chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 99537237 99537245 GCCCCTGC -------- 8 GENIC homozygous 50532989 13 99537245 99537246 A ATTTT 8 GENIC homozygous 50532991 13 99537248 99537249 G T 8 GENIC homozygous 50532993 13 99537250 99537251 T TGAAC 8 GENIC homozygous 50532995 13 99537251 99537252 T C 8 GENIC homozygous 50532997 13 99548764 99548765 A AAAG 22 GENIC homozygous 49866780 13 99562714 99562715 C - 12 GENIC homozygous 49866781 13 99562715 99562716 C T 12 GENIC homozygous 51255990 13 99627962 99627963 C A 15 GENIC homozygous 49866790 13 99639373 99639374 G - 20 GENIC homozygous 49866799 13 99639432 99639433 G C 20 GENIC homozygous 49973609 13 99639433 99639434 C A 21 GENIC homozygous 49973610 13 99639485 99639486 T - 19 GENIC homozygous 49866800 13 99661607 99661608 C CACACATACAT 15 GENIC homozygous 49866801 13 99673244 99673245 T - 14 GENIC homozygous 49866804 13 99673253 99673254 C A 17 GENIC homozygous 49866805 13 99673271 99673272 T A 16 GENIC homozygous 49866806 13 99673272 99673273 C A 16 GENIC homozygous 49866807 13 99673274 99673275 G A 16 GENIC homozygous 49866808 13 99673277 99673278 C T 16 GENIC homozygous 49866809 13 99673350 99673351 A AG 14 GENIC homozygous 49866810 13 99688377 99688378 G A 23 GENIC heterozygous 49866811 13 99688440 99688441 A G 17 GENIC heterozygous 49866812 13 99688448 99688449 G T 12 GENIC heterozygous 49866813 13 99692035 99692036 G - 14 GENIC homozygous 49866817 13 99701686 99701687 G GC 7 GENIC homozygous 49866822 13 99733338 99733339 G A 24 GENIC homozygous 49866827 13 99733432 99733433 A G 18 GENIC homozygous 49866828 13 99733461 99733462 G GAA 15 GENIC homozygous 50533066 13 99733471 99733474 ACC --- 15 GENIC homozygous 50533068 13 99760537 99760538 A AAAAAAAG 8 GENIC homozygous 49866833 13 99760957 99760958 T C 13 GENIC homozygous 49866841