chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	79554680	79554681	C	A	13	GENIC	homozygous	113887134
5	79555357	79555358	A	T	13	GENIC	homozygous	113887136
5	79555818	79555819	A	G	23	GENIC	homozygous	113887138
5	79557897	79557898	T	C	18	GENIC	homozygous	113887140
5	79558468	79558469	T	C	18	GENIC	homozygous	113887142
5	79559277	79559278	G	A	13	GENIC	homozygous	113887144
5	79559448	79559449	G	A	18	GENIC	homozygous	113887146
5	79559516	79559517	T	A	15	GENIC	homozygous	113887148
5	79559973	79559974	C	G	17	GENIC	homozygous	113887150
5	79560176	79560176		ATA	23	GENIC	homozygous	128202371
5	79560600	79560601	C	T	20	GENIC	homozygous	113887152
5	79560736	79560737	G	A	16	GENIC	homozygous	113887154
5	79560808	79560809	G	A	20	GENIC	homozygous	113887156
5	79561935	79561939	TCTC		11	GENIC	homozygous	128202372
5	79561970	79561971	G		10	GENIC	homozygous	128202373
5	79562406	79562407	T	C	14	GENIC	homozygous	113887158
5	79562666	79562667	A	G	18	GENIC	homozygous	113887160
5	79563467	79563468	A	T	13	GENIC	homozygous	113887163
5	79563522	79563523	T	C	14	GENIC	homozygous	113887166
5	79563879	79563880	G	A	22	GENIC	homozygous	113887168
5	79565156	79565157	A	C	22	GENIC	homozygous	113887170
5	79565390	79565392	TA		13	GENIC	homozygous	128202374
5	79565689	79565690	A	G	15	GENIC	homozygous	113887172
5	79568099	79568100	G	A	18	GENIC	homozygous	113887174
5	79568889	79568890	T		20	GENIC	possibly homozygous	128202375
5	79568635	79568636	T	C	17	GENIC	possibly homozygous	114412439