chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	27984359	27984360	T	C	29	GENIC	homozygous	109662152
2	27984517	27984518	A	T	24	GENIC	homozygous	109662154
2	27984741	27984742	G	C	28	GENIC	homozygous	109662156
2	27984829	27984830	G	C	29	GENIC	homozygous	109662158
2	27985723	27985724	T	C	30	GENIC	homozygous	109662160
2	27985823	27985824	A	G	23	GENIC	homozygous	109662162
2	27985882	27985883	G	A	27	GENIC	heterozygous	110497207
2	27985996	27985997	A	G	24	GENIC	homozygous	109662164
2	27986001	27986002	A	C	24	GENIC	homozygous	109662166
2	27986472	27986473	T	C	35	GENIC	homozygous	109662168
2	27986955	27986956	A	G	40	GENIC	homozygous	109662170
2	27987151	27987152	T	C	20	GENIC	homozygous	109662172
2	27987213	27987214	G	A	10	GENIC	homozygous	109662174
2	27987415	27987416	A	G	22	GENIC	homozygous	109662176
2	27987838	27987839	A	G	27	GENIC	homozygous	109662178
2	27988089	27988090	G	A	27	GENIC	possibly homozygous	109662180
2	27988116	27988117	G	A	24	GENIC	homozygous	109662182
2	27988193	27988194	T	A	22	GENIC	possibly homozygous	109662184
2	27988252	27988253	C	T	22	GENIC	homozygous	109662186
2	27988366	27988367	T	C	25	GENIC	homozygous	109662188
2	27988408	27988409	C	G	29	GENIC	homozygous	109662190
2	27989086	27989087	C	T	32	GENIC	homozygous	109662192
2	27990296	27990297	C	T	23	GENIC	homozygous	109662194
2	27990704	27990705	G	A	12	GENIC	homozygous	109662196
2	27990997	27990998	T	C	38	GENIC	possibly homozygous	109662198
2	27991701	27991702	G	A	20	GENIC	homozygous	109662200
2	27992072	27992073	C	T	37	GENIC	possibly homozygous	109662202
2	27992078	27992079	C	T	37	GENIC	possibly homozygous	109662204
2	27992443	27992444	A	G	26	GENIC	homozygous	109662208
2	27992514	27992515	A	C	26	GENIC	homozygous	109662210
2	27992703	27992704	T	C	47	GENIC	homozygous	109662212
2	27992810	27992811	G	A	43	GENIC	homozygous	109662214
2	27993000	27993001	A	G	28	GENIC	homozygous	109662216
2	27994878	27994879	C	G	15	GENIC	homozygous	109662218
2	27994987	27994988	C	A	22	GENIC	homozygous	109662220
2	27998101	27998102	A	G	45	GENIC	possibly homozygous	109662222
2	28000263	28000264	C	T	13	GENIC	homozygous	109662224
2	27995433	27995434	T	A	23	GENIC	heterozygous	111095038
2	27995429	27995430	T	A	20	GENIC	heterozygous	111095036