chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	160123496	160123497	T	C	10	GENIC	homozygous	114073873
5	160124033	160124034	T	A	27	GENIC	homozygous	118847336
5	160124368	160124369	T	C	20	GENIC	possibly homozygous	114073875
5	160124390	160124391	C	T	20	GENIC	possibly homozygous	114073876
5	160124554	160124555	C	G	13	GENIC	homozygous	114073877
5	160124910	160124911	G	A	6	GENIC	homozygous	114073881
5	160125583	160125584	C	T	14	GENIC	possibly homozygous	114073886
5	160125632	160125633	C	T	16	GENIC	homozygous	114073887
5	160125946	160125947	T	C	10	GENIC	homozygous	114073888
5	160126164	160126165	T	A	14	GENIC	homozygous	114604390
5	160126266	160126267	G	A	16	GENIC	homozygous	114073889
5	160126878	160126879	T	C	21	GENIC	homozygous	114073890
5	160127108	160127109	C	T	20	GENIC	homozygous	114073891
5	160127865	160127866	T	A	23	GENIC	homozygous	114073892
5	160131405	160131406	G	A	13	GENIC	homozygous	114073895
5	160133516	160133517	A	G	14	GENIC	homozygous	114073897
5	160135065	160135066	T	A	14	GENIC	homozygous	114073898
5	160135518	160135519	T	G	8	GENIC	heterozygous	114073902
5	160135535	160135536	C	T	7	GENIC	heterozygous	119087582
5	160136568	160136569	A	G	5	GENIC	homozygous	114073906
5	160138245	160138246	T	G	18	GENIC	homozygous	114073908
5	160138970	160138971	C	T	22	GENIC	homozygous	114073909
5	160139248	160139249	C	A	14	GENIC	homozygous	114073910
5	160140920	160140921	A	T	13	GENIC	homozygous	114073911
5	160143271	160143272	A	T	8	GENIC	homozygous	114073913
5	160145581	160145582	T	C	21	GENIC	possibly homozygous	114073916
5	160145654	160145655	T	C	32	GENIC	homozygous	114073917
5	160153881	160153882	C	T	17	GENIC	homozygous	114073920
5	160155879	160155880	C	T	5	GENIC	homozygous	114073921
5	160157260	160157261	C	G	12	GENIC	homozygous	114073925