chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 62848583 62848584 T C 34 GENIC homozygous 969417345 4 62848699 62848700 C T 22 GENIC homozygous 969417346 4 62849227 62849228 G A 34 GENIC homozygous 969417347 4 62850458 62850459 G A 23 GENIC homozygous 969417348 4 62851003 62851004 T C 23 GENIC homozygous 969417349 4 62853410 62853411 A G 25 GENIC homozygous 969417350 4 62853526 62853527 G A 34 GENIC homozygous 969417351 4 62853655 62853656 G T 34 GENIC homozygous 969417352 4 62853656 62853657 T C 34 GENIC homozygous 969417353 4 62853724 62853725 A G 28 GENIC homozygous 969417354 4 62856412 62856413 A G 33 GENIC homozygous 969417355 4 62857520 62857521 A T 23 GENIC homozygous 969417356 4 62857785 62857786 T A 24 GENIC homozygous 969417357 4 62857845 62857846 A G 26 GENIC homozygous 969417358 4 62857869 62857870 C T 23 GENIC homozygous 969417359 4 62858004 62858005 G T 25 GENIC homozygous 969417360 4 62858394 62858395 T C 31 GENIC homozygous 969417361 4 62858604 62858605 C T 37 GENIC homozygous 969417362 4 62859050 62859051 C A 24 GENIC homozygous 969417363 4 62859100 62859101 C T 39 GENIC homozygous 969417364 4 62859607 62859608 G A 42 GENIC homozygous 969417365 4 62859609 62859610 C T 41 GENIC homozygous 969417366 4 62859667 62859668 G A 43 GENIC homozygous 969417367 4 62859681 62859682 T C 47 GENIC homozygous 969417368 4 62859685 62859686 G A 48 GENIC homozygous 969417369 4 62859921 62859922 A G 34 GENIC homozygous 969417370