chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	209289179	209289180	G	GAGTT	4	GENIC	heterozygous	60515139
2	209289353	209289354	T	TTGTGTGTGTG	13	GENIC	heterozygous	59359478
2	209289353	209289354	T	TTGTGTGTGTGTG	13	GENIC	heterozygous	60515140
2	209289589	209289590	A	G	28	GENIC	homozygous	59359479
2	209290372	209290373	T	C	43	GENIC	homozygous	59359480
2	209291105	209291106	C	CA	10	GENIC	homozygous	59359481
2	209291326	209291327	T	G	16	GENIC	homozygous	59359482
2	209291805	209291806	T	A	1	GENIC	homozygous	59359483
2	209294159	209294160	A	C	23	GENIC	homozygous	59359487
2	209294370	209294371	A	T	29	GENIC	homozygous	59359488
2	209295227	209295230	CTG	---	2	GENIC	homozygous	59359489
2	209295233	209295236	TTT	---	1	GENIC	homozygous	59359490
2	209295291	209295292	G	GT	9	GENIC	homozygous	59359491
2	209295526	209295527	A	G	15	GENIC	homozygous	59359492
2	209295679	209295680	A	C	12	GENIC	homozygous	59359493
2	209296334	209296335	C	T	13	GENIC	homozygous	59359494
2	209297842	209297843	C	A	31	GENIC	homozygous	59359495
2	209299104	209299105	C	CTTT	8	GENIC	homozygous	59359496
2	209299266	209299267	C	CGT	17	GENIC	possibly homozygous	59359497
2	209299560	209299561	T	-	2	GENIC	homozygous	59359498
2	209299719	209299720	T	TAC	3	GENIC	heterozygous	59932787
2	209299762	209299763	C	T	12	GENIC	possibly homozygous	59359500
2	209300551	209300552	G	GA	13	GENIC	heterozygous	59932791
2	209300732	209300733	G	T	13	GENIC	homozygous	59359504
2	209301417	209301418	T	-	8	GENIC	homozygous	60515141
2	209301430	209301431	T	C	9	GENIC	possibly homozygous	59359506
2	209301671	209301672	C	CT	11	GENIC	homozygous	59359510
2	209304410	209304411	T	-	36	GENIC	homozygous	59359511
2	209305023	209305024	C	G	34	GENIC	homozygous	59359514
2	209305894	209305895	T	C	23	GENIC	homozygous	59359515
2	209306430	209306431	A	ATGTGTG	22	GENIC	homozygous	59359516
2	209307718	209307719	C	T	33	GENIC	homozygous	59359517
2	209299530	209299531	C	CT	3	GENIC	heterozygous	60895788