chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	7101500	7101501	T	TTGTG	5	INTERGENIC	heterozygous	52352846
10	7101511	7101513	TG	--	5	INTERGENIC	heterozygous	52795683
10	7104973	7104974	G	A	10	INTERGENIC	heterozygous	51801498
10	7109084	7109085	C	-	5	INTERGENIC	heterozygous	52479692
10	7127532	7127534	GA	--	16	GENIC	heterozygous	52312572
10	7155296	7155297	A	AGT	14	GENIC	possibly homozygous	51613030
10	7155296	7155297	A	AGTGT	14	GENIC	heterozygous	51801548
10	7164188	7164190	TG	--	23	GENIC	heterozygous	51613051
10	7170073	7170074	G	-	15	GENIC	homozygous	51316234
10	7170079	7170080	G	-	15	GENIC	homozygous	51316235
10	7170083	7170084	G	-	14	GENIC	homozygous	51316236
10	7170087	7170088	G	-	13	GENIC	homozygous	51316237
10	7170092	7170129	ACCTCTCACTTCTTTTCCCTCTCTTCCTCCCGACCTG	-------------------------------------	18	GENIC	homozygous	52352864
10	7192034	7192035	G	GT	35	GENIC	homozygous	51316245
10	7192074	7192075	A	G	31	GENIC	homozygous	51316246
10	7192090	7192091	A	AT	26	GENIC	homozygous	51316247