geneid | 9918 |
---|---|
ensemblid | ENSG00000010292.13 |
hgncid | 24305 |
symbol | NCAPD2 |
name | non-SMC condensin I complex subunit D2 |
refseq_nuc | NM_014865.4 |
refseq_prot | NP_055680.3 |
ensembl_nuc | ENST00000315579.10 |
ensembl_prot | ENSP00000325017.5 |
mane_status | MANE Select |
chr | chr12 |
start | 6494102 |
end | 6531955 |
strand | + |
ver | v1.2 |
region | chr12:6494102-6531955 |
region5000 | chr12:6489102-6536955 |
regionname0 | NCAPD2_chr12_6494102_6531955 |
regionname5000 | NCAPD2_chr12_6489102_6536955 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1401 | 210 | 71 | 41 | 72 | 3 | 23 | 60 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002 | 1/1 | 1401 | 85 | 2 | 14 | 52 | 6 | 9 | 38 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003 | 0/0 | 1401 | 78 | 4 | 7 | 56 | 3 | 8 | 37 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0004 | 0/0 | 1401 | 17 | 1 | 5 | 2 | 3 | 6 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0005 | 0/0 | 1401 | 12 | 0 | 0 | 10 | 0 | 2 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0006 | 0/0 | 1401 | 8 | 0 | 8 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0007 | 0/0 | 1401 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0008 | 0/0 | 1401 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0009 | 0/0 | 1401 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0010 | 0/0 | 1401 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0011 | 0/0 | 1401 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0012 | 0/0 | 48 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0013 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0014 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0015 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0016 | 0/0 | 1401 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0017 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0018 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0019 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4206 | 123 | 41 | 29 | 38 | 3 | 12 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0002 | 1/0 | 4206 | 81 | 2 | 13 | 50 | 6 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0003 | 0/0 | 4206 | 70 | 3 | 6 | 51 | 3 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0004 | 0/0 | 4206 | 58 | 14 | 8 | 28 | 0 | 8 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0005 | 0/0 | 4206 | 17 | 1 | 5 | 2 | 3 | 6 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0006 | 0/0 | 4206 | 12 | 0 | 0 | 10 | 0 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0007 | 0/0 | 4206 | 12 | 10 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0008 | 0/0 | 4206 | 8 | 0 | 8 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0009 | 0/0 | 4206 | 7 | 0 | 1 | 6 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0010 | 0/0 | 4206 | 6 | 0 | 0 | 5 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0011 | 0/0 | 4206 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0012 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0013 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0014 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0015 | 0/0 | 4206 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0016 | 0/0 | 4206 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0017 | 0/0 | 4206 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0018 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0019 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0020 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0021 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0022 | 0/1 | 4206 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0023 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0024 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0025 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0026 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0027 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0028 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0029 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0030 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0031 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0032 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0033 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0034 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0035 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
c0036 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 620 | 131 | 16 | 21 | 68 | 10 | 15 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0002 | 0/1 | 620 | 110 | 33 | 25 | 38 | 3 | 10 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0003 | 0/0 | 620 | 96 | 8 | 15 | 60 | 3 | 10 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0004 | 0/0 | 620 | 43 | 1 | 8 | 27 | 0 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0005 | 0/0 | 621 | 11 | 9 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0006 | 0/0 | 621 | 11 | 6 | 1 | 0 | 0 | 4 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0007 | 0/0 | 619 | 6 | 3 | 2 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0008 | 0/0 | 620 | 6 | 5 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0009 | 0/0 | 620 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0010 | 0/0 | 621 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0011 | 0/0 | 620 | 3 | 1 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0012 | 0/0 | 621 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0013 | 0/0 | 621 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0014 | 0/0 | 619 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0015 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
t0016 | 0/0 | 620 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
g0404 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4206 | 123 | 41 | 29 | 38 | 3 | 12 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004 | 0/0 | 4206 | 58 | 14 | 8 | 28 | 0 | 8 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0007 | 0/0 | 4206 | 12 | 10 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0009 | 0/0 | 4206 | 7 | 0 | 1 | 6 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0011 | 0/0 | 4206 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0026 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0028 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0030 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0031 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0032 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0033 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0002 | 1/0 | 4206 | 81 | 2 | 13 | 50 | 6 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0018 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0019 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0021 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0022 | 0/1 | 4206 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0003 | 0/0 | 4206 | 70 | 3 | 6 | 51 | 3 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0010 | 0/0 | 4206 | 6 | 0 | 0 | 5 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0015 | 0/0 | 4206 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0004c0005 | 0/0 | 4206 | 17 | 1 | 5 | 2 | 3 | 6 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0005c0006 | 0/0 | 4206 | 12 | 0 | 0 | 10 | 0 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0006c0008 | 0/0 | 4206 | 8 | 0 | 8 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0007c0014 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0007c0016 | 0/0 | 4206 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0008c0013 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0009c0012 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0010c0017 | 0/0 | 4206 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0011c0035 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0012c0034 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0013c0029 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0014c0027 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0015c0025 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0016c0023 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0017c0024 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0018c0020 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0019c0036 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 4825 | 104 | 30 | 25 | 37 | 3 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0001t0003 | 0/0 | 4825 | 5 | 4 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0001t0006 | 0/0 | 4826 | 7 | 3 | 1 | 0 | 0 | 3 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0001t0007 | 0/0 | 4824 | 6 | 3 | 2 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0001t0015 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004t0001 | 0/0 | 4825 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004t0004 | 0/0 | 4825 | 41 | 0 | 7 | 27 | 0 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004t0008 | 0/0 | 4825 | 6 | 5 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004t0009 | 0/0 | 4825 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004t0010 | 0/0 | 4826 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0004t0011 | 0/0 | 4825 | 3 | 1 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0007t0004 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0007t0005 | 0/0 | 4826 | 9 | 7 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0007t0012 | 0/0 | 4826 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0009t0001 | 0/0 | 4825 | 7 | 0 | 1 | 6 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0011t0001 | 0/0 | 4825 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0026t0006 | 0/0 | 4826 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0028t0009 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0030t0002 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0031t0001 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0032t0016 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0001c0033t0004 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0002t0001 | 1/0 | 4825 | 81 | 2 | 13 | 50 | 6 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0018t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0019t0001 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0021t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0002c0022t0002 | 0/1 | 4825 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0003t0003 | 0/0 | 4825 | 66 | 3 | 5 | 48 | 3 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0003t0013 | 0/0 | 4826 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0003t0014 | 0/0 | 4824 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0010t0001 | 0/0 | 4825 | 5 | 0 | 0 | 5 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0010t0003 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0003c0015t0003 | 0/0 | 4825 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0004c0005t0001 | 0/0 | 4825 | 17 | 1 | 5 | 2 | 3 | 6 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0005c0006t0003 | 0/0 | 4825 | 12 | 0 | 0 | 10 | 0 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0006c0008t0003 | 0/0 | 4825 | 8 | 0 | 8 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0007c0014t0001 | 0/0 | 4825 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0007c0016t0001 | 0/0 | 4825 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0008c0013t0002 | 0/0 | 4825 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0009c0012t0006 | 0/0 | 4826 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0010c0017t0003 | 0/0 | 4825 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0011c0035t0001 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0012c0034t0005 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0013c0029t0002 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0014c0027t0005 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0015c0025t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0016c0023t0001 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0017c0024t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0018c0020t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
a0019c0036t0001 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | copy fasta | chr12 | 6489102 | 6536955 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0015g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0010g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0011g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0011g0404 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0012g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0011t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0011t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0011t0001g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0026t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0028t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0030t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0031t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0032t0016g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0033t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0018t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0019t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0021t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0022t0002g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0014g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0014g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0015t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0015t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0014t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0014t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0014t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0016t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0016t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0008c0013t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0008c0013t0002g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0009c0012t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0009c0012t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0009c0012t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0010c0017t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0010c0017t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0011c0035t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0012c0034t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0013c0029t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0014c0027t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0015c0025t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0016c0023t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0017c0024t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0018c0020t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0019c0036t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00099 | hp2 | a0004 | c0005 | t0001 | g0247 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0297 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00140 | hp2 | a0016 | c0023 | t0001 | g0152 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00280 | hp1 | a0003 | c0003 | t0003 | g0064 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0011 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00323 | hp1 | a0004 | c0005 | t0001 | g0251 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0094 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00408 | hp2 | a0003 | c0003 | t0003 | g0079 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00423 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00423 | hp2 | a0003 | c0003 | t0003 | g0068 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00438 | hp2 | a0005 | c0006 | t0003 | g0183 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00544 | hp2 | a0003 | c0003 | t0003 | g0039 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00558 | hp1 | a0001 | c0004 | t0004 | g0200 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00597 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0028 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0058 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00642 | hp1 | a0001 | c0009 | t0001 | g0340 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00673 | hp1 | a0003 | c0010 | t0001 | g0087 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00733 | hp1 | a0004 | c0005 | t0001 | g0245 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00735 | hp2 | a0006 | c0008 | t0003 | g0051 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01069 | hp1 | a0004 | c0005 | t0001 | g0244 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01070 | hp1 | a0003 | c0003 | t0014 | g0089 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0362 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01074 | hp2 | a0004 | c0005 | t0001 | g0256 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01081 | hp1 | a0002 | c0019 | t0001 | g0118 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01099 | hp1 | a0003 | c0003 | t0003 | g0091 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01106 | hp1 | a0006 | c0008 | t0003 | g0002 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0370 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01109 | hp1 | a0006 | c0008 | t0003 | g0002 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0364 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01168 | hp1 | a0003 | c0003 | t0003 | g0095 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01168 | hp2 | a0001 | c0004 | t0011 | g0404 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01169 | hp1 | a0003 | c0003 | t0003 | g0093 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01192 | hp2 | a0001 | c0007 | t0005 | g0277 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01243 | hp1 | a0001 | c0033 | t0004 | g0193 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01243 | hp2 | a0004 | c0005 | t0001 | g0249 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01255 | hp1 | a0011 | c0035 | t0001 | g0252 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01257 | hp1 | a0006 | c0008 | t0003 | g0060 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01257 | hp2 | a0001 | c0004 | t0004 | g0208 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01258 | hp2 | a0001 | c0004 | t0004 | g0209 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01261 | hp1 | a0001 | c0007 | t0005 | g0275 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01261 | hp2 | a0003 | c0003 | t0003 | g0098 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0366 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01346 | hp2 | a0004 | c0005 | t0001 | g0241 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0338 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01358 | hp2 | a0001 | c0004 | t0004 | g0210 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01361 | hp1 | a0006 | c0008 | t0003 | g0069 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0379 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0328 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0334 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0103 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0122 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0353 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01884 | hp2 | a0001 | c0028 | t0009 | g0261 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01891 | hp1 | a0003 | c0015 | t0003 | g0085 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0388 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01928 | hp2 | a0006 | c0008 | t0003 | g0040 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01934 | hp2 | a0003 | c0003 | t0003 | g0092 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01943 | hp1 | a0001 | c0004 | t0004 | g0206 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01943 | hp2 | a0006 | c0008 | t0003 | g0002 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01952 | hp2 | a0001 | c0004 | t0004 | g0212 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01975 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01975 | hp2 | a0006 | c0008 | t0003 | g0042 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0359 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01978 | hp2 | a0001 | c0004 | t0004 | g0221 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01981 | hp1 | a0001 | c0004 | t0004 | g0222 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0378 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01993 | hp2 | a0003 | c0015 | t0003 | g0084 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02015 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0071 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0372 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02040 | hp2 | a0003 | c0003 | t0003 | g0057 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0375 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02055 | hp2 | a0001 | c0007 | t0012 | g0402 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02056 | hp2 | a0003 | c0003 | t0003 | g0081 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02071 | hp1 | a0003 | c0003 | t0003 | g0059 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02074 | hp1 | a0003 | c0010 | t0001 | g0074 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02080 | hp1 | a0010 | c0017 | t0003 | g0062 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02083 | hp1 | a0003 | c0003 | t0003 | g0027 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02083 | hp2 | a0002 | c0018 | t0001 | g0166 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02129 | hp1 | a0003 | c0010 | t0001 | g0047 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02132 | hp1 | a0003 | c0003 | t0003 | g0043 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02132 | hp2 | a0002 | c0021 | t0001 | g0117 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0393 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02155 | hp1 | a0003 | c0003 | t0003 | g0026 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02155 | hp2 | a0003 | c0003 | t0003 | g0038 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0386 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0383 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0381 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0374 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0358 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02451 | hp1 | a0001 | c0004 | t0008 | g0227 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02451 | hp2 | a0001 | c0007 | t0005 | g0016 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02523 | hp2 | a0018 | c0020 | t0001 | g0146 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02602 | hp1 | a0004 | c0005 | t0001 | g0250 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02615 | hp2 | a0014 | c0027 | t0005 | g0257 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02622 | hp1 | a0007 | c0014 | t0001 | g0296 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02622 | hp2 | a0001 | c0004 | t0010 | g0272 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0352 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02647 | hp1 | a0001 | c0007 | t0005 | g0273 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02647 | hp2 | a0009 | c0012 | t0006 | g0260 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02683 | hp1 | a0004 | c0005 | t0001 | g0243 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0389 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02717 | hp1 | a0001 | c0007 | t0005 | g0274 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02717 | hp2 | a0003 | c0003 | t0003 | g0070 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0332 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02738 | hp1 | a0003 | c0003 | t0003 | g0099 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02738 | hp2 | a0003 | c0003 | t0003 | g0096 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0365 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0267 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02818 | hp1 | a0001 | c0004 | t0010 | g0270 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0190 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02886 | hp2 | a0001 | c0004 | t0009 | g0239 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02895 | hp1 | a0001 | c0011 | t0001 | g0022 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02895 | hp2 | a0001 | c0007 | t0005 | g0280 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02896 | hp1 | a0001 | c0011 | t0001 | g0400 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02896 | hp2 | a0009 | c0012 | t0006 | g0259 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02897 | hp1 | a0001 | c0011 | t0001 | g0022 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02897 | hp2 | a0009 | c0012 | t0006 | g0258 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02922 | hp1 | a0001 | c0007 | t0005 | g0279 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0384 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0387 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02970 | hp1 | a0001 | c0004 | t0008 | g0226 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02970 | hp2 | a0012 | c0034 | t0005 | g0278 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0335 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03017 | hp2 | a0001 | c0004 | t0004 | g0216 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0385 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03041 | hp2 | a0001 | c0007 | t0004 | g0269 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03098 | hp1 | a0001 | c0004 | t0008 | g0224 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03098 | hp2 | a0001 | c0004 | t0008 | g0228 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03139 | hp1 | a0001 | c0004 | t0010 | g0271 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03139 | hp2 | a0001 | c0004 | t0009 | g0238 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03195 | hp1 | a0001 | c0007 | t0005 | g0016 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03195 | hp2 | a0001 | c0031 | t0001 | g0189 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0380 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03209 | hp2 | a0007 | c0016 | t0001 | g0294 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03225 | hp2 | a0008 | c0013 | t0002 | g0399 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03239 | hp1 | a0001 | c0030 | t0002 | g0303 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0376 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03486 | hp1 | a0007 | c0016 | t0001 | g0295 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03490 | hp1 | a0003 | c0003 | t0003 | g0065 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0264 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03491 | hp1 | a0004 | c0005 | t0001 | g0246 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0265 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0363 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0382 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0397 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03540 | hp1 | a0003 | c0003 | t0003 | g0082 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03579 | hp1 | a0001 | c0011 | t0001 | g0401 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03654 | hp1 | a0004 | c0005 | t0001 | g0242 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0045 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0266 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03688 | hp2 | a0005 | c0006 | t0003 | g0151 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03704 | hp1 | a0001 | c0004 | t0004 | g0195 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0023 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03710 | hp2 | a0001 | c0026 | t0006 | g0268 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03834 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0115 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03927 | hp1 | a0001 | c0004 | t0004 | g0211 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03927 | hp2 | a0003 | c0003 | t0003 | g0063 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03942 | hp1 | a0003 | c0010 | t0003 | g0217 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0346 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04115 | hp2 | a0001 | c0004 | t0004 | g0220 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04184 | hp1 | a0004 | c0005 | t0001 | g0248 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04184 | hp2 | a0001 | c0004 | t0004 | g0214 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04199 | hp1 | a0001 | c0004 | t0011 | g0403 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04199 | hp2 | a0001 | c0004 | t0004 | g0213 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04204 | hp1 | a0001 | c0032 | t0016 | g0291 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04204 | hp2 | a0004 | c0005 | t0001 | g0254 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04228 | hp1 | a0005 | c0006 | t0003 | g0125 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0119 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18522 | hp2 | a0001 | c0004 | t0011 | g0012 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18612 | hp1 | a0001 | c0004 | t0004 | g0194 | EAS | CHB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18612 | hp2 | a0003 | c0003 | t0003 | g0046 | EAS | CHB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18906 | hp2 | a0007 | c0014 | t0001 | g0292 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18939 | hp2 | a0001 | c0004 | t0004 | g0207 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18940 | hp2 | a0001 | c0004 | t0004 | g0219 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18941 | hp1 | a0001 | c0004 | t0004 | g0234 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18944 | hp2 | a0005 | c0006 | t0003 | g0120 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18945 | hp1 | a0001 | c0009 | t0001 | g0396 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18946 | hp1 | a0003 | c0003 | t0003 | g0036 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18948 | hp1 | a0003 | c0003 | t0014 | g0075 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18950 | hp1 | a0001 | c0009 | t0001 | g0197 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18950 | hp2 | a0003 | c0010 | t0001 | g0073 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18951 | hp1 | a0005 | c0006 | t0003 | g0112 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18952 | hp1 | a0001 | c0004 | t0004 | g0236 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18952 | hp2 | a0003 | c0003 | t0003 | g0078 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18954 | hp1 | a0001 | c0004 | t0004 | g0192 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18956 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18957 | hp1 | a0003 | c0003 | t0003 | g0034 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0055 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18960 | hp1 | a0005 | c0006 | t0003 | g0123 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18963 | hp2 | a0003 | c0003 | t0003 | g0033 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18965 | hp1 | a0003 | c0003 | t0003 | g0061 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18966 | hp1 | a0003 | c0003 | t0013 | g0080 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18966 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18967 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18968 | hp1 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18969 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18970 | hp1 | a0005 | c0006 | t0003 | g0124 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18970 | hp2 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18971 | hp1 | a0003 | c0003 | t0003 | g0032 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18971 | hp2 | a0001 | c0004 | t0004 | g0218 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18972 | hp1 | a0001 | c0004 | t0004 | g0203 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0392 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18973 | hp1 | a0003 | c0003 | t0003 | g0067 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18973 | hp2 | a0001 | c0004 | t0004 | g0237 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18974 | hp1 | a0003 | c0003 | t0003 | g0083 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18974 | hp2 | a0003 | c0003 | t0003 | g0054 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18975 | hp1 | a0003 | c0003 | t0003 | g0037 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0050 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0398 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18978 | hp2 | a0005 | c0006 | t0003 | g0141 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18982 | hp1 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18984 | hp1 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18984 | hp2 | a0005 | c0006 | t0003 | g0132 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18986 | hp1 | a0013 | c0029 | t0002 | g0323 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18986 | hp2 | a0003 | c0003 | t0003 | g0048 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18988 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18988 | hp2 | a0001 | c0004 | t0004 | g0201 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18989 | hp2 | a0001 | c0004 | t0004 | g0230 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0377 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18992 | hp2 | a0001 | c0004 | t0004 | g0231 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18995 | hp1 | a0005 | c0006 | t0003 | g0150 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18999 | hp1 | a0001 | c0009 | t0001 | g0215 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18999 | hp2 | a0003 | c0003 | t0003 | g0044 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19000 | hp1 | a0001 | c0004 | t0008 | g0223 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19002 | hp1 | a0005 | c0006 | t0003 | g0130 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19003 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19004 | hp2 | a0001 | c0004 | t0004 | g0014 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19010 | hp1 | a0001 | c0004 | t0004 | g0199 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19010 | hp2 | a0001 | c0009 | t0001 | g0198 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19012 | hp1 | a0001 | c0004 | t0004 | g0202 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19030 | hp2 | a0004 | c0005 | t0001 | g0255 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19043 | hp1 | a0008 | c0013 | t0002 | g0017 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19043 | hp2 | a0019 | c0036 | t0001 | g0394 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19054 | hp1 | a0003 | c0003 | t0003 | g0030 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19054 | hp2 | a0001 | c0004 | t0004 | g0204 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0395 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19058 | hp1 | a0001 | c0009 | t0001 | g0196 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19058 | hp2 | a0003 | c0003 | t0003 | g0052 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19060 | hp1 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19062 | hp1 | a0010 | c0017 | t0003 | g0056 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19063 | hp1 | a0017 | c0024 | t0001 | g0167 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19063 | hp2 | a0001 | c0004 | t0004 | g0233 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19066 | hp1 | a0005 | c0006 | t0003 | g0121 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19067 | hp1 | a0003 | c0003 | t0003 | g0077 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0371 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19068 | hp1 | a0004 | c0005 | t0001 | g0015 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0391 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19070 | hp2 | a0001 | c0004 | t0004 | g0232 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19074 | hp2 | a0015 | c0025 | t0001 | g0163 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19077 | hp2 | a0001 | c0004 | t0004 | g0205 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19078 | hp1 | a0001 | c0009 | t0001 | g0229 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19079 | hp1 | a0001 | c0004 | t0004 | g0014 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0076 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0072 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19081 | hp1 | a0003 | c0003 | t0013 | g0097 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19081 | hp2 | a0004 | c0005 | t0001 | g0015 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19083 | hp1 | a0003 | c0010 | t0001 | g0088 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19084 | hp2 | a0003 | c0003 | t0003 | g0024 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0336 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19087 | hp2 | a0001 | c0004 | t0004 | g0235 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19091 | hp1 | a0001 | c0004 | t0004 | g0005 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0053 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19240 | hp1 | a0001 | c0004 | t0009 | g0240 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19240 | hp2 | a0008 | c0013 | t0002 | g0017 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | ASW | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20129 | hp2 | a0001 | c0007 | t0012 | g0281 | AFR | ASW | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20752 | hp1 | a0004 | c0005 | t0001 | g0253 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0333 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20805 | hp2 | a0003 | c0003 | t0003 | g0090 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20905 | hp1 | a0001 | c0004 | t0004 | g0191 | SAS | GIH | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | GIH | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0390 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02109 | hp2 | a0001 | c0004 | t0008 | g0225 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02486 | hp1 | a0001 | c0007 | t0005 | g0276 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0360 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0367 | AFR | USA | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | USA | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0066 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA21309 | hp1 | a0007 | c0014 | t0001 | g0293 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA21309 | hp2 | a0003 | c0003 | t0003 | g0035 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
homoSapiens_chm13v2 | hp1 | a0002 | c0022 | t0002 | g0144 | REF | REF | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0101 | REF | REF | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6495103
|
C | G | 1 | a0019 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.5C>G | p.Ala2Gly | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/32 | 81/4825 | 5/4206 | 2/1401 | chr12 | 6495103 | ||
chr12:6495106
|
C | A | 1 | a0019 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.8C>A | p.Pro3His | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/32 | 84/4825 | 8/4206 | 3/1401 | chr12 | 6495106 | ||
chr12:6495165
|
G | T | 1 | a0011 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.67G>T | p.Val23Leu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/32 | 143/4825 | 67/4206 | 23/1401 | chr12 | 6495165 | ||
chr12:6509734
|
C | T | 1 | a0012 | 1 | HG02970.hp2 | stop_gained | HIGH | c.145C>T | p.Arg49* | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/32 | 221/4825 | 145/4206 | 49/1401 | chr12 | 6509734 | ||
chr12:6510118
|
C | G | 13 | a0001a0003a0004others(10): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
missense_variant | MODERATE | c.247C>G | p.Gln83Glu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/32 | 323/4825 | 247/4206 | 83/1401 | chr12 | 6510118 | ||
chr12:6514329
|
C | G | 1 | a0015 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.652C>G | p.Pro218Ala | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 7/32 | 728/4825 | 652/4206 | 218/1401 | chr12 | 6514329 | ||
chr12:6517440
|
T | C | 1 | a0018 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1261T>C | p.Cys421Arg | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 11/32 | 1337/4825 | 1261/4206 | 421/1401 | chr12 | 6517440 | ||
chr12:6521008
|
G | C | 1 | a0019 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1612G>C | p.Glu538Gln | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/32 | 1688/4825 | 1612/4206 | 538/1401 | chr12 | 6521008 | ||
chr12:6521803
|
G | A | 1 | a0014 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1720G>A | p.Ala574Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/32 | 1796/4825 | 1720/4206 | 574/1401 | chr12 | 6521803 | ||
chr12:6521909
|
G | C | 1 | a0010 | 2 | HG02080.hp1 NA19062.hp1 |
missense_variant | MODERATE | c.1826G>C | p.Arg609Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/32 | 1902/4825 | 1826/4206 | 609/1401 | chr12 | 6521909 | ||
chr12:6526108
|
G | A | 2 | a0004a0011 | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
missense_variant | MODERATE | c.2389G>A | p.Val797Met | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/32 | 2465/4825 | 2389/4206 | 797/1401 | chr12 | 6526108 | ||
chr12:6526311
|
C | T | 1 | a0017 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.2506C>T | p.Pro836Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 20/32 | 2582/4825 | 2506/4206 | 836/1401 | chr12 | 6526311 | ||
chr12:6526312
|
C | T | 1 | a0008 | 3 | HG03225.hp2 NA19043.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.2507C>T | p.Pro836Leu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 20/32 | 2583/4825 | 2507/4206 | 836/1401 | chr12 | 6526312 | ||
chr12:6528985
|
G | A | 1 | a0013 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.3518G>A | p.Arg1173His | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/32 | 3594/4825 | 3518/4206 | 1173/1401 | chr12 | 6528985 | ||
chr12:6529593
|
G | T | 1 | a0007 | 5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.3653G>T | p.Arg1218Leu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 28/32 | 3729/4825 | 3653/4206 | 1218/1401 | chr12 | 6529593 | ||
chr12:6530815
|
C | G | 4 | a0003a0005a0006others(1): Show | 100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
missense_variant&splice_region_variant | MODERATE | c.3962C>G | p.Thr1321Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 30/32 | 4038/4825 | 3962/4206 | 1321/1401 | chr12 | 6530815 | ||
chr12:6530960
|
A | G | 1 | a0009 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.4004A>G | p.Asn1335Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/32 | 4080/4825 | 4004/4206 | 1335/1401 | chr12 | 6530960 | ||
chr12:6531003
|
T | A | 1 | a0016 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.4047T>A | p.His1349Gln | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/32 | 4123/4825 | 4047/4206 | 1349/1401 | chr12 | 6531003 | ||
chr12:6531353
|
G | A | 1 | a0006 | 8 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(5): Show |
missense_variant | MODERATE | c.4147G>A | p.Glu1383Lys | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 4223/4825 | 4147/4206 | 1383/1401 | chr12 | 6531353 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6510114
|
T | C | 1 | a0002c0018 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.243T>C | p.Thr81Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/32 | 319/4825 | 243/4206 | 81/1401 | chr12 | 6510114 | ||
chr12:6510732
|
T | C | 1 | a0003c0015 | 2 | HG01891.hp1 HG01993.hp2 |
synonymous_variant | LOW | c.366T>C | p.Tyr122Tyr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/32 | 442/4825 | 366/4206 | 122/1401 | chr12 | 6510732 | ||
chr12:6511229
|
A | C | 1 | a0001c0033 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.564A>C | p.Ser188Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/32 | 640/4825 | 564/4206 | 188/1401 | chr12 | 6511229 | ||
chr12:6514334
|
T | C | 1 | a0002c0019 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.657T>C | p.Thr219Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 7/32 | 733/4825 | 657/4206 | 219/1401 | chr12 | 6514334 | ||
chr12:6514875
|
C | A | 1 | a0001c0026 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.942C>A | p.Ile314Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/32 | 1018/4825 | 942/4206 | 314/1401 | chr12 | 6514875 | ||
chr12:6517616
|
C | T | 1 | a0001c0032 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.1341C>T | p.Ala447Ala | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 12/32 | 1417/4825 | 1341/4206 | 447/1401 | chr12 | 6517616 | ||
chr12:6521091
|
C | A | 1 | a0007c0016 | 2 | HG03209.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1695C>A | p.Ile565Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/32 | 1771/4825 | 1695/4206 | 565/1401 | chr12 | 6521091 | ||
chr12:6522003
|
C | A | 14 | a0001c0001a0001c0026a0001c0028others(11): Show | 234 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
synonymous_variant | LOW | c.1920C>A | p.Ile640Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/32 | 1996/4825 | 1920/4206 | 640/1401 | chr12 | 6522003 | ||
chr12:6525651
|
C | T | 1 | a0001c0030 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2283C>T | p.Thr761Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/32 | 2359/4825 | 2283/4206 | 761/1401 | chr12 | 6525651 | ||
chr12:6526188
|
G | A | 1 | a0002c0021 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.2469G>A | p.Ser823Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/32 | 2545/4825 | 2469/4206 | 823/1401 | chr12 | 6526188 | ||
chr12:6528679
|
T | C | 26 | a0001c0001a0001c0004a0001c0007others(23): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
splice_region_variant&synonymous_variant | LOW | c.3300T>C | p.Arg1100Arg | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 26/32 | 3376/4825 | 3300/4206 | 1100/1401 | chr12 | 6528679 | ||
chr12:6528775
|
C | T | 2 | a0004c0005a0011c0035 | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
synonymous_variant | LOW | c.3396C>T | p.Ser1132Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 26/32 | 3472/4825 | 3396/4206 | 1132/1401 | chr12 | 6528775 | ||
chr12:6528950
|
C | T | 8 | a0001c0001a0001c0026a0001c0030others(5): Show | 134 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(131): Show |
synonymous_variant | LOW | c.3483C>T | p.Asn1161Asn | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/32 | 3559/4825 | 3483/4206 | 1161/1401 | chr12 | 6528950 | ||
chr12:6528977
|
C | A | 1 | a0001c0031 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3510C>A | p.Ile1170Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/32 | 3586/4825 | 3510/4206 | 1170/1401 | chr12 | 6528977 | ||
chr12:6529922
|
A | G | 23 | a0001c0001a0001c0004a0001c0007others(20): Show | 327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.3801A>G | p.Val1267Val | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/32 | 3877/4825 | 3801/4206 | 1267/1401 | chr12 | 6529922 | ||
chr12:6529949
|
T | G | 3 | a0001c0007a0012c0034a0014c0027 | 14 | HG01192.hp2 HG01261.hp1 HG02055.hp2 others(11): Show |
synonymous_variant | LOW | c.3828T>G | p.Pro1276Pro | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/32 | 3904/4825 | 3828/4206 | 1276/1401 | chr12 | 6529949 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6531496
|
T | G | 1 | a0001c0001t0015 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 84 | chr12 | 6531496 | |||||
chr12:6531503
|
CT | C | 2 | a0001c0001t0007a0003c0003t0014 | 8 | HG01070.hp1 HG01975.hp1 HG01993.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*99delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 99 | INFO_REALIGN_3_PRIME | chr12 | 6531503 | ||||
chr12:6531508
|
T | TA | 2 | a0001c0004t0010a0001c0007t0012 | 5 | HG02055.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*96_*97insA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 97 | chr12 | 6531508 | |||||
chr12:6531509
|
T | A | 2 | a0001c0004t0010a0001c0007t0012 | 5 | HG02055.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*97T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 97 | chr12 | 6531509 | |||||
chr12:6531509
|
T | TA | 3 | a0001c0007t0005a0012c0034t0005a0014c0027t0005 | 11 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*97_*98insA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 98 | chr12 | 6531509 | |||||
chr12:6531510
|
T | A | 17 | a0001c0001t0002a0001c0001t0015a0001c0004t0004others(14): Show | 175 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*98T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 98 | chr12 | 6531510 | |||||
chr12:6531510
|
T | TA | 4 | a0001c0001t0006a0001c0026t0006a0003c0003t0013others(1): Show | 13 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*98_*99insA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 99 | chr12 | 6531510 | |||||
chr12:6531511
|
T | A | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(28): Show | 299 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*99T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 99 | chr12 | 6531511 | |||||
chr12:6531528
|
G | A | 1 | a0001c0007t0012 | 2 | HG02055.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 116 | chr12 | 6531528 | |||||
chr12:6531678
|
G | A | 2 | a0001c0004t0009a0001c0028t0009 | 4 | HG01884.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*266G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 266 | chr12 | 6531678 | |||||
chr12:6531744
|
T | C | 11 | a0001c0004t0004a0001c0004t0008a0001c0004t0009others(8): Show | 69 | HG00558.hp1 HG01192.hp2 HG01243.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*332T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 332 | chr12 | 6531744 | |||||
chr12:6531810
|
A | T | 9 | a0001c0001t0003a0003c0003t0003a0003c0003t0013others(6): Show | 100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*398A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 398 | chr12 | 6531810 | |||||
chr12:6531828
|
C | T | 1 | a0001c0032t0016 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*416C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 416 | chr12 | 6531828 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6494160
|
A | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
splice_region_variant&intron_variant | LOW | c.-24+6A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494160 | ||||||
chr12:6494234
|
A | G | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-24+80A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494234 | ||||||
chr12:6494247
|
A | G | 133 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(130): Show | 139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-24+93A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494247 | ||||||
chr12:6494307
|
T | A | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-24+153T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494307 | ||||||
chr12:6494307
|
TTGTTAAG others(30): Show |
T | 175 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(172): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-24+211_-24+247del others(37): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr12 | 6494307 | |||||
chr12:6494371
|
G | T | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+217G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494371 | ||||||
chr12:6494440
|
T | C | 1 | a0003c0003t0003g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-24+286T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494440 | ||||||
chr12:6494590
|
G | T | 3 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240 | 3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-24+436G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494590 | ||||||
chr12:6494751
|
G | A | 133 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(130): Show | 139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-23-325G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494751 | ||||||
chr12:6494910
|
A | G | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.-23-166A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494910 | ||||||
chr12:6495019
|
A | G | 13 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(10): Show | 14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23-57A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6495019 | ||||||
chr12:6495249
|
T | G | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+24T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495249 | ||||||
chr12:6495252
|
C | T | 122 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(119): Show | 128 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.127+27C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495252 | ||||||
chr12:6495287
|
C | G | 1 | a0008c0013t0002g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+62C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495287 | ||||||
chr12:6495920
|
T | C | 1 | a0003c0003t0003g0024 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127+695T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495920 | ||||||
chr12:6495939
|
C | A | 130 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(127): Show | 135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.127+714C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495939 | ||||||
chr12:6495989
|
A | G | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+764A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495989 | ||||||
chr12:6496021
|
C | G | 1 | a0008c0013t0002g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+796C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496021 | ||||||
chr12:6496039
|
T | C | 164 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(161): Show | 172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.127+814T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496039 | ||||||
chr12:6496059
|
C | CT | 144 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(141): Show | 153 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.127+850dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6496059 | |||||
chr12:6496115
|
T | C | 1 | a0002c0002t0001g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127+890T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496115 | ||||||
chr12:6496121
|
G | A | 1 | a0001c0007t0004g0269 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127+896G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496121 | ||||||
chr12:6496217
|
A | G | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.127+992A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496217 | ||||||
chr12:6496348
|
C | T | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+1123C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496348 | ||||||
chr12:6496375
|
C | G | 133 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(130): Show | 139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.127+1150C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496375 | ||||||
chr12:6496401
|
G | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+1176G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496401 | ||||||
chr12:6496490
|
T | A | 122 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(119): Show | 128 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.127+1265T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496490 | ||||||
chr12:6496529
|
A | G | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+1304A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496529 | ||||||
chr12:6496539
|
C | T | 1 | a0001c0001t0002g0398 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.127+1314C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496539 | ||||||
chr12:6496645
|
G | A | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+1420G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496645 | ||||||
chr12:6496846
|
G | A | 122 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(119): Show | 128 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.127+1621G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496846 | ||||||
chr12:6497019
|
G | A | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+1794G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497019 | ||||||
chr12:6497283
|
T | G | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+2058T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497283 | ||||||
chr12:6497299
|
C | CT | 388 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(385): Show | 412 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(409): Show |
intron_variant | MODIFIER | c.127+2085dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497299 | |||||
chr12:6497299
|
C | CTT | 18 | a0001c0009t0001g0229a0004c0005t0001g0015a0004c0005t0001g0241others(15): Show | 19 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+2084_127+2085d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497299 | |||||
chr12:6497327
|
G | A | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+2102G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497327 | ||||||
chr12:6497452
|
C | G | 2 | a0003c0010t0001g0087a0003c0010t0001g0088 | 2 | HG00673.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.127+2227C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497452 | ||||||
chr12:6497536
|
T | A | 1 | a0002c0002t0001g0102 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.127+2311T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497536 | ||||||
chr12:6497562
|
G | T | 1 | a0001c0001t0003g0397 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127+2337G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497562 | ||||||
chr12:6497620
|
T | TTTG | 124 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(121): Show | 130 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.127+2411_127+2413d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497620 | |||||
chr12:6497649
|
T | TC | 403 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(400): Show | 428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.127+2426dupC | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497649 | |||||
chr12:6497680
|
C | T | 2 | a0001c0001t0002g0395a0001c0009t0001g0396 | 2 | NA18945.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.127+2455C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497680 | ||||||
chr12:6497780
|
G | A | 1 | a0003c0003t0003g0025 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.127+2555G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497780 | ||||||
chr12:6497852
|
G | C | 175 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(172): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.127+2627G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497852 | ||||||
chr12:6497918
|
C | CT | 124 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(121): Show | 130 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.127+2706dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497918 | |||||
chr12:6497918
|
C | CTT | 11 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+2705_127+2706d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497918 | |||||
chr12:6498002
|
G | C | 133 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(130): Show | 139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.127+2777G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498002 | ||||||
chr12:6498198
|
T | C | 31 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(28): Show | 33 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.127+2973T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498198 | ||||||
chr12:6498272
|
A | G | 1 | a0001c0004t0008g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127+3047A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498272 | ||||||
chr12:6498281
|
A | G | 1 | a0001c0001t0002g0393 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.127+3056A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498281 | ||||||
chr12:6498478
|
A | G | 1 | a0004c0005t0001g0256 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.127+3253A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498478 | ||||||
chr12:6498615
|
C | CT | 25 | a0001c0001t0002g0391a0001c0001t0002g0392a0001c0007t0004g0269others(22): Show | 27 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.127+3401dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6498615 | |||||
chr12:6498694
|
G | A | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+3469G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498694 | ||||||
chr12:6498732
|
T | C | 133 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(130): Show | 139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.127+3507T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498732 | ||||||
chr12:6498774
|
A | AT | 31 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(28): Show | 33 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.127+3555dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6498774 | |||||
chr12:6498855
|
C | T | 1 | a0003c0015t0003g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127+3630C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498855 | ||||||
chr12:6498879
|
C | T | 1 | a0005c0006t0003g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.127+3654C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498879 | ||||||
chr12:6498885
|
T | C | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+3660T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498885 | ||||||
chr12:6499203
|
C | A | 1 | a0002c0002t0001g0103 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.127+3978C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499203 | ||||||
chr12:6499388
|
G | A | 1 | a0001c0032t0016g0291 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127+4163G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499388 | ||||||
chr12:6499403
|
C | T | 2 | a0001c0001t0002g0389a0001c0001t0002g0390 | 2 | HG01123.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.127+4178C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499403 | ||||||
chr12:6499411
|
G | A | 1 | a0003c0003t0003g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.127+4186G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499411 | ||||||
chr12:6499441
|
G | A | 13 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(10): Show | 14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.127+4216G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499441 | ||||||
chr12:6499554
|
A | AT | 5 | a0001c0004t0008g0224a0001c0004t0008g0225a0001c0004t0008g0226others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+4337dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6499554 | |||||
chr12:6499612
|
G | A | 130 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(127): Show | 135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.127+4387G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499612 | ||||||
chr12:6499701
|
A | G | 1 | a0001c0007t0005g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127+4476A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499701 | ||||||
chr12:6499724
|
A | G | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127+4499A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499724 | ||||||
chr12:6499793
|
G | A | 1 | a0004c0005t0001g0241 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127+4568G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499793 | ||||||
chr12:6499860
|
C | G | 2 | a0001c0001t0002g0387a0001c0001t0002g0388 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127+4635C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499860 | ||||||
chr12:6499978
|
C | T | 1 | a0001c0001t0002g0386 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127+4753C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499978 | ||||||
chr12:6499994
|
A | G | 1 | a0001c0001t0002g0385 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127+4769A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499994 | ||||||
chr12:6500006
|
C | G | 7 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+4781C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500006 | ||||||
chr12:6500154
|
G | C | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | HG02523.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.127+4929G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500154 | ||||||
chr12:6500337
|
G | T | 113 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(110): Show | 118 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.127+5112G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500337 | ||||||
chr12:6500580
|
C | G | 1 | a0002c0002t0001g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127+5355C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500580 | ||||||
chr12:6500596
|
T | C | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127+5371T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500596 | ||||||
chr12:6500598
|
A | G | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+5373A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500598 | ||||||
chr12:6500802
|
A | G | 2 | a0003c0015t0003g0084a0003c0015t0003g0085 | 2 | HG01891.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.127+5577A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500802 | ||||||
chr12:6500952
|
C | T | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+5727C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500952 | ||||||
chr12:6501056
|
CT | C | 158 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0299others(155): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.127+5848delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501056 | |||||
chr12:6501056
|
CTT | C | 7 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(4): Show | 8 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+5847_127+5848d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501056 | |||||
chr12:6501056
|
CTTT | C | 11 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(8): Show | 11 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+5846_127+5848d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501056 | |||||
chr12:6501134
|
C | G | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+5909C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501134 | ||||||
chr12:6501217
|
C | T | 1 | a0003c0003t0003g0083 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.127+5992C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501217 | ||||||
chr12:6501227
|
A | AT | 53 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0194others(50): Show | 60 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.127+6034dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
A | ATT | 39 | a0001c0004t0004g0014a0001c0004t0004g0213a0001c0004t0004g0214others(36): Show | 42 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.127+6033_127+6034d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
AT | A | 61 | a0001c0001t0006g0267a0001c0004t0001g0012a0001c0004t0001g0190others(58): Show | 66 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.127+6034delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
ATT | A | 14 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(11): Show | 14 | HG01070.hp1 HG01884.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.127+6033_127+6034d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
ATTTT | A | 23 | a0001c0001t0002g0290a0001c0001t0002g0366a0001c0001t0002g0367others(20): Show | 23 | HG00597.hp1 HG01106.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.127+6031_127+6034d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
ATTTTT | A | 95 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(92): Show | 100 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.127+6030_127+6034d others(7): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
ATTTTTTT others(1): Show |
A | 10 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+6027_127+6034d others(10): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501227
|
ATTTTTTT others(2): Show |
A | 29 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0007t0004g0269others(26): Show | 31 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+6026_127+6034d others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | |||||
chr12:6501259
|
T | G | 130 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(127): Show | 135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.127+6034T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501259 | ||||||
chr12:6501262
|
G | T | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+6037G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501262 | ||||||
chr12:6501265
|
G | T | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127+6040G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501265 | ||||||
chr12:6501277
|
C | T | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+6052C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501277 | ||||||
chr12:6501319
|
C | T | 1 | a0001c0001t0002g0365 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127+6094C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501319 | ||||||
chr12:6501350
|
G | C | 1 | a0001c0001t0002g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127+6125G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501350 | ||||||
chr12:6501479
|
C | T | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+6254C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501479 | ||||||
chr12:6501489
|
T | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+6264T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501489 | ||||||
chr12:6501560
|
G | A | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+6335G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501560 | ||||||
chr12:6501567
|
G | C | 1 | a0001c0004t0008g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127+6342G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501567 | ||||||
chr12:6501600
|
A | G | 2 | a0003c0003t0003g0065a0003c0003t0003g0099 | 2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.127+6375A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501600 | ||||||
chr12:6501794
|
T | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+6569T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501794 | ||||||
chr12:6501901
|
A | G | 1 | a0001c0004t0008g0223 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.127+6676A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501901 | ||||||
chr12:6501912
|
T | C | 121 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(118): Show | 126 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.127+6687T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501912 | ||||||
chr12:6501954
|
C | G | 1 | a0002c0002t0001g0102 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.127+6729C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501954 | ||||||
chr12:6502002
|
T | G | 1 | a0004c0005t0001g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127+6777T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502002 | ||||||
chr12:6502041
|
C | T | 3 | a0001c0004t0004g0212a0001c0004t0004g0222a0001c0004t0008g0223 | 3 | HG01952.hp2 HG01981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.127+6816C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502041 | ||||||
chr12:6502244
|
T | C | 1 | a0001c0004t0008g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127+7019T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502244 | ||||||
chr12:6502322
|
G | A | 7 | a0001c0001t0002g0289a0001c0001t0002g0301a0001c0001t0002g0302others(4): Show | 8 | HG01169.hp2 HG02809.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+7097G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502322 | ||||||
chr12:6502345
|
A | G | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+7120A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502345 | ||||||
chr12:6502364
|
T | G | 1 | a0001c0030t0002g0303 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127+7139T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502364 | ||||||
chr12:6502447
|
A | G | 1 | a0003c0003t0003g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127+7222A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502447 | ||||||
chr12:6502503
|
C | T | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-7214C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502503 | ||||||
chr12:6502534
|
T | C | 11 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(8): Show | 12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-7183T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502534 | ||||||
chr12:6502553
|
G | A | 175 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(172): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.128-7164G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502553 | ||||||
chr12:6502674
|
G | A | 1 | a0002c0002t0001g0106 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.128-7043G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502674 | ||||||
chr12:6502716
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.128-7001G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502716 | ||||||
chr12:6502789
|
C | T | 45 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(42): Show | 49 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.128-6928C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502789 | ||||||
chr12:6502798
|
A | G | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-6919A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502798 | ||||||
chr12:6502837
|
T | TTTG | 288 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(285): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.128-6861_128-6859d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6502837 | |||||
chr12:6502837
|
TTTG | T | 10 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(7): Show | 11 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-6861_128-6859d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6502837 | |||||
chr12:6502847
|
T | TTG | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-6868_128-6867d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6502847 | |||||
chr12:6502948
|
G | A | 119 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(116): Show | 124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-6769G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502948 | ||||||
chr12:6503008
|
C | CT | 55 | a0001c0004t0004g0211a0001c0004t0004g0220a0001c0004t0004g0221others(52): Show | 57 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.128-6688dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503008 | |||||
chr12:6503008
|
CT | C | 103 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(100): Show | 107 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.128-6688delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503008 | |||||
chr12:6503008
|
CTT | C | 23 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(20): Show | 24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-6689_128-6688d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503008 | |||||
chr12:6503014
|
T | G | 7 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-6703T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503014 | ||||||
chr12:6503020
|
T | G | 23 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(20): Show | 24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-6697T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503020 | ||||||
chr12:6503024
|
T | G | 23 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(20): Show | 24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-6693T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503024 | ||||||
chr12:6503077
|
C | G | 13 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(10): Show | 14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-6640C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503077 | ||||||
chr12:6503134
|
C | T | 4 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(1): Show | 4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-6583C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503134 | ||||||
chr12:6503274
|
A | AT | 406 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(403): Show | 431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.128-6442dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503274 | |||||
chr12:6503293
|
T | C | 1 | a0001c0001t0002g0377 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.128-6424T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503293 | ||||||
chr12:6503319
|
A | AT | 406 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(403): Show | 431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
intron_variant | MODIFIER | c.128-6398_128-6397i others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503319 | ||||||
chr12:6503410
|
C | T | 45 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(42): Show | 49 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.128-6307C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503410 | ||||||
chr12:6503599
|
G | A | 82 | a0001c0001t0002g0358a0003c0003t0003g0001a0003c0003t0003g0007others(79): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.128-6118G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503599 | ||||||
chr12:6503676
|
C | T | 2 | a0001c0001t0002g0356a0001c0001t0002g0357 | 2 | NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.128-6041C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503676 | ||||||
chr12:6503717
|
G | C | 94 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(91): Show | 99 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.128-6000G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503717 | ||||||
chr12:6503770
|
A | AT | 13 | a0001c0004t0004g0221a0002c0002t0001g0105a0002c0002t0001g0133others(10): Show | 13 | HG01978.hp2 NA18945.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.128-5931dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503770 | |||||
chr12:6503770
|
AT | A | 156 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(153): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.128-5931delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503770 | |||||
chr12:6503786
|
T | A | 259 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(256): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.128-5931T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503786 | ||||||
chr12:6503787
|
A | T | 46 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(43): Show | 50 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(47): Show |
intron_variant | MODIFIER | c.128-5930A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503787 | ||||||
chr12:6503904
|
G | C | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5813G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503904 | ||||||
chr12:6503907
|
G | A | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-5810G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503907 | ||||||
chr12:6503910
|
A | G | 175 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(172): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.128-5807A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503910 | ||||||
chr12:6504003
|
G | T | 57 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0004g0005others(54): Show | 61 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.128-5714G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504003 | ||||||
chr12:6504092
|
T | G | 1 | a0019c0036t0001g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-5625T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504092 | ||||||
chr12:6504118
|
G | A | 119 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(116): Show | 124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-5599G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504118 | ||||||
chr12:6504155
|
C | T | 1 | a0001c0007t0005g0279 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128-5562C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504155 | ||||||
chr12:6504170
|
C | CATATATA others(99): Show |
1 | a0001c0001t0006g0267 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.128-5528_128-5527i others(108): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504170 | |||||
chr12:6504170
|
CATATATA others(55): Show |
C | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-5534_128-5473d others(64): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504170 | |||||
chr12:6504174
|
TATATATA others(43): Show |
T | 48 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(45): Show | 52 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(49): Show |
intron_variant | MODIFIER | c.128-5535_128-5486d others(52): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504174 | |||||
chr12:6504176
|
TATATACA others(35): Show |
T | 3 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240 | 3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.128-5535_128-5494d others(44): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504176 | |||||
chr12:6504176
|
TATATACA others(41): Show |
T | 6 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0004g0194others(3): Show | 6 | HG01243.hp1 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-5535_128-5488d others(50): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504176 | |||||
chr12:6504180
|
T | TACATATA others(87): Show |
1 | a0004c0005t0001g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.128-5520_128-5519i others(96): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504180 | |||||
chr12:6504180
|
T | TACATATA others(89): Show |
3 | a0004c0005t0001g0251a0004c0005t0001g0253a0011c0035t0001g0252 | 3 | HG00323.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.128-5520_128-5519i others(98): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504180 | |||||
chr12:6504180
|
T | TACATATA others(115): Show |
1 | a0004c0005t0001g0256 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.128-5520_128-5519i others(124): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504180 | |||||
chr12:6504182
|
C | CAT | 24 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0100others(21): Show | 27 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.128-5501_128-5500d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
C | CATAT | 11 | a0002c0002t0001g0102a0002c0002t0001g0129a0002c0002t0001g0139others(8): Show | 11 | HG02015.hp1 HG02135.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-5503_128-5500d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
C | CATATAT | 7 | a0002c0002t0001g0131a0002c0002t0001g0142a0002c0002t0001g0145others(4): Show | 7 | HG00621.hp2 HG00673.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-5505_128-5500d others(8): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
C | CATATATA others(1): Show |
4 | a0002c0002t0001g0004a0002c0002t0001g0159a0002c0002t0001g0177others(1): Show | 6 | NA18941.hp2 NA18968.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-5507_128-5500d others(10): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
C | CATATATA others(3): Show |
1 | a0002c0002t0001g0157 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.128-5509_128-5500d others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
C | T | 1 | a0002c0002t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.128-5535C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504182 | ||||||
chr12:6504182
|
CAT | C | 3 | a0002c0002t0001g0107a0002c0002t0001g0115a0002c0002t0001g0164 | 3 | HG02040.hp1 HG02258.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.128-5501_128-5500d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
CATAT | C | 2 | a0002c0002t0001g0009a0002c0002t0001g0143 | 3 | HG00099.hp1 HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.128-5503_128-5500d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504182
|
CATATATA others(43): Show |
C | 1 | a0001c0001t0002g0346 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.128-5523_128-5474d others(52): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | |||||
chr12:6504184
|
T | TATATATA others(85): Show |
1 | a0004c0005t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.128-5520_128-5519i others(94): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504184 | |||||
chr12:6504184
|
T | TATATATA others(87): Show |
6 | a0004c0005t0001g0015a0004c0005t0001g0246a0004c0005t0001g0247others(3): Show | 7 | HG00099.hp2 HG01243.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-5520_128-5519i others(96): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504184 | |||||
chr12:6504184
|
T | TATATATA others(117): Show |
2 | a0004c0005t0001g0241a0004c0005t0001g0243 | 2 | HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.128-5520_128-5519i others(126): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504184 | |||||
chr12:6504186
|
T | TATATATA others(85): Show |
1 | a0004c0005t0001g0244 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.128-5520_128-5519i others(94): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504186 | |||||
chr12:6504186
|
TATATATA others(31): Show |
T | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.128-5511_128-5474d others(40): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504186 | |||||
chr12:6504188
|
T | TACATATA others(105): Show |
3 | a0009c0012t0006g0258a0009c0012t0006g0259a0009c0012t0006g0260 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.128-5528_128-5527i others(114): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | |||||
chr12:6504188
|
T | TATATATA others(83): Show |
1 | a0004c0005t0001g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128-5520_128-5519i others(92): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | |||||
chr12:6504188
|
T | TATATATA others(83): Show |
1 | a0004c0005t0001g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128-5520_128-5519i others(92): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | |||||
chr12:6504188
|
TATATATA others(29): Show |
T | 7 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-5509_128-5474d others(38): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | |||||
chr12:6504190
|
T | C | 1 | a0001c0001t0006g0267 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.128-5527T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504190 | ||||||
chr12:6504194
|
TATATATA others(23): Show |
T | 1 | a0019c0036t0001g0394 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-5503_128-5474d others(32): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504194 | |||||
chr12:6504196
|
T | TATATACA others(83): Show |
1 | a0001c0001t0006g0263 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.128-5516_128-5515i others(92): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504196 | |||||
chr12:6504196
|
TATATATA others(21): Show |
T | 103 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(100): Show | 108 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.128-5501_128-5474d others(30): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504196 | |||||
chr12:6504197
|
A | G | 1 | a0001c0007t0005g0275 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.128-5520A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504197 | ||||||
chr12:6504198
|
T | C | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5519T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504198 | ||||||
chr12:6504198
|
T | TATACATA others(79): Show |
2 | a0001c0001t0006g0262a0001c0028t0009g0261 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.128-5516_128-5515i others(88): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504198 | |||||
chr12:6504198
|
TATATATA others(19): Show |
T | 12 | a0001c0001t0002g0329a0001c0001t0002g0330a0001c0001t0002g0352others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-5499_128-5474d others(28): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504198 | |||||
chr12:6504199
|
A | G | 10 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(7): Show | 11 | HG01192.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-5518A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504199 | ||||||
chr12:6504200
|
T | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-5517T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504200 | ||||||
chr12:6504202
|
T | C | 2 | a0001c0001t0002g0391a0001c0001t0002g0392 | 2 | NA18972.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.128-5515T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504202 | ||||||
chr12:6504202
|
T | TATATATA others(117): Show |
1 | a0001c0001t0006g0266 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-5506_128-5505i others(126): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504202 | |||||
chr12:6504204
|
T | C | 4 | a0001c0001t0006g0263a0009c0012t0006g0258a0009c0012t0006g0259others(1): Show | 4 | HG02630.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-5513T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504204 | ||||||
chr12:6504204
|
T | TACATATA others(103): Show |
1 | a0001c0026t0006g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.128-5512_128-5511i others(112): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504204 | |||||
chr12:6504204
|
T | TATATATA others(115): Show |
2 | a0001c0001t0006g0264a0001c0001t0006g0265 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.128-5506_128-5505i others(124): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504204 | |||||
chr12:6504206
|
T | C | 2 | a0001c0001t0006g0262a0001c0028t0009g0261 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.128-5511T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504206 | ||||||
chr12:6504208
|
TATATATA others(9): Show |
T | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5499_128-5484d others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504208 | |||||
chr12:6504212
|
T | C | 2 | a0004c0005t0001g0242a0004c0005t0001g0243 | 2 | HG02683.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.128-5505T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504212 | ||||||
chr12:6504212
|
T | TAG | 4 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0133others(1): Show | 4 | HG02165.hp2 NA18945.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5504_128-5503i others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504212 | |||||
chr12:6504214
|
T | C | 14 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(11): Show | 15 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.128-5503T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504214 | ||||||
chr12:6504215
|
A | ACACATAT others(55): Show |
3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5502_128-5501i others(64): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504215 | ||||||
chr12:6504216
|
T | C | 13 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0244others(10): Show | 14 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-5501T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504216 | ||||||
chr12:6504216
|
TAG | T | 8 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(5): Show | 9 | HG01192.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-5499_128-5498d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504216 | |||||
chr12:6504217
|
A | G | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5500A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504217 | ||||||
chr12:6504218
|
G | C | 5 | a0001c0004t0011g0403a0001c0004t0011g0404a0004c0005t0001g0245others(2): Show | 5 | HG00733.hp1 HG01074.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-5499G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504218 | ||||||
chr12:6504218
|
G | T | 29 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(26): Show | 30 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-5499G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504218 | ||||||
chr12:6504220
|
T | C | 4 | a0001c0004t0011g0403a0001c0004t0011g0404a0004c0005t0001g0245others(1): Show | 4 | HG00733.hp1 HG01168.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5497T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504220 | ||||||
chr12:6504222
|
T | C | 1 | a0001c0007t0005g0274 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.128-5495T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504222 | ||||||
chr12:6504224
|
G | C | 9 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(6): Show | 10 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-5493G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504224 | ||||||
chr12:6504224
|
G | T | 43 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(40): Show | 44 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.128-5493G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504224 | ||||||
chr12:6504226
|
T | G | 1 | a0002c0002t0001g0136 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.128-5491T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504226 | ||||||
chr12:6504228
|
T | C | 3 | a0001c0001t0002g0378a0001c0011t0001g0022a0001c0011t0001g0400 | 4 | HG01981.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5489T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504228 | ||||||
chr12:6504228
|
T | TATATATA others(27): Show |
2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-5482_128-5481i others(36): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504228 | |||||
chr12:6504230
|
T | C | 65 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(62): Show | 69 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.128-5487T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504230 | ||||||
chr12:6504230
|
T | G | 4 | a0002c0002t0001g0003a0002c0002t0001g0129a0002c0002t0001g0134others(1): Show | 6 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-5487T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504230 | ||||||
chr12:6504232
|
T | C | 115 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(112): Show | 121 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.128-5485T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504232 | ||||||
chr12:6504233
|
A | G | 3 | a0002c0002t0001g0127a0002c0002t0001g0128a0014c0027t0005g0257 | 3 | HG02615.hp2 NA18977.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.128-5484A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504233 | ||||||
chr12:6504234
|
T | C | 119 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(116): Show | 124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-5483T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504234 | ||||||
chr12:6504239
|
A | G | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5478A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504239 | ||||||
chr12:6504424
|
G | A | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-5293G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504424 | ||||||
chr12:6504453
|
C | T | 1 | a0001c0001t0002g0351 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128-5264C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504453 | ||||||
chr12:6504598
|
G | A | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.128-5119G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504598 | ||||||
chr12:6504924
|
T | G | 2 | a0003c0003t0003g0030a0003c0003t0003g0031 | 2 | NA18984.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.128-4793T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504924 | ||||||
chr12:6504933
|
C | T | 5 | a0007c0014t0001g0292a0007c0014t0001g0293a0007c0014t0001g0296others(2): Show | 5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-4784C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504933 | ||||||
chr12:6504990
|
T | C | 119 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(116): Show | 124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-4727T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504990 | ||||||
chr12:6505015
|
A | G | 45 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(42): Show | 49 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.128-4702A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505015 | ||||||
chr12:6505220
|
C | T | 13 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(10): Show | 14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-4497C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505220 | ||||||
chr12:6505290
|
T | C | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-4427T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505290 | ||||||
chr12:6505300
|
A | G | 1 | a0002c0002t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.128-4417A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505300 | ||||||
chr12:6505304
|
G | A | 3 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240 | 3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.128-4413G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505304 | ||||||
chr12:6505355
|
C | T | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-4362C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505355 | ||||||
chr12:6505361
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.128-4356C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505361 | ||||||
chr12:6505391
|
C | T | 3 | a0001c0004t0004g0208a0001c0004t0004g0209a0001c0004t0004g0210 | 3 | HG01257.hp2 HG01258.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.128-4326C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505391 | ||||||
chr12:6505575
|
G | A | 1 | a0004c0005t0001g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128-4142G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505575 | ||||||
chr12:6505656
|
C | T | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-4061C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505656 | ||||||
chr12:6505688
|
A | T | 4 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240others(1): Show | 4 | HG02886.hp2 HG03139.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-4029A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505688 | ||||||
chr12:6505779
|
C | T | 1 | a0001c0001t0015g0382 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.128-3938C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505779 | ||||||
chr12:6505846
|
C | CAG | 314 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(311): Show | 332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.128-3870_128-3869d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6505846 | |||||
chr12:6505986
|
G | T | 57 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0004g0005others(54): Show | 61 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.128-3731G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505986 | ||||||
chr12:6506036
|
G | A | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-3681G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506036 | ||||||
chr12:6506041
|
C | T | 1 | a0001c0001t0002g0355 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-3676C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506041 | ||||||
chr12:6506361
|
G | T | 32 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(29): Show | 36 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.128-3356G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506361 | ||||||
chr12:6506446
|
C | T | 20 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(17): Show | 21 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.128-3271C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506446 | ||||||
chr12:6506470
|
G | A | 1 | a0003c0003t0003g0032 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.128-3247G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506470 | ||||||
chr12:6506482
|
C | T | 1 | a0003c0003t0003g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.128-3235C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506482 | ||||||
chr12:6506515
|
A | G | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-3202A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506515 | ||||||
chr12:6506518
|
A | G | 1 | a0003c0003t0003g0031 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.128-3199A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506518 | ||||||
chr12:6506522
|
A | G | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-3195A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506522 | ||||||
chr12:6506552
|
T | C | 14 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(11): Show | 15 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-3165T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506552 | ||||||
chr12:6506695
|
A | T | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-3022A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506695 | ||||||
chr12:6506709
|
G | A | 8 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-3008G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506709 | ||||||
chr12:6506715
|
C | A | 1 | a0001c0004t0008g0223 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.128-3002C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506715 | ||||||
chr12:6506784
|
G | A | 1 | a0007c0016t0001g0295 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.128-2933G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506784 | ||||||
chr12:6506921
|
G | A | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-2796G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506921 | ||||||
chr12:6506954
|
G | T | 48 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(45): Show | 50 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-2763G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506954 | ||||||
chr12:6506972
|
A | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-2745A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506972 | ||||||
chr12:6507057
|
G | A | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-2660G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507057 | ||||||
chr12:6507090
|
T | G | 2 | a0002c0002t0001g0113a0015c0025t0001g0163 | 2 | NA18955.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.128-2627T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507090 | ||||||
chr12:6507157
|
T | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0129a0002c0002t0001g0160 | 5 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2560T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507157 | ||||||
chr12:6507341
|
C | T | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-2376C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507341 | ||||||
chr12:6507554
|
G | A | 2 | a0001c0001t0002g0366a0001c0001t0002g0367 | 2 | HG01346.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.128-2163G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507554 | ||||||
chr12:6507840
|
C | T | 1 | a0001c0004t0004g0231 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.128-1877C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507840 | ||||||
chr12:6507841
|
GA | G | 9 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-1869delA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6507841 | |||||
chr12:6507869
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.128-1848G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507869 | ||||||
chr12:6508043
|
T | G | 3 | a0003c0003t0003g0033a0003c0003t0003g0066a0003c0003t0003g0083 | 3 | NA18955.hp2 NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.128-1674T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508043 | ||||||
chr12:6508183
|
G | A | 1 | a0002c0002t0001g0106 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.128-1534G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508183 | ||||||
chr12:6508185
|
T | C | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-1532T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508185 | ||||||
chr12:6508206
|
T | C | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-1511T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508206 | ||||||
chr12:6508340
|
A | G | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-1377A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508340 | ||||||
chr12:6508393
|
C | T | 293 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(290): Show | 310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.128-1324C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508393 | ||||||
chr12:6508533
|
A | G | 1 | a0001c0007t0012g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.128-1184A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508533 | ||||||
chr12:6508902
|
C | T | 1 | a0001c0004t0008g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.128-815C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508902 | ||||||
chr12:6509023
|
C | T | 1 | a0001c0001t0002g0328 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.128-694C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509023 | ||||||
chr12:6509074
|
C | CTT | 16 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(13): Show | 17 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.128-629_128-628dup others(2): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6509074 | |||||
chr12:6509074
|
CT | C | 25 | a0001c0001t0002g0018a0001c0001t0002g0301a0001c0001t0002g0305others(22): Show | 25 | HG00642.hp2 HG01168.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-628delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6509074 | |||||
chr12:6509138
|
G | GT | 4 | a0001c0004t0008g0224a0001c0004t0008g0225a0001c0004t0008g0226others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-578dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6509138 | |||||
chr12:6509188
|
G | A | 1 | a0002c0021t0001g0117 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.128-529G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509188 | ||||||
chr12:6509490
|
G | A | 1 | a0001c0033t0004g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-227G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509490 | ||||||
chr12:6509508
|
C | T | 5 | a0003c0003t0003g0057a0003c0003t0003g0058a0003c0003t0003g0078others(2): Show | 5 | HG00621.hp1 HG02040.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-209C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509508 | ||||||
chr12:6509705
|
C | T | 81 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(78): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-12C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509705 | ||||||
chr12:6509888
|
T | C | 106 | a0001c0004t0011g0403a0001c0004t0011g0404a0001c0007t0012g0281others(103): Show | 114 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.203+96T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/31 | chr12 | 6509888 | ||||||
chr12:6509915
|
TCTA | T | 131 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(128): Show | 136 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.203+126_203+128del others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr12 | 6509915 | |||||
chr12:6509998
|
C | T | 4 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(1): Show | 4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-77C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/31 | chr12 | 6509998 | ||||||
chr12:6510151
|
G | A | 1 | a0001c0004t0008g0227 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.262+18G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/31 | chr12 | 6510151 | ||||||
chr12:6510236
|
T | A | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.262+103T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/31 | chr12 | 6510236 | ||||||
chr12:6510236
|
T | C | 83 | a0001c0004t0011g0403a0001c0004t0011g0404a0003c0003t0003g0001others(80): Show | 89 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.262+103T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/31 | chr12 | 6510236 | ||||||
chr12:6510857
|
G | C | 11 | a0001c0004t0004g0005a0001c0004t0004g0014a0001c0004t0004g0199others(8): Show | 14 | NA18941.hp1 NA18952.hp1 NA18968.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+47G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/31 | chr12 | 6510857 | ||||||
chr12:6510971
|
C | T | 1 | a0003c0003t0014g0089 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.445-139C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/31 | chr12 | 6510971 | ||||||
chr12:6510997
|
C | T | 2 | a0002c0002t0001g0103a0016c0023t0001g0152 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.445-113C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/31 | chr12 | 6510997 | ||||||
chr12:6511329
|
G | T | 234 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(231): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.587+77G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511329 | ||||||
chr12:6511334
|
G | GT | 9 | a0001c0001t0002g0357a0001c0009t0001g0229a0002c0002t0001g0168others(6): Show | 9 | HG02056.hp1 HG02074.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+92dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6511334 | |||||
chr12:6511340
|
T | G | 1 | a0001c0004t0011g0403 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.587+88T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511340 | ||||||
chr12:6511343
|
T | G | 5 | a0002c0002t0001g0004a0002c0002t0001g0131a0002c0002t0001g0142others(2): Show | 7 | HG00621.hp2 NA18941.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+91T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511343 | ||||||
chr12:6511346
|
T | G | 5 | a0002c0002t0001g0004a0002c0002t0001g0131a0002c0002t0001g0142others(2): Show | 7 | HG00621.hp2 NA18941.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+94T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511346 | ||||||
chr12:6511386
|
G | A | 2 | a0002c0002t0001g0113a0008c0013t0002g0399 | 2 | HG03225.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.587+134G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511386 | ||||||
chr12:6511436
|
A | G | 307 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(304): Show | 325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.587+184A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511436 | ||||||
chr12:6511457
|
C | T | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.587+205C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511457 | ||||||
chr12:6511472
|
A | G | 2 | a0001c0011t0001g0022a0001c0011t0001g0400 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.587+220A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511472 | ||||||
chr12:6511541
|
C | A | 1 | a0001c0001t0002g0331 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587+289C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511541 | ||||||
chr12:6511552
|
C | G | 1 | a0003c0003t0003g0061 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.587+300C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511552 | ||||||
chr12:6511613
|
G | A | 237 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(234): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.587+361G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511613 | ||||||
chr12:6511753
|
G | A | 1 | a0003c0003t0003g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587+501G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511753 | ||||||
chr12:6511866
|
G | A | 1 | a0001c0004t0009g0239 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.587+614G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511866 | ||||||
chr12:6511980
|
G | A | 1 | a0001c0004t0004g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.587+728G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511980 | ||||||
chr12:6512056
|
T | C | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.587+804T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512056 | ||||||
chr12:6512085
|
C | T | 154 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(151): Show | 161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.587+833C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512085 | ||||||
chr12:6512112
|
A | T | 1 | a0001c0001t0002g0360 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+860A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512112 | ||||||
chr12:6512114
|
A | C | 1 | a0001c0001t0002g0360 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+862A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512114 | ||||||
chr12:6512146
|
C | T | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587+894C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512146 | ||||||
chr12:6512188
|
C | T | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.587+936C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512188 | ||||||
chr12:6512272
|
C | CA | 12 | a0001c0004t0008g0223a0001c0009t0001g0229a0002c0002t0001g0127others(9): Show | 12 | HG01192.hp1 HG02622.hp1 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.587+1041dupA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512272 | |||||
chr12:6512272
|
CA | C | 23 | a0001c0001t0002g0379a0001c0004t0001g0012a0001c0004t0001g0190others(20): Show | 24 | HG01192.hp2 HG01261.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.587+1041delA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512272 | |||||
chr12:6512272
|
CAA | C | 223 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(220): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.587+1040_587+1041d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512272 | |||||
chr12:6512276
|
A | G | 2 | a0003c0003t0003g0054a0003c0003t0003g0077 | 2 | NA18974.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.587+1024A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512276 | ||||||
chr12:6512292
|
A | T | 2 | a0001c0001t0002g0342a0001c0001t0002g0343 | 2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.587+1040A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512292 | ||||||
chr12:6512308
|
TAGAC | T | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.587+1066_587+1069d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512308 | |||||
chr12:6512314
|
G | A | 1 | a0001c0001t0002g0346 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.587+1062G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512314 | ||||||
chr12:6512314
|
GACAGACA others(1): Show |
G | 4 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(1): Show | 4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+1070_587+1077d others(10): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512314 | |||||
chr12:6512318
|
GACAA | G | 7 | a0001c0001t0002g0376a0001c0004t0004g0191a0001c0004t0008g0224others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+1070_587+1073d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512318 | |||||
chr12:6512398
|
A | G | 1 | a0001c0011t0001g0401 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.587+1146A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512398 | ||||||
chr12:6512475
|
A | G | 131 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(128): Show | 136 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.587+1223A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512475 | ||||||
chr12:6512485
|
C | T | 1 | a0003c0003t0003g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.587+1233C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512485 | ||||||
chr12:6512535
|
C | T | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587+1283C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512535 | ||||||
chr12:6512680
|
A | G | 4 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(1): Show | 4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+1428A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512680 | ||||||
chr12:6512716
|
C | T | 1 | a0001c0004t0009g0238 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.587+1464C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512716 | ||||||
chr12:6512945
|
A | G | 307 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(304): Show | 325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.588-1320A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512945 | ||||||
chr12:6513065
|
TAA | T | 11 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(8): Show | 11 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.588-1198_588-1197d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513065 | |||||
chr12:6513180
|
T | C | 247 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(244): Show | 261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.588-1085T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513180 | ||||||
chr12:6513232
|
T | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.588-1033T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513232 | ||||||
chr12:6513239
|
C | T | 1 | a0004c0005t0001g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-1026C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513239 | ||||||
chr12:6513361
|
T | C | 7 | a0002c0002t0001g0147a0002c0002t0001g0148a0002c0002t0001g0154others(4): Show | 7 | HG00438.hp1 HG00673.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.588-904T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513361 | ||||||
chr12:6513444
|
G | A | 1 | a0003c0003t0003g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588-821G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513444 | ||||||
chr12:6513622
|
T | C | 1 | a0002c0002t0001g0106 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.588-643T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513622 | ||||||
chr12:6513715
|
C | CT | 9 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0267others(6): Show | 9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.588-532dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(7): Show |
2 | a0001c0004t0010g0270a0001c0004t0010g0271 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588-545_588-532dup others(14): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(8): Show |
13 | a0001c0004t0010g0272a0001c0007t0005g0280a0004c0005t0001g0015others(10): Show | 14 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-546_588-532dup others(15): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(9): Show |
9 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0279others(6): Show | 10 | HG00733.hp1 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.588-547_588-532dup others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0342a0001c0001t0002g0343a0001c0007t0005g0275others(4): Show | 7 | HG01099.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.588-548_588-532dup others(17): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(11): Show |
22 | a0001c0001t0002g0019a0001c0001t0002g0305a0001c0001t0002g0306others(19): Show | 23 | HG01069.hp2 HG01081.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.588-549_588-532dup others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(12): Show |
48 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0020others(45): Show | 52 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(13): Show |
24 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(21): Show | 24 | HG00642.hp1 HG01358.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(14): Show |
14 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0287others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(21): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(15): Show |
4 | a0001c0001t0002g0351a0001c0001t0002g0354a0001c0001t0002g0355others(1): Show | 4 | HG03453.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(22): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0373 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.588-532_588-531ins others(24): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
C | CTTTTTTT others(27): Show |
1 | a0001c0007t0012g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-532_588-531ins others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
CT | C | 80 | a0001c0001t0002g0309a0001c0004t0011g0404a0003c0003t0003g0001others(77): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.588-532delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513715
|
CTTTT | C | 52 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(49): Show | 56 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(53): Show |
intron_variant | MODIFIER | c.588-535_588-532del others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | |||||
chr12:6513735
|
T | C | 307 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(304): Show | 325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.588-530T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513735 | ||||||
chr12:6513747
|
G | C | 11 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(8): Show | 12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.588-518G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513747 | ||||||
chr12:6513751
|
T | C | 1 | a0001c0007t0012g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-514T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513751 | ||||||
chr12:6513784
|
C | T | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-481C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513784 | ||||||
chr12:6513842
|
A | T | 7 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0103others(4): Show | 10 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.588-423A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513842 | ||||||
chr12:6513931
|
G | A | 120 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(117): Show | 129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.588-334G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513931 | ||||||
chr12:6514041
|
T | A | 3 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0002g0368 | 3 | NA18944.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.588-224T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514041 | ||||||
chr12:6514138
|
A | G | 1 | a0003c0003t0003g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588-127A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514138 | ||||||
chr12:6514216
|
A | G | 120 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(117): Show | 125 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.588-49A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514216 | ||||||
chr12:6514223
|
T | C | 251 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(248): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.588-42T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514223 | ||||||
chr12:6514625
|
C | T | 1 | a0002c0002t0001g0177 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.839+38C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 8/31 | chr12 | 6514625 | ||||||
chr12:6514945
|
G | A | 1 | a0003c0003t0003g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.987+25G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6514945 | ||||||
chr12:6514973
|
T | C | 120 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(117): Show | 125 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.987+53T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6514973 | ||||||
chr12:6515200
|
T | C | 5 | a0007c0014t0001g0292a0007c0014t0001g0293a0007c0014t0001g0296others(2): Show | 5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+280T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515200 | ||||||
chr12:6515269
|
C | T | 128 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(125): Show | 133 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.987+349C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515269 | ||||||
chr12:6515374
|
G | A | 11 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(8): Show | 12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+454G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515374 | ||||||
chr12:6515401
|
T | C | 1 | a0001c0001t0002g0370 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.987+481T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515401 | ||||||
chr12:6515465
|
G | A | 1 | a0001c0033t0004g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.987+545G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515465 | ||||||
chr12:6515500
|
C | A | 1 | a0004c0005t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.987+580C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515500 | ||||||
chr12:6515572
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.987+652T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515572 | ||||||
chr12:6515640
|
A | G | 95 | a0001c0004t0011g0403a0001c0004t0011g0404a0002c0002t0001g0164others(92): Show | 101 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.987+720A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515640 | ||||||
chr12:6515843
|
T | C | 3 | a0007c0014t0001g0292a0007c0014t0001g0293a0007c0014t0001g0296 | 3 | HG02622.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+923T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515843 | ||||||
chr12:6515844
|
A | AG | 3 | a0007c0014t0001g0292a0007c0014t0001g0293a0007c0014t0001g0296 | 3 | HG02622.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+924_987+925ins others(1): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515844 | ||||||
chr12:6515877
|
G | A | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.988-951G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515877 | ||||||
chr12:6515964
|
A | G | 262 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(259): Show | 275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.988-864A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515964 | ||||||
chr12:6516050
|
G | T | 5 | a0001c0004t0008g0225a0001c0004t0008g0226a0001c0004t0008g0227others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-778G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516050 | ||||||
chr12:6516065
|
G | A | 1 | a0001c0001t0002g0366 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.988-763G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516065 | ||||||
chr12:6516067
|
G | A | 8 | a0003c0003t0003g0008a0003c0003t0003g0028a0003c0003t0003g0032others(5): Show | 9 | HG00597.hp2 HG00609.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-761G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516067 | ||||||
chr12:6516073
|
G | C | 2 | a0003c0003t0003g0065a0003c0003t0003g0099 | 2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.988-755G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516073 | ||||||
chr12:6516119
|
C | T | 105 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(102): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.988-709C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516119 | ||||||
chr12:6516145
|
G | A | 118 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(115): Show | 123 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.988-683G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516145 | ||||||
chr12:6516167
|
A | G | 266 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(263): Show | 280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.988-661A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516167 | ||||||
chr12:6516206
|
C | A | 5 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401others(2): Show | 6 | HG02622.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-622C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516206 | ||||||
chr12:6516216
|
C | A | 5 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401others(2): Show | 6 | HG02622.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-612C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516216 | ||||||
chr12:6516245
|
T | C | 1 | a0002c0002t0001g0164 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.988-583T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516245 | ||||||
chr12:6516317
|
T | C | 39 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(36): Show | 42 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-511T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516317 | ||||||
chr12:6516318
|
ATGGT | A | 39 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(36): Show | 42 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-509_988-506del others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516318 | ||||||
chr12:6516324
|
AAATCCT | A | 39 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(36): Show | 42 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-503_988-498del others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516324 | ||||||
chr12:6516704
|
A | G | 2 | a0001c0001t0002g0356a0001c0001t0002g0357 | 2 | NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.988-124A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516704 | ||||||
chr12:6516763
|
T | C | 6 | a0007c0014t0001g0292a0007c0014t0001g0293a0007c0014t0001g0296others(3): Show | 6 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-65T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516763 | ||||||
chr12:6517033
|
A | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0361a0001c0001t0002g0362others(2): Show | 6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1185+8A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 10/31 | chr12 | 6517033 | ||||||
chr12:6517066
|
C | T | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1185+41C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 10/31 | chr12 | 6517066 | ||||||
chr12:6517203
|
G | C | 312 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(309): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1186-162G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 10/31 | chr12 | 6517203 | ||||||
chr12:6517698
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1408+15C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 12/31 | chr12 | 6517698 | ||||||
chr12:6517994
|
T | C | 1 | a0004c0005t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1589+35T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6517994 | ||||||
chr12:6518120
|
T | G | 1 | a0002c0002t0001g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1589+161T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518120 | ||||||
chr12:6518190
|
G | A | 312 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(309): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1589+231G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518190 | ||||||
chr12:6518218
|
C | T | 1 | a0002c0002t0001g0010 | 2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1589+259C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518218 | ||||||
chr12:6518402
|
A | G | 1 | a0001c0001t0002g0315 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1589+443A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518402 | ||||||
chr12:6518492
|
A | G | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1589+533A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518492 | ||||||
chr12:6518503
|
A | AGTTTTTT others(9): Show |
5 | a0001c0001t0006g0263a0001c0001t0006g0267a0001c0028t0009g0261others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+545_1589+560d others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518503 | |||||
chr12:6518504
|
G | GT | 23 | a0001c0009t0001g0197a0001c0009t0001g0198a0001c0009t0001g0215others(20): Show | 23 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589+575dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTT | 14 | a0001c0004t0004g0200a0001c0004t0004g0201a0001c0004t0004g0202others(11): Show | 14 | HG00558.hp1 HG01257.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1589+571_1589+575d others(7): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(2): Show |
25 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0289others(22): Show | 27 | HG00408.hp1 HG00741.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(3): Show |
31 | a0001c0001t0002g0006a0001c0001t0002g0019a0001c0001t0002g0297others(28): Show | 33 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(4): Show |
10 | a0001c0001t0002g0021a0001c0001t0002g0308a0001c0001t0002g0324others(7): Show | 11 | HG00733.hp2 HG01934.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(13): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(5): Show |
5 | a0001c0001t0002g0290a0001c0001t0002g0330a0001c0001t0002g0346others(2): Show | 5 | HG01069.hp2 HG01346.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(14): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(6): Show |
3 | a0001c0001t0002g0325a0001c0001t0002g0362a0001c0001t0002g0381 | 3 | HG00639.hp1 HG01071.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(15): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(7): Show |
1 | a0001c0001t0002g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(8): Show |
2 | a0001c0001t0003g0384a0001c0001t0003g0397 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(17): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(9): Show |
1 | a0001c0001t0003g0339 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(10): Show |
1 | a0001c0001t0003g0375 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(11): Show |
3 | a0001c0001t0002g0353a0001c0001t0002g0354a0001c0001t0002g0388 | 3 | HG01884.hp1 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(12): Show |
1 | a0001c0001t0002g0355 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1589+550_1589+551i others(21): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(13): Show |
3 | a0001c0001t0002g0352a0001c0001t0002g0364a0001c0001t0002g0383 | 3 | HG01109.hp2 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(22): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(17): Show |
2 | a0001c0001t0002g0351a0001c0001t0003g0344 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(26): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(19): Show |
2 | a0001c0001t0007g0335a0001c0001t0007g0374 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(28): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(21): Show |
2 | a0001c0001t0007g0380a0001c0001t0015g0382 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(30): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(22): Show |
2 | a0001c0001t0002g0347a0001c0001t0002g0349 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(31): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(25): Show |
1 | a0001c0001t0002g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(27): Show |
2 | a0001c0001t0002g0304a0001c0001t0002g0348 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(36): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(34): Show |
2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(43): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(35): Show |
3 | a0001c0001t0002g0282a0001c0001t0002g0287a0001c0001t0002g0288 | 3 | HG02145.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(44): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(39): Show |
1 | a0001c0001t0002g0283 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(48): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTGT others(41): Show |
1 | a0001c0001t0002g0284 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1589+550_1589+551i others(50): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTT | 11 | a0001c0004t0004g0191a0001c0004t0004g0194a0001c0004t0004g0205others(8): Show | 11 | HG01243.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1589+570_1589+575d others(8): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT | 9 | a0001c0004t0004g0192a0001c0004t0004g0207a0001c0004t0004g0210others(6): Show | 9 | HG01358.hp2 HG01361.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1589+569_1589+575d others(9): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(2): Show |
11 | a0001c0001t0002g0371a0001c0031t0001g0189a0004c0005t0001g0015others(8): Show | 12 | HG00323.hp1 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1589+567_1589+575d others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(3): Show |
10 | a0001c0001t0002g0307a0001c0004t0001g0012a0001c0004t0001g0190others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1589+566_1589+575d others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(4): Show |
5 | a0001c0007t0012g0281a0003c0003t0003g0035a0003c0003t0003g0070others(2): Show | 5 | HG01255.hp1 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+565_1589+575d others(13): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(5): Show |
1 | a0007c0014t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1589+564_1589+575d others(14): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(10): Show |
3 | a0001c0001t0006g0264a0001c0001t0006g0266a0001c0026t0006g0268 | 3 | HG03490.hp2 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1589+557_1589+558i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0006g0265 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1589+557_1589+558i others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(6): Show |
5 | a0003c0015t0003g0084a0003c0015t0003g0085a0004c0005t0001g0241others(2): Show | 5 | HG01346.hp2 HG01891.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+563_1589+575d others(15): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(7): Show |
1 | a0003c0003t0003g0025 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1589+562_1589+575d others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0006g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1589+560_1589+561i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(9): Show |
1 | a0003c0003t0003g0065 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1589+560_1589+575d others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(10): Show |
11 | a0003c0003t0003g0001a0003c0003t0003g0026a0003c0003t0003g0043others(8): Show | 13 | HG00408.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1589+559_1589+575d others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(11): Show |
16 | a0001c0001t0002g0387a0003c0003t0003g0008a0003c0003t0003g0027others(13): Show | 17 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1589+558_1589+575d others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(12): Show |
14 | a0003c0003t0003g0029a0003c0003t0003g0030a0003c0003t0003g0033others(11): Show | 14 | HG02056.hp2 HG03669.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.1589+557_1589+575d others(21): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(13): Show |
1 | a0005c0006t0003g0130 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1589+556_1589+575d others(22): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(14): Show |
3 | a0005c0006t0003g0123a0005c0006t0003g0141a0005c0006t0003g0150 | 3 | NA18960.hp1 NA18978.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1589+555_1589+575d others(23): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(15): Show |
6 | a0003c0003t0003g0038a0003c0003t0003g0067a0003c0003t0003g0099others(3): Show | 6 | HG02129.hp1 HG02155.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+554_1589+575d others(24): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(16): Show |
5 | a0003c0003t0003g0007a0003c0003t0003g0032a0003c0003t0003g0053others(2): Show | 6 | NA18948.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+553_1589+575d others(25): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(17): Show |
5 | a0003c0003t0003g0048a0003c0003t0003g0049a0003c0003t0003g0052others(2): Show | 5 | HG00621.hp1 HG02040.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+552_1589+575d others(26): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(18): Show |
1 | a0003c0003t0003g0050 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1589+551_1589+575d others(27): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(21): Show |
2 | a0003c0003t0003g0094a0003c0003t0013g0097 | 2 | HG00323.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1589+548_1589+575d others(30): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(22): Show |
1 | a0006c0008t0003g0002 | 3 | HG01106.hp1 HG01109.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1589+547_1589+575d others(31): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(23): Show |
2 | a0003c0003t0003g0098a0006c0008t0003g0051 | 2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1589+546_1589+575d others(32): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
G | GTTTTTTT others(25): Show |
1 | a0003c0003t0003g0024 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1589+575_1589+576i others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
GTT | G | 10 | a0001c0007t0005g0016a0001c0007t0005g0273a0001c0007t0005g0274others(7): Show | 11 | HG00423.hp2 HG01070.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1589+574_1589+575d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
GTTT | G | 8 | a0001c0001t0002g0331a0001c0001t0002g0337a0001c0001t0002g0341others(5): Show | 8 | HG01099.hp1 HG02080.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589+573_1589+575d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
GTTTT | G | 12 | a0001c0004t0004g0005a0001c0004t0004g0014a0001c0004t0004g0199others(9): Show | 15 | HG00544.hp2 NA18941.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.1589+572_1589+575d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518504
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0004t0004g0195 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1589+566_1589+575d others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | |||||
chr12:6518505
|
T | TTTTTTTT others(8): Show |
1 | a0009c0012t0006g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1589+560_1589+561i others(17): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518505 | |||||
chr12:6518508
|
T | TTTGTTTT others(3): Show |
2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+551_1589+552i others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518508 | |||||
chr12:6518508
|
T | TTTTTTTT others(3): Show |
1 | a0001c0004t0010g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1589+558_1589+559i others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518508 | |||||
chr12:6518511
|
T | G | 1 | a0017c0024t0001g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1589+552T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518511 | ||||||
chr12:6518513
|
T | G | 5 | a0001c0001t0002g0331a0001c0001t0002g0337a0001c0001t0002g0341others(2): Show | 5 | HG02080.hp2 HG02293.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+554T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518513 | ||||||
chr12:6518515
|
T | G | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+556T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518515 | ||||||
chr12:6518517
|
T | TTTTTTTT others(10): Show |
1 | a0003c0010t0003g0217 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1589+574_1589+575i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518517 | |||||
chr12:6518519
|
T | G | 2 | a0001c0001t0002g0345a0001c0001t0002g0377 | 2 | NA18990.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1589+560T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518519 | ||||||
chr12:6518525
|
T | G | 1 | a0001c0004t0010g0271 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1589+566T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518525 | ||||||
chr12:6518533
|
T | TTTTTTTT others(7): Show |
1 | a0004c0005t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1589+575_1589+576i others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518533 | |||||
chr12:6518630
|
C | T | 3 | a0001c0001t0002g0322a0010c0017t0003g0056a0010c0017t0003g0062 | 3 | HG02071.hp2 HG02080.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1589+671C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518630 | ||||||
chr12:6518723
|
A | G | 312 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(309): Show | 330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1589+764A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518723 | ||||||
chr12:6518809
|
C | T | 5 | a0001c0001t0002g0297a0001c0001t0002g0313a0001c0001t0002g0360others(2): Show | 5 | HG00140.hp1 HG01081.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+850C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518809 | ||||||
chr12:6518833
|
T | C | 1 | a0002c0002t0001g0105 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1589+874T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518833 | ||||||
chr12:6518949
|
G | A | 3 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240 | 3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1589+990G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518949 | ||||||
chr12:6518967
|
C | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0361a0001c0001t0002g0362others(2): Show | 6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+1008C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518967 | ||||||
chr12:6518972
|
A | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0361a0001c0001t0002g0362others(2): Show | 6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+1013A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518972 | ||||||
chr12:6518982
|
T | C | 105 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(102): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1589+1023T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518982 | ||||||
chr12:6519029
|
GC | G | 5 | a0001c0004t0008g0224a0001c0004t0008g0225a0001c0004t0008g0226others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+1071delC | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519029 | ||||||
chr12:6519031
|
G | A | 1 | a0014c0027t0005g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1589+1072G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519031 | ||||||
chr12:6519033
|
C | A | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1589+1074C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519033 | ||||||
chr12:6519111
|
C | T | 1 | a0003c0010t0001g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1589+1152C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519111 | ||||||
chr12:6519133
|
G | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+1174G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519133 | ||||||
chr12:6519195
|
T | C | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589+1236T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519195 | ||||||
chr12:6519267
|
A | C | 3 | a0001c0001t0007g0335a0001c0001t0007g0374a0001c0001t0007g0380 | 3 | HG02258.hp1 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1589+1308A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519267 | ||||||
chr12:6519315
|
C | T | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+1356C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519315 | ||||||
chr12:6519382
|
A | G | 1 | a0007c0014t0001g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1589+1423A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519382 | ||||||
chr12:6519484
|
C | T | 1 | a0002c0002t0001g0105 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1590-1502C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519484 | ||||||
chr12:6519609
|
T | C | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1590-1377T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519609 | ||||||
chr12:6519947
|
G | C | 223 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(220): Show | 234 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1590-1039G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519947 | ||||||
chr12:6519954
|
T | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1590-1032T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519954 | ||||||
chr12:6520100
|
A | G | 313 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(310): Show | 331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1590-886A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520100 | ||||||
chr12:6520115
|
A | C | 1 | a0004c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1590-871A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520115 | ||||||
chr12:6520181
|
T | TA | 161 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(158): Show | 171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1590-794dupA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520181 | |||||
chr12:6520181
|
T | TAA | 34 | a0001c0001t0002g0290a0001c0001t0002g0372a0001c0001t0006g0267others(31): Show | 35 | HG00438.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1590-795_1590-794d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520181 | |||||
chr12:6520191
|
A | AT | 8 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240others(5): Show | 9 | HG00673.hp2 HG02523.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1590-795_1590-794i others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520191 | ||||||
chr12:6520192
|
AT | A | 8 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1590-793delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520192 | ||||||
chr12:6520193
|
T | A | 214 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(211): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1590-793T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520193 | ||||||
chr12:6520195
|
T | A | 32 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(29): Show | 32 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1590-791T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520195 | ||||||
chr12:6520265
|
A | G | 1 | a0003c0003t0003g0031 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1590-721A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520265 | ||||||
chr12:6520304
|
T | G | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1590-682T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520304 | ||||||
chr12:6520322
|
G | A | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1590-664G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520322 | ||||||
chr12:6520379
|
ACCACAGG others(15): Show |
A | 94 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(91): Show | 100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1590-589_1590-568d others(24): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520379 | |||||
chr12:6520389
|
CACACCAT others(59): Show |
C | 11 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(8): Show | 11 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1590-589_1590-524d others(68): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520389 | |||||
chr12:6520397
|
T | C | 9 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(6): Show | 9 | NA18945.hp2 NA18953.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.1590-589T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520397 | ||||||
chr12:6520439
|
A | G | 1 | a0003c0003t0003g0044 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1590-547A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520439 | ||||||
chr12:6520491
|
C | T | 1 | a0001c0004t0008g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1590-495C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520491 | ||||||
chr12:6520492
|
G | A | 1 | a0004c0005t0001g0241 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1590-494G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520492 | ||||||
chr12:6520670
|
T | A | 1 | a0002c0002t0001g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1590-316T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520670 | ||||||
chr12:6520717
|
C | G | 5 | a0007c0014t0001g0292a0007c0014t0001g0293a0007c0014t0001g0296others(2): Show | 5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1590-269C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520717 | ||||||
chr12:6520918
|
A | C | 1 | a0002c0002t0001g0172 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1590-68A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520918 | ||||||
chr12:6521312
|
C | T | 1 | a0001c0001t0002g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1714+202C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521312 | ||||||
chr12:6521313
|
G | A | 3 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240 | 3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1714+203G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521313 | ||||||
chr12:6521461
|
T | C | 105 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(102): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1715-337T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521461 | ||||||
chr12:6521570
|
C | A | 6 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1715-228C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521570 | ||||||
chr12:6521584
|
A | AG | 318 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(315): Show | 336 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1715-213dupG | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr12 | 6521584 | |||||
chr12:6521692
|
AAAG | A | 4 | a0003c0003t0003g0023a0003c0003t0003g0065a0003c0003t0003g0099others(1): Show | 4 | HG02738.hp1 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715-99_1715-97del others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr12 | 6521692 | |||||
chr12:6521748
|
C | A | 1 | a0007c0014t0001g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1715-50C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521748 | ||||||
chr12:6521748
|
C | T | 1 | a0001c0001t0002g0337 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1715-50C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521748 | ||||||
chr12:6521750
|
C | T | 1 | a0001c0033t0004g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1715-48C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521750 | ||||||
chr12:6522051
|
C | G | 1 | a0002c0021t0001g0117 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1954+14C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522051 | ||||||
chr12:6522142
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1954+105C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522142 | ||||||
chr12:6522183
|
G | A | 34 | a0003c0003t0003g0001a0003c0003t0003g0008a0003c0003t0003g0028others(31): Show | 39 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1954+146G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522183 | ||||||
chr12:6522229
|
C | T | 1 | a0003c0003t0003g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1954+192C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522229 | ||||||
chr12:6522238
|
ATCTTGGA others(2): Show |
A | 2 | a0001c0001t0002g0020a0001c0001t0002g0358 | 3 | HG00741.hp1 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1954+206_1954+214d others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr12 | 6522238 | |||||
chr12:6522344
|
T | C | 1 | a0001c0001t0002g0312 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1954+307T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522344 | ||||||
chr12:6522457
|
G | A | 318 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(315): Show | 336 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1955-371G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522457 | ||||||
chr12:6522559
|
G | A | 118 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(115): Show | 123 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1955-269G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522559 | ||||||
chr12:6522568
|
G | A | 5 | a0001c0004t0008g0224a0001c0004t0008g0225a0001c0004t0008g0226others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1955-260G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522568 | ||||||
chr12:6522722
|
G | A | 104 | a0001c0001t0006g0262a0001c0001t0006g0263a0001c0001t0006g0264others(101): Show | 110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1955-106G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522722 | ||||||
chr12:6523054
|
A | C | 1 | a0001c0001t0002g0379 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2129+52A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 16/31 | chr12 | 6523054 | ||||||
chr12:6523095
|
A | C | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2129+93A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 16/31 | chr12 | 6523095 | ||||||
chr12:6523238
|
C | T | 1 | a0014c0027t0005g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2130-24C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 16/31 | chr12 | 6523238 | ||||||
chr12:6523398
|
G | GT | 8 | a0001c0009t0001g0198a0001c0009t0001g0215a0002c0002t0001g0105others(5): Show | 8 | HG01123.hp1 HG02056.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.2214+69dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | |||||
chr12:6523398
|
G | GTT | 18 | a0001c0001t0002g0304a0001c0004t0004g0234a0004c0005t0001g0015others(15): Show | 19 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2214+68_2214+69dup others(2): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | |||||
chr12:6523398
|
G | GTTT | 52 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(49): Show | 57 | HG00558.hp1 HG01168.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.2214+67_2214+69dup others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | |||||
chr12:6523398
|
G | GTTTT | 204 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(201): Show | 215 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.2214+66_2214+69dup others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | |||||
chr12:6523398
|
G | GTTTTT | 36 | a0001c0001t0002g0286a0001c0001t0002g0290a0001c0001t0002g0316others(33): Show | 37 | HG00621.hp1 HG01123.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2214+65_2214+69dup others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | |||||
chr12:6523484
|
G | A | 1 | a0003c0003t0003g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2214+138G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523484 | ||||||
chr12:6523643
|
C | T | 1 | a0004c0005t0001g0244 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2214+297C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523643 | ||||||
chr12:6523650
|
A | G | 4 | a0002c0002t0001g0103a0002c0002t0001g0173a0002c0002t0001g0180others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2214+304A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523650 | ||||||
chr12:6523725
|
T | G | 1 | a0002c0002t0001g0147 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2214+379T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523725 | ||||||
chr12:6523759
|
A | G | 37 | a0001c0001t0002g0304a0001c0004t0001g0012a0001c0004t0001g0190others(34): Show | 39 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2214+413A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523759 | ||||||
chr12:6523803
|
C | A | 94 | a0003c0003t0003g0001a0003c0003t0003g0007a0003c0003t0003g0008others(91): Show | 100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2214+457C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523803 | ||||||
chr12:6523882
|
G | A | 3 | a0002c0002t0001g0174a0002c0002t0001g0181a0018c0020t0001g0146 | 3 | HG00438.hp1 HG02523.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2214+536G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523882 | ||||||
chr12:6524066
|
G | A | 8 | a0003c0003t0003g0030a0003c0003t0003g0031a0003c0003t0003g0034others(5): Show | 8 | NA18948.hp1 NA18954.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.2214+720G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524066 | ||||||
chr12:6524345
|
A | G | 1 | a0001c0004t0004g0207 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2214+999A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524345 | ||||||
chr12:6524369
|
G | A | 5 | a0001c0009t0001g0196a0001c0009t0001g0197a0001c0009t0001g0198others(2): Show | 5 | NA18950.hp1 NA18999.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.2214+1023G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524369 | ||||||
chr12:6524394
|
A | G | 1 | a0002c0002t0001g0164 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2214+1048A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524394 | ||||||
chr12:6524414
|
C | T | 11 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(8): Show | 12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2214+1068C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524414 | ||||||
chr12:6524455
|
T | C | 36 | a0001c0001t0002g0304a0001c0004t0001g0012a0001c0004t0001g0190others(33): Show | 39 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2214+1109T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524455 | ||||||
chr12:6524648
|
C | CA | 140 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(137): Show | 146 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.2215-912dupA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6524648 | |||||
chr12:6524648
|
C | CAA | 14 | a0001c0001t0002g0305a0001c0001t0002g0309a0001c0001t0002g0317others(11): Show | 14 | HG01168.hp2 HG01433.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.2215-913_2215-912d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6524648 | |||||
chr12:6524648
|
CA | C | 19 | a0001c0004t0004g0206a0001c0004t0008g0224a0001c0004t0008g0226others(16): Show | 20 | HG00323.hp1 HG01943.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2215-912delA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6524648 | |||||
chr12:6524709
|
A | C | 4 | a0001c0001t0002g0331a0001c0001t0002g0337a0001c0001t0002g0341others(1): Show | 4 | HG02080.hp2 HG02293.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.2215-874A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524709 | ||||||
chr12:6524817
|
C | T | 3 | a0001c0011t0001g0022a0001c0011t0001g0400a0001c0011t0001g0401 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2215-766C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524817 | ||||||
chr12:6524936
|
T | G | 1 | a0001c0004t0004g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2215-647T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524936 | ||||||
chr12:6525286
|
C | T | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2215-297C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6525286 | ||||||
chr12:6525323
|
C | G | 13 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(10): Show | 14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2215-260C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6525323 | ||||||
chr12:6525526
|
A | C | 2 | a0001c0004t0011g0403a0001c0004t0011g0404 | 2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2215-57A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6525526 | ||||||
chr12:6525818
|
G | T | 1 | a0003c0003t0003g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2348+102G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6525818 | ||||||
chr12:6525848
|
T | C | 1 | a0001c0004t0004g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2348+132T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6525848 | ||||||
chr12:6525950
|
A | G | 1 | a0001c0004t0004g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2349-118A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6525950 | ||||||
chr12:6526000
|
A | G | 39 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(36): Show | 43 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.2349-68A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6526000 | ||||||
chr12:6526039
|
C | T | 4 | a0001c0001t0006g0264a0001c0001t0006g0265a0001c0001t0006g0266others(1): Show | 4 | HG03490.hp2 HG03492.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2349-29C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6526039 | ||||||
chr12:6526208
|
G | A | 17 | a0004c0005t0001g0015a0004c0005t0001g0241a0004c0005t0001g0242others(14): Show | 18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.2481+8G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/31 | chr12 | 6526208 | ||||||
chr12:6526242
|
C | T | 2 | a0001c0001t0002g0341a0001c0001t0007g0336 | 2 | NA19085.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2481+42C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/31 | chr12 | 6526242 | ||||||
chr12:6526266
|
A | G | 1 | a0001c0001t0002g0351 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482-21A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/31 | chr12 | 6526266 | ||||||
chr12:6526401
|
A | T | 319 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(316): Show | 337 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.2566+30A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 20/31 | chr12 | 6526401 | ||||||
chr12:6526629
|
G | C | 11 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(8): Show | 12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2734+14G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 21/31 | chr12 | 6526629 | ||||||
chr12:6526643
|
G | A | 1 | a0003c0003t0003g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2734+28G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 21/31 | chr12 | 6526643 | ||||||
chr12:6526727
|
G | A | 1 | a0004c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2734+112G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 21/31 | chr12 | 6526727 | ||||||
chr12:6527135
|
G | A | 4 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(1): Show | 4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2907+72G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527135 | ||||||
chr12:6527219
|
C | T | 1 | a0001c0004t0004g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2907+156C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527219 | ||||||
chr12:6527226
|
G | A | 51 | a0001c0004t0004g0005a0001c0004t0004g0013a0001c0004t0004g0014others(48): Show | 55 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(52): Show |
intron_variant | MODIFIER | c.2907+163G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527226 | ||||||
chr12:6527244
|
C | A | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2907+181C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527244 | ||||||
chr12:6527549
|
A | T | 2 | a0010c0017t0003g0056a0010c0017t0003g0062 | 2 | HG02080.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2908-228A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527549 | ||||||
chr12:6527572
|
G | A | 1 | a0001c0004t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2908-205G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527572 | ||||||
chr12:6527702
|
T | C | 1 | a0016c0023t0001g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2908-75T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527702 | ||||||
chr12:6527733
|
T | C | 1 | a0003c0003t0003g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2908-44T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527733 | ||||||
chr12:6528108
|
G | A | 1 | a0001c0001t0002g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3143+17G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 24/31 | chr12 | 6528108 | ||||||
chr12:6528110
|
A | AC | 21 | a0001c0001t0002g0318a0001c0001t0002g0322a0001c0001t0002g0337others(18): Show | 21 | HG01192.hp1 HG01243.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.3143+24dupC | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr12 | 6528110 | |||||
chr12:6528114
|
C | A | 1 | a0007c0014t0001g0292 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3143+23C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 24/31 | chr12 | 6528114 | ||||||
chr12:6528434
|
G | A | 1 | a0002c0002t0001g0164 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3299+106G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 25/31 | chr12 | 6528434 | ||||||
chr12:6528586
|
T | C | 1 | a0001c0009t0001g0340 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3300-93T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 25/31 | chr12 | 6528586 | ||||||
chr12:6528936
|
G | C | 1 | a0003c0003t0003g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3478-9G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 26/31 | chr12 | 6528936 | ||||||
chr12:6529081
|
C | T | 2 | a0001c0007t0012g0281a0001c0007t0012g0402 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3572+42C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529081 | ||||||
chr12:6529184
|
C | T | 108 | a0001c0031t0001g0189a0003c0003t0003g0001a0003c0003t0003g0007others(105): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.3572+145C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529184 | ||||||
chr12:6529383
|
G | T | 4 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3573-130G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529383 | ||||||
chr12:6529393
|
CAG | C | 13 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272others(10): Show | 14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3573-119_3573-118d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529393 | ||||||
chr12:6529450
|
G | A | 1 | a0002c0002t0001g0148 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3573-63G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529450 | ||||||
chr12:6529481
|
C | T | 1 | a0002c0018t0001g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3573-32C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529481 | ||||||
chr12:6529500
|
C | T | 129 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(126): Show | 134 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.3573-13C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529500 | ||||||
chr12:6529727
|
T | C | 20 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0284others(17): Show | 20 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.3654-48T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 28/31 | chr12 | 6529727 | ||||||
chr12:6529736
|
G | A | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3654-39G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 28/31 | chr12 | 6529736 | ||||||
chr12:6530056
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3837+98G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530056 | ||||||
chr12:6530121
|
T | TCCAGTTC others(334): Show |
1 | a0002c0002t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3837+177_3837+178i others(343): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr12 | 6530121 | |||||
chr12:6530125
|
G | A | 3 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012 | 3 | HG02886.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3837+167G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530125 | ||||||
chr12:6530224
|
G | C | 1 | a0002c0002t0001g0153 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3837+266G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530224 | ||||||
chr12:6530271
|
C | T | 1 | a0003c0003t0003g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3837+313C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530271 | ||||||
chr12:6530272
|
T | C | 1 | a0003c0003t0003g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3837+314T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530272 | ||||||
chr12:6530330
|
T | G | 1 | a0002c0002t0001g0164 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3838-361T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530330 | ||||||
chr12:6530440
|
T | C | 4 | a0001c0004t0009g0238a0001c0004t0009g0239a0001c0004t0009g0240others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3838-251T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530440 | ||||||
chr12:6530544
|
T | C | 1 | a0002c0002t0001g0169 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3838-147T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530544 | ||||||
chr12:6530595
|
T | G | 1 | a0001c0007t0012g0402 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3838-96T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530595 | ||||||
chr12:6530873
|
G | T | 3 | a0001c0004t0010g0270a0001c0004t0010g0271a0001c0004t0010g0272 | 3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3965-48G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 30/31 | chr12 | 6530873 | ||||||
chr12:6531097
|
C | A | 1 | a0001c0009t0001g0198 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4120+21C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531097 | ||||||
chr12:6531101
|
G | A | 114 | a0001c0004t0001g0012a0001c0004t0001g0190a0001c0004t0011g0012others(111): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.4120+25G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531101 | ||||||
chr12:6531212
|
G | A | 11 | a0001c0007t0004g0269a0001c0007t0005g0016a0001c0007t0005g0273others(8): Show | 12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.4121-115G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531212 | ||||||
chr12:6531277
|
C | T | 2 | a0001c0001t0002g0297a0002c0022t0002g0144 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4121-50C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531277 |