chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23941489	23941490	G	A	38	GENIC	homozygous	115286191
12	23942728	23942729	C	G	35	GENIC	homozygous	115286193
12	23942947	23942948	C	T	31	GENIC	homozygous	115286195
12	23943269	23943270	G	A	36	GENIC	homozygous	115469773
12	23943683	23943684	T	G	31	GENIC	homozygous	115286197
12	23944550	23944551	T	A	29	GENIC	homozygous	115422062
12	23944595	23944596	A	G	16	GENIC	homozygous	115510214
12	23944640	23944641	T	C	13	GENIC	homozygous	115560691
12	23944835	23944836	T	G	39	GENIC	homozygous	115286199
12	23945077	23945078	T	C	36	GENIC	homozygous	115286201
12	23945614	23945615	T	C	36	GENIC	homozygous	115286205
12	23945914	23945915	C	T	35	GENIC	homozygous	115286207
12	23946266	23946267	A	G	20	GENIC	homozygous	115286209
12	23946560	23946561	C	T	25	GENIC	homozygous	115286213
12	23946574	23946575	T	A	29	GENIC	homozygous	115438578
12	23946601	23946602	C	A	33	GENIC	homozygous	115438579
12	23946605	23946606	T	C	36	GENIC	homozygous	115438580
12	23946652	23946653	C	G	28	GENIC	possibly homozygous	115469777
12	23946802	23946803	G	A	36	GENIC	homozygous	115422064
12	23947790	23947791	A	C	37	GENIC	homozygous	115286215
12	23947916	23947917	C	A	29	GENIC	homozygous	115286217
12	23948186	23948187	T	A	40	GENIC	homozygous	115286219
12	23948728	23948729	C	A	23	GENIC	homozygous	115286221
12	23948832	23948833	T	C	31	GENIC	homozygous	115286223
12	23949064	23949065	A	C	35	GENIC	possibly homozygous	115286225
12	23949295	23949296	T	A	33	GENIC	homozygous	115286227
12	23949833	23949834	A	T	35	GENIC	homozygous	115286229
12	23950222	23950223	T	C	36	GENIC	homozygous	115286231
12	23950339	23950340	C	T	29	GENIC	homozygous	115286233
12	23951204	23951205	A	G	28	GENIC	homozygous	115286235
12	23951318	23951319	G	A	20	GENIC	homozygous	115286237
12	23951481	23951482	C	T	30	GENIC	homozygous	115438584
12	23951823	23951824	C	T	48	GENIC	homozygous	115286239
12	23952517	23952518	G	A	50	GENIC	homozygous	115286243