chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 8982984 8982985 G A 17 GENIC possibly homozygous 993163435 3 8983559 8983560 C T 21 GENIC homozygous 993163436 3 8984267 8984268 T A 24 GENIC homozygous 993163437 3 8984305 8984306 T A 26 GENIC homozygous 993163438 3 8985027 8985028 A G 20 GENIC homozygous 993163439 3 8987027 8987028 G C 27 GENIC homozygous 993163440 3 8989345 8989346 T C 23 GENIC homozygous 993163441 3 8990633 8990634 T C 27 GENIC possibly homozygous 993163442 3 8992378 8992379 A G 25 GENIC homozygous 993163443 3 8992637 8992638 A G 23 GENIC homozygous 993163444 3 8994846 8994847 G A 22 GENIC possibly homozygous 993163445 3 8995179 8995180 T G 4 GENIC homozygous 993163446 3 8997340 8997341 A G 17 GENIC homozygous 993163447 3 8998857 8998858 G A 20 GENIC homozygous 993163448 3 9003419 9003420 G A 31 GENIC homozygous 993163449 3 9004965 9004966 T G 19 GENIC homozygous 993163450 3 9005689 9005690 G A 32 GENIC possibly homozygous 993163451 3 9006532 9006533 T C 21 GENIC homozygous 993163452 3 9006846 9006847 T C 30 GENIC possibly homozygous 993163453 3 9007888 9007889 C T 22 GENIC possibly homozygous 993163454 3 9008743 9008744 C T 23 GENIC homozygous 993163455 3 9009469 9009470 A G 29 GENIC homozygous 993163456 3 9009628 9009629 T C 21 GENIC heterozygous 993163457 3 9010711 9010712 C T 13 GENIC homozygous 993163458 3 9011122 9011123 G A 33 GENIC homozygous 993163459