chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44370081	44370082	T	C	30	GENIC	possibly homozygous	139150205
12	44370302	44370302		CA	6	GENIC	homozygous	139058208
12	44370656	44370657	C	T	16	GENIC	homozygous	139150206
12	44370834	44370835	A	G	16	GENIC	homozygous	139150207
12	44372629	44372630	C	T	21	GENIC	possibly homozygous	139150208
12	44373256	44373257	T	G	26	GENIC	homozygous	139150209
12	44373495	44373496	T	C	25	GENIC	homozygous	139150210
12	44374124	44374125	A	G	22	GENIC	homozygous	139150211
12	44374398	44374399	A		28	GENIC	homozygous	139058209
12	44374864	44374865	G	A	27	GENIC	homozygous	139150212
12	44376135	44376136	A	G	23	GENIC	homozygous	139150213
12	44376565	44376566	G	T	24	GENIC	possibly homozygous	139150214
12	44376631	44376632	G	A	22	GENIC	homozygous	139150215
12	44377159	44377160	A	G	29	GENIC	homozygous	139150216
12	44377328	44377329	T	A	29	GENIC	homozygous	139150217
12	44377492	44377493	C	T	27	GENIC	homozygous	139150218
12	44377624	44377625	G	A	24	GENIC	homozygous	139150219
12	44377819	44377820	C	T	23	GENIC	homozygous	139150220
12	44377977	44377978	A	G	21	GENIC	homozygous	139150221
12	44378166	44378167	C	T	24	GENIC	homozygous	139150222
12	44378479	44378480	G	A	24	GENIC	homozygous	139150223
12	44379364	44379365	A	T	22	GENIC	homozygous	139150224
12	44379396	44379397	A	G	23	GENIC	homozygous	139150225
12	44380054	44380055	G	A	24	GENIC	homozygous	139150226
12	44380070	44380071	C	T	26	GENIC	homozygous	139150227
12	44380526	44380527	C	T	29	GENIC	possibly homozygous	139150228
12	44380744	44380745	A	G	15	GENIC	homozygous	139150229
12	44380819	44380820	G	A	15	GENIC	homozygous	139150230
12	44381909	44381910	C		20	GENIC	homozygous	139058210
12	44382439	44382440	T	C	23	GENIC	homozygous	139150231
12	44383072	44383073	G	A	17	GENIC	homozygous	139150232
12	44383110	44383111	C	T	17	GENIC	homozygous	139150233
12	44383207	44383208	T	C	23	GENIC	homozygous	139150234