chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59538811	59538812	C	T	46	GENIC	homozygous	116608215
10	59538839	59538840	C	A	49	GENIC	possibly homozygous	116608217
10	59541405	59541406	G	A	35	GENIC	homozygous	116608219
10	59541656	59541657	G	A	49	GENIC	homozygous	116608221
10	59541954	59541955	G	A	43	GENIC	possibly homozygous	116608223
10	59542518	59542519	G	C	35	GENIC	homozygous	116608225
10	59543679	59543680	G	A	43	GENIC	homozygous	116608227
10	59544290	59544291	A	G	40	GENIC	homozygous	116608229
10	59544481	59544482	C	G	72	GENIC	homozygous	116608231
10	59544828	59544829	C	T	29	GENIC	homozygous	116608233
10	59544916	59544917	T	C	22	GENIC	homozygous	116608235
10	59544963	59544964	T	C	41	GENIC	homozygous	116608237
10	59545376	59545377	A	G	53	GENIC	homozygous	116608239
10	59545505	59545506	T	C	61	GENIC	homozygous	116608241
10	59545952	59545953	C	T	33	GENIC	homozygous	116608243
10	59546908	59546909	G	A	38	GENIC	homozygous	116608245
10	59547174	59547175	T	A	45	GENIC	homozygous	116608247
10	59548770	59548771	T	C	45	GENIC	homozygous	116608249
10	59548771	59548772	G	T	45	GENIC	homozygous	116608251
10	59550147	59550148	A	C	40	GENIC	homozygous	116608253
10	59550549	59550550	G	T	58	GENIC	homozygous	116608255
10	59550628	59550629	G	A	66	GENIC	homozygous	116608257
10	59551996	59551997	A	G	67	GENIC	homozygous	116608259
10	59553251	59553252	G	A	28	GENIC	homozygous	116608261
10	59553283	59553284	C	T	34	GENIC	homozygous	116608263
10	59553968	59553969	G	A	38	GENIC	homozygous	116608265
10	59554080	59554081	T	G	33	GENIC	homozygous	116608267
10	59554498	59554499	A	G	41	GENIC	homozygous	116608269
10	59554951	59554952	G	A	48	GENIC	homozygous	116608271
10	59557050	59557051	A	G	59	GENIC	homozygous	116608273
10	59557436	59557437	G	A	28	GENIC	homozygous	116608275
10	59557987	59557988	T	C	47	GENIC	homozygous	116608277
10	59558325	59558326	A	G	41	GENIC	homozygous	116608279
10	59558638	59558639	C	T	29	GENIC	homozygous	116608281
10	59559539	59559540	T	C	34	GENIC	homozygous	116608283