chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 61165885 61165886 G T 18 GENIC homozygous 803447265 7 61167719 61167720 C A 12 GENIC heterozygous 803447266 7 61168429 61168430 T C 17 GENIC homozygous 803447267 7 61169135 61169136 T C 24 GENIC homozygous 803447268 7 61170045 61170046 A G 15 GENIC homozygous 803447269 7 61171532 61171533 T C 30 GENIC homozygous 803447270 7 61171989 61171990 A G 16 GENIC homozygous 803447271 7 61172256 61172257 A G 12 GENIC homozygous 803447272 7 61174065 61174066 C G 30 GENIC homozygous 803447273 7 61176288 61176289 T C 35 GENIC homozygous 803447274 7 61178568 61178569 G A 13 GENIC homozygous 803447275 7 61180789 61180790 A G 18 GENIC homozygous 803447276 7 61181538 61181539 T C 20 GENIC homozygous 803447277 7 61181684 61181685 T G 36 GENIC homozygous 803447278 7 61182215 61182216 G A 25 GENIC homozygous 803447279 7 61182827 61182828 G A 11 GENIC homozygous 803447280 7 61183211 61183212 T C 37 GENIC homozygous 803447281 7 61184439 61184440 T C 9 GENIC homozygous 803447282 7 61184448 61184449 T C 9 GENIC homozygous 803447283 7 61187301 61187302 C T 19 GENIC homozygous 803447284 7 61187610 61187611 C T 40 GENIC homozygous 803447285 7 61188392 61188393 C G 23 GENIC homozygous 803447286 7 61192106 61192107 T C 28 GENIC homozygous 803447287 7 61192493 61192494 C T 25 GENIC heterozygous 803447288 7 61193407 61193408 C T 26 GENIC homozygous 803447289 7 61193684 61193685 T C 21 GENIC homozygous 803447290 7 61194178 61194179 A G 22 GENIC homozygous 803447291 7 61194377 61194378 T G 15 GENIC homozygous 803447292 7 61197278 61197279 A G 37 GENIC homozygous 803447293 7 61197809 61197810 A G 30 GENIC homozygous 803447294 7 61198433 61198434 C G 25 GENIC homozygous 803447295 7 61198601 61198602 T A 22 GENIC homozygous 803447296 7 61198813 61198814 G A 18 GENIC possibly homozygous 803447297