chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 31694654 31694655 T C 8 GENIC homozygous 115812390 11 31694813 31694814 G T 18 GENIC homozygous 115812392 11 31695708 31695709 A G 14 GENIC homozygous 115812394 11 31696294 31696295 C G 37 GENIC homozygous 115812396 11 31696330 31696331 T C 40 GENIC homozygous 116035374 11 31696757 31696758 A G 23 GENIC homozygous 116035376 11 31697220 31697221 C T 21 GENIC homozygous 116035378 11 31697393 31697394 A G 24 GENIC homozygous 115812400 11 31697767 31697768 A T 40 GENIC homozygous 116035380 11 31698450 31698451 A G 26 GENIC homozygous 115812402 11 31699233 31699234 A G 25 GENIC homozygous 115812404 11 31699289 31699290 G A 31 GENIC homozygous 116035382 11 31700631 31700632 T C 33 GENIC homozygous 115812406 11 31700713 31700714 C G 45 GENIC homozygous 115812408 11 31701245 31701246 A G 28 GENIC homozygous 115812410 11 31701336 31701337 C G 24 GENIC homozygous 115812412 11 31701509 31701510 C T 30 GENIC homozygous 116035384 11 31701579 31701580 A G 30 GENIC homozygous 115812414 11 31702225 31702226 C T 28 GENIC homozygous 116035386 11 31702613 31702614 T C 24 GENIC homozygous 115812416 11 31702797 31702798 C T 26 GENIC homozygous 115812418 11 31702916 31702917 T C 20 GENIC homozygous 115812420 11 31704027 31704028 G A 34 GENIC homozygous 116035388 11 31705451 31705452 A G 31 GENIC homozygous 115812424 11 31706330 31706331 G A 28 GENIC homozygous 115812430 11 31706697 31706698 T A 27 GENIC homozygous 115812432 11 31706930 31706931 C T 23 GENIC homozygous 116035390 11 31708283 31708284 C T 23 GENIC homozygous 115812440 11 31710094 31710095 G A 16 GENIC homozygous 115812444 11 31711900 31711901 C T 42 GENIC homozygous 116035392