chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14400656	14400657	T	C	29	GENIC	possibly homozygous	67597134
12	14400785	14400786	G	A	34	GENIC	homozygous	67597135
12	14400794	14400795	T	C	33	GENIC	homozygous	67597136
12	14401019	14401020	G	A	25	GENIC	homozygous	67597137
12	14401107	14401108	C	G	27	GENIC	homozygous	67597138
12	14401154	14401155	G	A	30	GENIC	homozygous	67597139
12	14402151	14402152	T	A	28	GENIC	homozygous	67597141
12	14402171	14402172	G	A	24	GENIC	homozygous	67597142
12	14402268	14402269	T	C	31	GENIC	homozygous	67597143
12	14402583	14402584	T	C	22	GENIC	homozygous	67597144
12	14402615	14402616	A	G	18	GENIC	homozygous	67612325
12	14403217	14403218	C	T	27	GENIC	homozygous	67597147
12	14403938	14403939	C	T	20	GENIC	homozygous	67597148
12	14404009	14404010	G	A	25	GENIC	homozygous	67597149
12	14404165	14404166	G	A	32	GENIC	homozygous	67597150
12	14404173	14404174	G	A	34	GENIC	homozygous	67597151
12	14404189	14404190	A	G	38	GENIC	homozygous	67612334
12	14404353	14404354	C	T	25	GENIC	homozygous	67597152
12	14405123	14405124	G	T	12	GENIC	homozygous	67597154
12	14406783	14406784	C	T	28	GENIC	homozygous	67597155
12	14406952	14406953	T	C	24	GENIC	homozygous	67597156
12	14406957	14406958	G	A	22	GENIC	possibly homozygous	67597157
12	14407259	14407260	T	C	17	GENIC	homozygous	67597158
12	14407290	14407291	G	T	23	GENIC	homozygous	67597159
12	14408306	14408307	T	C	23	GENIC	homozygous	67612338
12	14408405	14408406	A	C	30	GENIC	homozygous	67597160
12	14406847	14406848	C	T	30	GENIC	homozygous	66647486
12	14406110	14406111	A	G	25	GENIC	homozygous	66647484
12	14409347	14409348	A	C	26	GENIC	homozygous	66647490
12	14410692	14410693	T	C	21	GENIC	possibly homozygous	83096425