chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40341047 40341048 T C 1 GENIC homozygous 567482242 12 40341058 40341059 G A 5 GENIC homozygous 567482243 12 40341213 40341214 A C 9 GENIC homozygous 567482244 12 40341986 40341987 T - 15 GENIC homozygous 708946068 12 40342338 40342339 G A 20 GENIC homozygous 567482245 12 40342426 40342427 A G 30 GENIC homozygous 567482246 12 40342687 40342689 CA -- 25 GENIC heterozygous 708946069 12 40342760 40342761 A G 17 GENIC possibly homozygous 567482247 12 40349984 40349985 G GCACACACACACACACACA 3 GENIC homozygous 708946072 12 40350848 40350849 C CCACACA 6 GENIC heterozygous 708946074 12 40354386 40354387 G A 19 GENIC homozygous 567482248 12 40355056 40355060 GTGT ---- 5 GENIC heterozygous 708946075 12 40358199 40358200 T TC 24 GENIC homozygous 708946076 12 40358206 40358207 T TC 25 GENIC homozygous 708946077 12 40358210 40358211 G GC 29 GENIC homozygous 708946078 12 40358269 40358270 C CTG 6 GENIC homozygous 708946081 12 40358443 40358444 C G 28 GENIC homozygous 567482249 12 40358445 40358446 C G 29 GENIC homozygous 567482250 12 40359068 40359069 C CA 19 GENIC heterozygous 708946082 12 40363893 40363897 GTGT ---- 1 GENIC homozygous 708946084 12 40364121 40364122 A - 7 GENIC homozygous 708946087 12 40364133 40364134 C CA 1 GENIC homozygous 708946089 12 40364774 40364775 C T 27 GENIC homozygous 567482251 12 40364782 40364783 A C 27 GENIC homozygous 567482252