chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 156584774 156584775 T C 27 GENIC homozygous 114068301 5 156586601 156586602 A T 30 GENIC homozygous 114068303 5 156587409 156587410 T C 25 GENIC homozygous 114068305 5 156587917 156587918 T C 35 GENIC homozygous 114068307 5 156588803 156588804 T C 39 GENIC homozygous 114068308 5 156592419 156592420 C T 16 GENIC homozygous 114068310 5 156593434 156593435 A C 18 GENIC homozygous 118847069 5 156593941 156593942 T C 28 GENIC homozygous 114068312 5 156593942 156593943 T C 29 GENIC homozygous 114068314 5 156597238 156597239 T C 29 GENIC homozygous 114068318 5 156597521 156597522 G A 28 GENIC homozygous 114068320 5 156599704 156599705 A G 29 GENIC homozygous 114068322 5 156599741 156599742 C T 33 GENIC homozygous 118847071 5 156600070 156600071 T G 28 GENIC homozygous 114068328 5 156600096 156600097 A C 30 GENIC homozygous 114068330 5 156602012 156602013 G A 18 GENIC homozygous 114068338 5 156602468 156602469 A G 22 GENIC homozygous 114068340 5 156602519 156602520 C T 29 GENIC homozygous 118847074 5 156602520 156602521 T A 29 GENIC homozygous 118847076 5 156604127 156604128 A G 20 GENIC homozygous 114068342 5 156606606 156606607 G A 34 GENIC homozygous 114068343 5 156606894 156606895 C G 34 GENIC homozygous 114068345 5 156607553 156607554 C T 25 GENIC homozygous 114068347 5 156607589 156607590 T C 35 GENIC homozygous 114068349 5 156607631 156607632 C T 25 GENIC homozygous 114068351 5 156608078 156608079 A G 23 GENIC homozygous 114068353 5 156608309 156608310 A G 21 GENIC homozygous 114068355