chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	135080527	135080528	C	T	12	GENIC	homozygous	135673365
1	135080850	135080851	G	A	20	GENIC	homozygous	135673366
1	135081709	135081710	C	T	22	GENIC	homozygous	135673367
1	135083651	135083651		GTGGTG	13	GENIC	homozygous	135430343
1	135085741	135085742	A	G	15	GENIC	homozygous	135673368
1	135088608	135088610	AC		12	GENIC	homozygous	135430344
1	135096294	135096295	G	T	14	GENIC	homozygous	135673369
1	135099688	135099689	C	T	11	GENIC	homozygous	135673370
1	135101379	135101380	G	A	15	GENIC	homozygous	135673371
1	135103258	135103259	A	G	23	GENIC	homozygous	135673372
1	135104234	135104235	T	G	22	GENIC	homozygous	135673373
1	135105651	135105652	A	G	20	GENIC	homozygous	135673374
1	135106645	135106647	TG		19	GENIC	homozygous	135430345
1	135107699	135107700	T	C	20	GENIC	homozygous	135673375
1	135109657	135109658	A	C	17	GENIC	homozygous	135673376
1	135109667	135109668	G	A	19	GENIC	homozygous	135673377
1	135109856	135109857	G	A	25	GENIC	homozygous	135673378
1	135109865	135109866	T	C	25	GENIC	homozygous	135673379
1	135110654	135110655	T	A	19	GENIC	homozygous	135673380
1	135112661	135112662	A	G	15	GENIC	homozygous	135673381
1	135114612	135114613	C	A	20	GENIC	homozygous	135673382
1	135117669	135117670	C	T	21	GENIC	possibly homozygous	135673383
1	135120606	135120607	T	C	24	GENIC	homozygous	135673384
1	135120869	135120869		C	5	GENIC	homozygous	135430346
1	135120990	135120991	T	C	22	GENIC	homozygous	135673385
1	135121529	135121530	C	T	15	GENIC	homozygous	135673386
1	135111635	135111636	G		17	GENIC	homozygous	402964455
1	135111635	135111636	G	C	17	GENIC	heterozygous	153797378