chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	5309139	5309140	T	G	19	GENIC	homozygous	139430066
14	5309205	5309206	A	C	20	GENIC	homozygous	139430067
14	5309276	5309277	A	T	22	GENIC	homozygous	139430068
14	5309991	5309992	G	A	16	GENIC	homozygous	139430070
14	5311223	5311224	A	G	25	GENIC	homozygous	142427309
14	5309707	5309708	T	G	13	GENIC	homozygous	142427306
14	5310849	5310850	C	T	22	GENIC	homozygous	142427307
14	5310999	5311000	G	A	22	GENIC	homozygous	142427308
14	5311245	5311246	T	C	21	GENIC	homozygous	142427310
14	5311419	5311420	T	C	29	GENIC	homozygous	142427311
14	5311743	5311744	G	C	22	GENIC	homozygous	142427312
14	5311901	5311902	T	C	27	GENIC	homozygous	142427313
14	5312083	5312084	A	T	21	GENIC	homozygous	142427314
14	5312084	5312085	A	T	21	GENIC	homozygous	142427315
14	5312137	5312138	C	T	31	GENIC	homozygous	142427316
14	5312396	5312397	T	C	30	GENIC	homozygous	142427317
14	5312410	5312411	G	C	31	GENIC	homozygous	142427318
14	5312411	5312412	T	A	31	GENIC	homozygous	142427319
14	5312681	5312682	T	C	30	GENIC	homozygous	142427320
14	5312708	5312709	A	G	29	GENIC	homozygous	142427321
14	5312794	5312795	G	T	19	GENIC	homozygous	142427322
14	5313069	5313070	A	G	25	GENIC	homozygous	142427323
14	5313160	5313161	T	C	18	GENIC	homozygous	142427324
14	5313382	5313383	T	G	27	GENIC	homozygous	142427325
14	5313476	5313477	C	G	19	GENIC	homozygous	142427326
14	5313577	5313578	A	G	20	GENIC	homozygous	142427327
14	5313803	5313804	C	A	15	GENIC	homozygous	142427328
14	5313807	5313808	G	C	15	GENIC	homozygous	142427329
14	5313871	5313872	T	C	12	GENIC	homozygous	142427330
14	5313995	5313996	C	T	23	GENIC	homozygous	142427331
14	5314008	5314009	G	T	22	GENIC	homozygous	142427332
14	5314018	5314019	C	A	22	GENIC	homozygous	142427333
14	5314031	5314032	G	T	20	GENIC	homozygous	142427334
14	5315002	5315003	C	T	22	GENIC	homozygous	142427335
14	5312409	5312409		C	30	GENIC	homozygous	142417980
14	5315011	5315012	G		21	GENIC	homozygous	142417981
14	5313857	5313858	A		9	GENIC	homozygous	139375482