chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	78168841	78168842	G	C	31	GENIC	homozygous	116643339
10	78169772	78169773	C	A	29	GENIC	homozygous	116643341
10	78169947	78169948	C	T	16	GENIC	homozygous	116643343
10	78170011	78170012	C	G	27	GENIC	homozygous	116643345
10	78170040	78170041	T	A	26	GENIC	homozygous	116643347
10	78170146	78170147	A	G	20	GENIC	homozygous	116643349
10	78170397	78170398	C	T	20	GENIC	homozygous	116643351
10	78170444	78170445	G	A	23	GENIC	homozygous	116643353
10	78170510	78170511	C	T	20	GENIC	homozygous	116643355
10	78170557	78170558	G	A	18	GENIC	homozygous	116643357
10	78170677	78170678	A	G	33	GENIC	homozygous	116643359
10	78170693	78170694	A	G	36	GENIC	homozygous	116643361
10	78170727	78170728	C	G	31	GENIC	homozygous	116643363
10	78170886	78170887	T	C	59	GENIC	homozygous	116643365
10	78170992	78170993	T	C	47	GENIC	homozygous	116643367
10	78171164	78171165	C	A	22	GENIC	homozygous	116643369
10	78171207	78171208	A	G	24	GENIC	homozygous	116643371
10	78171305	78171306	C	T	17	GENIC	homozygous	116643373
10	78171354	78171355	T	C	18	GENIC	homozygous	116643375
10	78171474	78171475	T	C	16	GENIC	homozygous	116643377
10	78171512	78171513	T	C	22	GENIC	homozygous	116643379
10	78171515	78171516	C	G	19	GENIC	homozygous	116643381
10	78171520	78171521	G	T	17	GENIC	homozygous	116643383
10	78171683	78171684	A	G	15	GENIC	homozygous	116643385
10	78171809	78171810	G	T	17	GENIC	homozygous	116643387
10	78171818	78171819	C	T	17	GENIC	homozygous	116643389
10	78171819	78171820	A	G	17	GENIC	homozygous	116643391
10	78171864	78171865	T	C	21	GENIC	homozygous	116643393
10	78171891	78171892	A	G	17	GENIC	homozygous	116643395
10	78171932	78171933	A	C	9	GENIC	homozygous	116643397