chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40341047 40341048 T C 23 GENIC homozygous 661483203 12 40341058 40341059 G A 25 GENIC homozygous 661483204 12 40341213 40341214 A C 24 GENIC homozygous 661483205 12 40341986 40341987 T - 14 GENIC homozygous 763986448 12 40342338 40342339 G A 21 GENIC homozygous 661483206 12 40342426 40342427 A G 28 GENIC homozygous 661483207 12 40342760 40342761 A G 35 GENIC homozygous 661483208 12 40349984 40349985 G GCACACACACACACACACA 3 GENIC homozygous 763986451 12 40350572 40350573 T - 13 GENIC heterozygous 763986452 12 40350849 40350851 CA -- 5 GENIC heterozygous 763986454 12 40354386 40354387 G A 26 GENIC homozygous 661483209 12 40355056 40355060 GTGT ---- 3 GENIC homozygous 763986456 12 40358199 40358200 T TC 23 GENIC homozygous 763986457 12 40358206 40358207 T TC 22 GENIC homozygous 763986458 12 40358210 40358211 G GC 23 GENIC homozygous 763986459 12 40358443 40358444 C G 21 GENIC homozygous 661483210 12 40358445 40358446 C G 22 GENIC homozygous 661483211 12 40363893 40363897 GTGT ---- 8 GENIC homozygous 763986461 12 40364121 40364122 A - 5 GENIC homozygous 763986464 12 40364133 40364134 C CA 6 GENIC heterozygous 763986466 12 40364134 40364136 AA -- 6 GENIC heterozygous 763986465 12 40364774 40364775 C T 24 GENIC homozygous 661483212 12 40364782 40364783 A C 27 GENIC homozygous 661483213