chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	27097879	27097880	T	C	13	GENIC	heterozygous	50152177
12	27099192	27099193	G	A	19	GENIC	homozygous	50152185
12	27099227	27099228	A	G	15	GENIC	possibly homozygous	50152187
12	27100319	27100320	C	CTTTTT	2	GENIC	heterozygous	50152199
12	27101672	27101673	T	-	4	GENIC	homozygous	50152209
12	27101782	27101783	G	A	8	GENIC	homozygous	50374170
12	27102556	27102557	T	C	15	GENIC	possibly homozygous	50152221
12	27103026	27103027	G	C	27	GENIC	possibly homozygous	50152225
12	27103150	27103151	T	C	23	GENIC	possibly homozygous	50152227
12	27103676	27103677	C	CT	9	GENIC	homozygous	50374172
12	27103830	27103834	ATAG	----	12	GENIC	possibly homozygous	50374176
12	27104730	27104731	G	A	13	GENIC	homozygous	50374178
12	27105044	27105045	T	A	5	GENIC	homozygous	50374180
12	27105046	27105047	A	C	5	GENIC	homozygous	50374182
12	27105921	27105922	T	C	24	GENIC	homozygous	50152244
12	27106288	27106289	G	A	11	GENIC	homozygous	50374184
12	27106388	27106389	T	A	23	GENIC	possibly homozygous	50152250
12	27106767	27106768	G	A	27	GENIC	possibly homozygous	50374186
12	27107062	27107063	G	A	6	GENIC	homozygous	50152260
12	27107070	27107071	T	TGTGG	7	GENIC	homozygous	50152262
12	27107075	27107076	A	G	9	GENIC	homozygous	50374188
12	27108010	27108011	A	G	9	GENIC	possibly homozygous	50152270
12	27108121	27108124	TCT	---	1	GENIC	homozygous	50539535
12	27108332	27108333	A	C	11	GENIC	homozygous	50374190
12	27109205	27109206	A	-	22	GENIC	homozygous	50374192