chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	153774644	153774645	G	T	27	GENIC	possibly homozygous	112890371
4	153776483	153776484	G	A	78	GENIC	heterozygous	113061292
4	153776733	153776734	T	C	61	GENIC	homozygous	112890372
4	153777091	153777092	C	T	66	GENIC	homozygous	112890373
4	153777965	153777966	C	T	61	GENIC	homozygous	112890374
4	153778240	153778241	G	T	33	GENIC	homozygous	112890375
4	153778328	153778329	A	T	44	GENIC	homozygous	112890376
4	153780804	153780805	T	C	50	GENIC	homozygous	112890377
4	153783531	153783532	T	C	33	GENIC	homozygous	112890380
4	153784338	153784339	T	C	44	GENIC	homozygous	112890381
4	153785894	153785895	C	T	37	GENIC	homozygous	112890382
4	153786361	153786362	G	T	22	GENIC	homozygous	112890383
4	153787656	153787657	C	G	89	GENIC	heterozygous	112890384
4	153789676	153789677	G	A	50	GENIC	homozygous	112890385
4	153790568	153790569	C	T	35	GENIC	homozygous	112890386
4	153790870	153790871	G	A	47	GENIC	homozygous	112890387
4	153790952	153790953	A	G	44	GENIC	homozygous	112890388
4	153790976	153790977	A	C	44	GENIC	homozygous	112890389
4	153788085	153788086	G	T	34	GENIC	heterozygous	113563065
4	153788077	153788078	G	T	33	GENIC	possibly homozygous	113183139
4	153788081	153788082	G	T	34	GENIC	possibly homozygous	113563063
4	153788084	153788085	C	T	33	GENIC	heterozygous	113563064