chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30759952	30759953	G		7	GENIC	possibly homozygous	403281034
10	30759952	30759953	G	C	7	GENIC	heterozygous	403281035
10	30765488	30765493	CCTCC		4	GENIC	homozygous	142199236
10	30799480	30799481	A		8	GENIC	homozygous	403281037
10	30799480	30799481	A	G	8	GENIC	heterozygous	403281038
10	30799482	30799483	G		8	GENIC	homozygous	403281039
10	30799482	30799483	G	A	8	GENIC	heterozygous	403281040
10	30808447	30808448	C	T	19	GENIC	homozygous	138755245
10	30794588	30794589	T	C	14	GENIC	homozygous	142228813
10	30783592	30783593	T	C	11	GENIC	homozygous	138755240
10	30795995	30795996	A	T	25	GENIC	homozygous	138755241
10	30807354	30807355	T	C	17	GENIC	homozygous	138755242
10	30807418	30807419	G	A	16	GENIC	homozygous	138755243
10	30808133	30808134	T	G	14	GENIC	homozygous	138755244
10	30808928	30808929	G	A	18	GENIC	homozygous	138755246
10	30809059	30809060	C	T	19	GENIC	homozygous	138755247
10	30809861	30809862	A	G	17	GENIC	homozygous	138755248
10	30810018	30810019	G	A	22	GENIC	homozygous	138755249
10	30810046	30810047	G	T	22	GENIC	homozygous	138755250
10	30810291	30810292	C	G	25	GENIC	homozygous	138755251
10	30810375	30810376	G	A	20	GENIC	homozygous	138755252
10	30810495	30810496	A	G	19	GENIC	homozygous	138755253
10	30810560	30810560		A	18	GENIC	homozygous	138676405
10	30810989	30810990	C	T	23	GENIC	homozygous	138755254
10	30812991	30812992	G	A	20	GENIC	homozygous	138755258
10	30811210	30811211	A		16	GENIC	homozygous	138676406
10	30811796	30811797	G		15	GENIC	homozygous	138676407
10	30811457	30811458	A	G	17	GENIC	homozygous	138755255
10	30812549	30812550	T	G	16	GENIC	homozygous	138755256
10	30812563	30812564	C	T	17	GENIC	homozygous	138755257
10	30813472	30813473	G	A	10	GENIC	homozygous	138755259
10	30813875	30813876	T	C	10	GENIC	homozygous	138755260
10	30814233	30814234	C	T	8	GENIC	homozygous	138755261
10	30814383	30814384	A	G	17	GENIC	homozygous	138755262
10	30814461	30814462	G	A	24	GENIC	homozygous	138755263