chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116406396	116406397	C	T	38	GENIC	homozygous	116669247
8	116407471	116407472	T	C	13	GENIC	homozygous	116669249
8	116407733	116407734	T	C	31	GENIC	heterozygous	116669253
8	116407737	116407738	T	C	30	GENIC	heterozygous	116669255
8	116410462	116410463	G	A	35	GENIC	homozygous	116669257
8	116411870	116411871	C	T	24	GENIC	homozygous	116669259
8	116412085	116412086	A	T	22	GENIC	homozygous	116669261
8	116412247	116412248	T	C	21	GENIC	homozygous	116669263
8	116412502	116412503	T	C	26	GENIC	homozygous	116669265
8	116413929	116413930	T	G	28	GENIC	homozygous	116669267
8	116414757	116414758	T	C	35	GENIC	homozygous	116669269
8	116416752	116416753	A	G	27	GENIC	homozygous	116669271
8	116417175	116417176	G	A	20	GENIC	homozygous	116669273
8	116417766	116417767	T	C	27	GENIC	possibly homozygous	116669275
8	116419996	116419997	C	A	32	GENIC	homozygous	116669277
8	116420174	116420175	C	T	23	GENIC	homozygous	116669279
8	116420762	116420763	G	A	20	GENIC	homozygous	116669281
8	116420834	116420835	G	A	31	GENIC	homozygous	116669283
8	116421135	116421136	C	T	25	GENIC	homozygous	116669285
8	116421298	116421299	A	G	22	GENIC	homozygous	116669287
8	116421299	116421300	T	C	22	GENIC	homozygous	116669289
8	116421494	116421495	A	G	30	GENIC	homozygous	116669291
8	116423091	116423092	T	C	15	GENIC	homozygous	116669293
8	116423126	116423127	C	A	19	GENIC	homozygous	116669295