chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 157613853 157613854 G T 5 GENIC homozygous 985001527 4 157614185 157614186 T G 17 GENIC homozygous 985001528 4 157614774 157614775 A T 11 GENIC homozygous 985001529 4 157614977 157614978 A C 16 GENIC homozygous 985001530 4 157616535 157616536 C A 15 GENIC homozygous 985001531 4 157619978 157619979 G T 18 GENIC homozygous 985001532 4 157620744 157620745 T C 24 GENIC homozygous 985001533 4 157621147 157621148 C T 9 GENIC homozygous 985001534 4 157623083 157623084 G A 18 GENIC homozygous 985001535 4 157625710 157625711 C T 19 GENIC homozygous 985001536 4 157626447 157626448 T C 13 GENIC homozygous 985001537 4 157627043 157627044 T C 24 GENIC homozygous 985001538 4 157629525 157629526 T C 36 GENIC homozygous 985001539 4 157630918 157630919 G T 17 GENIC homozygous 985001540 4 157631950 157631951 A G 17 GENIC homozygous 985001541 4 157632657 157632658 T C 23 GENIC homozygous 985001542 4 157633500 157633501 A G 8 GENIC homozygous 985001543 4 157634098 157634099 T C 17 GENIC homozygous 985001544 4 157635239 157635240 A C 19 GENIC homozygous 985001545 4 157635295 157635296 C T 12 GENIC homozygous 985001546 4 157638495 157638496 T C 24 GENIC homozygous 985001547 4 157639657 157639658 G C 23 GENIC homozygous 985001548 4 157644216 157644217 C G 12 GENIC homozygous 985001549