chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40895607	40895608	T	G	2	INTERGENIC	homozygous	50323470
12	40895965	40895966	A	G	17	INTERGENIC	homozygous	50204973
12	40896064	40896065	T	C	7	INTERGENIC	homozygous	50323472
12	40896245	40896246	C	A	10	INTERGENIC	homozygous	50323474
12	40896537	40896538	C	T	13	INTERGENIC	heterozygous	50323476
12	40896637	40896639	GG	--	2	INTERGENIC	homozygous	50204976
12	40897027	40897028	G	GCC	1	INTERGENIC	homozygous	50204977
12	40897363	40897364	G	-	12	INTERGENIC	homozygous	50323484
12	40897415	40897416	A	AT	18	INTERGENIC	homozygous	50204979
12	40897731	40897732	G	A	14	INTERGENIC	possibly homozygous	50323486
12	40897786	40897789	TTC	---	1	INTERGENIC	homozygous	50204980
12	40897892	40897893	T	-	8	INTERGENIC	possibly homozygous	50323492
12	40898147	40898148	A	G	23	INTERGENIC	possibly homozygous	50323494
12	40898314	40898315	T	G	11	INTERGENIC	possibly homozygous	50323496
12	40899089	40899090	G	A	16	INTERGENIC	possibly homozygous	50323500
12	40899794	40899795	C	T	23	GENIC	homozygous	50204981
12	40901018	40901019	T	C	6	GENIC	heterozygous	50204984
12	40901189	40901190	A	G	21	GENIC	possibly homozygous	50204985
12	40902655	40902656	A	G	4	INTERGENIC	homozygous	50204988
12	40902811	40902812	T	TA	2	INTERGENIC	homozygous	50204991
12	40902820	40902821	C	A	4	INTERGENIC	homozygous	50204992
12	40904654	40904655	T	A	2	INTERGENIC	homozygous	50323506
12	40906569	40906570	C	T	10	INTERGENIC	homozygous	50323508
12	40907708	40907709	C	-	3	INTERGENIC	heterozygous	50381700
12	40908430	40908431	A	G	19	INTERGENIC	homozygous	50204997
12	40908985	40908986	G	A	18	INTERGENIC	possibly homozygous	50323510
12	40909696	40909697	G	A	7	INTERGENIC	heterozygous	50205001
12	40910416	40910417	C	CTTCCTTGCCCGGACCT	2	INTERGENIC	homozygous	50205002
12	40912021	40912022	C	T	17	GENIC	possibly homozygous	50323518
12	40912070	40912071	T	C	19	GENIC	possibly homozygous	50205005
12	40913010	40913011	G	A	24	GENIC	possibly homozygous	50323520
12	40914306	40914307	T	C	14	GENIC	homozygous	50205006
12	40914573	40914574	G	T	17	GENIC	possibly homozygous	50205007
12	40917344	40917345	A	G	9	GENIC	heterozygous	50205012
12	40917592	40917593	T	TG	1	GENIC	homozygous	50205013
12	40917780	40917781	T	C	1	GENIC	homozygous	50205014
12	40918310	40918312	TG	--	5	GENIC	homozygous	50323532
12	40922135	40922136	C	G	26	GENIC	homozygous	50205016
12	40922816	40922817	G	A	21	GENIC	possibly homozygous	50205017
12	40923777	40923778	C	A	20	GENIC	possibly homozygous	50205019
12	40924190	40924191	C	CCTCT	9	GENIC	homozygous	50205020
12	40925841	40925842	A	C	19	GENIC	homozygous	50205023
12	40926067	40926068	G	GTGT	1	GENIC	homozygous	50205024
12	40931799	40931800	A	G	8	GENIC	heterozygous	50452544
12	40932816	40932817	G	T	20	GENIC	possibly homozygous	50205035
12	40932910	40932911	T	C	18	GENIC	possibly homozygous	50205036
12	40915594	40915595	G	T	22	GENIC	possibly homozygous	50827551
12	40933022	40933023	A	G	6	GENIC	homozygous	50543803
12	40934552	40934553	C	A	8	GENIC	homozygous	50323547
12	40937983	40937984	C	A	7	GENIC	possibly homozygous	50205038
12	40950247	40950248	G	GT	4	GENIC	homozygous	50205054
12	40953275	40953276	G	A	8	GENIC	possibly homozygous	50205059