chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31780513	31780514	C	T	24	GENIC	homozygous	115812496
11	31785262	31785263	T	C	10	GENIC	homozygous	115960364
11	31785559	31785560	C	T	22	GENIC	homozygous	115812498
11	31788111	31788112	T	C	32	GENIC	homozygous	115812500
11	31788588	31788589	T	C	31	GENIC	homozygous	115812502
11	31789989	31789990	A	G	24	GENIC	homozygous	115812508
11	31792308	31792309	G	A	23	GENIC	homozygous	115812510
11	31793069	31793070	G	A	19	GENIC	homozygous	115812512
11	31795123	31795124	A	G	39	GENIC	homozygous	115812514
11	31795699	31795700	A	G	27	GENIC	homozygous	115812516
11	31797255	31797256	G	A	18	GENIC	homozygous	115812518
11	31798066	31798067	T	C	26	GENIC	homozygous	115812520
11	31798159	31798160	G	T	23	GENIC	homozygous	115812522
11	31798209	31798210	T	C	21	GENIC	homozygous	115812524
11	31798292	31798293	T	C	17	GENIC	homozygous	115812526
11	31799631	31799632	G	A	16	GENIC	homozygous	115812528
11	31800475	31800476	A	T	14	GENIC	homozygous	115812530
11	31800983	31800984	C	T	25	GENIC	homozygous	115812532
11	31801916	31801917	T	C	23	GENIC	homozygous	115812534
11	31801989	31801990	G	A	24	GENIC	homozygous	115812536
11	31803317	31803318	C	T	14	GENIC	homozygous	115812538
11	31803796	31803797	G	C	12	GENIC	homozygous	115812540
11	31804551	31804552	T	C	6	GENIC	homozygous	115812542
11	31805267	31805268	T	A	12	GENIC	homozygous	115812544