chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	45821636	45821637	T	C	38	GENIC	homozygous	139152565
12	45822814	45822815	A	G	34	GENIC	possibly homozygous	139152566
12	45823129	45823130	A	G	42	GENIC	homozygous	139152567
12	45823777	45823807	CTCTCTCTCTCTCTCTCGCTCTCGCTCTCG		20	GENIC	homozygous	139058876
12	45823829	45823835	CACACA		24	GENIC	homozygous	139058877
12	45824294	45824295	C	A	29	GENIC	homozygous	139152568
12	45824379	45824380	G	C	27	GENIC	homozygous	139152569
12	45825487	45825488	T	C	26	GENIC	homozygous	139152570
12	45825520	45825521	G	A	22	GENIC	homozygous	139152571
12	45825704	45825705	G	A	48	GENIC	homozygous	139152572
12	45826292	45826293	T	C	43	GENIC	homozygous	139152573
12	45826675	45826675		CCTTCTG	21	GENIC	homozygous	139058878
12	45826764	45826765	T	C	18	GENIC	homozygous	139152574
12	45827016	45827017	G	A	29	GENIC	homozygous	139152575
12	45827401	45827402	G	A	30	GENIC	homozygous	139152576
12	45828127	45828128	A	G	38	GENIC	homozygous	139152577
12	45828841	45828842	A	G	33	GENIC	homozygous	139152578
12	45828930	45828931	A	C	32	GENIC	homozygous	139152579
12	45828931	45828932	A	G	34	GENIC	homozygous	139152580
12	45829003	45829004	A	G	39	GENIC	homozygous	139152581
12	45829025	45829025		GCTAT	43	GENIC	homozygous	139058879
12	45829121	45829134	CCTAGCAAGCGCA		45	GENIC	homozygous	139058880
12	45829205	45829206	T	G	29	GENIC	possibly homozygous	139152582
12	45830327	45830328	G	A	35	GENIC	homozygous	139152583
12	45830373	45830374	G	A	30	GENIC	homozygous	139152584
12	45830879	45830880	G	A	38	GENIC	homozygous	139152585
12	45831342	45831343	A	G	33	GENIC	homozygous	139152586