chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	120778166	120778167	G		14	GENIC	possibly homozygous	403118449
4	120778166	120778167	G	A	14	GENIC	heterozygous	403118450
4	120833772	120833780	TCTCTGTG		11	GENIC	heterozygous	140995718
4	120833777	120833778	G		6	GENIC	heterozygous	403118451
4	120833777	120833778	G	C	6	GENIC	heterozygous	403118452
4	120833779	120833780	G		6	GENIC	heterozygous	403118453
4	120833779	120833780	G	C	6	GENIC	heterozygous	403118454
4	120833781	120833782	G		6	GENIC	heterozygous	403118455
4	120833781	120833782	G	C	6	GENIC	heterozygous	403118456
4	120837234	120837235	A	G	25	GENIC	possibly homozygous	403888540
4	120839699	120839700	C	G	36	GENIC	heterozygous	403118460
4	120839699	120839700	C		36	GENIC	heterozygous	403118461
4	120839701	120839702	C	G	36	GENIC	heterozygous	137194530
4	120839703	120839704	C	G	37	GENIC	heterozygous	137194531
4	120839707	120839708	C	G	39	GENIC	heterozygous	137194532
4	120839709	120839710	C	G	39	GENIC	heterozygous	137194533
4	120885412	120885413	A	C	48	GENIC	homozygous	144683851