chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	44170398	44170399	G	A	8	GENIC	possibly homozygous	47114123
17	44170930	44170931	C	T	16	GENIC	heterozygous	47114125
17	44171674	44171675	T	C	11	GENIC	homozygous	47114134
17	44171685	44171686	G	A	10	GENIC	homozygous	47114135
17	44171743	44171744	T	C	12	GENIC	possibly homozygous	47114137
17	44171870	44171871	T	A	16	GENIC	possibly homozygous	47114139
17	44172344	44172345	T	-	15	GENIC	possibly homozygous	47114140
17	44172777	44172778	C	T	2	GENIC	heterozygous	47114142
17	44173079	44173080	T	TTA	2	GENIC	homozygous	47114143
17	44173117	44173118	T	-	5	GENIC	heterozygous	47114145
17	44173436	44173437	T	C	7	GENIC	possibly homozygous	47114147
17	44173673	44173674	A	G	15	GENIC	possibly homozygous	47114152
17	44173964	44173965	G	A	13	GENIC	possibly homozygous	47114154
17	44174166	44174167	G	A	24	GENIC	possibly homozygous	47114156
17	44175057	44175058	G	A	32	GENIC	possibly homozygous	47114157
17	44175605	44175606	A	G	20	GENIC	homozygous	47114159
17	44175685	44175686	G	A	19	GENIC	heterozygous	47114161
17	44175775	44175776	A	G	18	GENIC	homozygous	47114163
17	44176302	44176303	T	C	15	GENIC	homozygous	47114165
17	44176870	44176871	G	A	22	GENIC	possibly homozygous	47114167
17	44177664	44177665	G	C	19	GENIC	possibly homozygous	47114172