chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120527025	120527026	C	T	11	GENIC	homozygous	146202012
7	120527155	120527156	G	C	14	GENIC	homozygous	138197420
7	120527202	120527203	C	A	13	GENIC	homozygous	403224321
7	120527204	120527205	C	A	13	GENIC	homozygous	146202013
7	120527212	120527213	C	T	14	GENIC	homozygous	138197421
7	120527214	120527215	C	G	14	GENIC	homozygous	138197422
7	120527217	120527218	C	T	14	GENIC	homozygous	138197423
7	120528137	120528138	G	A	14	GENIC	homozygous	146202014
7	120528383	120528384	C	T	24	GENIC	homozygous	146202015
7	120529082	120529083	C	T	15	GENIC	homozygous	146202016
7	120531974	120531975	C	T	11	GENIC	homozygous	146202017
7	120532653	120532654	A	G	16	GENIC	homozygous	138197428
7	120533251	120533252	G	A	6	GENIC	homozygous	146202018
7	120533252	120533253	C	T	6	GENIC	homozygous	146202019
7	120535587	120535588	T	C	20	GENIC	homozygous	138197432
7	120531807	120531808	G	C	12	GENIC	homozygous	154479552
7	120532675	120532675		AGGCCTGATTCAG	14	GENIC	homozygous	137977958
7	120535998	120535999	G	A	24	GENIC	homozygous	146202020
7	120536271	120536272	T	C	21	GENIC	homozygous	146202021
7	120536369	120536370	A	G	13	GENIC	homozygous	146202022
7	120536555	120536556	T	C	13	GENIC	homozygous	146202023
7	120536773	120536774	C	T	18	GENIC	homozygous	146202024
7	120536891	120536892	C	A	13	GENIC	homozygous	146202025
7	120531807	120531808	G	T	12	GENIC	heterozygous	154479553
7	120536310	120536310		CTGGGTTCTTT	21	GENIC	homozygous	146186510