chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	55099975	55099976	G	A	34	GENIC	homozygous	146989446
11	55100009	55100010	G	A	36	GENIC	homozygous	146989447
11	55100062	55100063	A	C	58	GENIC	homozygous	146989448
11	55100607	55100608	C	T	66	GENIC	homozygous	146989449
11	55100719	55100720	A	G	57	GENIC	homozygous	146989450
11	55100782	55100783	A	G	63	GENIC	homozygous	146989451
11	55101130	55101131	G	A	50	GENIC	homozygous	146989452
11	55101379	55101380	C	T	41	GENIC	homozygous	146989453
11	55101782	55101783	C	T	47	GENIC	homozygous	146989454
11	55102257	55102258	C	T	41	GENIC	homozygous	146989455
11	55103077	55103078	C	T	56	GENIC	homozygous	138995915
11	55105510	55105511	C	A	68	GENIC	homozygous	146989456
11	55106499	55106500	G	A	48	GENIC	homozygous	146989457
11	55109258	55109259	C	T	50	GENIC	homozygous	146989458
11	55111412	55111413	A	G	54	GENIC	homozygous	146989459
11	55111428	55111429	A	G	53	GENIC	homozygous	138995949
11	55112472	55112473	T	C	45	GENIC	homozygous	138995951
11	55112943	55112944	A	G	43	GENIC	homozygous	146989460
11	55113251	55113252	G	A	40	GENIC	homozygous	146989461
11	55108811	55108824	CCGATTCCTGCCG		38	GENIC	homozygous	146978191