chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 23538304 23538305 A G 42 GENIC homozygous 139250251 13 23540948 23540949 C T 49 GENIC homozygous 147014462 13 23543828 23543829 C T 46 GENIC homozygous 147014463 13 23544059 23544060 T 36 GENIC possibly homozygous 403332434 13 23544059 23544060 T C 36 GENIC heterozygous 403332435 13 23544058 23544059 G 36 GENIC possibly homozygous 403332432 13 23544058 23544059 G A 36 GENIC heterozygous 403332433 13 23544291 23544292 C G 49 GENIC homozygous 147014464 13 23545266 23545267 G C 41 GENIC homozygous 139250257 13 23547332 23547333 G A 56 GENIC homozygous 147014465 13 23547345 23547346 G T 53 GENIC homozygous 147014466 13 23547349 23547350 C T 53 GENIC homozygous 147014467 13 23547462 23547463 T C 51 GENIC homozygous 139250263 13 23547577 23547578 C T 54 GENIC homozygous 139250264 13 23547615 23547616 T A 49 GENIC homozygous 143562251 13 23548646 23548647 G C 49 GENIC homozygous 143562252 13 23548682 23548683 C G 48 GENIC homozygous 139250267 13 23549074 23549075 T A 52 GENIC homozygous 147014468 13 23550522 23550523 T A 40 GENIC homozygous 147014469 13 23550789 23550790 T C 58 GENIC homozygous 139250274 13 23551345 23551346 T G 44 GENIC homozygous 147014470 13 23544478 23544478 TC 22 GENIC homozygous 147006487 13 23544458 23544458 TA 22 GENIC homozygous 142341526 13 23546063 23546094 CCAGCAGGGAGATCAGTTTCAAAGCACTGTT 36 GENIC homozygous 147006488 13 23546696 23546705 CTCCTCCTG 23 GENIC homozygous 143546265 13 23550150 23550151 C 51 GENIC heterozygous 143546266 13 23550150 23550151 C T 51 GENIC homozygous 154768837