chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	10276413	10276414	A	T	36	GENIC	possibly homozygous	112658139
15	10276649	10276650	C	A	54	GENIC	homozygous	112449236
15	10276807	10276808	T	A	42	GENIC	homozygous	118868748
15	10277025	10277026	C	T	54	GENIC	possibly homozygous	112449240
15	10277031	10277032	C	A	59	GENIC	homozygous	113161348
15	10276821	10276822	C	T	42	GENIC	homozygous	118868750
15	10276984	10276985	C	G	37	GENIC	homozygous	118868752
15	10276989	10276990	G	A	40	GENIC	homozygous	118868754
15	10277026	10277027	T	A	57	GENIC	possibly homozygous	118944662
15	10277410	10277411	G	T	23	GENIC	homozygous	112981214
15	10278025	10278026	C	A	50	GENIC	possibly homozygous	112658141
15	10277073	10277074	C	A	62	GENIC	homozygous	112875985
15	10278244	10278245	A	G	37	GENIC	homozygous	112875988
15	10278269	10278270	C	G	14	GENIC	homozygous	112875990
15	10278363	10278364	C	A	47	GENIC	homozygous	112449242
15	10286161	10286162	C	T	60	GENIC	heterozygous	118944663
15	10286163	10286164	G	T	61	GENIC	heterozygous	118944664
15	10286195	10286196	C	A	59	GENIC	heterozygous	118868756
15	10286202	10286203	C	T	62	GENIC	heterozygous	118868758
15	10286529	10286530	T	G	73	GENIC	homozygous	112449244
15	10287337	10287338	A	G	52	GENIC	homozygous	112449246
15	10289061	10289062	C	T	48	GENIC	homozygous	112449248
15	10289079	10289080	C	G	50	GENIC	homozygous	112449250
15	10299432	10299433	G	A	52	GENIC	heterozygous	119031168
15	10299452	10299453	A	G	48	GENIC	heterozygous	119031170
15	10311801	10311802	A	T	18	GENIC	homozygous	118868760
15	10311905	10311906	A	G	10	GENIC	homozygous	118868762
15	10312188	10312189	C	A	9	GENIC	homozygous	118868766
15	10312201	10312202	T	A	21	GENIC	homozygous	118868768