chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	9915664	9915665	A	C	11	GENIC	heterozygous	113023222
15	9958908	9958909	C	A	16	GENIC	homozygous	112658129
15	9958948	9958949	T	A	16	GENIC	homozygous	112449171
15	9959092	9959093	T	A	11	GENIC	homozygous	112658132
15	10001270	10001271	T	G	23	GENIC	homozygous	112449186
15	10001273	10001274	C	A	25	GENIC	homozygous	112449188
15	10049173	10049174	G	A	31	GENIC	homozygous	112449190
15	10049272	10049273	C	T	30	GENIC	homozygous	112449192
15	10049368	10049369	A	G	38	GENIC	homozygous	112449194
15	10049489	10049490	C	T	25	GENIC	homozygous	112449196
15	10049584	10049585	A	C	22	GENIC	homozygous	112449198
15	10125968	10125969	G	T	18	GENIC	homozygous	112449200
15	10125970	10125971	C	T	17	GENIC	homozygous	112449202
15	10125971	10125972	T	A	19	GENIC	homozygous	112449205
15	10125983	10125984	G	T	15	GENIC	homozygous	112449207
15	10125985	10125986	T	A	15	GENIC	homozygous	112449209
15	10125990	10125991	T	G	16	GENIC	homozygous	112449211
15	10127526	10127527	A	G	26	GENIC	homozygous	113023225
15	10138731	10138732	C	T	26	GENIC	homozygous	112999405
15	10157059	10157060	G	T	25	GENIC	homozygous	112449213
15	10160610	10160611	G	C	17	GENIC	homozygous	112658134
15	10170618	10170619	G	T	35	GENIC	homozygous	112449215
15	10190552	10190553	C	A	22	GENIC	homozygous	112449222
15	10190769	10190770	G	A	25	GENIC	homozygous	112449224
15	10190848	10190849	C	A	20	GENIC	homozygous	112449226
15	10190982	10190983	T	C	21	GENIC	homozygous	112449228
15	10190983	10190984	G	T	22	GENIC	homozygous	112449230
15	10258075	10258076	G	A	25	GENIC	heterozygous	113023228