chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116406396	116406397	C	T	53	GENIC	homozygous	116669247
8	116407471	116407472	T	C	33	GENIC	homozygous	116669249
8	116410462	116410463	G	A	70	GENIC	homozygous	116669257
8	116411870	116411871	C	T	14	GENIC	homozygous	116669259
8	116412085	116412086	A	T	15	GENIC	homozygous	116669261
8	116412247	116412248	T	C	38	GENIC	homozygous	116669263
8	116412502	116412503	T	C	35	GENIC	homozygous	116669265
8	116413929	116413930	T	G	55	GENIC	homozygous	116669267
8	116414757	116414758	T	C	45	GENIC	homozygous	116669269
8	116416752	116416753	A	G	40	GENIC	homozygous	116669271
8	116417175	116417176	G	A	40	GENIC	homozygous	116669273
8	116417766	116417767	T	C	43	GENIC	homozygous	116669275
8	116419996	116419997	C	A	53	GENIC	homozygous	116669277
8	116420174	116420175	C	T	60	GENIC	homozygous	116669279
8	116420762	116420763	G	A	58	GENIC	homozygous	116669281
8	116420834	116420835	G	A	52	GENIC	homozygous	116669283
8	116421135	116421136	C	T	69	GENIC	homozygous	116669285
8	116421298	116421299	A	G	27	GENIC	homozygous	116669287
8	116421299	116421300	T	C	29	GENIC	homozygous	116669289
8	116421494	116421495	A	G	55	GENIC	homozygous	116669291
8	116423091	116423092	T	C	57	GENIC	homozygous	116669293
8	116423126	116423127	C	A	63	GENIC	homozygous	116669295