chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 1325903 1325904 C T 20 GENIC homozygous 137987501 7 1325903 1325904 C 20 GENIC heterozygous 403198243 7 1326847 1326848 T 11 GENIC homozygous 403198244 7 1326847 1326848 T C 11 GENIC heterozygous 403198245 7 1326851 1326852 T 11 GENIC homozygous 403198246 7 1326851 1326852 T G 11 GENIC heterozygous 403198247 7 1326911 1326912 A G 9 GENIC homozygous 154435418 7 1328707 1328708 G A 26 GENIC homozygous 137987502 7 1329130 1329131 G A 11 GENIC homozygous 137987503 7 1333139 1333140 A G 27 GENIC homozygous 137987504 7 1334012 1334013 T 23 GENIC heterozygous 403198250 7 1334012 1334013 T A 23 GENIC homozygous 403198251 7 1334014 1334015 T 23 GENIC heterozygous 403198252 7 1334014 1334015 T A 23 GENIC homozygous 403198253 7 1334016 1334017 T 23 GENIC heterozygous 403198254 7 1334016 1334017 T A 23 GENIC homozygous 403198255 7 1334018 1334019 T 23 GENIC heterozygous 403198256 7 1334018 1334019 T A 23 GENIC homozygous 403198257 7 1334177 1334178 C T 21 GENIC homozygous 137987507 7 1334411 1334412 G A 20 GENIC homozygous 137987508 7 1334903 1334904 C T 23 GENIC homozygous 137987509 7 1335942 1335943 A C 17 GENIC homozygous 137987510 7 1336393 1336394 G A 17 GENIC homozygous 137987511 7 1336789 1336790 C A 15 GENIC homozygous 137987512 7 1337223 1337224 G A 22 GENIC homozygous 137987513 7 1338380 1338381 C T 3 GENIC homozygous 137987514 7 1338382 1338383 C A 2 GENIC homozygous 137987515 7 1339460 1339461 C G 18 GENIC possibly homozygous 137987516 7 1339846 1339847 C T 28 GENIC homozygous 137987517 7 1330286 1330287 A G 4 GENIC heterozygous 140893339 7 1328761 1328761 GGATCCCTT 29 GENIC homozygous 137932494 7 1330288 1330289 G A 4 GENIC heterozygous 140893340