chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 86368276 86368277 G C 60 GENIC homozygous 116667506 10 86368594 86368595 A T 53 GENIC homozygous 116667508 10 86368648 86368649 C G 46 GENIC homozygous 116667510 10 86368812 86368813 A 54 GENIC homozygous 128841973 10 86369686 86369686 G 28 GENIC homozygous 128841974 10 86369961 86369962 G A 47 GENIC homozygous 116667512 10 86369979 86369980 G T 49 GENIC possibly homozygous 116667514 10 86370259 86370260 G C 65 GENIC homozygous 116667516 10 86370298 86370299 G A 53 GENIC homozygous 116667518 10 86370362 86370362 G 52 GENIC homozygous 128841975 10 86371088 86371089 T C 61 GENIC homozygous 116667520 10 86372434 86372435 A G 48 GENIC homozygous 116816163 10 86373326 86373328 GC 20 GENIC possibly homozygous 128841976 10 86374945 86374945 GTGT 55 GENIC homozygous 128841977 10 86375960 86375961 C T 67 GENIC homozygous 116667522 10 86375993 86375994 G T 76 GENIC homozygous 116667524 10 86376413 86376414 C T 68 GENIC homozygous 116667526 10 86376816 86376817 G A 56 GENIC homozygous 116667528 10 86376960 86376961 C G 60 GENIC possibly homozygous 116667530 10 86377033 86377034 C T 63 GENIC possibly homozygous 116667532 10 86377901 86377902 A G 66 GENIC homozygous 116667534 10 86378371 86378372 C T 69 GENIC homozygous 116667536 10 86378531 86378531 T 61 GENIC homozygous 128841978 10 86379008 86379009 T C 59 GENIC homozygous 116667538 10 86379009 86379010 C T 59 GENIC homozygous 116667540 10 86379291 86379292 A G 57 GENIC homozygous 116667542 10 86380100 86380101 A G 70 GENIC homozygous 116667544 10 86382097 86382098 G T 52 GENIC homozygous 116667546 10 86382185 86382186 G A 49 GENIC homozygous 116667548 10 86384122 86384123 G T 4 GENIC homozygous 134437979 10 86384006 86384007 G A 30 GENIC homozygous 118005151 10 86373314 86373315 G C 23 GENIC homozygous 117227679 10 86384094 86384095 C T 10 GENIC homozygous 128872810