chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 9236256 9236257 C T 26 GENIC homozygous 130048733 20 9236491 9236492 C G 32 GENIC homozygous 130048736 20 9236557 9236558 G A 30 GENIC homozygous 130048738 20 9236610 9236611 C A 26 GENIC homozygous 130048741 20 9236749 9236750 T C 20 GENIC homozygous 130048744 20 9236802 9236803 C T 22 GENIC homozygous 130048747 20 9236831 9236832 C T 20 GENIC homozygous 130048750 20 9236844 9236845 A G 23 GENIC homozygous 130048752 20 9237252 9237253 C 33 GENIC homozygous 129981972 20 9237267 9237268 C T 33 GENIC homozygous 130048755 20 9237280 9237281 T C 35 GENIC homozygous 130048758 20 9237283 9237284 A 36 GENIC homozygous 129981973 20 9237320 9237320 CTGGCACT 33 GENIC homozygous 129981974 20 9238391 9238392 A 9 GENIC homozygous 129981975 20 9239233 9239234 T C 26 GENIC homozygous 130048761 20 9239282 9239283 T C 26 GENIC homozygous 130048764 20 9239292 9239293 C G 30 GENIC homozygous 130048767