chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 23545038 23545039 A G 13 GENIC homozygous 893939497 12 23548240 23548241 T C 9 GENIC homozygous 893939498 12 23549188 23549189 G T 23 GENIC homozygous 893939499 12 23549411 23549412 T C 5 GENIC heterozygous 893939500 12 23549655 23549656 C T 31 GENIC homozygous 893939501 12 23549710 23549711 A G 14 GENIC homozygous 893939502 12 23549870 23549871 T C 21 GENIC homozygous 893939503 12 23550107 23550108 T C 23 GENIC homozygous 893939504 12 23550166 23550167 C T 19 GENIC homozygous 893939505 12 23550376 23550377 C T 13 GENIC heterozygous 893939506 12 23551097 23551098 T C 3 GENIC heterozygous 893939507 12 23551525 23551526 C T 17 GENIC homozygous 893939508 12 23552336 23552337 T C 18 GENIC homozygous 893939509 12 23552544 23552545 T C 17 GENIC homozygous 893939510 12 23552618 23552619 A G 21 GENIC homozygous 893939511 12 23553440 23553441 C T 13 GENIC homozygous 893939512 12 23553910 23553911 G A 21 GENIC homozygous 893939513 12 23554336 23554337 C T 16 GENIC heterozygous 893939514 12 23554434 23554435 T C 6 GENIC heterozygous 893939515 12 23554461 23554462 A T 4 GENIC heterozygous 893939516 12 23556166 23556167 C T 10 GENIC homozygous 893939517 12 23556684 23556685 G A 21 GENIC homozygous 893939518 12 23556747 23556748 T C 21 GENIC homozygous 893939519 12 23556790 23556791 A C 19 GENIC homozygous 893939520 12 23558051 23558052 A C 25 GENIC homozygous 893939521 12 23558550 23558551 C G 9 GENIC heterozygous 893939522