chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	70439296	70439297	G	A	42	GENIC	homozygous	116190345
7	70439914	70439915	C	T	47	GENIC	homozygous	115708976
7	70440420	70440421	C	T	148	GENIC	heterozygous	116190347
7	70441091	70441092	C	A	37	GENIC	homozygous	116190349
7	70441100	70441101	T	C	34	GENIC	homozygous	116190351
7	70441140	70441141	C	T	47	GENIC	heterozygous	116291578
7	70441806	70441807	A	G	54	GENIC	possibly homozygous	116190353
7	70442832	70442833	C	T	58	GENIC	homozygous	116190354
7	70443589	70443590	C	T	62	GENIC	possibly homozygous	116190356
7	70444787	70444788	A	G	44	GENIC	homozygous	116190358
7	70444803	70444804	T	C	43	GENIC	homozygous	115708978
7	70445070	70445071	C	T	27	GENIC	heterozygous	116190360
7	70445536	70445537	T	G	50	GENIC	homozygous	116190362
7	70445619	70445620	G	T	49	GENIC	homozygous	116190364
7	70445651	70445652	C	T	40	GENIC	homozygous	116190366
7	70446222	70446223	G	A	38	GENIC	homozygous	116190368
7	70446910	70446911	A	G	35	GENIC	homozygous	115708979
7	70447868	70447869	T	C	53	GENIC	homozygous	116190370
7	70449738	70449739	A	G	38	GENIC	homozygous	115708982
7	70450425	70450426	A	G	59	GENIC	homozygous	115708983
7	70451014	70451015	C	G	36	GENIC	homozygous	115708984
7	70451570	70451571	A	G	28	GENIC	homozygous	115708985
7	70453142	70453143	T	C	37	GENIC	homozygous	116190372
7	70453484	70453485	G	T	37	GENIC	homozygous	116190374
7	70453696	70453697	T	C	37	GENIC	possibly homozygous	115708986
7	70456380	70456381	C	T	55	GENIC	homozygous	116190376
7	70457411	70457412	G	A	48	GENIC	heterozygous	115708987
7	70457419	70457420	G	A	44	GENIC	heterozygous	116190380
7	70457427	70457428	G	A	43	GENIC	heterozygous	116190382
7	70458992	70458993	C	T	39	GENIC	homozygous	116190384