chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	73307022	73307023	T	G	13	GENIC	homozygous	108867095
1	73307161	73307162	A	T	9	GENIC	homozygous	108867096
1	73307220	73307221	G	T	13	GENIC	homozygous	108867097
1	73312458	73312459	A	T	11	GENIC	homozygous	109292449
1	73314471	73314472	A	G	14	GENIC	homozygous	109497322
1	73314634	73314635	C	G	7	GENIC	homozygous	108867098
1	73318632	73318633	T	G	20	GENIC	homozygous	109497324
1	73320248	73320249	T	C	16	GENIC	homozygous	108867105
1	73320249	73320250	T	C	16	GENIC	homozygous	108867106
1	73320367	73320368	A	G	29	GENIC	homozygous	109292454
1	73321062	73321063	C	T	22	GENIC	homozygous	108867108
1	73321243	73321244	G	A	15	GENIC	homozygous	109497325
1	73325327	73325328	G	A	12	GENIC	homozygous	109497326
1	73325417	73325418	C	G	20	GENIC	homozygous	109497327
1	73325548	73325549	C	T	21	GENIC	homozygous	109497328
1	73326369	73326370	A	G	30	GENIC	homozygous	108867113
1	73326413	73326414	G	A	29	GENIC	homozygous	109497329
1	73328628	73328629	A	T	18	GENIC	homozygous	108867114
1	73328803	73328804	C	G	9	GENIC	homozygous	108867115
1	73340778	73340779	C	T	16	GENIC	homozygous	109497335
1	73341971	73341972	G	A	20	GENIC	homozygous	109497336
1	73343739	73343740	C	T	15	GENIC	homozygous	109497337