chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	140043833	140043834	T	TC	5	GENIC	homozygous	54152370
7	140043994	140043995	C	T	1	GENIC	homozygous	54152372
7	140044450	140044451	G	T	5	GENIC	homozygous	54152374
7	140044470	140044471	G	A	5	GENIC	homozygous	54152376
7	140044503	140044504	C	A	6	GENIC	heterozygous	54152379
7	140044606	140044607	G	C	13	GENIC	possibly homozygous	54152381
7	140044794	140044795	C	CT	1	GENIC	homozygous	54152383
7	140044796	140044797	T	TGCACCCGGCCCCGTTTGGTAGCTCTG	1	GENIC	homozygous	54152385
7	140044805	140044806	T	C	5	GENIC	heterozygous	54152387
7	140044850	140044852	AG	--	18	GENIC	heterozygous	54152389
7	140045377	140045378	G	A	24	GENIC	heterozygous	54152391
7	140045706	140045707	G	A	4	GENIC	homozygous	54152393
7	140045754	140045755	A	G	12	GENIC	homozygous	54152395
7	140045756	140045757	T	C	11	GENIC	homozygous	54152397
7	140046106	140046107	T	C	15	GENIC	homozygous	54152399
7	140046546	140046548	AA	--	3	GENIC	homozygous	54152401
7	140046695	140046696	C	T	3	GENIC	homozygous	54152403
7	140046842	140046843	A	G	24	GENIC	heterozygous	54152405
7	140046920	140046921	G	A	16	GENIC	homozygous	54152407
7	140046928	140046929	C	T	21	GENIC	homozygous	54152409
7	140047019	140047020	A	G	20	GENIC	homozygous	54152411
7	140047073	140047074	G	A	19	GENIC	homozygous	54152412
7	140047644	140047645	A	G	17	GENIC	possibly homozygous	54152414
7	140048213	140048214	G	A	4	GENIC	heterozygous	54152416
7	140048250	140048251	G	A	13	GENIC	heterozygous	54152418