chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90400501	90400502	G	C	28	GENIC	homozygous	116676210
10	90400510	90400511	T	C	32	GENIC	homozygous	116676212
10	90406528	90406529	G	A	23	GENIC	homozygous	116904617
10	90407093	90407094	G	C	27	GENIC	homozygous	116676216
10	90407213	90407214	A	G	32	GENIC	homozygous	116904619
10	90407485	90407486	G	A	14	GENIC	homozygous	116676218
10	90408576	90408577	T	C	32	GENIC	homozygous	116904621
10	90409346	90409347	C	G	26	GENIC	possibly homozygous	117227976
10	90409399	90409400	A	G	22	GENIC	homozygous	117413162
10	90409478	90409479	C	T	28	GENIC	homozygous	116904623
10	90409902	90409903	G	T	12	GENIC	homozygous	116676222
10	90410024	90410025	G	A	38	GENIC	homozygous	116904625
10	90412560	90412561	C	T	35	GENIC	homozygous	116951312
10	90414204	90414205	C	T	22	GENIC	homozygous	116904627
10	90414650	90414651	G	A	23	GENIC	homozygous	116904629
10	90414912	90414913	T	C	37	GENIC	homozygous	116904631
10	90415390	90415391	A	T	31	GENIC	homozygous	116676238