chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	128800050	128800051	G	T	7	GENIC	heterozygous	52886977
8	128801364	128801365	A	G	8	GENIC	homozygous	52886978
8	128801696	128801697	A	AT	20	GENIC	possibly homozygous	52886979
8	128803490	128803507	GCCTGGGTCTGTGCATC	-----------------	4	GENIC	heterozygous	52886982
8	128803702	128803703	G	GA	4	GENIC	homozygous	52886983
8	128803705	128803706	T	A	4	GENIC	homozygous	53369604
8	128803706	128803707	G	GCAC	4	GENIC	homozygous	52886984
8	128803754	128803755	C	T	27	GENIC	homozygous	52886985
8	128804165	128804166	A	G	30	GENIC	possibly homozygous	52886986
8	128804687	128804688	A	G	17	GENIC	possibly homozygous	52886987
8	128804949	128804950	A	G	21	GENIC	possibly homozygous	52886988
8	128805055	128805056	T	C	12	GENIC	homozygous	52886989
8	128806345	128806346	A	T	13	GENIC	homozygous	52886990
8	128806917	128806918	G	A	22	GENIC	homozygous	52886991
8	128807350	128807351	C	T	23	GENIC	homozygous	52886992
8	128808346	128808347	T	C	29	GENIC	homozygous	52886996
8	128809380	128809381	G	A	14	GENIC	homozygous	52886997
8	128810072	128810073	T	G	17	GENIC	homozygous	52886998
8	128810546	128810547	G	A	10	GENIC	homozygous	52886999
8	128811224	128811225	T	G	1	GENIC	homozygous	52887003
8	128811226	128811227	T	G	2	GENIC	homozygous	52887004
8	128812750	128812751	A	-	2	GENIC	homozygous	53064661
8	128813274	128813275	T	C	13	GENIC	homozygous	52887006
8	128813286	128813287	C	T	12	GENIC	homozygous	52887007
8	128813866	128813867	C	CT	19	GENIC	homozygous	52887008
8	128814029	128814030	G	A	11	GENIC	homozygous	52887009
8	128814505	128814507	AA	--	3	GENIC	heterozygous	52887010
8	128814506	128814507	A	-	3	GENIC	heterozygous	53653078
8	128816936	128816938	AG	--	18	GENIC	homozygous	52887012
8	128817512	128817513	G	T	2	GENIC	heterozygous	52887015
8	128820223	128820224	C	T	15	GENIC	homozygous	52887016
8	128820520	128820521	A	C	10	GENIC	homozygous	52887017
8	128822299	128822300	C	T	17	GENIC	possibly homozygous	52887018
8	128824499	128824500	C	G	20	GENIC	possibly homozygous	52887019