chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	46862551	46862552	G	C	28	GENIC	homozygous	50221100
12	46863456	46863457	G	-	12	GENIC	homozygous	50221112
12	46863464	46863465	G	A	9	GENIC	homozygous	50221114
12	46863466	46863467	G	A	10	GENIC	heterozygous	50221116
12	46863472	46863473	G	A	11	GENIC	heterozygous	50221118
12	46863485	46863486	C	T	13	GENIC	heterozygous	50221120
12	46863498	46863499	G	GGATA	12	GENIC	heterozygous	50221122
12	46863516	46863517	A	G	18	GENIC	heterozygous	50387569
12	46863520	46863521	G	A	18	GENIC	heterozygous	50387570
12	46866454	46866455	T	C	44	GENIC	homozygous	50221158
12	46866955	46866956	C	T	30	GENIC	homozygous	50221169
12	46867209	46867210	T	C	28	GENIC	homozygous	50221171
12	46868251	46868254	TTT	---	19	GENIC	heterozygous	50342267
12	46868253	46868254	T	-	19	GENIC	heterozygous	50454206
12	46868695	46868696	T	C	40	GENIC	homozygous	50221186
12	46869986	46869987	G	GT	12	GENIC	heterozygous	50454207
12	46870098	46870099	T	C	41	GENIC	homozygous	50221196
12	46870235	46870236	C	G	36	GENIC	homozygous	50221198
12	46870492	46870493	T	G	33	GENIC	homozygous	50221202
12	46871443	46871444	G	A	48	GENIC	homozygous	50454208
12	46872400	46872401	T	TG	4	GENIC	homozygous	50221230
12	46873315	46873316	A	G	43	GENIC	homozygous	50221238
12	46873707	46873708	A	ATGTGTGTG	12	GENIC	homozygous	50342285
12	46875142	46875143	A	C	36	GENIC	homozygous	50221247
12	46875244	46875245	T	TTGTGTG	24	GENIC	homozygous	50221249
12	46875265	46875266	C	T	42	GENIC	heterozygous	50221251
12	46876427	46876432	GCCCC	-----	19	GENIC	homozygous	50221257