chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95386210	95386211	G	A	28	GENIC	homozygous	69504891
10	95386716	95386717	C	T	22	GENIC	homozygous	69504894
10	95386752	95386753	A	T	14	GENIC	homozygous	68186964
10	95387143	95387144	A	G	31	GENIC	homozygous	68186967
10	95386608	95386609	T	C	22	GENIC	homozygous	68186957
10	95386711	95386712	A	G	22	GENIC	homozygous	68186961
10	95387836	95387837	C	G	24	GENIC	homozygous	68186971
10	95388095	95388096	G	A	27	GENIC	homozygous	68186974
10	95388663	95388664	T	C	8	GENIC	homozygous	68186982
10	95388759	95388760	G	A	11	GENIC	homozygous	69504897
10	95389225	95389226	G	A	24	GENIC	homozygous	68186986
10	95391254	95391255	T	C	24	GENIC	homozygous	68187050
10	95391320	95391321	A	G	15	GENIC	homozygous	69504900
10	95391438	95391439	G	A	11	GENIC	homozygous	68187057
10	95391753	95391754	A	G	20	GENIC	homozygous	69504906
10	95392127	95392128	C	T	11	GENIC	homozygous	68187069
10	95391314	95391315	G	A	21	GENIC	possibly homozygous	69280441
10	95391462	95391463	G	A	13	GENIC	homozygous	68932563
10	95392635	95392636	T	C	36	GENIC	homozygous	68471410
10	95393104	95393105	T	C	19	GENIC	homozygous	68187073
10	95393278	95393279	C	T	17	GENIC	possibly homozygous	68187085
10	95393538	95393539	T	C	28	GENIC	homozygous	69504912
10	95394933	95394934	T	C	5	GENIC	homozygous	68187096
10	95394975	95394976	G	A	13	GENIC	homozygous	69504918
10	95395521	95395522	C	A	22	GENIC	homozygous	69504921
10	95396775	95396776	T	G	13	GENIC	homozygous	68187104
10	95396787	95396788	A	G	13	GENIC	homozygous	68187108
10	95398334	95398335	C	T	31	GENIC	homozygous	69504924
10	95393228	95393229	C	T	16	GENIC	heterozygous	82706004
10	95393371	95393372	A	G	21	GENIC	heterozygous	82706005
10	95393373	95393374	G	A	21	GENIC	heterozygous	82706006