chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51361633	51361634	G	A	36	GENIC	homozygous	115355234
12	51361751	51361752	G	A	50	GENIC	homozygous	115355235
12	51362529	51362530	G	A	43	GENIC	homozygous	115355236
12	51362940	51362941	C	T	36	GENIC	homozygous	115355237
12	51363462	51363463	T	C	36	GENIC	homozygous	115355238
12	51363991	51363992	T	C	49	GENIC	homozygous	115355239
12	51364586	51364587	G	A	33	GENIC	homozygous	115355240
12	51364942	51364943	G	A	37	GENIC	homozygous	115355241
12	51365239	51365240	G	A	26	GENIC	homozygous	115355242
12	51365609	51365610	C	T	15	GENIC	homozygous	115487174
12	51366050	51366051	T	A	25	GENIC	homozygous	115444502
12	51366250	51366251	T	A	31	GENIC	homozygous	115355243
12	51366392	51366393	C	G	53	GENIC	homozygous	115355244
12	51366493	51366494	T	C	32	GENIC	heterozygous	118274997
12	51366495	51366496	A	G	34	GENIC	heterozygous	115355245
12	51366783	51366784	A	G	18	GENIC	possibly homozygous	118274998
12	51366858	51366859	T	C	35	GENIC	homozygous	115487175
12	51367165	51367166	T	C	25	GENIC	possibly homozygous	115355246