chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	110505285	110505287	AG	--	14	GENIC	homozygous	52801371
8	110505499	110505500	A	G	18	GENIC	homozygous	52801373
8	110505850	110505851	T	C	21	GENIC	homozygous	52801375
8	110506194	110506198	AAAC	----	17	GENIC	homozygous	52801377
8	110506226	110506227	T	G	18	GENIC	homozygous	52801379
8	110507429	110507430	C	T	31	GENIC	homozygous	52801381
8	110507474	110507475	G	GT	13	GENIC	heterozygous	53454151
8	110507475	110507476	T	-	13	GENIC	heterozygous	53034144
8	110508137	110508138	T	A	19	GENIC	homozygous	52801383
8	110509566	110509567	C	G	10	GENIC	homozygous	52801385
8	110509832	110509833	T	-	31	GENIC	possibly homozygous	53367561
8	110509843	110509844	T	A	35	GENIC	homozygous	53034148
8	110510196	110510197	C	T	33	GENIC	homozygous	52801391
8	110510273	110510274	T	TGTCC	18	GENIC	homozygous	52801393
8	110511904	110511905	C	A	20	GENIC	homozygous	52801397
8	110512631	110512632	A	G	25	GENIC	homozygous	52801399
8	110513064	110513065	C	T	33	GENIC	homozygous	52801401
8	110513555	110513556	T	-	8	GENIC	homozygous	52801403
8	110513564	110513568	TTTT	----	8	GENIC	possibly homozygous	53522465