chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	36695761	36695769	TCATAGTG	--------	11	GENIC	homozygous	54357350
7	36697156	36697157	C	T	25	GENIC	homozygous	54357352
7	36697228	36697229	C	A	22	GENIC	homozygous	53876337
7	36697963	36697964	T	C	7	GENIC	homozygous	53876341
7	36698137	36698138	C	-	10	GENIC	homozygous	53876344
7	36701493	36701495	CT	--	24	GENIC	homozygous	54357354
7	36701579	36701580	A	G	9	GENIC	homozygous	53876356
7	36701805	36701822	TGAATAAAGCTACAGGA	-----------------	15	GENIC	homozygous	54193208
7	36701847	36701848	C	T	12	GENIC	homozygous	54357356
7	36702241	36702242	T	C	25	GENIC	homozygous	53876365
7	36702391	36702392	A	G	19	GENIC	homozygous	53876367
7	36702517	36702518	A	G	30	GENIC	homozygous	54193209
7	36702829	36702830	A	T	28	GENIC	homozygous	54357358
7	36703156	36703169	AAAAAAAAAAAAA	-------------	13	GENIC	homozygous	54357360
7	36703180	36703194	CAAAAAAAAAAAAA	--------------	19	GENIC	homozygous	54357362
7	36703624	36703625	C	T	28	GENIC	homozygous	54357364
7	36705972	36705973	C	CCAT	22	GENIC	homozygous	53876377
7	36706046	36706050	TTGA	----	19	GENIC	homozygous	54193211
7	36706281	36706282	A	G	30	GENIC	homozygous	53876379
7	36706483	36706484	C	T	24	GENIC	homozygous	54357366
7	36706515	36706519	TTTT	----	21	GENIC	homozygous	53876385
7	36707210	36707211	C	T	19	GENIC	homozygous	54357368
7	36707271	36707272	T	TG	21	GENIC	homozygous	53876386
7	36709116	36709117	C	A	22	GENIC	homozygous	54193213
7	36709516	36709517	A	AC	11	GENIC	homozygous	53876392
7	36710201	36710202	G	A	19	GENIC	homozygous	53876395
7	36711099	36711100	C	T	17	GENIC	homozygous	53876398
7	36711151	36711152	A	-	16	GENIC	homozygous	54968974
7	36711353	36711354	G	A	21	GENIC	homozygous	54193217
7	36711466	36711467	A	G	6	GENIC	homozygous	54193218
7	36711521	36711522	G	A	7	GENIC	homozygous	54193220
7	36706524	36706525	T	G	23	GENIC	homozygous	55273497