chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23929276	23929277	T	A	31	GENIC	homozygous	115438568
12	23934909	23934910	C	A	28	GENIC	homozygous	115286165
12	23932395	23932396	A	G	32	GENIC	homozygous	115286157
12	23932517	23932518	A	G	31	GENIC	homozygous	115286159
12	23933452	23933453	C	T	33	GENIC	homozygous	115286161
12	23934283	23934284	A	G	27	GENIC	homozygous	115286163
12	23935174	23935175	T	C	34	GENIC	homozygous	115286167
12	23935511	23935512	A	C	28	GENIC	heterozygous	118336934
12	23935522	23935523	T	C	27	GENIC	heterozygous	118336935
12	23935569	23935570	C	T	29	GENIC	homozygous	118261914
12	23935380	23935381	G	C	32	GENIC	possibly homozygous	118261910
12	23935381	23935382	T	C	33	GENIC	possibly homozygous	118261911
12	23935386	23935387	G	A	35	GENIC	possibly homozygous	118261912
12	23935391	23935392	A	G	35	GENIC	homozygous	118261913
12	23935495	23935496	A	G	33	GENIC	heterozygous	118341338
12	23935498	23935499	T	C	30	GENIC	heterozygous	118341339
12	23935637	23935638	A	G	25	GENIC	homozygous	115469767
12	23935690	23935691	T	C	19	GENIC	homozygous	118261915
12	23935700	23935701	G	C	19	GENIC	homozygous	118261916
12	23935916	23935917	T	A	15	GENIC	possibly homozygous	115438572
12	23936264	23936265	T	A	34	GENIC	homozygous	115286169
12	23936390	23936391	C	T	26	GENIC	homozygous	115286171
12	23936432	23936433	T	C	27	GENIC	homozygous	115286173
12	23936687	23936688	T	C	35	GENIC	homozygous	115286175
12	23937094	23937095	C	T	40	GENIC	homozygous	115286177
12	23937572	23937573	T	A	52	GENIC	homozygous	115286179
12	23937838	23937839	T	A	31	GENIC	homozygous	115286181
12	23935797	23935798	G	A	26	GENIC	homozygous	115492981
12	23936091	23936092	T	G	18	GENIC	homozygous	115422060
12	23937521	23937522	C	T	50	GENIC	possibly homozygous	115703397
12	23935822	23935823	A	G	24	GENIC	homozygous	115653533