chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11648525	11648526	A	G	18	GENIC	homozygous	115437517
12	11665047	11665048	A	G	68	GENIC	heterozygous	115256108
12	11665078	11665079	G	A	55	GENIC	heterozygous	115256110
12	11665283	11665284	A	T	47	GENIC	heterozygous	115256120
12	11665293	11665294	C	T	51	GENIC	heterozygous	115256122
12	11665349	11665350	A	G	39	GENIC	heterozygous	115256124
12	11665830	11665831	G	A	48	GENIC	heterozygous	115256126
12	11665884	11665885	C	A	31	GENIC	heterozygous	115256128
12	11665885	11665886	T	G	30	GENIC	heterozygous	115256130
12	11665946	11665947	C	T	30	GENIC	heterozygous	115256132
12	11665947	11665948	G	A	31	GENIC	heterozygous	115256134
12	11665966	11665967	G	A	41	GENIC	heterozygous	115256136
12	11666034	11666035	C	G	57	GENIC	heterozygous	115256138
12	11666089	11666090	G	T	60	GENIC	heterozygous	115256140
12	11666437	11666438	C	T	25	GENIC	heterozygous	115256144
12	11666449	11666450	G	T	22	GENIC	heterozygous	115256146
12	11666508	11666509	T	C	11	GENIC	homozygous	115514168
12	11667296	11667297	T	A	27	GENIC	heterozygous	115415623
12	11667315	11667316	C	T	30	GENIC	heterozygous	115415625
12	11667324	11667325	T	G	27	GENIC	heterozygous	115415627
12	11668563	11668564	A	G	32	GENIC	heterozygous	115415631
12	11669411	11669412	A	C	36	GENIC	heterozygous	115482373
12	11669413	11669414	C	A	37	GENIC	heterozygous	115482374
12	11669420	11669421	A	G	32	GENIC	heterozygous	115256152
12	11669490	11669491	C	T	33	GENIC	heterozygous	115491518
12	11669498	11669499	T	C	27	GENIC	heterozygous	115491520
12	11669500	11669501	A	G	26	GENIC	heterozygous	115491522
12	11669511	11669512	A	C	28	GENIC	heterozygous	115491524
12	11677195	11677196	T	A	19	GENIC	homozygous	115256154