chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32170632321706323G15GENIChomozygous127859506
32172348121723481T7GENIChomozygous130278479
32172359921723600TG10GENICheterozygous111504302
32172359921723599G10GENICheterozygous131837837
32174614821746149G11GENIChomozygous127859515
32174615421746154T12GENIChomozygous127859516
32174619321746194CT10GENIChomozygous111504330
32174619621746197G10GENIChomozygous127859517
32174621421746214C9GENIChomozygous127859518
32174749821747499CA10GENIChomozygous111504331
32174750421747505A12GENIChomozygous127859519
32174751021747511GC14GENIChomozygous111504333
32174753221747533CA16GENIChomozygous111504335
32174755121747553TG16GENIChomozygous127859520
32174760921747610G1GENIChomozygous129888256
32174771621747716T1GENIChomozygous127859521
32174774621747753TCCCCCC1GENIChomozygous133473027
32174792821747929A4GENIChomozygous127859522
32174804721748047G4GENIChomozygous127859523
32174812321748124G4GENIChomozygous127859524
32174816621748167G10GENIChomozygous127859525
32175257021752570A18GENIChomozygous127859526
32176841921768419TGGGG6GENIChomozygous127859528
32176842021768420TTTAGCTCAGTGGTAGAGCGCTTGCCTAGC7GENIChomozygous127859529
32176842321768424GA9GENIChomozygous121755751