chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54090169	54090170	T	C	21	GENIC	homozygous	138334996
8	54090194	54090195	A	G	24	GENIC	homozygous	138334997
8	54090658	54090659	G	A	29	GENIC	homozygous	138334998
8	54091759	54091760	A	G	25	GENIC	homozygous	138334999
8	54094182	54094183	G	A	29	GENIC	homozygous	138335000
8	54092437	54092437		CGAGG	19	GENIC	homozygous	138246072
8	54094512	54094513	G		36	GENIC	homozygous	138246073
8	54095638	54095642	TGAA		27	GENIC	homozygous	138246074
8	54100339	54100340	C	G	20	GENIC	homozygous	138335001
8	54100659	54100660	A	G	30	GENIC	homozygous	138335002
8	54101341	54101342	G	A	13	GENIC	homozygous	138335003
8	54101352	54101479	CCGGACTCAATCTTTTGACATTACCTTTTTTTTTTTTTTTCTTTTCTTTTTTTTCGGAGCTGGGGACCAAACCCAGAGCCTTGTGCTTGCCAGGCAAGTGCTCTACCACTGAGCTAAATCCCCATCC		12	GENIC	homozygous	138246075
8	54104214	54104215	T	C	21	GENIC	homozygous	138335004
8	54104399	54104400	G	A	26	GENIC	homozygous	138335005
8	54104727	54104728	C	G	23	GENIC	homozygous	138335006