chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 125744277 125744278 A C 10 GENIC homozygous 631475488 7 125744898 125744899 G A 20 GENIC possibly homozygous 631475489 7 125745046 125745047 T A 17 GENIC homozygous 631475490 7 125745150 125745151 A T 13 GENIC homozygous 631475491 7 125745717 125745718 G T 6 GENIC homozygous 631475492 7 125745937 125745938 G A 11 GENIC possibly homozygous 631475493 7 125746484 125746485 A G 20 GENIC possibly homozygous 631475494 7 125746618 125746619 G A 18 GENIC homozygous 631475495 7 125747534 125747535 C T 24 GENIC possibly homozygous 631475496 7 125747571 125747572 G A 3 GENIC heterozygous 631475497 7 125748329 125748330 A G 12 GENIC homozygous 631475498 7 125748927 125748928 G A 28 GENIC possibly homozygous 631475499 7 125749012 125749013 G A 25 GENIC possibly homozygous 631475500 7 125749414 125749415 A G 15 GENIC homozygous 631475501 7 125749466 125749467 T TG 11 GENIC possibly homozygous 745671685 7 125751521 125751522 A ATT 1 GENIC homozygous 745671687 7 125752000 125752001 T C 24 GENIC possibly homozygous 631475502 7 125752756 125752757 G A 15 GENIC possibly homozygous 631475503 7 125753897 125753898 C T 11 GENIC heterozygous 631475504 7 125753949 125753950 G A 9 GENIC homozygous 631475505 7 125754274 125754275 A G 23 GENIC homozygous 631475506 7 125754320 125754321 C T 15 GENIC heterozygous 631475507 7 125754367 125754368 C T 14 GENIC homozygous 631475508 7 125754379 125754380 G C 14 GENIC heterozygous 631475509 7 125755157 125755158 G A 3 GENIC heterozygous 631475510 7 125755666 125755667 C T 17 GENIC homozygous 631475511 7 125755703 125755704 C T 16 GENIC homozygous 631475512 7 125756500 125756501 T C 7 GENIC homozygous 631475513 7 125756849 125756850 A G 9 GENIC homozygous 631475514 7 125757153 125757154 T TA 2 GENIC heterozygous 745671688