chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	92476836	92476837	G	GA	8	GENIC	heterozygous	54573913
7	92477123	92477124	T	TA	14	GENIC	homozygous	54023211
7	92477809	92477810	A	AATTCCTGTTAAAATAG	10	GENIC	homozygous	54023212
7	92479132	92479138	CTCTCT	------	16	GENIC	heterozygous	54023214
7	92482713	92482717	AGAC	----	8	GENIC	homozygous	54023215
7	92482746	92482747	G	A	17	GENIC	heterozygous	54573915
7	92483544	92483545	G	A	25	GENIC	homozygous	54023216
7	92483666	92483667	A	ACTCT	17	GENIC	homozygous	54023217
7	92484643	92484644	T	C	35	GENIC	homozygous	54023218
7	92485013	92485015	TA	--	3	GENIC	homozygous	54023219
7	92485062	92485063	A	ATG	8	GENIC	homozygous	54023220
7	92488724	92488725	T	-	14	GENIC	homozygous	54023222
7	92490902	92490903	C	CA	12	GENIC	homozygous	54023223
7	92492106	92492107	G	T	17	GENIC	heterozygous	54573917
7	92493780	92493782	AC	--	14	GENIC	possibly homozygous	54023224
7	92496095	92496096	G	GA	13	GENIC	homozygous	54023225
7	92496600	92496601	C	T	26	GENIC	homozygous	54023226
7	92498650	92498651	A	G	19	GENIC	homozygous	54023227
7	92500065	92500066	T	C	26	GENIC	homozygous	54023228
7	92501487	92501489	CA	--	3	GENIC	homozygous	54023229
7	92479134	92479138	CTCT	----	16	GENIC	heterozygous	54486032
7	92479359	92479363	TGTA	----	17	GENIC	heterozygous	54486034
7	92503082	92503083	C	CTA	1	GENIC	homozygous	54023230
7	92508721	92508722	G	A	28	GENIC	homozygous	54486038