chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23956027	23956028	A	G	53	GENIC	homozygous	115286245
12	23956663	23956664	T	C	47	GENIC	homozygous	115286247
12	23958260	23958384	AGGAATGTGTTCAGTGGGACTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAA		38	GENIC	homozygous	128973013
12	23958508	23958509	G	A	58	GENIC	homozygous	115286249
12	23959056	23959057	G	A	44	GENIC	homozygous	115286251
12	23959336	23959347	TTTTCTTTTTG		33	GENIC	heterozygous	128973014
12	23959855	23959855		TGCTTGCTA	24	GENIC	homozygous	128973015
12	23959857	23959857		CAAGCGCTCTACCACTGAGCTAAATCCCC	23	GENIC	homozygous	128973016
12	23960295	23960296	A	C	46	GENIC	homozygous	115286253
12	23960947	23960953	GTGTGC		21	GENIC	possibly homozygous	128973017
12	23961678	23961679	T	A	53	GENIC	homozygous	115510216
12	23964126	23964127	G	A	45	GENIC	homozygous	115286255
12	23965489	23965490	C	T	36	GENIC	homozygous	115286259
12	23968549	23968550	C	A	46	GENIC	homozygous	115286261
12	23961880	23961881	G	T	45	GENIC	homozygous	115469778
12	23969359	23969375	CTCTCACACACACACA		21	GENIC	heterozygous	133254138
12	23973275	23973276	C	T	48	GENIC	homozygous	115286265
12	23975336	23975337	A	G	53	GENIC	homozygous	115469780
12	23979405	23979406	G	A	11	GENIC	heterozygous	118301180
12	23976538	23976539	C	T	33	GENIC	homozygous	115422070
12	23982041	23982042	C	G	40	GENIC	homozygous	115286281
12	23983262	23983263	C	T	47	GENIC	homozygous	115469782
12	23986286	23986287	G	C	6	GENIC	homozygous	118301186
12	23986307	23986308	G	C	2	GENIC	homozygous	118301187
12	23986312	23986313	G	C	3	GENIC	homozygous	118261922
12	23986359	23986360	T	C	17	GENIC	homozygous	115469784
12	23969437	23969438	C	T	41	GENIC	homozygous	115446259
12	23985124	23985124		GT	34	GENIC	homozygous	131115468
12	23985235	23985243	TGTGTCTG		25	GENIC	homozygous	131115469
12	23986233	23986235	GG		2	GENIC	homozygous	131115470