chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 157613725 157613726 G A 47 GENIC homozygous 802788520 4 157613853 157613854 G T 34 GENIC homozygous 802788521 4 157614185 157614186 T G 31 GENIC homozygous 802788522 4 157614774 157614775 A T 19 GENIC possibly homozygous 802788523 4 157614977 157614978 A C 16 GENIC homozygous 802788524 4 157616535 157616536 C A 22 GENIC homozygous 802788525 4 157619978 157619979 G T 15 GENIC homozygous 802788526 4 157620744 157620745 T C 22 GENIC homozygous 802788527 4 157621147 157621148 C T 29 GENIC homozygous 802788528 4 157623083 157623084 G A 28 GENIC homozygous 802788529 4 157625710 157625711 C T 29 GENIC homozygous 802788530 4 157626447 157626448 T C 38 GENIC homozygous 802788531 4 157627043 157627044 T C 24 GENIC homozygous 802788532 4 157629525 157629526 T C 24 GENIC homozygous 802788533 4 157630918 157630919 G T 18 GENIC possibly homozygous 802788534 4 157631950 157631951 A G 23 GENIC homozygous 802788535 4 157632657 157632658 T C 26 GENIC homozygous 802788536 4 157633500 157633501 A G 28 GENIC homozygous 802788537 4 157634098 157634099 T C 22 GENIC homozygous 802788538 4 157635239 157635240 A C 24 GENIC homozygous 802788539 4 157635295 157635296 C T 25 GENIC homozygous 802788540 4 157638495 157638496 T C 24 GENIC homozygous 802788541 4 157639657 157639658 G C 17 GENIC homozygous 802788542 4 157644216 157644217 C G 17 GENIC homozygous 802788543 4 157644340 157644341 T C 26 GENIC possibly homozygous 802788544