chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37984803	37984804	G	C	3	GENIC	homozygous	115543864
12	37985062	37985063	C	G	12	GENIC	homozygous	115322283
12	37985253	37985254	G	A	15	GENIC	homozygous	115322285
12	37985396	37985397	G	A	23	GENIC	homozygous	115476063
12	37985747	37985748	T	A	15	GENIC	homozygous	115322287
12	37986361	37986362	G	A	22	GENIC	homozygous	115476065
12	37986520	37986521	T	C	32	GENIC	homozygous	115322289
12	37986744	37986745	T	C	22	GENIC	homozygous	115322291
12	37987191	37987192	C	T	5	GENIC	homozygous	115493924
12	37987458	37987459	A	G	12	GENIC	homozygous	115322299
12	37987738	37987739	C	T	23	GENIC	homozygous	115476067
12	37988257	37988258	G	A	25	GENIC	homozygous	115493926
12	37988305	37988306	A	G	26	GENIC	homozygous	115476069
12	37988367	37988368	T	G	30	GENIC	homozygous	115476071
12	37988493	37988494	T	C	17	GENIC	homozygous	115322305
12	37988494	37988495	A	G	16	GENIC	homozygous	115322307
12	37989391	37989392	T	C	27	GENIC	homozygous	115322309
12	38005437	38005438	C	T	18	GENIC	homozygous	115476079
12	38008498	38008499	A	G	21	GENIC	homozygous	115322325
12	38010484	38010485	C	G	19	GENIC	homozygous	115322329
12	38011281	38011282	T	A	15	GENIC	homozygous	115322331
12	38003780	38003781	A	G	11	GENIC	homozygous	115440239
12	38008274	38008275	T	G	14	GENIC	homozygous	115440241
12	38008916	38008917	T	C	16	GENIC	homozygous	115440242
12	38004257	38004258	C	T	22	GENIC	heterozygous	115692134
12	38013334	38013335	A	G	23	GENIC	homozygous	115476081
12	38013932	38013933	T	C	25	GENIC	homozygous	115426410
12	38014285	38014286	T	C	16	GENIC	homozygous	115476083
12	38014296	38014297	C	T	15	GENIC	homozygous	115476085
12	38015758	38015759	T	A	20	GENIC	homozygous	115322337
12	38015759	38015760	A	T	20	GENIC	homozygous	115322339
12	38020059	38020060	T	C	12	GENIC	homozygous	115493930
12	38020061	38020062	T	G	14	GENIC	homozygous	115322343