chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11631338	11631339	T	C	25	GENIC	homozygous	47365551
17	11631363	11631364	A	AG	20	GENIC	homozygous	47365553
17	11632644	11632645	A	AAG	25	GENIC	homozygous	47365555
17	11632880	11632881	G	GT	9	GENIC	homozygous	47702931
17	11632894	11632895	A	T	10	GENIC	homozygous	47702933
17	11633103	11633104	G	GT	10	GENIC	homozygous	47365559
17	11633134	11633135	A	G	13	GENIC	homozygous	47365561
17	11633207	11633208	G	GTTT	5	GENIC	heterozygous	47722354
17	11634441	11634442	A	AACAC	11	GENIC	heterozygous	47792441
17	11634442	11634448	ACACAC	------	11	GENIC	heterozygous	47722356
17	11634444	11634448	ACAC	----	11	GENIC	heterozygous	47722358
17	11636119	11636123	AAAA	----	1	GENIC	homozygous	47722360
17	11636252	11636253	T	C	40	GENIC	homozygous	47365567
17	11636325	11636326	T	-	7	GENIC	homozygous	47020543
17	11636855	11636858	TTA	---	10	GENIC	heterozygous	47365569
17	11637759	11637760	A	AAATAATAAT	2	GENIC	heterozygous	47020545
17	11637759	11637760	A	AAATAATAATAAT	2	GENIC	heterozygous	47722362
17	11638440	11638444	AAAA	----	8	GENIC	heterozygous	47020546
17	11638441	11638444	AAA	---	8	GENIC	possibly homozygous	47020547
17	11640315	11640316	A	-	15	GENIC	homozygous	47365571
17	11641941	11641942	T	C	46	GENIC	homozygous	47365573