chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90400501	90400502	G	C	7	GENIC	homozygous	116676210
10	90400510	90400511	T	C	7	GENIC	homozygous	116676212
10	90402111	90402112	A	T	23	GENIC	homozygous	116676214
10	90407093	90407094	G	C	42	GENIC	homozygous	116676216
10	90407485	90407486	G	A	30	GENIC	homozygous	116676218
10	90408763	90408764	G	T	35	GENIC	homozygous	116676220
10	90409902	90409903	G	T	21	GENIC	homozygous	116676222
10	90410159	90410160	G	T	30	GENIC	homozygous	116676224
10	90410177	90410178	C	T	33	GENIC	homozygous	116676226
10	90410978	90410979	G	T	19	GENIC	homozygous	116820967
10	90412225	90412226	G	T	22	GENIC	homozygous	116676228
10	90412290	90412291	C	T	16	GENIC	homozygous	116676230
10	90413388	90413389	C	T	23	GENIC	homozygous	116676232
10	90413412	90413413	G	A	22	GENIC	homozygous	116676234
10	90415163	90415164	G	A	29	GENIC	homozygous	116676236
10	90415390	90415391	A	T	38	GENIC	homozygous	116676238
10	90415408	90415409	G	T	35	GENIC	homozygous	116676240