chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 14098962 14098963 T A 41 GENIC homozygous 115262269 12 14099465 14099466 G A 37 GENIC homozygous 115262271 12 14101920 14101921 A G 40 GENIC homozygous 115262273 12 14102285 14102286 C T 26 GENIC possibly homozygous 115262275 12 14106879 14106880 A G 35 GENIC homozygous 115262277 12 14133701 14133702 G C 8 GENIC heterozygous 115262279 12 14133712 14133713 G T 5 GENIC heterozygous 115262281 12 14134702 14134703 T G 29 GENIC homozygous 115262283 12 14137946 14137947 G T 27 GENIC homozygous 115262285 12 14137996 14137997 T C 28 GENIC homozygous 115262287 12 14141004 14141005 G A 31 GENIC homozygous 115262289 12 14141017 14141018 A G 27 GENIC homozygous 115262291 12 14141723 14141724 A T 19 GENIC homozygous 115262293 12 14143938 14143939 A G 37 GENIC homozygous 115262295 12 14144576 14144577 A C 25 GENIC homozygous 115262297 12 14145606 14145607 C T 36 GENIC homozygous 115262299 12 14146083 14146084 A C 33 GENIC homozygous 115262301 12 14146459 14146460 T C 28 GENIC homozygous 115262303 12 14146598 14146599 A G 20 GENIC homozygous 115437980 12 14133702 14133703 G C 8 GENIC heterozygous 115510032 12 14144676 14144677 C T 27 GENIC homozygous 115437979 12 14147052 14147053 T C 26 GENIC homozygous 115262305 12 14147291 14147292 T C 23 GENIC homozygous 115262307 12 14147916 14147917 C T 28 GENIC homozygous 115262309 12 14148349 14148350 G T 20 GENIC homozygous 115262311 12 14148606 14148607 T C 29 GENIC homozygous 115262315 12 14148659 14148660 C T 27 GENIC homozygous 115262317 12 14149546 14149547 T A 28 GENIC homozygous 115262319 12 14153018 14153019 G A 23 GENIC homozygous 115262321 12 14156467 14156468 A G 20 GENIC homozygous 115363028 12 14156478 14156479 C A 21 GENIC possibly homozygous 115262323