chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110680853	110680854	C	T	132	GENIC	heterozygous	118013450
10	110680915	110680916	T	C	144	GENIC	heterozygous	118013452
10	110680967	110680968	C	T	48	GENIC	heterozygous	118013453
10	110710651	110710652	C	A	25	GENIC	homozygous	117232692
10	110710814	110710815	T	G	31	GENIC	homozygous	117313475
10	110710928	110710929	T	G	18	GENIC	homozygous	118013454
10	110710930	110710931	T	C	18	GENIC	homozygous	117035998
10	110711004	110711005	G	T	17	GENIC	homozygous	117036000
10	110713215	110713216	G	C	27	GENIC	homozygous	116721000
10	110713476	110713477	C	G	18	GENIC	homozygous	118013455
10	110713632	110713633	C	A	12	GENIC	homozygous	117201164
10	110713842	110713843	T	G	4	GENIC	homozygous	118054444
10	110714227	110714228	A	C	5	GENIC	homozygous	117036004
10	110714517	110714518	A	C	4	GENIC	homozygous	118013457
10	110714747	110714748	A	T	9	GENIC	homozygous	118013458
10	110738581	110738582	G	A	29	GENIC	homozygous	117201166
10	110745160	110745161	C	A	37	GENIC	homozygous	116721002
10	110745763	110745764	G	A	8	GENIC	homozygous	118013459
10	110745767	110745768	C	A	9	GENIC	possibly homozygous	118013460
10	110738585	110738586	G	C	25	GENIC	homozygous	117201168