chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39390812	39390813	C	T	29	GENIC	homozygous	116870029
10	39390875	39390876	G	A	25	GENIC	homozygous	116870031
10	39394852	39394853	G	T	28	GENIC	possibly homozygous	116870033
10	39397384	39397385	C	A	12	GENIC	homozygous	116870035
10	39399414	39399414		ATGCTCACTTACTCTCT	10	GENIC	homozygous	128809190
10	39401239	39401240	A		27	GENIC	homozygous	128809191
10	39401243	39401244	T		26	GENIC	homozygous	128809192
10	39401246	39401247	A		26	GENIC	homozygous	128809193
10	39401258	39401262	GGTG		24	GENIC	homozygous	128809194
10	39401344	39401345	A		19	GENIC	homozygous	128809197
10	39401350	39401351	C		20	GENIC	homozygous	128809198
10	39401378	39401378		T	13	GENIC	homozygous	128809199
10	39401411	39401411		A	12	GENIC	homozygous	128809200
10	39401414	39401414		T	12	GENIC	homozygous	128809201
10	39401473	39401473		G	17	GENIC	homozygous	128809203
10	39401481	39401481		G	17	GENIC	homozygous	128809204
10	39401500	39401500		G	16	GENIC	homozygous	128809205
10	39401502	39401503	C	T	16	GENIC	homozygous	117217692
10	39401505	39401505		C	15	GENIC	homozygous	128809206
10	39401603	39401603		T	15	GENIC	homozygous	128809207
10	39401657	39401658	G	T	20	GENIC	homozygous	116566833
10	39401659	39401660	T	G	21	GENIC	homozygous	116566835
10	39401810	39401810		T	16	GENIC	homozygous	128809212
10	39401634	39401634		T	16	GENIC	homozygous	128809208
10	39401649	39401649		C	16	GENIC	homozygous	128809209
10	39401697	39401698	T		27	GENIC	homozygous	128809210
10	39401799	39401799		T	21	GENIC	homozygous	128809211
10	39401816	39401816		G	16	GENIC	homozygous	128809213
10	39401892	39401893	A		14	GENIC	homozygous	128809214
10	39401913	39401914	G	T	16	GENIC	homozygous	116566837
10	39401916	39401917	T		16	GENIC	homozygous	128809215
10	39402702	39402703	G	A	17	GENIC	homozygous	116870039
10	39403862	39403870	AGCCTGTC		25	GENIC	homozygous	128809216