chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 124382016 124382017 T - 26 GENIC heterozygous 54513653 7 124382451 124382453 CC -- 29 GENIC homozygous 54093493 7 124382686 124382687 A ATT 21 GENIC homozygous 54093495 7 124383212 124383213 G A 30 GENIC homozygous 54093497 7 124383854 124383855 C T 27 GENIC homozygous 54093499 7 124386305 124386306 C T 34 GENIC possibly homozygous 54093501 7 124386427 124386428 C T 31 GENIC heterozygous 54093503 7 124386748 124386749 C T 26 GENIC homozygous 54093504 7 124388115 124388116 T G 36 GENIC homozygous 54093506 7 124388401 124388402 T C 34 GENIC homozygous 54093508 7 124388645 124388646 G A 30 GENIC homozygous 54093510 7 124389535 124389536 G A 28 GENIC homozygous 54093512 7 124389691 124389692 T TAA 27 GENIC homozygous 54093514 7 124389854 124389855 T G 37 GENIC homozygous 54093516 7 124389865 124389866 T C 39 GENIC homozygous 54093517 7 124390195 124390196 T G 31 GENIC homozygous 54093519 7 124390205 124390206 C T 32 GENIC homozygous 54093521 7 124390532 124390533 G T 18 GENIC homozygous 54093523 7 124390735 124390736 T G 30 GENIC homozygous 54093525 7 124390916 124390917 G A 52 GENIC homozygous 54093527 7 124393697 124393698 G A 15 GENIC homozygous 54093537 7 124391341 124391342 A G 41 GENIC homozygous 54093529 7 124391690 124391691 G A 32 GENIC heterozygous 54093531 7 124392722 124392723 T TCC 28 GENIC homozygous 54093535 7 124393999 124394000 T A 32 GENIC heterozygous 54093539 7 124394073 124394074 T TA 19 GENIC possibly homozygous 54093541 7 124394696 124394697 C T 26 GENIC homozygous 54093543 7 124394727 124394728 C T 37 GENIC homozygous 54093545 7 124396849 124396850 A G 24 GENIC homozygous 54093547 7 124397409 124397410 A G 34 GENIC homozygous 54093549 7 124398091 124398092 T C 45 GENIC homozygous 54093551 7 124398339 124398340 C A 45 GENIC homozygous 54093553 7 124398850 124398851 T - 1 GENIC homozygous 54093555