chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	111434032	111434033	T	G	39	GENIC	homozygous	138182501
7	111435627	111435628	C		24	GENIC	homozygous	137974364
7	111435904	111435905	T	G	33	GENIC	homozygous	138182503
7	111436688	111436689	T	C	29	GENIC	homozygous	138182504
7	111439764	111439765	A	G	39	GENIC	homozygous	138182505
7	111440277	111440278	T	C	29	GENIC	homozygous	138182506
7	111440484	111440485	T	G	34	GENIC	homozygous	138182507
7	111435890	111435891	T		37	GENIC	heterozygous	141922627
7	111435888	111435889	T	G	38	GENIC	heterozygous	154492307
7	111435890	111435891	T	G	37	GENIC	homozygous	154492308
7	111435888	111435889	T		38	GENIC	homozygous	403222447
7	111437032	111437032		A	30	GENIC	homozygous	141922628
7	111439084	111439085	A	G	46	GENIC	homozygous	145635124
7	111439821	111439822	T	C	43	GENIC	homozygous	145635125
7	111440743	111440743		TGATGA	26	GENIC	homozygous	137974365
7	111444102	111444103	C	T	40	GENIC	homozygous	138182510
7	111445066	111445067	A	G	47	GENIC	homozygous	138182511
7	111445339	111445451	AAACTCTTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAGAATAAAAAAAAAAAAAAA		10	GENIC	homozygous	137974368
7	111445686	111445687	A	T	28	GENIC	possibly homozygous	138182512
7	111446216	111446217	T	C	37	GENIC	homozygous	138182513
7	111446223	111446224	G	A	39	GENIC	homozygous	138182514
7	111446586	111446586		T	13	GENIC	possibly homozygous	143350756
7	111446750	111446751	G	A	38	GENIC	homozygous	138182515
7	111447329	111447330	A	G	39	GENIC	homozygous	138182516
7	111447881	111447882	G	A	38	GENIC	homozygous	145635126
7	111448987	111448988	G	A	44	GENIC	homozygous	138182517
7	111449453	111449454	C	T	37	GENIC	homozygous	138182518
7	111452535	111452536	C	G	26	GENIC	homozygous	145635127
7	111451168	111451169	G		40	GENIC	possibly homozygous	145610123