chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	43065010	43065011	A	G	15	GENIC	possibly homozygous	50210460
12	43065584	43065585	C	G	5	GENIC	heterozygous	50210461
12	43065585	43065586	C	T	6	GENIC	heterozygous	50210462
12	43065586	43065587	A	G	6	GENIC	heterozygous	50210463
12	43065890	43065891	T	C	10	GENIC	heterozygous	50469168
12	43066303	43066304	C	T	5	GENIC	heterozygous	50210467
12	43066313	43066314	T	C	8	GENIC	homozygous	50210469
12	43066318	43066319	G	A	15	GENIC	heterozygous	50210470
12	43066757	43066758	A	G	12	GENIC	homozygous	50210472
12	43066771	43066772	C	G	16	GENIC	heterozygous	50210473
12	43067427	43067428	T	C	5	GENIC	heterozygous	50210478
12	43067496	43067497	G	GACAAAACAAA	1	GENIC	homozygous	50544514
12	43067698	43067699	C	G	17	GENIC	possibly homozygous	50210479
12	43068077	43068078	T	C	25	GENIC	homozygous	50210480
12	43068233	43068234	G	A	19	GENIC	possibly homozygous	50210481
12	43068249	43068250	G	A	18	GENIC	homozygous	50210482
12	43068610	43068611	T	C	27	GENIC	homozygous	50210483
12	43068760	43068761	T	C	26	GENIC	homozygous	50210485
12	43068792	43068793	T	A	24	GENIC	possibly homozygous	50210486
12	43068985	43068986	G	A	32	GENIC	possibly homozygous	50210487
12	43069098	43069099	G	A	25	GENIC	homozygous	50210488
12	43069413	43069414	T	G	1	GENIC	homozygous	50210489
12	43069742	43069743	T	C	17	GENIC	possibly homozygous	50210492
12	43070420	43070421	G	C	5	GENIC	heterozygous	50210493
12	43072066	43072067	T	A	1	GENIC	homozygous	50210494
12	43072103	43072107	TGTG	----	6	GENIC	heterozygous	50210495
12	43073154	43073155	C	T	2	GENIC	homozygous	50210496
12	43073342	43073343	C	T	22	GENIC	homozygous	50210497