chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	40734863	40734864	G	A	29	GENIC	homozygous	110329840
18	40735502	40735503	C	T	24	GENIC	homozygous	110329842
18	40744081	40744082	A	T	13	GENIC	homozygous	110329844
18	40746561	40746562	T	A	38	GENIC	homozygous	110329846
18	40747645	40747646	A	G	29	GENIC	homozygous	110329848
18	40748034	40748035	C	T	32	GENIC	homozygous	110329850
18	40748546	40748547	A	C	30	GENIC	homozygous	110329852
18	40748884	40748885	T	C	27	GENIC	homozygous	110329854
18	40750646	40750647	C	A	19	GENIC	homozygous	110329856
18	40750779	40750780	C	G	17	GENIC	homozygous	110329858
18	40751180	40751181	T	G	15	GENIC	homozygous	110329860
18	40754337	40754338	G	C	24	GENIC	homozygous	110329862
18	40759063	40759064	C	G	32	GENIC	homozygous	110329864
18	40770741	40770742	T	G	29	GENIC	homozygous	110329866
18	40773867	40773868	A	G	35	GENIC	homozygous	110463699
18	40777236	40777237	G	C	19	GENIC	homozygous	110329868
18	40778954	40778955	C	A	14	GENIC	homozygous	110329870
18	40783790	40783791	A	G	16	GENIC	homozygous	110329872
18	40784397	40784398	A	G	28	GENIC	homozygous	110329874
18	40784877	40784878	G	A	23	GENIC	homozygous	110463702
18	40786418	40786419	T	G	17	GENIC	homozygous	110329876
18	40788667	40788668	C	T	18	GENIC	homozygous	110463704
18	40791435	40791436	G	A	27	GENIC	homozygous	110329878