chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116406396	116406397	C	T	32	GENIC	homozygous	116669247
8	116407471	116407472	T	C	32	GENIC	homozygous	116669249
8	116407733	116407734	T	C	23	GENIC	heterozygous	116669253
8	116407737	116407738	T	C	23	GENIC	heterozygous	116669255
8	116407817	116407818	C	T	33	GENIC	homozygous	116988061
8	116410430	116410431	G	T	41	GENIC	homozygous	116988062
8	116410462	116410463	G	A	46	GENIC	homozygous	116669257
8	116411870	116411871	C	T	8	GENIC	homozygous	116669259
8	116412247	116412248	T	C	30	GENIC	homozygous	116669263
8	116412502	116412503	T	C	28	GENIC	homozygous	116669265
8	116413929	116413930	T	G	35	GENIC	homozygous	116669267
8	116414757	116414758	T	C	24	GENIC	homozygous	116669269
8	116420174	116420175	C	T	41	GENIC	homozygous	116669279
8	116420593	116420594	T	C	29	GENIC	homozygous	116886435
8	116420762	116420763	G	A	29	GENIC	homozygous	116669281
8	116421494	116421495	A	G	35	GENIC	homozygous	116669291
8	116423126	116423127	C	A	39	GENIC	possibly homozygous	116669295