chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2197688605197688605TC13GENICheterozygous132808715
2197688606197688606C13GENICheterozygous127723250
2197688700197688701TC14GENIChomozygous110199772
2197689407197689407TTTATTTA9GENIChomozygous127723251
2197689944197689944TAGATGTCAA14GENIChomozygous127723253
2197691253197691254T20GENICheterozygous131299131
2197691938197691939GA14GENIChomozygous110199773
2197695601197695601A16GENIChomozygous127723254
2197697135197697136CT19GENIChomozygous110199781
2197697652197697653TG24GENIChomozygous110199782
2197697795197697796AG19GENIChomozygous110199783
2197700277197700278C5GENIChomozygous127723255
2197691349197691350TC14GENICheterozygous132950263
2197691363197691364CT13GENICheterozygous132950264
2197702634197702635TA19GENICheterozygous132578490
2197703308197703309GA26GENICpossibly homozygous110199792
2197704746197704747GA3GENIChomozygous131834485
2197705613197705614C19GENIChomozygous127723258
2197705696197705696G12GENIChomozygous127723259
2197705706197705706T14GENIChomozygous127723260
2197705746197705746A9GENIChomozygous127723261
2197705759197705759C8GENIChomozygous127723262
2197705822197705823AT6GENIChomozygous110199793
2197705830197705831C5GENIChomozygous127723263
2197705836197705837C4GENIChomozygous127723264
2197705927197705927G1GENIChomozygous127723266
2197705934197705935A1GENIChomozygous127723267
2197705945197705945C1GENIChomozygous127723268
2197706094197706094A15GENIChomozygous127723269
2197704530197704531TC2GENIChomozygous127833587
2197710968197710969GT6GENIChomozygous127833590
2197704691197704691G3GENIChomozygous130253971
2197704706197704707GT3GENIChomozygous130274753
2197705851197705852GT3GENIChomozygous111355494
2197715675197715676CA25GENIChomozygous110199794
2197717096197717097GT36GENIChomozygous110199795
2197717766197717766TGTGTGTG29GENICpossibly homozygous127723270
2197718380197718381A11GENIChomozygous127723271
2197720164197720209GGTTGCCTAGTGATCCTGAGGAAGCTGATGTGTTATTCCCCAAGT15GENIChomozygous127723272