chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	29016490	29016491	G	A	15	GENIC	homozygous	116750921
10	29018152	29018153	G	A	23	GENIC	homozygous	116750923
10	29019149	29019150	A	G	29	GENIC	homozygous	116538954
10	29020207	29020208	G	A	7	GENIC	homozygous	117001324
10	29021659	29021660	T	C	19	GENIC	homozygous	116750925
10	29021920	29021921	G	A	20	GENIC	homozygous	116538960
10	29022284	29022285	C	A	30	GENIC	homozygous	116538962
10	29022289	29022290	G	A	30	GENIC	homozygous	116538964
10	29022314	29022315	A	C	29	GENIC	homozygous	116538966
10	29022452	29022453	C	T	9	GENIC	homozygous	116538968
10	29023684	29023685	G	A	29	GENIC	homozygous	116750927
10	29023793	29023794	A	G	15	GENIC	homozygous	116538970
10	29023920	29023921	C	T	24	GENIC	homozygous	116538974
10	29023983	29023984	C	T	18	GENIC	homozygous	116538976
10	29023987	29023988	C	T	18	GENIC	homozygous	116538980
10	29024192	29024193	C	T	17	GENIC	homozygous	116538988
10	29024412	29024413	T	C	14	GENIC	homozygous	116750929
10	29024656	29024657	C	A	17	GENIC	homozygous	116750931
10	29024884	29024885	G	A	23	GENIC	homozygous	116538990
10	29025155	29025156	C	G	12	GENIC	homozygous	116538992
10	29025212	29025213	T	G	21	GENIC	homozygous	116750933