chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	8846319	8846320	C	T	20	GENIC	possibly homozygous	137999220
7	8847781	8847781		CTGT	29	GENIC	homozygous	137934483
7	8849049	8849050	A	G	13	GENIC	homozygous	137999221
7	8849221	8849222	T	C	4	GENIC	homozygous	137999222
7	8849904	8849905	G	A	26	GENIC	homozygous	137999223
7	8849931	8849932	G	C	22	GENIC	homozygous	137999224
7	8849977	8849978	G	C	19	GENIC	homozygous	137999225
7	8849988	8849989	C	T	18	GENIC	homozygous	137999226
7	8851046	8851047	T	C	20	GENIC	homozygous	137999227
7	8851785	8851786	A	T	25	GENIC	homozygous	137999228
7	8851812	8851813	G	T	29	GENIC	homozygous	137999229
7	8852034	8852034		CACAGCCGCGGCCCAG	19	GENIC	homozygous	137934493
7	8852600	8852600		AC	17	GENIC	homozygous	137934494
7	8852670	8852671	C	T	22	GENIC	homozygous	137999230
7	8852840	8852841	G	A	22	GENIC	homozygous	137999231
7	8852916	8852917	A	G	19	GENIC	homozygous	137999232
7	8853141	8853142	G	T	21	GENIC	homozygous	137999233
7	8853707	8853709	CA		12	GENIC	homozygous	137934495
7	8854663	8854664	T	G	27	GENIC	homozygous	137999234
7	8855216	8855217	C	A	7	GENIC	homozygous	137999235
7	8855480	8855481	A	G	15	GENIC	homozygous	137999237
7	8855788	8855789	C	T	20	GENIC	homozygous	137999238
7	8855868	8855869	T	C	18	GENIC	homozygous	137999239
7	8855992	8855993	T	C	19	GENIC	homozygous	137999240