chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	23884457	23884457		TTCT	18	GENIC	homozygous	140215833
18	23885911	23885912	T	A	19	GENIC	homozygous	140286899
18	23887193	23887194	A	G	22	GENIC	homozygous	140286900
18	23887393	23887394	G	A	14	GENIC	homozygous	140286901
18	23888389	23888390	C	T	13	GENIC	homozygous	140286902
18	23889184	23889185	T	C	24	GENIC	homozygous	140286903
18	23890752	23890753	T	G	12	GENIC	homozygous	140286904
18	23892157	23892158	G	A	17	GENIC	homozygous	140286905
18	23892177	23892178	C	T	17	GENIC	homozygous	140286906
18	23893675	23893676	A	G	27	GENIC	homozygous	140286907
18	23894111	23894112	C	G	25	GENIC	possibly homozygous	140286908
18	23894725	23894726	C	T	8	GENIC	homozygous	140286909
18	23894819	23894827	GCTGCTCT		12	GENIC	homozygous	140215834
18	23894827	23894828	T	A	12	GENIC	homozygous	140286910
18	23894985	23894986	A	G	14	GENIC	possibly homozygous	140286911
18	23896720	23896721	T	C	17	GENIC	homozygous	140286912
18	23898742	23898743	C	T	15	GENIC	homozygous	140286913
18	23898798	23898799	G	A	14	GENIC	homozygous	140286914
18	23898927	23898928	G	A	24	GENIC	homozygous	140286915
18	23899225	23899226	T	G	17	GENIC	homozygous	140286916
18	23899499	23899500	T	A	16	GENIC	homozygous	140286917
18	23903255	23903256	G	A	26	GENIC	homozygous	140286918
18	23903692	23903693	G	A	15	GENIC	homozygous	140286919
18	23903883	23903884	C	T	22	GENIC	homozygous	140286920
18	23906844	23906845	T	C	15	GENIC	homozygous	140286921
18	23909673	23909674	C	T	17	GENIC	homozygous	140286922
18	23909836	23909837	G	A	19	GENIC	homozygous	140286923
18	23910017	23910018	G	T	22	GENIC	homozygous	140286924
18	23910227	23910228	C	A	21	GENIC	homozygous	140286925
18	23910870	23910870		CTGCCTCTGCCT	15	GENIC	homozygous	140215835
18	23911002	23911002		CTGCCTCTC	14	GENIC	homozygous	140215836
18	23912563	23912564	G		13	GENIC	homozygous	140215837
18	23913498	23913498		C	11	GENIC	homozygous	140215838
18	23913872	23913872		CA	14	GENIC	homozygous	140215839