chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	78165268	78165269	T	A	12	GENIC	homozygous	108139675
1	78165303	78165304	A	G	10	GENIC	homozygous	108872124
1	78166214	78166215	A	G	28	GENIC	homozygous	108872125
1	78167226	78167227	C	T	21	GENIC	homozygous	108872126
1	78168892	78168893	C	T	1	GENIC	homozygous	108139676
1	78169243	78169244	T	C	47	GENIC	homozygous	108139677
1	78170757	78170758	C	G	37	GENIC	homozygous	108139680
1	78170834	78170835	A	C	21	GENIC	homozygous	108139681
1	78178498	78178499	A	T	39	GENIC	homozygous	108872130
1	78178815	78178816	C	T	37	GENIC	homozygous	108872131
1	78179398	78179399	C	T	23	GENIC	homozygous	108872132
1	78179527	78179528	A	G	23	GENIC	homozygous	108872133
1	78179835	78179836	T	C	26	GENIC	homozygous	108872134
1	78181184	78181185	A	G	34	GENIC	homozygous	108872136
1	78182822	78182823	C	T	28	GENIC	homozygous	108872137
1	78169242	78169243	C	T	47	GENIC	homozygous	120481015
1	78169904	78169905	G	A	11	GENIC	homozygous	120472110
1	78169906	78169907	A	C	12	GENIC	homozygous	120472111