chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	1145754	1145755	C	T	43	GENIC	homozygous	110568911
18	1147524	1147525	G	A	35	GENIC	homozygous	110512406
18	1149235	1149236	G	A	46	GENIC	homozygous	110512408
18	1150212	1150213	G	A	51	GENIC	homozygous	119577900
18	1150215	1150216	A	G	51	GENIC	homozygous	119577901
18	1150741	1150742	C	T	51	GENIC	homozygous	110568915
18	1151800	1151801	T	C	40	GENIC	homozygous	110568922
18	1151818	1151819	T	C	37	GENIC	homozygous	110568925
18	1153112	1153113	A	G	34	GENIC	homozygous	110640989
18	1154081	1154082	C	T	40	GENIC	homozygous	110512410
18	1154197	1154198	G	A	36	GENIC	homozygous	110568930
18	1150214	1150215	A	T	51	GENIC	homozygous	119509952
18	1150223	1150224	T	C	53	GENIC	homozygous	119509954
18	1150244	1150245	G	T	48	GENIC	homozygous	119509956
18	1153223	1153223		TAATCT	30	GENIC	homozygous	131202381
18	1155032	1155033	T		45	GENIC	homozygous	131202382
18	1157771	1157772	A	C	34	GENIC	homozygous	110512415
18	1159924	1159925	C	T	37	GENIC	homozygous	110512419
18	1161274	1161275	G	A	53	GENIC	homozygous	110512422
18	1163594	1163595	C	T	44	GENIC	possibly homozygous	110670167
18	1164008	1164009	C	T	48	GENIC	homozygous	110670169
18	1164254	1164255	T	A	43	GENIC	homozygous	110568935
18	1166253	1166254	G	A	41	GENIC	homozygous	110670171
18	1166290	1166291	G	A	26	GENIC	homozygous	110512426
18	1166573	1166574	T	C	27	GENIC	homozygous	119509958
18	1166795	1166796	C	T	38	GENIC	possibly homozygous	119509962
18	1166830	1166831	T	C	36	GENIC	homozygous	119509966
18	1167080	1167081	T	A	36	GENIC	homozygous	110670173
18	1168284	1168285	G	T	38	GENIC	possibly homozygous	110512428
18	1170490	1170491	T	G	36	GENIC	possibly homozygous	110512430
18	1170779	1170780	T		36	GENIC	homozygous	131754991
18	1172637	1172638	G	A	65	GENIC	homozygous	110512432
18	1175223	1175223		TTTCAGA	53	GENIC	homozygous	131202386