chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241359454241359455CT72GENICheterozygous108773976
1241359484241359485CT79GENICheterozygous109571277
1241359509241359510GT80GENICheterozygous108591056
1241359946241359947CG74GENICheterozygous108591057
1241360724241360725CA56GENICheterozygous108773977
1241360777241360778CT29GENICheterozygous108773978
1241451632241451633CA38GENIChomozygous109541549
1241406388241406389CT13GENIChomozygous109541544
1241451315241451316GA36GENIChomozygous109541545
1241451622241451623CT34GENIChomozygous109541547
1241451993241451994TG32GENIChomozygous109541550
1241452095241452096GA35GENIChomozygous109541552
1241452332241452333CT32GENIChomozygous109541554
1241452693241452694AT21GENIChomozygous109541555
1241453088241453089AG26GENICheterozygous109541559
1241453092241453093AG25GENICheterozygous109057521
1241453096241453097AG27GENICheterozygous109541560
1241453100241453101AG27GENICheterozygous109571278
1241453518241453519GC23GENIChomozygous109541561
1241453693241453694AG35GENIChomozygous109541563
1241454252241454253TC21GENIChomozygous109541565
1241454326241454327GA17GENIChomozygous108591058
1241454391241454392GA7GENIChomozygous109571279
1241454714241454715CT20GENIChomozygous109541566
1241455077241455078TC48GENIChomozygous109541568
1241456140241456141GA19GENIChomozygous109541569
1241456421241456422TC19GENIChomozygous109541571
1241456536241456537AG26GENIChomozygous109541572
1241457061241457062CT25GENIChomozygous109541574
1241457586241457587TC37GENIChomozygous109541576
1241457834241457835CT20GENIChomozygous109541577
1241457900241457901CT23GENIChomozygous109541579
1241458149241458150AG32GENIChomozygous109541580
1241458432241458433TC16GENIChomozygous109541582
1241458571241458572GA21GENIChomozygous109541583
1241458702241458703GA16GENIChomozygous109541586
1241459925241459926AG21GENIChomozygous109541588
1241459963241459964TA18GENIChomozygous109541589
1241460305241460306AC20GENIChomozygous109541591
1241460704241460705AG26GENIChomozygous109541592