chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94969629	94969630	C	T	21	GENIC	homozygous	116827029
10	94970003	94970004	T	A	18	GENIC	homozygous	116827031
10	94970252	94970253	T	C	20	GENIC	homozygous	116827033
10	94970343	94970344	C	T	20	GENIC	homozygous	116955665
10	94971125	94971127	GG		18	GENIC	homozygous	131709429
10	94972685	94972686	T	C	28	GENIC	homozygous	116955667
10	94972917	94972918	G	C	24	GENIC	homozygous	116955669
10	94973330	94973331	G		25	GENIC	homozygous	128847917
10	94973142	94973142		T	10	GENIC	homozygous	128847913
10	94973171	94973171		C	9	GENIC	homozygous	128847914
10	94973244	94973244		C	18	GENIC	homozygous	128847915
10	94973250	94973251	C		20	GENIC	homozygous	128847916
10	94972923	94972924	A	G	23	GENIC	homozygous	116686698
10	94973337	94973338	G		23	GENIC	homozygous	128847918
10	94973385	94973385		G	21	GENIC	homozygous	128847919
10	94973449	94973449		C	10	GENIC	homozygous	128847920
10	94973485	94973486	T		18	GENIC	homozygous	128847921
10	94973541	94973542	A	C	24	GENIC	homozygous	116827039
10	94973548	94973549	C		26	GENIC	homozygous	128847922
10	94973553	94973553		C	26	GENIC	homozygous	128847923
10	94973560	94973562	TA		27	GENIC	homozygous	128847924
10	94973569	94973570	T		28	GENIC	homozygous	128847925
10	94973580	94973581	C		27	GENIC	homozygous	128847926
10	94973582	94973583	T	A	27	GENIC	homozygous	116827041
10	94974066	94974067	C	G	28	GENIC	homozygous	116955671
10	94974276	94974277	G	A	17	GENIC	homozygous	116955673
10	94974871	94974872	T	C	24	GENIC	homozygous	116955675
10	94976359	94976360	G	A	28	GENIC	homozygous	116955676
10	94976472	94976473	C	G	25	GENIC	homozygous	116955677
10	94976645	94976645		A	9	GENIC	possibly homozygous	131709433
10	94978935	94978936	A		33	GENIC	homozygous	132694308