chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3995757	3995758	A	C	15	INTERGENIC	homozygous	45730052
20	3995774	3995775	A	G	13	INTERGENIC	homozygous	45374464
20	3996471	3996472	T	G	9	GENIC	heterozygous	45374466
20	3996830	3996831	C	G	10	GENIC	homozygous	45730053
20	3997873	3997874	A	AG	3	GENIC	heterozygous	45374473
20	3998443	3998444	G	A	16	GENIC	heterozygous	45730056
20	3998760	3998761	A	G	17	GENIC	possibly homozygous	45374475
20	3999135	3999136	C	T	13	GENIC	homozygous	45730057
20	3999950	3999951	T	TA	5	GENIC	heterozygous	45730058
20	4001601	4001602	G	C	8	GENIC	homozygous	45730059
20	4001894	4001895	G	A	11	GENIC	possibly homozygous	45730060
20	4003086	4003087	C	T	1	GENIC	homozygous	45374480
20	4003200	4003201	C	G	13	GENIC	possibly homozygous	45730061
20	4004135	4004136	T	C	6	GENIC	homozygous	45374485
20	4004426	4004428	GG	--	4	GENIC	heterozygous	45620596
20	4004755	4004756	T	G	5	GENIC	homozygous	45374488
20	4004756	4004757	C	A	5	GENIC	homozygous	45374489
20	4004763	4004764	C	T	5	GENIC	heterozygous	45374490
20	4005284	4005285	G	A	18	GENIC	possibly homozygous	45374491
20	4005434	4005435	C	T	21	GENIC	possibly homozygous	45730062
20	4006217	4006218	A	G	5	GENIC	heterozygous	45374494
20	4006440	4006441	A	G	13	GENIC	heterozygous	45374495
20	4006549	4006550	G	A	11	GENIC	heterozygous	45374497
20	4007628	4007629	A	C	4	GENIC	homozygous	45374498
20	4008294	4008295	C	T	13	GENIC	possibly homozygous	45374499
20	4008958	4008960	GT	--	1	GENIC	homozygous	45838325
20	4009398	4009399	G	-	4	GENIC	heterozygous	45374500
20	4008973	4008974	G	A	2	GENIC	homozygous	45818336