chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40341047 40341048 T C 18 GENIC homozygous 635732064 12 40341058 40341059 G A 17 GENIC homozygous 635732065 12 40341986 40341987 T - 12 GENIC homozygous 748319035 12 40342338 40342339 G A 30 GENIC homozygous 635732066 12 40342426 40342427 A G 32 GENIC homozygous 635732067 12 40342687 40342689 CA -- 24 GENIC heterozygous 748319036 12 40342760 40342761 A G 31 GENIC homozygous 635732068 12 40347980 40347981 T - 33 GENIC heterozygous 748319037 12 40349985 40349987 CA -- 12 GENIC heterozygous 748319039 12 40358199 40358200 T TC 22 GENIC possibly homozygous 748319042 12 40358206 40358207 T TC 25 GENIC homozygous 748319043 12 40358210 40358211 G GC 23 GENIC homozygous 748319044 12 40358269 40358270 C CTG 12 GENIC heterozygous 748319047 12 40358280 40358282 TG -- 12 GENIC heterozygous 748319046 12 40358443 40358444 C G 33 GENIC homozygous 635732069 12 40358445 40358446 C G 33 GENIC homozygous 635732070 12 40359068 40359069 C CA 39 GENIC heterozygous 748319048 12 40364133 40364134 C CA 3 GENIC heterozygous 748319050 12 40364134 40364136 AA -- 3 GENIC heterozygous 748319049