chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109528931	109528932	A	G	12	GENIC	heterozygous	116718537
10	109529995	109529996	C	A	19	GENIC	heterozygous	116718539
10	109530529	109530530	G	A	27	GENIC	heterozygous	116718541
10	109530659	109530660	G	C	23	GENIC	heterozygous	116718543
10	109530960	109530960		T	22	GENIC	heterozygous	128860524
10	109531858	109531859	A	C	26	GENIC	heterozygous	116718545
10	109532324	109532325	A	G	23	GENIC	heterozygous	116718547
10	109532860	109532861	G	A	23	GENIC	heterozygous	116718549
10	109533199	109533200	T	C	21	GENIC	heterozygous	116718551
10	109534587	109534588	G	A	12	GENIC	heterozygous	116718553
10	109534704	109534705	T	C	15	GENIC	heterozygous	116718555
10	109535201	109535202	C	T	13	GENIC	heterozygous	116718557
10	109535688	109535689	A	G	29	GENIC	heterozygous	116718559
10	109535769	109535772	AGT		24	GENIC	heterozygous	128860525
10	109535798	109535799	G	A	24	GENIC	heterozygous	116909575
10	109535847	109535848	C	G	23	GENIC	heterozygous	116718561
10	109535940	109535941	T	G	16	GENIC	heterozygous	116718563
10	109536319	109536319		GTGTGT	11	GENIC	heterozygous	128860526
10	109536535	109536535		TTGTT	16	GENIC	heterozygous	128860527
10	109539468	109539469	G	C	17	GENIC	heterozygous	116718565