chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3995632	3995633	G	A	21	INTERGENIC	possibly homozygous	45374463
20	3995774	3995775	A	G	18	INTERGENIC	homozygous	45374464
20	3996374	3996375	G	A	22	GENIC	homozygous	45374465
20	3996471	3996472	T	G	31	GENIC	homozygous	45374466
20	3996647	3996648	C	T	33	GENIC	homozygous	45374467
20	3996651	3996652	G	A	33	GENIC	homozygous	45374468
20	3997138	3997144	GTGTGT	------	9	GENIC	homozygous	45854844
20	3997871	3997874	GGA	---	13	GENIC	homozygous	45374470
20	3998001	3998002	T	TA	12	GENIC	heterozygous	45374474
20	3998002	3998003	A	-	12	GENIC	heterozygous	45620594
20	3998760	3998761	A	G	42	GENIC	homozygous	45374475
20	4001368	4001369	A	G	29	GENIC	homozygous	45374476
20	4001887	4001888	A	-	21	GENIC	homozygous	45374477
20	4002638	4002639	T	A	37	GENIC	homozygous	45374479
20	4003086	4003087	C	T	13	GENIC	homozygous	45374480
20	4003498	4003499	A	AAG	8	GENIC	possibly homozygous	45374481
20	4003554	4003555	G	C	15	GENIC	homozygous	45374484
20	4004135	4004136	T	C	38	GENIC	homozygous	45374485
20	4004426	4004428	GG	--	23	GENIC	heterozygous	45620596
20	4004427	4004428	G	-	23	GENIC	possibly homozygous	45374486
20	4004589	4004590	G	A	19	GENIC	homozygous	45374487
20	4004755	4004756	T	G	30	GENIC	homozygous	45374488
20	4004756	4004757	C	A	29	GENIC	homozygous	45374489
20	4004763	4004764	C	T	29	GENIC	homozygous	45374490
20	4005284	4005285	G	A	22	GENIC	homozygous	45374491
20	4005568	4005569	T	TACAC	8	GENIC	possibly homozygous	45891145
20	4005577	4005579	AC	--	8	GENIC	heterozygous	45374493
20	4006217	4006218	A	G	23	GENIC	homozygous	45374494
20	4006440	4006441	A	G	24	GENIC	homozygous	45374495
20	4006512	4006515	AAA	---	3	GENIC	heterozygous	45374496
20	4006549	4006550	G	A	16	GENIC	possibly homozygous	45374497
20	4007628	4007629	A	C	21	GENIC	homozygous	45374498
20	4008294	4008295	C	T	19	GENIC	homozygous	45374499
20	4008958	4008960	GT	--	2	GENIC	homozygous	45838325
20	4008973	4008974	G	A	8	GENIC	homozygous	45818336
20	4009398	4009399	G	-	28	GENIC	homozygous	45374500