chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	73938858	73938859	G	C	12	GENIC	homozygous	115990387
11	73939195	73939196	A	G	21	GENIC	homozygous	116248206
11	73939939	73939940	T	A	13	GENIC	homozygous	115990389
11	73940206	73940207	C	T	19	GENIC	homozygous	116248208
11	73941157	73941158	G	T	8	GENIC	homozygous	115990393
11	73941294	73941295	G	T	14	GENIC	homozygous	116054341
11	73941306	73941307	C	T	17	GENIC	homozygous	116054343
11	73942777	73942778	C	T	16	GENIC	homozygous	115990399
11	73944181	73944182	C	T	12	GENIC	homozygous	116248210
11	73947753	73947754	T	C	22	GENIC	homozygous	116248212
11	73948991	73948992	C	T	18	GENIC	homozygous	116248214
11	73949379	73949380	T	A	24	GENIC	homozygous	116248216
11	73951473	73951474	G	A	43	GENIC	homozygous	115990407
11	73952998	73952999	T	C	22	GENIC	homozygous	116248218
11	73953489	73953490	C	T	19	GENIC	homozygous	116248220
11	73953549	73953550	G	A	16	GENIC	homozygous	116248222
11	73953581	73953582	G	A	18	GENIC	homozygous	115990409
11	73956053	73956054	C	T	25	GENIC	homozygous	116308702
11	73956974	73956975	C	T	20	GENIC	homozygous	115990413
11	73960118	73960119	T	A	22	GENIC	homozygous	115990415
11	73961112	73961113	G	A	27	GENIC	possibly homozygous	116248224
11	73961242	73961243	A	G	26	GENIC	homozygous	115990421
11	73961408	73961409	G	A	28	GENIC	homozygous	116248226
11	73961978	73961979	C	T	26	GENIC	homozygous	116248228
11	73962191	73962192	G	A	22	GENIC	homozygous	115990423
11	73962288	73962289	G	A	16	GENIC	homozygous	115990425
11	73962628	73962629	T	A	13	GENIC	homozygous	115990427
11	73963258	73963259	T	G	5	GENIC	homozygous	115990429
11	73948262	73948263	A	C	7	GENIC	heterozygous	116388885