chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	111477209	111477210	G	C	16	GENIC	homozygous	115154547
6	111477596	111477597	T	G	19	GENIC	homozygous	115154549
6	111477775	111477776	A	G	10	GENIC	homozygous	115154551
6	111477962	111477963	G	C	19	GENIC	homozygous	115154553
6	111478382	111478383	T	G	23	GENIC	homozygous	118575139
6	111478447	111478448	C	T	27	GENIC	homozygous	115154561
6	111478449	111478450	G	A	25	GENIC	homozygous	115154563
6	111478551	111478552	C	T	19	GENIC	homozygous	115154565
6	111478766	111478767	A	G	22	GENIC	homozygous	115154567
6	111479360	111479361	C	T	15	GENIC	homozygous	115154570
6	111479664	111479665	A	G	21	GENIC	homozygous	115154572
6	111479806	111479807	G	A	18	GENIC	homozygous	115154574
6	111480069	111480070	C	T	34	GENIC	possibly homozygous	115154576
6	111480093	111480094	A	G	36	GENIC	homozygous	115154578
6	111480357	111480358	C	T	39	GENIC	homozygous	115154580
6	111480406	111480407	G	A	35	GENIC	homozygous	115154582
6	111480449	111480450	G	A	29	GENIC	homozygous	115154584
6	111480611	111480612	T	C	40	GENIC	homozygous	115154586
6	111480630	111480631	T	C	37	GENIC	homozygous	115154588
6	111480894	111480895	C	T	26	GENIC	homozygous	115154590
6	111481514	111481515	G	A	35	GENIC	possibly homozygous	115154592
6	111481601	111481602	A	G	42	GENIC	homozygous	115154594
6	111482981	111482982	T	C	25	GENIC	homozygous	115154598
6	111483352	111483353	A	G	20	GENIC	homozygous	115154600
6	111483811	111483812	C	T	20	GENIC	homozygous	115154602
6	111484855	111484856	G	A	21	GENIC	homozygous	115154604
6	111485417	111485418	T	C	20	GENIC	possibly homozygous	115154606
6	111485516	111485517	C	T	19	GENIC	homozygous	115154610
6	111485625	111485626	A	C	22	GENIC	homozygous	115154612
6	111485846	111485847	T	C	31	GENIC	homozygous	115154614
6	111486035	111486036	G	A	27	GENIC	homozygous	115154616