chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 26031412 26031413 T C 60 GENIC possibly homozygous 783021353 19 26031966 26031967 A C 54 GENIC possibly homozygous 783021354 19 26033859 26033860 C G 23 GENIC heterozygous 783021355 19 26037654 26037655 T C 53 GENIC homozygous 783021356 19 26037998 26037999 G C 49 GENIC homozygous 783021357 19 26039540 26039541 C T 51 GENIC homozygous 783021358 19 26042129 26042130 T C 47 GENIC possibly homozygous 783021359 19 26042606 26042607 G A 46 GENIC heterozygous 783021360 19 26044593 26044594 T C 62 GENIC possibly homozygous 783021361 19 26046276 26046277 T C 55 GENIC homozygous 783021362 19 26047360 26047361 C T 61 GENIC heterozygous 783021363 19 26047366 26047367 C A 72 GENIC heterozygous 783021364 19 26047414 26047415 C T 97 GENIC heterozygous 783021365 19 26047416 26047417 A C 89 GENIC heterozygous 783021366 19 26047460 26047461 C T 58 GENIC heterozygous 783021367 19 26047661 26047662 G A 45 GENIC homozygous 783021368 19 26050915 26050916 T C 48 GENIC homozygous 783021369 19 26051251 26051252 T G 64 GENIC possibly homozygous 783021370 19 26053368 26053369 A G 33 GENIC possibly homozygous 783021371