geneid | 9436 |
---|---|
ensemblid | ENSG00000096264.14 |
hgncid | 6732 |
symbol | NCR2 |
name | natural cytotoxicity triggering receptor 2 |
refseq_nuc | NM_004828.4 |
refseq_prot | NP_004819.2 |
ensembl_nuc | ENST00000373089.10 |
ensembl_prot | ENSP00000362181.5 |
mane_status | MANE Select |
chr | chr6 |
start | 41335608 |
end | 41350889 |
strand | + |
ver | v1.2 |
region | chr6:41335608-41350889 |
region5000 | chr6:41330608-41355889 |
regionname0 | NCR2_chr6_41335608_41350889 |
regionname5000 | NCR2_chr6_41330608_41355889 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 276 | 203 | 7 | 53 | 98 | 13 | 32 | 70 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0002 | 1/1 | 276 | 90 | 41 | 11 | 26 | 0 | 10 | 19 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0003 | 0/0 | 276 | 70 | 5 | 4 | 57 | 2 | 2 | 50 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0004 | 0/0 | 276 | 22 | 20 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0005 | 0/0 | 276 | 12 | 4 | 4 | 0 | 2 | 2 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0006 | 0/0 | 276 | 11 | 7 | 0 | 2 | 1 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0007 | 0/0 | 276 | 8 | 4 | 2 | 2 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0008 | 0/0 | 276 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0009 | 0/0 | 276 | 5 | 1 | 1 | 2 | 0 | 1 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0010 | 0/0 | 276 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0011 | 0/0 | 276 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0012 | 0/0 | 276 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0013 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0014 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0015 | 0/0 | 276 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 831 | 203 | 7 | 53 | 98 | 13 | 32 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0002 | 1/1 | 831 | 88 | 39 | 11 | 26 | 0 | 10 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0003 | 0/0 | 831 | 69 | 5 | 4 | 56 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0004 | 0/0 | 831 | 22 | 20 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0005 | 0/0 | 831 | 11 | 7 | 0 | 2 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0006 | 0/0 | 831 | 9 | 2 | 3 | 0 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0007 | 0/0 | 831 | 8 | 4 | 2 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0008 | 0/0 | 831 | 6 | 6 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0009 | 0/0 | 831 | 5 | 1 | 1 | 2 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0010 | 0/0 | 831 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0011 | 0/0 | 831 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0012 | 0/0 | 831 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0013 | 0/0 | 831 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0014 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0015 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0016 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0017 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0018 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
c0019 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 295 | 321 | 43 | 62 | 166 | 15 | 35 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
t0002 | 1/1 | 295 | 112 | 53 | 16 | 27 | 2 | 12 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
t0003 | 0/0 | 295 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
t0004 | 0/0 | 295 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
t0005 | 0/0 | 295 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
t0006 | 0/0 | 295 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 46 | 1 | 9 | 28 | 3 | 5 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0002 | 0/0 | 38 | 2 | 4 | 23 | 2 | 7 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0003 | 0/0 | 36 | 1 | 3 | 29 | 2 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0004 | 0/0 | 32 | 2 | 12 | 10 | 0 | 8 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0005 | 1/1 | 24 | 1 | 5 | 16 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0006 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0007 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0008 | 0/0 | 9 | 2 | 4 | 0 | 1 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0013 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 831 | 203 | 7 | 53 | 98 | 13 | 32 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0002c0002 | 1/1 | 831 | 88 | 39 | 11 | 26 | 0 | 10 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0002c0013 | 0/0 | 831 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0003c0003 | 0/0 | 831 | 69 | 5 | 4 | 56 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0003c0017 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0004c0004 | 0/0 | 831 | 22 | 20 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0005c0006 | 0/0 | 831 | 9 | 2 | 3 | 0 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0005c0011 | 0/0 | 831 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0006c0005 | 0/0 | 831 | 11 | 7 | 0 | 2 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0007c0007 | 0/0 | 831 | 8 | 4 | 2 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0008c0008 | 0/0 | 831 | 6 | 6 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0009c0009 | 0/0 | 831 | 5 | 1 | 1 | 2 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0010c0010 | 0/0 | 831 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0011c0012 | 0/0 | 831 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0012c0018 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0012c0019 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0013c0014 | 0/0 | 831 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0014c0015 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0015c0016 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1125 | 201 | 7 | 53 | 98 | 12 | 31 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0001c0001t0004 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0001c0001t0006 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0002c0002t0002 | 1/1 | 1125 | 86 | 37 | 11 | 26 | 0 | 10 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0002c0002t0003 | 0/0 | 1125 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0002c0013t0002 | 0/0 | 1125 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0003c0003t0001 | 0/0 | 1125 | 68 | 5 | 4 | 55 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0003c0003t0005 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0003c0017t0001 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0004c0004t0001 | 0/0 | 1125 | 22 | 20 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0005c0006t0002 | 0/0 | 1125 | 9 | 2 | 3 | 0 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0005c0011t0002 | 0/0 | 1125 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0006c0005t0001 | 0/0 | 1125 | 11 | 7 | 0 | 2 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0007c0007t0001 | 0/0 | 1125 | 8 | 4 | 2 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0008c0008t0002 | 0/0 | 1125 | 6 | 6 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0009c0009t0001 | 0/0 | 1125 | 2 | 0 | 0 | 1 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0009c0009t0002 | 0/0 | 1125 | 3 | 1 | 1 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0010c0010t0001 | 0/0 | 1125 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0011c0012t0001 | 0/0 | 1125 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0012c0018t0002 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0012c0019t0002 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0013c0014t0001 | 0/0 | 1125 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0014c0015t0001 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
a0015c0016t0002 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | copy fasta | chr6 | 41330608 | 41355889 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 43 | 1 | 8 | 27 | 3 | 4 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0002 | 0/0 | 38 | 2 | 4 | 23 | 2 | 7 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0004 | 0/0 | 32 | 2 | 12 | 10 | 0 | 8 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0007 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0008 | 0/0 | 9 | 2 | 4 | 0 | 1 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0005 | 1/1 | 24 | 1 | 5 | 16 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0002t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0002c0013t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0003 | 0/0 | 34 | 1 | 3 | 27 | 2 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0003t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0003c0017t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0006 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0004c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0005c0011t0002g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0006c0005t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0006c0005t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0006c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0006c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0006c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0006c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0007c0007t0001g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0007c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0007c0007t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0007c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0008c0008t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0008c0008t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0008c0008t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0008c0008t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0009c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0009c0009t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0009c0009t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0009c0009t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0009c0009t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0010c0010t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0010c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0011c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0011c0012t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0012c0018t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0012c0019t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0013c0014t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0014c0015t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
a0015c0016t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00140 | hp1 | a0005 | c0006 | t0002 | g0039 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00140 | hp2 | a0005 | c0006 | t0002 | g0071 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00423 | hp2 | a0010 | c0010 | t0001 | g0019 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00438 | hp1 | a0006 | c0005 | t0001 | g0109 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00642 | hp1 | a0007 | c0007 | t0001 | g0095 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00738 | hp2 | a0005 | c0006 | t0002 | g0035 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00741 | hp1 | a0005 | c0011 | t0002 | g0025 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01081 | hp1 | a0009 | c0009 | t0002 | g0150 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0057 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01175 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01192 | hp2 | a0005 | c0006 | t0002 | g0035 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01255 | hp1 | a0007 | c0007 | t0001 | g0012 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0051 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0045 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01517 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01934 | hp2 | a0004 | c0004 | t0001 | g0065 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02004 | hp1 | a0005 | c0006 | t0002 | g0074 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02004 | hp2 | a0013 | c0014 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0055 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02055 | hp2 | a0002 | c0002 | t0003 | g0048 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02071 | hp2 | a0007 | c0007 | t0001 | g0122 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02129 | hp2 | a0006 | c0005 | t0001 | g0101 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02145 | hp1 | a0005 | c0011 | t0002 | g0025 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02257 | hp1 | a0006 | c0005 | t0001 | g0016 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02258 | hp2 | a0008 | c0008 | t0002 | g0043 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02280 | hp1 | a0002 | c0013 | t0002 | g0015 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02451 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02572 | hp1 | a0008 | c0008 | t0002 | g0098 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0048 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02615 | hp2 | a0003 | c0003 | t0001 | g0070 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02622 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02630 | hp1 | a0004 | c0004 | t0001 | g0068 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02723 | hp1 | a0006 | c0005 | t0001 | g0016 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02735 | hp2 | a0005 | c0006 | t0002 | g0090 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02809 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0099 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02922 | hp1 | a0007 | c0007 | t0001 | g0012 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02922 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02965 | hp1 | a0008 | c0008 | t0002 | g0042 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02970 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02970 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03017 | hp1 | a0006 | c0005 | t0001 | g0108 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03041 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03098 | hp1 | a0015 | c0016 | t0002 | g0149 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03098 | hp2 | a0004 | c0004 | t0001 | g0056 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03130 | hp2 | a0007 | c0007 | t0001 | g0012 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03139 | hp1 | a0005 | c0011 | t0002 | g0025 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03139 | hp2 | a0003 | c0003 | t0001 | g0051 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03195 | hp1 | a0006 | c0005 | t0001 | g0024 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03195 | hp2 | a0002 | c0013 | t0002 | g0015 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03209 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03225 | hp1 | a0008 | c0008 | t0002 | g0042 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03453 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0082 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0154 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03491 | hp1 | a0009 | c0009 | t0001 | g0094 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03516 | hp2 | a0008 | c0008 | t0002 | g0043 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03540 | hp2 | a0004 | c0004 | t0001 | g0059 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03579 | hp1 | a0006 | c0005 | t0001 | g0024 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03579 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0018 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0023 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0023 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0001 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0089 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG04228 | hp2 | a0005 | c0006 | t0002 | g0039 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18522 | hp2 | a0006 | c0005 | t0001 | g0016 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18906 | hp1 | a0004 | c0004 | t0001 | g0066 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18946 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18952 | hp1 | a0003 | c0003 | t0005 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18952 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18956 | hp1 | a0007 | c0007 | t0001 | g0125 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18959 | hp1 | a0011 | c0012 | t0001 | g0052 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18963 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18973 | hp1 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18985 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18992 | hp2 | a0003 | c0017 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18993 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18994 | hp1 | a0011 | c0012 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18995 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19000 | hp1 | a0009 | c0009 | t0001 | g0102 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19004 | hp2 | a0014 | c0015 | t0001 | g0130 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19005 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19006 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19006 | hp2 | a0009 | c0009 | t0002 | g0146 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19010 | hp1 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19030 | hp1 | a0009 | c0009 | t0002 | g0148 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19043 | hp1 | a0005 | c0006 | t0002 | g0093 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19043 | hp2 | a0007 | c0007 | t0001 | g0012 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19054 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19057 | hp1 | a0010 | c0010 | t0001 | g0058 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19063 | hp2 | a0010 | c0010 | t0001 | g0019 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19065 | hp2 | a0010 | c0010 | t0001 | g0019 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19067 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19070 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19074 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19076 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19078 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19081 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19082 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19090 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19240 | hp1 | a0007 | c0007 | t0001 | g0012 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA19240 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | ASW | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20805 | hp2 | a0006 | c0005 | t0001 | g0141 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02109 | hp1 | a0006 | c0005 | t0001 | g0024 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02486 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02559 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG02559 | hp2 | a0012 | c0019 | t0002 | g0084 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03471 | hp1 | a0008 | c0008 | t0002 | g0152 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG03471 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG06807 | hp1 | a0006 | c0005 | t0001 | g0016 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
HG06807 | hp2 | a0005 | c0006 | t0002 | g0083 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
NA21309 | hp2 | a0012 | c0018 | t0002 | g0085 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0005 | REF | REF | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0005 | REF | REF | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41336093
|
A | G | 1 | a0012 | 2 | HG02559.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.59A>G | p.Gln20Arg | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 328/1125 | 59/831 | 20/276 | chr6 | 41336093 | ||
chr6:41336125
|
G | A | 1 | a0008 | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
missense_variant | MODERATE | c.91G>A | p.Val31Met | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 360/1125 | 91/831 | 31/276 | chr6 | 41336125 | ||
chr6:41336257
|
A | G | 3 | a0003a0004a0010 | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
missense_variant | MODERATE | c.223A>G | p.Met75Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 492/1125 | 223/831 | 75/276 | chr6 | 41336257 | ||
chr6:41336401
|
G | A | 1 | a0013 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.367G>A | p.Val123Ile | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 636/1125 | 367/831 | 123/276 | chr6 | 41336401 | ||
chr6:41341814
|
T | C | 7 | a0001a0006a0007others(4): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
missense_variant | MODERATE | c.415T>C | p.Ser139Pro | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/5 | 684/1125 | 415/831 | 139/276 | chr6 | 41341814 | ||
chr6:41341887
|
G | C | 1 | a0008 | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
missense_variant | MODERATE | c.488G>C | p.Arg163Thr | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/5 | 757/1125 | 488/831 | 163/276 | chr6 | 41341887 | ||
chr6:41342050
|
C | T | 2 | a0011a0014 | 3 | NA18959.hp1 NA18994.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.545C>T | p.Thr182Met | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 814/1125 | 545/831 | 182/276 | chr6 | 41342050 | ||
chr6:41342109
|
G | A | 1 | a0015 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.604G>A | p.Val202Ile | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 873/1125 | 604/831 | 202/276 | chr6 | 41342109 | ||
chr6:41350686
|
T | A | 3 | a0003a0007a0009 | 83 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
missense_variant | MODERATE | c.653T>A | p.Ile218Lys | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 922/1125 | 653/831 | 218/276 | chr6 | 41350686 | ||
chr6:41350700
|
A | G | 10 | a0001a0003a0004others(7): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
missense_variant | MODERATE | c.667A>G | p.Met223Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 936/1125 | 667/831 | 223/276 | chr6 | 41350700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41342087
|
G | A | 1 | a0003c0017 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.582G>A | p.Val194Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 851/1125 | 582/831 | 194/276 | chr6 | 41342087 | ||
chr6:41342093
|
G | A | 1 | a0002c0013 | 2 | HG02280.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.588G>A | p.Val196Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 857/1125 | 588/831 | 196/276 | chr6 | 41342093 | ||
chr6:41350840
|
T | C | 1 | a0005c0011 | 3 | HG00741.hp1 HG02145.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.807T>C | p.Asp269Asp | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 1076/1125 | 807/831 | 269/276 | chr6 | 41350840 | ||
chr6:41350849
|
T | C | 1 | a0012c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.816T>C | p.Asp272Asp | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 1085/1125 | 816/831 | 272/276 | chr6 | 41350849 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41335782
|
G | A | 1 | a0001c0001t0004 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 95 | chr6 | 41335782 | |||||
chr6:41335833
|
T | C | 1 | a0003c0003t0005 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 44 | chr6 | 41335833 | |||||
chr6:41335854
|
T | C | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(11): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 23 | chr6 | 41335854 | |||||
chr6:41335854
|
T | G | 1 | a0002c0002t0003 | 2 | HG02055.hp2 HG02572.hp2 |
5_prime_UTR_variant | MODIFIER | c.-23T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 23 | chr6 | 41335854 | |||||
chr6:41335867
|
A | C | 1 | a0001c0001t0006 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 10 | chr6 | 41335867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41335994
|
G | A | 1 | a0011c0012t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.52+66G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41335994 | ||||||
chr6:41336046
|
G | A | 30 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(27): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.53-41G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41336046 | ||||||
chr6:41336049
|
C | T | 1 | a0001c0001t0001g0029 | 3 | NA18966.hp2 NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.53-38C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41336049 | ||||||
chr6:41336067
|
G | A | 30 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(27): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.53-20G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41336067 | ||||||
chr6:41336479
|
G | A | 1 | a0002c0002t0002g0034 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.394+51G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336479 | ||||||
chr6:41336503
|
C | T | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+75C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336503 | ||||||
chr6:41336505
|
A | G | 1 | a0008c0008t0002g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394+77A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336505 | ||||||
chr6:41336529
|
G | A | 1 | a0003c0003t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.394+101G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336529 | ||||||
chr6:41336885
|
G | GA | 30 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(27): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.394+465dupA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41336885 | |||||
chr6:41336953
|
G | A | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+525G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336953 | ||||||
chr6:41336978
|
T | C | 1 | a0003c0003t0001g0054 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.394+550T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336978 | ||||||
chr6:41337099
|
C | G | 1 | a0002c0002t0002g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.394+671C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337099 | ||||||
chr6:41337125
|
T | C | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+697T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337125 | ||||||
chr6:41337197
|
A | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.394+769A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337197 | ||||||
chr6:41337231
|
AG | A | 4 | a0002c0002t0002g0050a0009c0009t0002g0148a0009c0009t0002g0150others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+804delG | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337231 | ||||||
chr6:41337264
|
C | T | 7 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0049others(4): Show | 15 | HG00621.hp1 HG00733.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+836C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337264 | ||||||
chr6:41337337
|
T | C | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+909T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337337 | ||||||
chr6:41337351
|
G | C | 1 | a0003c0003t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394+923G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337351 | ||||||
chr6:41337415
|
G | A | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+987G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337415 | ||||||
chr6:41337434
|
C | A | 1 | a0001c0001t0001g0079 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.394+1006C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337434 | ||||||
chr6:41337447
|
T | C | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+1019T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337447 | ||||||
chr6:41337494
|
C | T | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+1066C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337494 | ||||||
chr6:41337579
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.394+1151G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337579 | ||||||
chr6:41337582
|
A | G | 1 | a0002c0002t0003g0048 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.394+1154A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337582 | ||||||
chr6:41337631
|
T | A | 2 | a0002c0002t0002g0081a0002c0002t0002g0082 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.394+1203T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337631 | ||||||
chr6:41337669
|
T | G | 1 | a0005c0006t0002g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.394+1241T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337669 | ||||||
chr6:41337714
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394+1286C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337714 | ||||||
chr6:41337716
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(64): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.394+1288G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337716 | ||||||
chr6:41338005
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0100a0006c0005t0001g0101 | 4 | HG02080.hp1 HG02129.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+1577T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338005 | ||||||
chr6:41338121
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.394+1693C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338121 | ||||||
chr6:41338222
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.394+1794C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338222 | ||||||
chr6:41338236
|
A | T | 1 | a0005c0006t0002g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394+1808A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338236 | ||||||
chr6:41338238
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0026others(19): Show | 64 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.394+1810G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338238 | ||||||
chr6:41338265
|
C | CA | 4 | a0002c0002t0002g0050a0009c0009t0002g0148a0009c0009t0002g0150others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+1839dupA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41338265 | |||||
chr6:41338270
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118 | 13 | HG00735.hp2 HG01346.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.394+1842G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338270 | ||||||
chr6:41338449
|
A | T | 1 | a0003c0003t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.394+2021A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338449 | ||||||
chr6:41338451
|
C | G | 2 | a0002c0002t0002g0041a0002c0002t0002g0092 | 3 | HG02055.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.394+2023C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338451 | ||||||
chr6:41338552
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.394+2124A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338552 | ||||||
chr6:41338792
|
G | A | 1 | a0007c0007t0001g0012 | 5 | HG01255.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+2364G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338792 | ||||||
chr6:41338886
|
T | C | 1 | a0002c0002t0002g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.394+2458T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338886 | ||||||
chr6:41338957
|
G | A | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+2529G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338957 | ||||||
chr6:41339101
|
G | A | 1 | a0005c0006t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394+2673G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339101 | ||||||
chr6:41339147
|
C | A | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2647C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339147 | ||||||
chr6:41339169
|
C | T | 4 | a0002c0002t0002g0050a0009c0009t0002g0148a0009c0009t0002g0150others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-2625C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339169 | ||||||
chr6:41339186
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(70): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.395-2608G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339186 | ||||||
chr6:41339207
|
G | A | 2 | a0003c0003t0001g0030a0003c0003t0001g0031 | 4 | NA19000.hp2 NA19006.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2587G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339207 | ||||||
chr6:41339220
|
C | A | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2574C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339220 | ||||||
chr6:41339223
|
G | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.395-2571G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339223 | ||||||
chr6:41339250
|
T | C | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.395-2544T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339250 | ||||||
chr6:41339305
|
G | A | 33 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(30): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.395-2489G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339305 | ||||||
chr6:41339360
|
A | G | 1 | a0002c0002t0002g0078 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.395-2434A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339360 | ||||||
chr6:41339523
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.395-2271T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339523 | ||||||
chr6:41339533
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.395-2261C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339533 | ||||||
chr6:41339546
|
G | A | 2 | a0001c0001t0001g0119a0003c0003t0001g0018 | 4 | HG03831.hp2 NA18946.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2248G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339546 | ||||||
chr6:41339739
|
G | T | 1 | a0007c0007t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.395-2055G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339739 | ||||||
chr6:41339773
|
T | C | 30 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(27): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.395-2021T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339773 | ||||||
chr6:41339856
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0017others(9): Show | 56 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.395-1938A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339856 | ||||||
chr6:41340130
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395-1664T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340130 | ||||||
chr6:41340147
|
C | CTTTA | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(59): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.395-1620_395-1617d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | |||||
chr6:41340147
|
C | CTTTATTT others(1): Show |
31 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0047others(28): Show | 91 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.395-1624_395-1617d others(10): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | |||||
chr6:41340147
|
C | CTTTATTT others(5): Show |
10 | a0002c0002t0002g0096a0002c0002t0002g0097a0003c0003t0001g0009others(7): Show | 18 | HG00621.hp2 HG01934.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.395-1628_395-1617d others(14): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | |||||
chr6:41340147
|
C | CTTTATTT others(9): Show |
17 | a0002c0002t0002g0034a0002c0002t0002g0036a0002c0002t0002g0086others(14): Show | 24 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.395-1632_395-1617d others(18): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | |||||
chr6:41340147
|
C | CTTTATTT others(13): Show |
15 | a0001c0001t0001g0029a0002c0002t0002g0010a0002c0002t0002g0021others(12): Show | 33 | HG00741.hp1 HG01081.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.395-1636_395-1617d others(22): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | |||||
chr6:41340147
|
C | CTTTATTT others(17): Show |
7 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0040others(4): Show | 14 | HG00140.hp1 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.395-1640_395-1617d others(26): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | |||||
chr6:41340225
|
G | A | 30 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(27): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.395-1569G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340225 | ||||||
chr6:41340351
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.395-1443G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340351 | ||||||
chr6:41340414
|
G | A | 4 | a0002c0002t0002g0037a0002c0002t0002g0041a0002c0002t0002g0092others(1): Show | 6 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.395-1380G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340414 | ||||||
chr6:41340425
|
C | G | 37 | a0002c0002t0002g0050a0003c0003t0001g0003a0003c0003t0001g0009others(34): Show | 101 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.395-1369C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340425 | ||||||
chr6:41340427
|
G | T | 1 | a0003c0003t0001g0064 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.395-1367G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340427 | ||||||
chr6:41340430
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.395-1364G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340430 | ||||||
chr6:41340491
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.395-1303C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340491 | ||||||
chr6:41340667
|
C | T | 7 | a0002c0002t0002g0050a0003c0003t0001g0051a0003c0003t0001g0153others(4): Show | 9 | HG01081.hp1 HG01496.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-1127C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340667 | ||||||
chr6:41341130
|
C | T | 4 | a0002c0002t0002g0050a0009c0009t0002g0148a0009c0009t0002g0150others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-664C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341130 | ||||||
chr6:41341153
|
C | T | 7 | a0002c0002t0002g0050a0003c0003t0001g0051a0003c0003t0001g0153others(4): Show | 9 | HG01081.hp1 HG01496.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-641C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341153 | ||||||
chr6:41341615
|
G | A | 31 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(28): Show | 93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.395-179G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341615 | ||||||
chr6:41341710
|
C | A | 3 | a0001c0001t0001g0029a0006c0005t0001g0016a0006c0005t0001g0024 | 10 | HG02109.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.395-84C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341710 | ||||||
chr6:41341782
|
C | T | 1 | a0001c0001t0001g0028 | 3 | HG00609.hp2 HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.395-12C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341782 | ||||||
chr6:41341947
|
C | T | 1 | a0005c0006t0002g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530+18C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/4 | chr6 | 41341947 | ||||||
chr6:41341960
|
G | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(75): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.530+31G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/4 | chr6 | 41341960 | ||||||
chr6:41342293
|
T | C | 13 | a0002c0002t0002g0010a0002c0002t0002g0021a0002c0002t0002g0022others(10): Show | 28 | HG00140.hp1 HG01361.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.644+144T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342293 | ||||||
chr6:41342483
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG00639.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.644+334C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342483 | ||||||
chr6:41342524
|
T | C | 1 | a0004c0004t0001g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.644+375T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342524 | ||||||
chr6:41342581
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.644+432C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342581 | ||||||
chr6:41342704
|
G | A | 1 | a0004c0004t0001g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.644+555G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342704 | ||||||
chr6:41342767
|
GA | G | 1 | a0005c0011t0002g0025 | 3 | HG00741.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+624delA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41342767 | |||||
chr6:41342791
|
T | TG | 5 | a0001c0001t0001g0027a0001c0001t0001g0114a0001c0001t0001g0119others(2): Show | 7 | HG00323.hp1 HG00733.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.644+643dupG | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41342791 | |||||
chr6:41342967
|
C | T | 8 | a0002c0002t0002g0023a0002c0002t0002g0036a0002c0002t0002g0038others(5): Show | 12 | HG02698.hp2 HG02735.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.644+818C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342967 | ||||||
chr6:41343037
|
T | C | 4 | a0002c0002t0002g0050a0009c0009t0002g0148a0009c0009t0002g0150others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+888T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343037 | ||||||
chr6:41343132
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(137): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.644+983A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343132 | ||||||
chr6:41343140
|
T | C | 1 | a0009c0009t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.644+991T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343140 | ||||||
chr6:41343167
|
C | T | 4 | a0002c0002t0002g0010a0002c0002t0002g0040a0002c0002t0002g0086others(1): Show | 11 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.644+1018C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343167 | ||||||
chr6:41343599
|
T | C | 3 | a0002c0002t0002g0014a0002c0002t0002g0049a0009c0009t0002g0146 | 8 | HG00621.hp1 NA18950.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.644+1450T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343599 | ||||||
chr6:41343625
|
G | T | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+1476G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343625 | ||||||
chr6:41343629
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.644+1480A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343629 | ||||||
chr6:41343648
|
G | A | 8 | a0002c0002t0002g0023a0002c0002t0002g0036a0002c0002t0002g0038others(5): Show | 12 | HG02698.hp2 HG02735.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.644+1499G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343648 | ||||||
chr6:41343685
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0004g0045 | 2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.644+1536T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343685 | ||||||
chr6:41343807
|
CT | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.644+1660delT | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41343807 | |||||
chr6:41343822
|
G | C | 34 | a0001c0001t0001g0029a0002c0002t0002g0096a0002c0002t0002g0097others(31): Show | 93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.644+1673G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343822 | ||||||
chr6:41343897
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(125): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.644+1748T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343897 | ||||||
chr6:41343900
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.644+1751A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343900 | ||||||
chr6:41343918
|
G | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(80): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.644+1769G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343918 | ||||||
chr6:41343939
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.644+1790A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343939 | ||||||
chr6:41343965
|
TCTCC | T | 4 | a0002c0002t0002g0050a0009c0009t0002g0148a0009c0009t0002g0150others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+1820_644+1823d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41343965 | |||||
chr6:41344083
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(121): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.644+1934A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344083 | ||||||
chr6:41344106
|
G | A | 1 | a0002c0002t0002g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.644+1957G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344106 | ||||||
chr6:41344154
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(81): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.644+2005T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344154 | ||||||
chr6:41344240
|
C | T | 5 | a0002c0002t0002g0050a0002c0002t0002g0096a0009c0009t0002g0148others(2): Show | 6 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+2091C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344240 | ||||||
chr6:41344484
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.644+2335G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344484 | ||||||
chr6:41344508
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0079 | 5 | NA18939.hp2 NA18956.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+2359C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344508 | ||||||
chr6:41344525
|
C | T | 10 | a0002c0002t0002g0010a0002c0002t0002g0021a0002c0002t0002g0022others(7): Show | 24 | HG01361.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.644+2376C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344525 | ||||||
chr6:41344554
|
A | T | 4 | a0002c0002t0002g0050a0002c0002t0002g0096a0009c0009t0002g0148others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+2405A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344554 | ||||||
chr6:41344664
|
T | C | 4 | a0008c0008t0002g0042a0008c0008t0002g0043a0008c0008t0002g0098others(1): Show | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.644+2515T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344664 | ||||||
chr6:41344681
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.644+2532G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344681 | ||||||
chr6:41344716
|
T | C | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+2567T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344716 | ||||||
chr6:41344794
|
C | T | 4 | a0001c0001t0001g0029a0006c0005t0001g0016a0006c0005t0001g0024others(1): Show | 11 | HG02109.hp1 HG02257.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.644+2645C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344794 | ||||||
chr6:41344796
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.644+2647C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344796 | ||||||
chr6:41344802
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.644+2653G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344802 | ||||||
chr6:41344838
|
G | C | 1 | a0001c0001t0001g0046 | 2 | HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.644+2689G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344838 | ||||||
chr6:41344983
|
G | A | 1 | a0004c0004t0001g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.644+2834G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344983 | ||||||
chr6:41344998
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.644+2849G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344998 | ||||||
chr6:41345118
|
A | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0134 | 4 | HG00323.hp1 HG00733.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+2969A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345118 | ||||||
chr6:41345244
|
C | G | 1 | a0005c0006t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.644+3095C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345244 | ||||||
chr6:41345322
|
C | A | 1 | a0002c0002t0002g0073 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.644+3173C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345322 | ||||||
chr6:41345427
|
G | A | 1 | a0005c0011t0002g0025 | 3 | HG00741.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+3278G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345427 | ||||||
chr6:41345427
|
G | C | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+3278G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345427 | ||||||
chr6:41345509
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.644+3360C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345509 | ||||||
chr6:41345572
|
C | T | 2 | a0005c0011t0002g0025a0009c0009t0001g0094 | 4 | HG00741.hp1 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+3423C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345572 | ||||||
chr6:41345589
|
C | G | 7 | a0001c0001t0001g0029a0003c0003t0001g0051a0003c0003t0001g0153others(4): Show | 15 | HG01496.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.644+3440C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345589 | ||||||
chr6:41345627
|
G | A | 4 | a0002c0002t0002g0050a0002c0002t0002g0096a0009c0009t0002g0148others(1): Show | 5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+3478G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345627 | ||||||
chr6:41345635
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0080others(9): Show | 32 | HG00099.hp1 HG01069.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.644+3486T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345635 | ||||||
chr6:41345648
|
T | C | 25 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(22): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.644+3499T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345648 | ||||||
chr6:41345728
|
T | A | 1 | a0003c0003t0001g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.644+3579T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345728 | ||||||
chr6:41345738
|
T | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.644+3589T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345738 | ||||||
chr6:41345752
|
T | C | 1 | a0003c0003t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.644+3603T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345752 | ||||||
chr6:41345770
|
G | A | 2 | a0005c0011t0002g0025a0009c0009t0001g0094 | 4 | HG00741.hp1 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+3621G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345770 | ||||||
chr6:41345796
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.644+3647C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345796 | ||||||
chr6:41345861
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.644+3712C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345861 | ||||||
chr6:41345892
|
G | A | 4 | a0001c0001t0001g0115a0003c0003t0001g0051a0003c0003t0001g0153others(1): Show | 5 | HG00639.hp1 HG01496.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+3743G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345892 | ||||||
chr6:41345899
|
A | G | 3 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154 | 4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+3750A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345899 | ||||||
chr6:41345922
|
C | T | 1 | a0015c0016t0002g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.644+3773C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345922 | ||||||
chr6:41345953
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.644+3804C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345953 | ||||||
chr6:41345971
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.644+3822A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345971 | ||||||
chr6:41346026
|
C | T | 1 | a0003c0003t0001g0033 | 2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.644+3877C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346026 | ||||||
chr6:41346098
|
G | A | 1 | a0004c0004t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.644+3949G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346098 | ||||||
chr6:41346112
|
A | G | 1 | a0003c0003t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.644+3963A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346112 | ||||||
chr6:41346133
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.644+3984T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346133 | ||||||
chr6:41346160
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.644+4011G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346160 | ||||||
chr6:41346183
|
A | G | 8 | a0002c0002t0002g0050a0002c0002t0002g0096a0003c0003t0001g0051others(5): Show | 12 | HG00741.hp1 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.644+4034A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346183 | ||||||
chr6:41346249
|
C | T | 1 | a0001c0001t0001g0026 | 3 | HG01168.hp2 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.644+4100C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346249 | ||||||
chr6:41346263
|
G | C | 8 | a0002c0002t0002g0050a0002c0002t0002g0096a0003c0003t0001g0051others(5): Show | 12 | HG00741.hp1 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.644+4114G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346263 | ||||||
chr6:41346272
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.644+4123T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346272 | ||||||
chr6:41346274
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.644+4125C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346274 | ||||||
chr6:41346286
|
G | A | 1 | a0002c0002t0002g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.644+4137G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346286 | ||||||
chr6:41346289
|
C | T | 7 | a0002c0002t0002g0050a0002c0002t0002g0096a0003c0003t0001g0051others(4): Show | 9 | HG01081.hp1 HG01496.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.644+4140C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346289 | ||||||
chr6:41346309
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.644+4160C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346309 | ||||||
chr6:41346376
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.644+4227G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346376 | ||||||
chr6:41346429
|
A | G | 4 | a0008c0008t0002g0042a0008c0008t0002g0043a0008c0008t0002g0098others(1): Show | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-4249A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346429 | ||||||
chr6:41346445
|
G | A | 1 | a0003c0003t0001g0061 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.645-4233G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346445 | ||||||
chr6:41346501
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.645-4177C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346501 | ||||||
chr6:41346568
|
G | A | 1 | a0012c0019t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.645-4110G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346568 | ||||||
chr6:41346597
|
T | G | 11 | a0001c0001t0001g0029a0002c0002t0002g0050a0002c0002t0002g0096others(8): Show | 20 | HG01081.hp1 HG01496.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.645-4081T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346597 | ||||||
chr6:41346671
|
G | A | 1 | a0003c0003t0001g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.645-4007G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346671 | ||||||
chr6:41346677
|
T | G | 8 | a0002c0002t0002g0050a0002c0002t0002g0088a0002c0002t0002g0096others(5): Show | 10 | HG01081.hp1 HG01496.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.645-4001T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346677 | ||||||
chr6:41346828
|
A | AGAGG | 9 | a0001c0001t0001g0029a0001c0001t0001g0129a0002c0002t0002g0036others(6): Show | 16 | HG02071.hp1 HG02559.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.645-3827_645-3824d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41346828 | |||||
chr6:41346828
|
A | AGAGGGAG others(1): Show |
1 | a0006c0005t0001g0024 | 3 | HG02109.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.645-3831_645-3824d others(10): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41346828 | |||||
chr6:41346828
|
AGAGG | A | 10 | a0001c0001t0001g0123a0002c0002t0002g0082a0003c0003t0001g0051others(7): Show | 15 | HG00642.hp1 HG00673.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.645-3827_645-3824d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41346828 | |||||
chr6:41346844
|
G | A | 1 | a0002c0002t0002g0049 | 2 | NA18950.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.645-3834G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346844 | ||||||
chr6:41347086
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.645-3592G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347086 | ||||||
chr6:41347107
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(139): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.645-3571T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347107 | ||||||
chr6:41347169
|
C | T | 11 | a0002c0002t0002g0034a0002c0002t0002g0037a0002c0002t0002g0041others(8): Show | 18 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.645-3509C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347169 | ||||||
chr6:41347217
|
A | C | 2 | a0010c0010t0001g0019a0010c0010t0001g0058 | 4 | HG00423.hp2 NA19057.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.645-3461A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347217 | ||||||
chr6:41347220
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.645-3458G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347220 | ||||||
chr6:41347246
|
A | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0080others(10): Show | 25 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.645-3432A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347246 | ||||||
chr6:41347272
|
G | T | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-3406G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347272 | ||||||
chr6:41347474
|
T | C | 24 | a0003c0003t0001g0003a0003c0003t0001g0009a0003c0003t0001g0018others(21): Show | 70 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.645-3204T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347474 | ||||||
chr6:41347498
|
G | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-3180G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347498 | ||||||
chr6:41347572
|
C | T | 1 | a0009c0009t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.645-3106C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347572 | ||||||
chr6:41347614
|
G | C | 1 | a0006c0005t0001g0024 | 3 | HG02109.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.645-3064G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347614 | ||||||
chr6:41347732
|
G | C | 1 | a0002c0002t0002g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.645-2946G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347732 | ||||||
chr6:41347734
|
G | T | 1 | a0003c0003t0001g0032 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.645-2944G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347734 | ||||||
chr6:41347735
|
G | T | 1 | a0003c0003t0001g0032 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.645-2943G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347735 | ||||||
chr6:41347860
|
G | A | 6 | a0001c0001t0001g0126a0003c0003t0001g0051a0003c0003t0001g0154others(3): Show | 7 | HG01081.hp1 HG01496.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-2818G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347860 | ||||||
chr6:41347981
|
G | A | 1 | a0002c0002t0002g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.645-2697G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347981 | ||||||
chr6:41348034
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(105): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.645-2644G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348034 | ||||||
chr6:41348158
|
T | C | 2 | a0006c0005t0001g0024a0015c0016t0002g0149 | 4 | HG02109.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-2520T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348158 | ||||||
chr6:41348225
|
G | T | 1 | a0005c0006t0002g0039 | 2 | HG00140.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.645-2453G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348225 | ||||||
chr6:41348252
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.645-2426C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348252 | ||||||
chr6:41348433
|
T | C | 2 | a0003c0003t0001g0153a0007c0007t0001g0095 | 2 | HG00642.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.645-2245T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348433 | ||||||
chr6:41348465
|
C | CA | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.645-2203dupA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41348465 | |||||
chr6:41348473
|
A | AC | 12 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0080others(9): Show | 24 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.645-2205_645-2204i others(3): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348473 | ||||||
chr6:41348512
|
A | C | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-2166A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348512 | ||||||
chr6:41348659
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-2019G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348659 | ||||||
chr6:41348794
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.645-1884G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348794 | ||||||
chr6:41348816
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0080others(8): Show | 23 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.645-1862G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348816 | ||||||
chr6:41348941
|
G | T | 1 | a0002c0002t0002g0034 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.645-1737G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348941 | ||||||
chr6:41348952
|
C | A | 7 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(4): Show | 12 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-1726C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348952 | ||||||
chr6:41348962
|
C | T | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-1716C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348962 | ||||||
chr6:41349005
|
T | C | 7 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(4): Show | 12 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-1673T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349005 | ||||||
chr6:41349026
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-1652C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349026 | ||||||
chr6:41349075
|
T | TTTTTA | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-1602_645-1598d others(7): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41349075 | |||||
chr6:41349114
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(78): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.645-1564T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349114 | ||||||
chr6:41349135
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.645-1543T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349135 | ||||||
chr6:41349197
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-1481C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349197 | ||||||
chr6:41349514
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.645-1164C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349514 | ||||||
chr6:41349540
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.645-1138G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349540 | ||||||
chr6:41349553
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.645-1125A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349553 | ||||||
chr6:41349586
|
TC | T | 1 | a0006c0005t0001g0024 | 3 | HG02109.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.645-1091delC | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349586 | ||||||
chr6:41349689
|
C | G | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-989C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349689 | ||||||
chr6:41349697
|
C | T | 7 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(4): Show | 12 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-981C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349697 | ||||||
chr6:41349698
|
C | A | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-980C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349698 | ||||||
chr6:41349803
|
C | T | 4 | a0006c0005t0001g0016a0009c0009t0001g0094a0012c0018t0002g0085others(1): Show | 7 | HG02257.hp1 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.645-875C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349803 | ||||||
chr6:41349972
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-706G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349972 | ||||||
chr6:41349973
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-705C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349973 | ||||||
chr6:41349975
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-703C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349975 | ||||||
chr6:41349977
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-701T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349977 | ||||||
chr6:41349978
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-700T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349978 | ||||||
chr6:41349979
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-699C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349979 | ||||||
chr6:41349983
|
AGTTTGCC others(121): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-694_645-567del | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349983 | ||||||
chr6:41350026
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.645-652A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350026 | ||||||
chr6:41350066
|
C | T | 4 | a0008c0008t0002g0042a0008c0008t0002g0043a0008c0008t0002g0098others(1): Show | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-612C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350066 | ||||||
chr6:41350112
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-566C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350112 | ||||||
chr6:41350115
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-563C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350115 | ||||||
chr6:41350116
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-562T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350116 | ||||||
chr6:41350121
|
G | T | 4 | a0008c0008t0002g0042a0008c0008t0002g0043a0008c0008t0002g0098others(1): Show | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-557G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350121 | ||||||
chr6:41350122
|
A | AGAAAAAA others(122): Show |
1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-556_645-555ins others(129): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350122 | ||||||
chr6:41350180
|
C | T | 1 | a0003c0003t0001g0063 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.645-498C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350180 | ||||||
chr6:41350191
|
C | T | 1 | a0009c0009t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.645-487C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350191 | ||||||
chr6:41350256
|
G | A | 1 | a0010c0010t0001g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.645-422G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350256 | ||||||
chr6:41350319
|
G | A | 4 | a0008c0008t0002g0042a0008c0008t0002g0043a0008c0008t0002g0098others(1): Show | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-359G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350319 | ||||||
chr6:41350363
|
A | G | 8 | a0003c0003t0001g0051a0003c0003t0001g0153a0003c0003t0001g0154others(5): Show | 13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-315A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350363 | ||||||
chr6:41350445
|
G | A | 1 | a0005c0006t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.645-233G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350445 | ||||||
chr6:41350519
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-159T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350519 |