chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 39315789 39315790 T - 23 GENIC possibly homozygous 729889541 12 39315825 39315826 G A 22 GENIC homozygous 602252281 12 39316196 39316197 T C 32 GENIC homozygous 602252282 12 39317102 39317103 T C 32 GENIC homozygous 602252283 12 39317409 39317410 A G 30 GENIC homozygous 602252284 12 39317837 39317838 G A 31 GENIC homozygous 602252285 12 39317854 39317855 T C 31 GENIC homozygous 602252286 12 39318268 39318275 TGGTCAC ------- 24 GENIC homozygous 729889542 12 39318571 39318572 T C 24 GENIC homozygous 602252287 12 39318675 39318676 T C 22 GENIC homozygous 602252288 12 39319563 39319564 G A 27 GENIC homozygous 602252289 12 39319727 39319728 G GTTT 16 GENIC heterozygous 729889543 12 39319727 39319728 G GTTTT 16 GENIC heterozygous 729889544 12 39319835 39319836 A G 22 GENIC homozygous 602252290 12 39320000 39320008 ATGTGCAC -------- 31 GENIC homozygous 729889546 12 39320082 39320083 A C 22 GENIC homozygous 602252291 12 39320394 39320395 G A 26 GENIC homozygous 602252292 12 39321179 39321180 G A 28 GENIC homozygous 602252293 12 39321213 39321214 C T 28 GENIC homozygous 602252294 12 39321949 39321950 C T 26 GENIC homozygous 602252295 12 39322640 39322641 C T 17 GENIC homozygous 602252296 12 39322659 39322660 C T 15 GENIC homozygous 602252297 12 39322674 39322675 G A 11 GENIC homozygous 602252298 12 39322706 39322707 C T 5 GENIC heterozygous 603276588 12 39323213 39323214 T C 23 GENIC homozygous 602252299