chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93982940	93982941	G	A	21	GENIC	homozygous	51547902
10	93984045	93984046	G	-	20	GENIC	possibly homozygous	51547903
10	93985784	93985785	G	A	17	GENIC	homozygous	51547904
10	93986366	93986367	G	GAT	25	GENIC	homozygous	51547905
10	93987585	93987586	C	T	16	GENIC	possibly homozygous	51547907
10	93988977	93988978	A	T	20	GENIC	possibly homozygous	51547908
10	93990402	93990403	C	T	17	GENIC	possibly homozygous	51547909
10	93991439	93991440	G	A	21	GENIC	homozygous	51547910
10	93992201	93992202	A	G	18	GENIC	homozygous	51547911
10	93992804	93992805	G	A	22	GENIC	possibly homozygous	51547912
10	93993254	93993255	G	T	23	GENIC	possibly homozygous	51547913
10	93993388	93993389	C	T	22	GENIC	possibly homozygous	51547914
10	93993693	93993694	A	G	22	GENIC	possibly homozygous	51547915
10	93993988	93993989	T	C	2	GENIC	heterozygous	51547916
10	93994217	93994218	T	TC	22	GENIC	homozygous	51547917
10	93996010	93996011	G	A	24	GENIC	possibly homozygous	51547920
10	93996055	93996056	C	T	33	GENIC	homozygous	51547921
10	93996317	93996318	T	C	11	GENIC	possibly homozygous	51547922
10	93996871	93996872	G	A	15	GENIC	homozygous	51547923
10	93996995	93996996	G	A	5	GENIC	heterozygous	51547924
10	93997035	93997036	G	GACAC	5	GENIC	heterozygous	51547926
10	93997035	93997036	G	GACACACAC	5	GENIC	heterozygous	52324555
10	93998395	93998396	C	CA	4	GENIC	heterozygous	51547927
10	93998588	93998589	T	A	19	GENIC	homozygous	51547928
10	93999947	93999948	T	C	12	GENIC	homozygous	51547929
10	94000567	94000568	T	C	29	GENIC	possibly homozygous	51547930
10	94001690	94001691	T	C	18	GENIC	heterozygous	51547931
10	94002094	94002095	T	C	30	GENIC	possibly homozygous	51547932
10	94002200	94002201	A	G	23	GENIC	possibly homozygous	51547933
10	94002600	94002601	C	A	20	GENIC	possibly homozygous	51547934
10	94004680	94004681	A	C	16	GENIC	homozygous	51547935