chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94969629	94969630	C	T	27	GENIC	homozygous	116827029
10	94970003	94970004	T	A	21	GENIC	homozygous	116827031
10	94970252	94970253	T	C	25	GENIC	homozygous	116827033
10	94971015	94971016	G	A	33	GENIC	homozygous	116827035
10	94971125	94971127	GG		17	GENIC	homozygous	131709429
10	94971834	94971835	C	A	32	GENIC	homozygous	116827037
10	94972037	94972038	A		28	GENIC	homozygous	131709430
10	94973142	94973142		T	12	GENIC	homozygous	128847913
10	94973171	94973171		C	15	GENIC	homozygous	128847914
10	94973244	94973244		C	23	GENIC	homozygous	128847915
10	94973250	94973251	C		23	GENIC	homozygous	128847916
10	94973330	94973331	G		25	GENIC	homozygous	128847917
10	94973541	94973542	A	C	13	GENIC	homozygous	116827039
10	94973548	94973549	C		14	GENIC	homozygous	128847922
10	94973337	94973338	G		25	GENIC	homozygous	128847918
10	94973385	94973385		G	28	GENIC	homozygous	128847919
10	94973449	94973449		C	5	GENIC	homozygous	128847920
10	94973485	94973486	T		9	GENIC	homozygous	128847921
10	94972923	94972924	A	G	26	GENIC	homozygous	116686698
10	94973553	94973553		C	14	GENIC	homozygous	128847923
10	94973560	94973562	TA		18	GENIC	homozygous	128847924
10	94973569	94973570	T		18	GENIC	homozygous	128847925
10	94973580	94973581	C		16	GENIC	homozygous	128847926
10	94973582	94973583	T	A	17	GENIC	homozygous	116827041
10	94974263	94974263		A	19	GENIC	possibly homozygous	131709431
10	94974437	94974438	G	A	29	GENIC	homozygous	116827043
10	94976469	94976470	C	A	17	GENIC	homozygous	116827045
10	94977528	94977529	G	A	29	GENIC	homozygous	116827047
10	94976468	94976469	C		17	GENIC	homozygous	131709432
10	94976645	94976645		A	22	GENIC	possibly homozygous	131709433