chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104442503	104442504	G	A	18	GENIC	homozygous	61490089
1	104443196	104443197	T	A	31	GENIC	homozygous	61490090
1	104443201	104443202	G	A	32	GENIC	homozygous	61490091
1	104444174	104444175	A	AGTGTGTGTGTGTGTGT	7	GENIC	homozygous	62147949
1	104445688	104445689	G	GA	8	GENIC	homozygous	61490094
1	104445879	104445880	A	C	11	GENIC	homozygous	61490095
1	104446521	104446522	A	AACACACACACAC	6	GENIC	homozygous	62147951
1	104446762	104446763	T	TACACAC	7	GENIC	homozygous	61490096
1	104447099	104447100	A	C	13	GENIC	homozygous	61490098
1	104447449	104447450	A	G	17	GENIC	homozygous	61490099
1	104447697	104447709	CACACACACACA	------------	5	GENIC	homozygous	62147953
1	104448784	104448785	C	T	25	GENIC	homozygous	61490101
1	104448794	104448795	G	A	26	GENIC	homozygous	61490102
1	104448836	104448837	G	A	22	GENIC	homozygous	61490103
1	104448899	104448900	G	A	28	GENIC	homozygous	61490104
1	104449762	104449764	CA	--	2	GENIC	homozygous	62147955
1	104450391	104450392	T	C	22	GENIC	homozygous	61490107
1	104450737	104450738	A	C	28	GENIC	homozygous	61490108
1	104450933	104450934	C	T	24	GENIC	homozygous	61735084
1	104448837	104448838	G	A	22	GENIC	homozygous	61735082
1	104447544	104447545	C	CATCT	2	GENIC	homozygous	61299678