chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 91597213 91597214 C A 18 GENIC homozygous 50866373 11 91597538 91597539 C T 20 GENIC homozygous 50866374 11 91598001 91598002 C - 4 GENIC heterozygous 51241852 11 91598231 91598232 G T 19 GENIC homozygous 50866377 11 91598315 91598316 C T 10 GENIC homozygous 50866378 11 91598764 91598765 A T 19 GENIC homozygous 50866379 11 91599204 91599205 T C 28 GENIC homozygous 50866380 11 91599410 91599411 C T 19 GENIC homozygous 50866381 11 91599620 91599621 A G 17 GENIC homozygous 50866382 11 91599729 91599730 A - 15 GENIC homozygous 50866383 11 91599796 91599797 A G 19 GENIC homozygous 50866384 11 91599874 91599875 T C 18 GENIC homozygous 50866385 11 91600086 91600087 G A 18 GENIC homozygous 50866386 11 91600255 91600256 A G 20 GENIC homozygous 50866387 11 91600303 91600305 AC -- 18 GENIC homozygous 50866388 11 91600355 91600356 C - 25 GENIC heterozygous 51171356 11 91600469 91600470 T C 18 GENIC homozygous 50866389 11 91600484 91600486 CA -- 16 GENIC homozygous 50866390 11 91600737 91600738 G A 19 GENIC homozygous 50866391 11 91600741 91600742 A G 21 GENIC homozygous 50866392 11 91602310 91602311 A C 20 GENIC homozygous 50866397