A	G	45	GENIC	possibly homozygous	110157073
2	181660434	181660435	A	C	35	GENIC	homozygous	110157074
2	181660495	181660496	A	G	30	GENIC	homozygous	110157075
2	181660735	181660736	G	T	40	GENIC	possibly homozygous	110157076
2	181660820	181660821	T	A	33	GENIC	homozygous	110157077
2	181662485	181662486	A	G	33	GENIC	homozygous	110157078
2	181662568	181662569	T	C	30	GENIC	homozygous	110157079
2	181662613	181662614	C	T	27	GENIC	homozygous	110157080