chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	34350156	34350157	T	G	38	GENIC	homozygous	115642277
7	34350171	34350171		C	36	GENIC	homozygous	128451615
7	34350178	34350178		C	31	GENIC	homozygous	128451616
7	34350179	34350180	A	C	31	GENIC	homozygous	122754623
7	34350184	34350184		C	31	GENIC	homozygous	128451617
7	34350190	34350190		C	29	GENIC	homozygous	128451618
7	34350191	34350191		C	28	GENIC	homozygous	128451619
7	34350201	34350204	AAA		26	GENIC	homozygous	128451620
7	34350208	34350209	T	C	26	GENIC	homozygous	122754628
7	34350233	34350233		C	24	GENIC	homozygous	129936463
7	34350223	34350223		CA	25	GENIC	homozygous	129936460
7	34350228	34350228		C	27	GENIC	homozygous	129936461
7	34350231	34350231		A	24	GENIC	homozygous	129936462
7	34350237	34350238	T	C	23	GENIC	homozygous	122754633
7	34350242	34350245	CTG		20	GENIC	homozygous	129936464
7	34350249	34350251	TC		21	GENIC	homozygous	129936465
7	34350254	34350255	G	T	21	GENIC	homozygous	122754636
7	34350258	34350258		T	21	GENIC	homozygous	129936466
7	34350391	34350391		GTGTGTGTGAGAGT	29	GENIC	homozygous	128451621
7	34350478	34350479	T		19	GENIC	homozygous	128451622
7	34354814	34354814		G	19	GENIC	homozygous	128451623
7	34350278	34350279	T	G	23	GENIC	homozygous	116140775
7	34350282	34350283	C	G	24	GENIC	homozygous	116140777
7	34350283	34350284	C	T	25	GENIC	homozygous	116140779