chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	87114213	87114214	G	A	18	GENIC	homozygous	51029715
11	87114458	87114459	A	G	21	GENIC	homozygous	51029716
11	87114510	87114511	A	G	26	GENIC	homozygous	51029717
11	87114819	87114820	T	C	18	GENIC	homozygous	51029718
11	87114835	87114836	A	ACGCT	19	GENIC	homozygous	51192282
11	87114841	87114843	AT	--	17	GENIC	homozygous	51192283
11	87114859	87114860	T	TCACA	8	GENIC	homozygous	51192285
11	87115431	87115432	C	T	24	GENIC	homozygous	51029721
11	87115439	87115440	C	T	23	GENIC	homozygous	51029722
11	87116384	87116385	G	A	13	GENIC	homozygous	51029724
11	87116482	87116483	G	C	14	GENIC	homozygous	51029725
11	87116483	87116484	G	C	14	GENIC	homozygous	51029726
11	87116514	87116515	C	G	16	GENIC	homozygous	51029727
11	87117246	87117247	T	A	23	GENIC	homozygous	51029728
11	87117424	87117425	G	C	25	GENIC	homozygous	51029729
11	87117695	87117696	A	T	27	GENIC	homozygous	50857413
11	87118349	87118350	A	G	36	GENIC	homozygous	51029730
11	87118495	87118496	T	G	27	GENIC	homozygous	51029731
11	87118799	87118800	C	T	30	GENIC	homozygous	51029732
11	87118991	87118992	A	-	20	GENIC	homozygous	50857414
11	87119025	87119035	AAAAATATAT	----------	20	GENIC	homozygous	51192286
11	87119136	87119137	T	TTGG	8	GENIC	homozygous	50857416
11	87119703	87119704	C	T	22	GENIC	homozygous	51029734
11	87119720	87119721	C	G	25	GENIC	homozygous	51029735