chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 115962267 115962268 T C 13 GENIC homozygous 54072466 7 115962325 115962326 G C 8 GENIC homozygous 54072470 7 115962403 115962404 T C 14 GENIC homozygous 54072472 7 115965123 115965124 C T 11 GENIC homozygous 54072474 7 115965749 115965750 G C 9 GENIC homozygous 54072476 7 115966667 115966668 C - 12 GENIC homozygous 54072481 7 115966838 115966839 G A 13 GENIC homozygous 54072483 7 115967522 115967524 CC -- 10 GENIC homozygous 54072485 7 115967756 115967757 C - 10 GENIC homozygous 54072487 7 115967757 115967758 C G 10 GENIC homozygous 54920529 7 115968034 115968035 C T 8 GENIC homozygous 56483731 7 115968035 115968036 T C 8 GENIC homozygous 54920531 7 115969029 115969030 T C 8 GENIC homozygous 54670097 7 115970356 115970358 TG -- 24 GENIC heterozygous 54920533 7 115970359 115970360 A AG 24 GENIC heterozygous 54920535 7 115970394 115970395 G A 21 GENIC heterozygous 54072499 7 115970702 115970703 A - 15 GENIC homozygous 54072501 7 115970873 115970874 T C 8 GENIC homozygous 54072503 7 115971146 115971148 CT -- 11 GENIC homozygous 54072504 7 115972153 115972154 A G 24 GENIC homozygous 54072510 7 115972276 115972277 G C 22 GENIC homozygous 54072512 7 115973579 115973580 G GTCTCTC 11 GENIC homozygous 54072514 7 115973613 115973614 C G 16 GENIC homozygous 54072516 7 115975271 115975272 T C 7 GENIC homozygous 54072522