chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	76388751	76388752	A	G	18	GENIC	homozygous	111095127
17	76388771	76388772	T	C	19	GENIC	homozygous	111095129
17	76390205	76390206	C	T	14	GENIC	homozygous	111213312
17	76391417	76391418	G	A	19	GENIC	homozygous	111213313
17	76392282	76392283	G	A	13	GENIC	homozygous	111213314
17	76393095	76393096	T	C	21	GENIC	homozygous	111095135
17	76393324	76393325	A	G	23	GENIC	homozygous	111095139
17	76393939	76393940	G	T	26	GENIC	homozygous	111095141
17	76394796	76394797	C	T	28	GENIC	homozygous	111213315
17	76397807	76397808	A	G	22	GENIC	homozygous	111095147
17	76399543	76399544	C	T	24	GENIC	homozygous	111213317
17	76401736	76401737	A	G	22	GENIC	homozygous	111095151
17	76403612	76403613	G	A	22	GENIC	homozygous	111213318
17	76405084	76405085	T	C	29	GENIC	homozygous	111213319
17	76405406	76405407	G	T	24	GENIC	homozygous	111213320
17	76406122	76406123	T	C	16	GENIC	homozygous	111095157
17	76406326	76406327	T	C	28	GENIC	homozygous	111095159
17	76406394	76406395	A	G	25	GENIC	homozygous	111095161
17	76407295	76407296	A	C	28	GENIC	homozygous	111213321
17	76408153	76408154	C	T	22	GENIC	homozygous	111213322
17	76408918	76408919	G	T	23	GENIC	homozygous	111213323
17	76409142	76409143	G	A	19	GENIC	homozygous	111095163
17	76409773	76409774	A	G	21	GENIC	homozygous	111213324
17	76410090	76410091	A	C	12	GENIC	homozygous	111095166