geneid | 55093 |
---|---|
ensemblid | ENSG00000156795.8 |
hgncid | 25490 |
symbol | NTAQ1 |
name | N-terminal glutamine amidase 1 |
refseq_nuc | NM_018024.3 |
refseq_prot | NP_060494.1 |
ensembl_nuc | ENST00000287387.7 |
ensembl_prot | ENSP00000287387.2 |
mane_status | MANE Select |
chr | chr8 |
start | 123416774 |
end | 123442240 |
strand | + |
ver | v1.2 |
region | chr8:123416774-123442240 |
region5000 | chr8:123411774-123447240 |
regionname0 | NTAQ1_chr8_123416774_123442240 |
regionname5000 | NTAQ1_chr8_123411774_123447240 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 205 | 194 | 56 | 42 | 61 | 12 | 22 | 46 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0002 | 0/1 | 205 | 170 | 30 | 32 | 84 | 2 | 21 | 61 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0003 | 0/0 | 203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0004 | 0/0 | 205 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 618 | 192 | 56 | 41 | 60 | 12 | 22 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
c0002 | 0/1 | 618 | 169 | 30 | 32 | 83 | 2 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
c0003 | 0/0 | 618 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
c0004 | 0/0 | 618 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
c0005 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
c0006 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
c0007 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 902 | 183 | 46 | 41 | 62 | 11 | 22 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0002 | 0/1 | 902 | 170 | 30 | 32 | 84 | 2 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0003 | 0/0 | 902 | 6 | 5 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0004 | 0/0 | 902 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0005 | 0/0 | 902 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0006 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0007 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
t0008 | 0/0 | 902 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 4 | 3 | 2 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0007 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0017 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 618 | 192 | 56 | 41 | 60 | 12 | 22 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0004 | 0/0 | 618 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0005 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0002c0002 | 0/1 | 618 | 169 | 30 | 32 | 83 | 2 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0002c0007 | 0/0 | 618 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0003c0006 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0004c0003 | 0/0 | 618 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1519 | 179 | 46 | 40 | 60 | 11 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0001t0003 | 0/0 | 1519 | 6 | 5 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0001t0004 | 0/0 | 1519 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0001t0005 | 0/0 | 1519 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0001t0006 | 0/0 | 1519 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0001t0007 | 0/0 | 1519 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0001t0008 | 0/0 | 1519 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0004t0001 | 0/0 | 1519 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0001c0005t0001 | 0/0 | 1519 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0002c0002t0002 | 0/1 | 1519 | 169 | 30 | 32 | 83 | 2 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0002c0007t0002 | 0/0 | 1519 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0003c0006t0001 | 0/0 | 1513 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
a0004c0003t0001 | 0/0 | 1519 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | copy fasta | chr8 | 123411774 | 123447240 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 3 | 2 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0007 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0004g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0004t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0001c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0017 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0002c0007t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0003c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
a0004c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0105 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0100 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0175 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0106 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0107 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0157 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0097 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0164 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0178 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0262 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0172 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0185 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0069 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0184 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0165 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0135 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0151 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0144 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0147 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0186 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0177 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0173 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0161 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0133 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0176 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0112 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04115 | hp2 | a0004 | c0003 | t0001 | g0255 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0228 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0170 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0131 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18971 | hp2 | a0002 | c0007 | t0002 | g0120 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18997 | hp2 | a0003 | c0006 | t0001 | g0264 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19012 | hp2 | a0001 | c0005 | t0001 | g0261 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | ASW | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0091 | EUR | TSI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0190 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0134 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0017 | REF | REF | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0037 | REF | REF | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123416868
|
G | A | 1 | a0004 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.19G>A | p.Ala7Thr | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/6 | 95/1519 | 19/618 | 7/205 | chr8 | 123416868 | ||
chr8:123427934
|
A | G | 1 | a0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
missense_variant | MODERATE | c.94A>G | p.Ile32Val | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/6 | 170/1519 | 94/618 | 32/205 | chr8 | 123427934 | ||
chr8:123436496
|
A | G | 1 | a0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
missense_variant | MODERATE | c.278A>G | p.Asn93Ser | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 354/1519 | 278/618 | 93/205 | chr8 | 123436496 | ||
chr8:123436564
|
T | A | 1 | a0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
missense_variant | MODERATE | c.346T>A | p.Phe116Ile | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 422/1519 | 346/618 | 116/205 | chr8 | 123436564 | ||
chr8:123437226
|
C | T | 1 | a0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
missense_variant | MODERATE | c.400C>T | p.Arg134Cys | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/6 | 476/1519 | 400/618 | 134/205 | chr8 | 123437226 | ||
chr8:123437328
|
ACTGGAGG others(13): Show |
A | 1 | a0003 | 1 | NA18997.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.505_508+16delGGAGG others(15): Show |
p.Gly169fs | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/6 | 581/1519 | 505/618 | 169/205 | INFO_REALIGN_3_PRIME | chr8 | 123437328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123427993
|
T | C | 1 | a0001c0004 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.153T>C | p.Tyr51Tyr | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/6 | 229/1519 | 153/618 | 51/205 | chr8 | 123427993 | ||
chr8:123436506
|
T | C | 1 | a0001c0005 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.288T>C | p.Tyr96Tyr | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 364/1519 | 288/618 | 96/205 | chr8 | 123436506 | ||
chr8:123436593
|
G | A | 1 | a0002c0007 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.375G>A | p.Gln125Gln | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 451/1519 | 375/618 | 125/205 | chr8 | 123436593 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123416834
|
G | C | 1 | a0001c0001t0005 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/6 | 16 | chr8 | 123416834 | |||||
chr8:123441422
|
T | C | 2 | a0002c0002t0002a0002c0007t0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 7 | chr8 | 123441422 | |||||
chr8:123441529
|
T | C | 2 | a0001c0001t0006a0001c0001t0007 | 2 | HG02451.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 114 | chr8 | 123441529 | |||||
chr8:123441559
|
A | G | 2 | a0002c0002t0002a0002c0007t0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*144A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 144 | chr8 | 123441559 | |||||
chr8:123441626
|
C | T | 1 | a0001c0001t0003 | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*211C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 211 | chr8 | 123441626 | |||||
chr8:123441687
|
C | T | 1 | a0001c0001t0004 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*272C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 272 | chr8 | 123441687 | |||||
chr8:123441688
|
G | A | 1 | a0001c0001t0006 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 273 | chr8 | 123441688 | |||||
chr8:123441739
|
T | C | 2 | a0002c0002t0002a0002c0007t0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 324 | chr8 | 123441739 | |||||
chr8:123441767
|
T | C | 2 | a0002c0002t0002a0002c0007t0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*352T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 352 | chr8 | 123441767 | |||||
chr8:123441824
|
A | G | 2 | a0001c0001t0006a0001c0001t0007 | 2 | HG02451.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 409 | chr8 | 123441824 | |||||
chr8:123441855
|
C | T | 1 | a0001c0001t0008 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 440 | chr8 | 123441855 | |||||
chr8:123442235
|
A | G | 2 | a0002c0002t0002a0002c0007t0002 | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*820A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 820 | chr8 | 123442235 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123417010
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83+78G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417010 | ||||||
chr8:123417106
|
G | C | 1 | a0002c0002t0002g0029 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.83+174G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417106 | ||||||
chr8:123417155
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(99): Show | 123 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.83+223A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417155 | ||||||
chr8:123417214
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+282C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417214 | ||||||
chr8:123417244
|
C | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(24): Show | 30 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+312C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417244 | ||||||
chr8:123417250
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(228): Show | 296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.83+318G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417250 | ||||||
chr8:123417404
|
A | C | 1 | a0002c0002t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83+472A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417404 | ||||||
chr8:123417410
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+478A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417410 | ||||||
chr8:123417491
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.83+559G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417491 | ||||||
chr8:123417683
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(230): Show | 298 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.83+751A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417683 | ||||||
chr8:123417714
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.83+782C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417714 | ||||||
chr8:123417775
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.83+843G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417775 | ||||||
chr8:123418087
|
A | C | 1 | a0002c0002t0002g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.83+1155A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418087 | ||||||
chr8:123418223
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(95): Show | 119 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.83+1291G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418223 | ||||||
chr8:123418226
|
G | GAGGCCGA others(6): Show |
1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+1294_83+1295ins others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418226 | ||||||
chr8:123418268
|
T | G | 1 | a0002c0002t0002g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.83+1336T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418268 | ||||||
chr8:123418447
|
C | CA | 106 | a0001c0001t0001g0030a0001c0001t0001g0155a0001c0001t0001g0203others(103): Show | 143 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.83+1531dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123418447 | |||||
chr8:123418447
|
CA | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0056others(42): Show | 50 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.83+1531delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123418447 | |||||
chr8:123418454
|
A | T | 1 | a0001c0001t0003g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83+1522A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418454 | ||||||
chr8:123418457
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+1525A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418457 | ||||||
chr8:123418460
|
A | AT | 12 | a0002c0002t0002g0010a0002c0002t0002g0013a0002c0002t0002g0022others(9): Show | 18 | HG00642.hp1 HG00741.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.83+1528_83+1529ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418460 | ||||||
chr8:123418460
|
A | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0072others(33): Show | 39 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.83+1528A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418460 | ||||||
chr8:123418464
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.83+1532T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418464 | ||||||
chr8:123418474
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG01496.hp2 HG02683.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.83+1542A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418474 | ||||||
chr8:123418760
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+1828T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418760 | ||||||
chr8:123418838
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+1906A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418838 | ||||||
chr8:123418842
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+1910C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418842 | ||||||
chr8:123418871
|
A | T | 1 | a0002c0002t0002g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1939A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418871 | ||||||
chr8:123418873
|
G | T | 1 | a0002c0002t0002g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1941G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418873 | ||||||
chr8:123418874
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1942A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418874 | ||||||
chr8:123418876
|
G | A | 1 | a0002c0002t0002g0183 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.83+1944G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418876 | ||||||
chr8:123418878
|
G | A | 1 | a0002c0002t0002g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1946G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418878 | ||||||
chr8:123418920
|
C | T | 1 | a0002c0002t0002g0181 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83+1988C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418920 | ||||||
chr8:123418978
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2046G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418978 | ||||||
chr8:123418996
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.83+2064G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418996 | ||||||
chr8:123419045
|
G | A | 1 | a0002c0002t0002g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.83+2113G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419045 | ||||||
chr8:123419077
|
G | GT | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | HG00140.hp2 HG01255.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+2145_83+2146ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419077 | ||||||
chr8:123419078
|
G | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(286): Show | 360 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.83+2146G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419078 | ||||||
chr8:123419079
|
GGGTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2148_83+2163del others(16): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419079 | ||||||
chr8:123419081
|
G | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | HG00140.hp2 HG01255.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+2149G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419081 | ||||||
chr8:123419081
|
GTTTTTTT others(3): Show |
G | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 13 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.83+2175_83+2184del others(10): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(4): Show |
G | 7 | a0001c0001t0001g0034a0001c0001t0003g0031a0001c0001t0003g0032others(4): Show | 7 | HG01099.hp2 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+2174_83+2184del others(11): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83+2173_83+2184del others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0284a0002c0002t0002g0180 | 2 | HG01891.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.83+2172_83+2184del others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(7): Show |
G | 34 | a0001c0001t0001g0038a0001c0001t0001g0270a0001c0001t0001g0271others(31): Show | 34 | HG00609.hp1 HG00735.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.83+2171_83+2184del others(14): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(8): Show |
G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(178): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.83+2170_83+2184del others(15): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(9): Show |
G | 7 | a0001c0001t0001g0209a0001c0001t0001g0288a0002c0002t0002g0029others(4): Show | 7 | HG02622.hp1 NA18942.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+2169_83+2184del others(16): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(10): Show |
G | 2 | a0001c0001t0001g0072a0001c0001t0001g0096 | 2 | HG02056.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.83+2168_83+2184del others(17): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419081
|
GTTTTTTT others(11): Show |
G | 25 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0074others(22): Show | 28 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.83+2167_83+2184del others(18): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | |||||
chr8:123419097
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2165T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419097 | ||||||
chr8:123419098
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2166T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419098 | ||||||
chr8:123419104
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.83+2172T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419104 | ||||||
chr8:123419111
|
T | C | 8 | a0001c0001t0001g0034a0001c0001t0003g0031a0001c0001t0003g0032others(5): Show | 8 | HG01099.hp2 HG02451.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+2179T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419111 | ||||||
chr8:123419146
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+2214T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419146 | ||||||
chr8:123419159
|
T | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(24): Show | 30 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+2227T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419159 | ||||||
chr8:123419192
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(220): Show | 288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+2260A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419192 | ||||||
chr8:123419417
|
G | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+2485G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419417 | ||||||
chr8:123419677
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 345 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.83+2745T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419677 | ||||||
chr8:123419678
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83+2746G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419678 | ||||||
chr8:123419684
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83+2752A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419684 | ||||||
chr8:123419705
|
T | A | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.83+2773T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419705 | ||||||
chr8:123419733
|
G | GCCCCTCC others(10): Show |
1 | a0001c0001t0001g0270 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.83+2804_83+2805ins others(17): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | |||||
chr8:123419733
|
G | GCCCGCCC others(13): Show |
2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.83+2804_83+2805ins others(20): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | |||||
chr8:123419733
|
G | GCCCTCCC others(5): Show |
76 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0024others(73): Show | 93 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.83+2814_83+2825dup others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | |||||
chr8:123419733
|
G | GCCCTCCC others(9): Show |
25 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0205others(22): Show | 29 | HG00609.hp1 HG00673.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.83+2810_83+2825dup others(16): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | |||||
chr8:123419733
|
G | GCCCTCCC others(13): Show |
1 | a0001c0001t0001g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.83+2806_83+2825dup others(20): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | |||||
chr8:123419733
|
G | GCCCTCCC others(17): Show |
2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.83+2802_83+2825dup others(24): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | |||||
chr8:123419739
|
C | CCTCCCTC others(5): Show |
121 | a0001c0001t0001g0155a0001c0001t0001g0290a0002c0002t0002g0002others(118): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.83+2818_83+2819ins others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419739 | |||||
chr8:123419741
|
T | TCCCTCCC others(6): Show |
1 | a0002c0002t0002g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.83+2818_83+2819ins others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419741 | |||||
chr8:123419747
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.83+2815C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419747 | ||||||
chr8:123419750
|
C | CTCCTCCC others(10): Show |
1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2818_83+2819ins others(17): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419750 | ||||||
chr8:123419758
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2826T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419758 | ||||||
chr8:123419771
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2839T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419771 | ||||||
chr8:123419773
|
T | TTCCC | 4 | a0002c0002t0002g0013a0002c0002t0002g0162a0002c0002t0002g0163others(1): Show | 6 | HG02040.hp2 HG03239.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2857_83+2860dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419773 | |||||
chr8:123419773
|
T | TTCCCTCC others(1): Show |
213 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(210): Show | 276 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.83+2853_83+2860dup others(8): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419773 | |||||
chr8:123419773
|
T | TTCCCTCC others(5): Show |
3 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0102 | 3 | HG00323.hp1 HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.83+2849_83+2860dup others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419773 | |||||
chr8:123419775
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2843C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419775 | ||||||
chr8:123419777
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2845C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419777 | ||||||
chr8:123419948
|
T | C | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+3016T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419948 | ||||||
chr8:123420004
|
A | T | 1 | a0002c0002t0002g0029 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.83+3072A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420004 | ||||||
chr8:123420060
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+3128T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420060 | ||||||
chr8:123420061
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+3129C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420061 | ||||||
chr8:123420091
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+3159A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420091 | ||||||
chr8:123420126
|
T | G | 1 | a0002c0002t0002g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83+3194T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420126 | ||||||
chr8:123420157
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+3225T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420157 | ||||||
chr8:123420165
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.83+3233G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420165 | ||||||
chr8:123420328
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(291): Show | 365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.83+3396G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420328 | ||||||
chr8:123420330
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.83+3398C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420330 | ||||||
chr8:123420344
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+3412C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420344 | ||||||
chr8:123420457
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+3525A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420457 | ||||||
chr8:123420490
|
A | G | 2 | a0002c0002t0002g0165a0002c0002t0002g0166 | 2 | HG01167.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.83+3558A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420490 | ||||||
chr8:123420572
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0271 | 2 | NA18946.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.83+3640G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420572 | ||||||
chr8:123420590
|
C | CTTT | 116 | a0001c0001t0001g0155a0001c0001t0001g0226a0001c0001t0001g0227others(113): Show | 160 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.83+3675_83+3677dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | |||||
chr8:123420590
|
C | CTTTT | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(85): Show | 108 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.83+3674_83+3677dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | |||||
chr8:123420590
|
C | CTTTTT | 16 | a0001c0001t0001g0028a0001c0001t0001g0202a0001c0001t0001g0211others(13): Show | 17 | HG01192.hp2 HG01515.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.83+3673_83+3677dup others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | |||||
chr8:123420590
|
CT | C | 22 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0056others(19): Show | 24 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.83+3677delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | |||||
chr8:123420663
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(221): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.83+3731A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420663 | ||||||
chr8:123420785
|
T | TTTTA | 7 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0003g0031others(4): Show | 7 | HG01099.hp2 HG02572.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+3874_83+3877dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420785 | |||||
chr8:123420813
|
C | T | 1 | a0002c0002t0002g0020 | 2 | NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.83+3881C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420813 | ||||||
chr8:123420841
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.83+3909G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420841 | ||||||
chr8:123420918
|
C | T | 123 | a0001c0001t0001g0155a0001c0001t0001g0290a0002c0002t0002g0002others(120): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.83+3986C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420918 | ||||||
chr8:123420976
|
G | A | 1 | a0002c0002t0002g0105 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.83+4044G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420976 | ||||||
chr8:123421031
|
T | C | 123 | a0001c0001t0001g0155a0001c0001t0001g0290a0002c0002t0002g0002others(120): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.83+4099T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421031 | ||||||
chr8:123421063
|
G | A | 119 | a0001c0001t0001g0155a0001c0001t0001g0290a0002c0002t0002g0002others(116): Show | 162 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.83+4131G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421063 | ||||||
chr8:123421094
|
AT | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 354 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(351): Show |
intron_variant | MODIFIER | c.83+4169delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421094 | |||||
chr8:123421103
|
A | G | 1 | a0002c0002t0002g0181 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83+4171A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421103 | ||||||
chr8:123421106
|
C | G | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+4174C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421106 | ||||||
chr8:123421115
|
A | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0068 | 2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.83+4183A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421115 | ||||||
chr8:123421136
|
T | C | 123 | a0001c0001t0001g0155a0001c0001t0001g0290a0002c0002t0002g0002others(120): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.83+4204T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421136 | ||||||
chr8:123421172
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+4240C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421172 | ||||||
chr8:123421185
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.83+4253A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421185 | ||||||
chr8:123421187
|
T | C | 123 | a0001c0001t0001g0155a0001c0001t0001g0290a0002c0002t0002g0002others(120): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.83+4255T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421187 | ||||||
chr8:123421339
|
C | A | 122 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+4407C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421339 | ||||||
chr8:123421357
|
G | A | 5 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(2): Show | 5 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+4425G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421357 | ||||||
chr8:123421386
|
T | TAAGAATA others(345): Show |
1 | a0002c0002t0002g0013 | 3 | HG02040.hp2 HG03239.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.83+4470_83+4471ins others(352): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421386 | |||||
chr8:123421386
|
T | TAAGAATA others(346): Show |
1 | a0002c0002t0002g0199 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.83+4470_83+4471ins others(353): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421386 | |||||
chr8:123421512
|
C | CTTTT | 83 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0008others(80): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.83+4591_83+4594dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421512 | |||||
chr8:123421512
|
C | CTTTTT | 30 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(27): Show | 50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.83+4590_83+4594dup others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421512 | |||||
chr8:123421512
|
C | CTTTTTT | 7 | a0002c0002t0002g0019a0002c0002t0002g0104a0002c0002t0002g0153others(4): Show | 8 | HG00558.hp2 HG02071.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+4589_83+4594dup others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421512 | |||||
chr8:123421527
|
G | T | 1 | a0002c0002t0002g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.83+4595G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421527 | ||||||
chr8:123421571
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+4639C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421571 | ||||||
chr8:123421577
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83+4645C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421577 | ||||||
chr8:123421615
|
G | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 345 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.83+4683G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421615 | ||||||
chr8:123421620
|
C | T | 2 | a0002c0002t0002g0013a0002c0002t0002g0199 | 4 | HG02040.hp2 HG03239.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4688C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421620 | ||||||
chr8:123421694
|
C | CTT | 121 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(118): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.83+4773_83+4774dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421694 | |||||
chr8:123421751
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(243): Show | 313 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.83+4819T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421751 | ||||||
chr8:123421825
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+4893G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421825 | ||||||
chr8:123421849
|
C | CG | 122 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+4919dupG | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421849 | |||||
chr8:123421864
|
A | AT | 27 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(24): Show | 30 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+4941dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421864 | |||||
chr8:123421872
|
T | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0231a0001c0001t0001g0232 | 4 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4940T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421872 | ||||||
chr8:123421886
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.83+4954G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421886 | ||||||
chr8:123421932
|
G | A | 122 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+5000G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421932 | ||||||
chr8:123421984
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.83+5052T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421984 | ||||||
chr8:123422060
|
C | T | 122 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+5128C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422060 | ||||||
chr8:123422077
|
A | G | 6 | a0002c0002t0002g0005a0002c0002t0002g0133a0002c0002t0002g0134others(3): Show | 10 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+5145A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422077 | ||||||
chr8:123422109
|
C | CCTGT | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(243): Show | 313 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.83+5179_83+5180ins others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422109 | |||||
chr8:123422282
|
G | GT | 17 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(14): Show | 19 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.83+5361dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422282 | |||||
chr8:123422282
|
G | GTTT | 114 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(111): Show | 158 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.83+5359_83+5361dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422282 | |||||
chr8:123422282
|
G | GTTTT | 6 | a0002c0002t0002g0132a0002c0002t0002g0151a0002c0002t0002g0152others(3): Show | 6 | HG01884.hp1 HG02683.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+5358_83+5361dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422282 | |||||
chr8:123422495
|
T | C | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033 | 3 | HG01099.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84-5429T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422495 | ||||||
chr8:123422545
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0024others(58): Show | 77 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.84-5379G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422545 | ||||||
chr8:123422569
|
A | G | 122 | a0001c0001t0001g0290a0002c0002t0002g0002a0002c0002t0002g0003others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.84-5355A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422569 | ||||||
chr8:123422588
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-5336C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422588 | ||||||
chr8:123422606
|
G | GT | 24 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0049others(21): Show | 25 | HG00673.hp1 HG01433.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.84-5301dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | |||||
chr8:123422606
|
G | GTT | 6 | a0001c0001t0001g0095a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-5302_84-5301dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | |||||
chr8:123422606
|
G | GTTT | 6 | a0001c0001t0001g0265a0001c0001t0003g0031a0001c0001t0003g0032others(3): Show | 6 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-5303_84-5301dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | |||||
chr8:123422606
|
G | GTTTTTT | 12 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(9): Show | 14 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.84-5306_84-5301dup others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | |||||
chr8:123422606
|
GT | G | 8 | a0001c0001t0001g0226a0002c0002t0002g0012a0002c0002t0002g0018others(5): Show | 11 | HG01071.hp1 HG01071.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.84-5301delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | |||||
chr8:123422606
|
GTT | G | 114 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(111): Show | 155 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.84-5302_84-5301del others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | |||||
chr8:123422683
|
G | A | 1 | a0002c0002t0002g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.84-5241G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422683 | ||||||
chr8:123422737
|
G | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.84-5187G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422737 | ||||||
chr8:123422914
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.84-5010G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422914 | ||||||
chr8:123423049
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(117): Show | 144 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.84-4875G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423049 | ||||||
chr8:123423151
|
G | A | 121 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(118): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.84-4773G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423151 | ||||||
chr8:123423181
|
C | A | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84-4743C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423181 | ||||||
chr8:123423182
|
A | C | 1 | a0001c0001t0001g0288 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84-4742A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423182 | ||||||
chr8:123423187
|
G | A | 123 | a0001c0001t0006g0070a0001c0001t0007g0069a0002c0002t0002g0002others(120): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.84-4737G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423187 | ||||||
chr8:123423232
|
TCTCCCTC others(5): Show |
T | 10 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0003g0031others(7): Show | 10 | HG01099.hp2 HG02451.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-4675_84-4664del others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423232 | |||||
chr8:123423270
|
GTCTC | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033 | 3 | HG01099.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84-4648_84-4645del others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423270 | |||||
chr8:123423313
|
T | TTC | 275 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 345 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.84-4609_84-4608dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423313 | |||||
chr8:123423362
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-4562T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423362 | ||||||
chr8:123423362
|
T | TCCTTTCC others(50): Show |
3 | a0002c0002t0002g0106a0002c0002t0002g0108a0002c0002t0002g0109 | 3 | HG00741.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.84-4506_84-4505ins others(57): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423362 | |||||
chr8:123423370
|
C | G | 4 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(1): Show | 4 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-4554C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423370 | ||||||
chr8:123423381
|
C | CCCTTTCC others(12): Show |
25 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(22): Show | 28 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.84-4522_84-4504dup others(19): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423381 | |||||
chr8:123423381
|
C | CCCTTTCC others(31): Show |
1 | a0001c0001t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.84-4541_84-4504dup others(38): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423381 | |||||
chr8:123423381
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-4543C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423381 | ||||||
chr8:123423435
|
TTTTCTTT others(1): Show |
T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0023others(96): Show | 118 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.84-4477_84-4470del others(8): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423435 | |||||
chr8:123423475
|
T | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0268 | 3 | NA18978.hp2 NA18980.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.84-4449T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423475 | ||||||
chr8:123423574
|
C | T | 120 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(117): Show | 164 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-4350C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423574 | ||||||
chr8:123423612
|
G | A | 121 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(118): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.84-4312G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423612 | ||||||
chr8:123423629
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0275a0001c0001t0001g0276 | 5 | HG02109.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-4295C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423629 | ||||||
chr8:123423651
|
C | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0064others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-4273C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423651 | ||||||
chr8:123423765
|
A | G | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.84-4159A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423765 | ||||||
chr8:123423829
|
G | A | 124 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(121): Show | 168 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.84-4095G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423829 | ||||||
chr8:123423861
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.84-4063T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423861 | ||||||
chr8:123423870
|
T | TTTA | 124 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(121): Show | 168 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.84-4036_84-4034dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423870 | |||||
chr8:123423888
|
A | T | 1 | a0001c0001t0007g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.84-4036A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423888 | ||||||
chr8:123424027
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 347 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.84-3897T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424027 | ||||||
chr8:123424044
|
G | A | 1 | a0002c0002t0002g0192 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.84-3880G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424044 | ||||||
chr8:123424072
|
G | GTT | 33 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0072others(30): Show | 36 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.84-3835_84-3834dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | |||||
chr8:123424072
|
G | GTTT | 93 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(90): Show | 114 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.84-3836_84-3834dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | |||||
chr8:123424072
|
G | GTTTT | 19 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(16): Show | 21 | HG00558.hp1 HG01192.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.84-3837_84-3834dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | |||||
chr8:123424072
|
G | T | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.84-3852G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424072 | ||||||
chr8:123424072
|
GT | G | 108 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(105): Show | 152 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.84-3834delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | |||||
chr8:123424076
|
T | C | 1 | a0002c0002t0002g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-3848T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424076 | ||||||
chr8:123424089
|
T | G | 1 | a0002c0002t0002g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-3835T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424089 | ||||||
chr8:123424174
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-3750G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424174 | ||||||
chr8:123424195
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84-3729C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424195 | ||||||
chr8:123424214
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3710A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424214 | ||||||
chr8:123424247
|
AT | A | 123 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(120): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.84-3664delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424247 | |||||
chr8:123424273
|
T | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(271): Show | 344 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.84-3651T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424273 | ||||||
chr8:123424304
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-3620A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424304 | ||||||
chr8:123424322
|
A | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(23): Show | 29 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.84-3602A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424322 | ||||||
chr8:123424399
|
C | T | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.84-3525C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424399 | ||||||
chr8:123424419
|
T | A | 1 | a0002c0002t0002g0149 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.84-3505T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424419 | ||||||
chr8:123424522
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.84-3402G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424522 | ||||||
chr8:123424570
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-3354C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424570 | ||||||
chr8:123424602
|
AACCTCAG others(24): Show |
A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-3307_84-3277del others(31): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424602 | |||||
chr8:123424642
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-3282T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424642 | ||||||
chr8:123424696
|
C | T | 1 | a0002c0002t0002g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.84-3228C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424696 | ||||||
chr8:123424775
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3149C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424775 | ||||||
chr8:123424836
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84-3088A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424836 | ||||||
chr8:123424967
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.84-2957T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424967 | ||||||
chr8:123425049
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 347 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.84-2875T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425049 | ||||||
chr8:123425061
|
T | C | 1 | a0002c0002t0002g0185 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.84-2863T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425061 | ||||||
chr8:123425192
|
A | G | 1 | a0001c0001t0004g0011 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.84-2732A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425192 | ||||||
chr8:123425216
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.84-2708C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425216 | ||||||
chr8:123425248
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-2676C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425248 | ||||||
chr8:123425271
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.84-2653T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425271 | ||||||
chr8:123425380
|
C | A | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.84-2544C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425380 | ||||||
chr8:123425469
|
C | A | 6 | a0002c0002t0002g0005a0002c0002t0002g0133a0002c0002t0002g0134others(3): Show | 10 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-2455C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425469 | ||||||
chr8:123425470
|
A | C | 1 | a0002c0002t0002g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.84-2454A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425470 | ||||||
chr8:123425471
|
C | A | 1 | a0002c0002t0002g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.84-2453C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425471 | ||||||
chr8:123425471
|
CT | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0001t0001g0226others(6): Show | 9 | HG02895.hp2 HG02922.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-2439delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123425471 | |||||
chr8:123425472
|
T | C | 1 | a0002c0002t0002g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.84-2452T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425472 | ||||||
chr8:123425496
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 347 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.84-2428A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425496 | ||||||
chr8:123425560
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-2364G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425560 | ||||||
chr8:123425708
|
G | A | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.84-2216G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425708 | ||||||
chr8:123425735
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-2189C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425735 | ||||||
chr8:123425775
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-2149C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425775 | ||||||
chr8:123425822
|
C | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-2102C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425822 | ||||||
chr8:123425834
|
G | A | 1 | a0002c0002t0002g0180 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.84-2090G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425834 | ||||||
chr8:123426024
|
C | T | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(3): Show | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-1900C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426024 | ||||||
chr8:123426091
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-1833G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426091 | ||||||
chr8:123426375
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-1549G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426375 | ||||||
chr8:123426395
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-1529C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426395 | ||||||
chr8:123426480
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-1444A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426480 | ||||||
chr8:123426642
|
G | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-1282G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426642 | ||||||
chr8:123426651
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-1273T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426651 | ||||||
chr8:123426677
|
T | C | 1 | a0001c0001t0005g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.84-1247T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426677 | ||||||
chr8:123426747
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.84-1177A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426747 | ||||||
chr8:123426785
|
C | T | 1 | a0002c0002t0002g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.84-1139C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426785 | ||||||
chr8:123426786
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-1138A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426786 | ||||||
chr8:123426926
|
C | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-998C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426926 | ||||||
chr8:123426973
|
A | G | 1 | a0002c0002t0002g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.84-951A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426973 | ||||||
chr8:123426978
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84-946A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426978 | ||||||
chr8:123427139
|
G | T | 1 | a0002c0002t0002g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.84-785G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427139 | ||||||
chr8:123427154
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-770G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427154 | ||||||
chr8:123427217
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.84-707A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427217 | ||||||
chr8:123427225
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84-699G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427225 | ||||||
chr8:123427247
|
C | CT | 106 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(103): Show | 150 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.84-655dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | |||||
chr8:123427247
|
C | CTT | 20 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0107others(17): Show | 22 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.84-656_84-655dupTT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | |||||
chr8:123427247
|
CT | C | 45 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0072others(42): Show | 48 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.84-655delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | |||||
chr8:123427247
|
CTT | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(81): Show | 104 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.84-656_84-655delTT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | |||||
chr8:123427247
|
CTTT | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0203a0001c0001t0001g0216others(3): Show | 7 | HG01928.hp2 HG01975.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-657_84-655delTT others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | |||||
chr8:123427272
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.84-652G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427272 | ||||||
chr8:123427351
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.84-573C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427351 | ||||||
chr8:123427402
|
G | A | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.84-522G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427402 | ||||||
chr8:123427457
|
T | C | 10 | a0002c0002t0002g0003a0002c0002t0002g0137a0002c0002t0002g0139others(7): Show | 17 | HG00408.hp2 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.84-467T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427457 | ||||||
chr8:123427464
|
G | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0216a0001c0001t0001g0225others(1): Show | 5 | HG00609.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-460G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427464 | ||||||
chr8:123427475
|
T | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-449T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427475 | ||||||
chr8:123427503
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-421C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427503 | ||||||
chr8:123427578
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.84-346G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427578 | ||||||
chr8:123427789
|
A | G | 1 | a0002c0002t0002g0145 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.84-135A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427789 | ||||||
chr8:123427880
|
A | G | 1 | a0001c0001t0001g0283 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.84-44A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427880 | ||||||
chr8:123428086
|
TA | T | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.183+75delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428086 | |||||
chr8:123428096
|
A | AAAG | 132 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.183+74_183+76dupAA others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428096 | |||||
chr8:123428096
|
A | AAG | 136 | a0001c0001t0001g0030a0001c0001t0001g0089a0001c0001t0001g0226others(133): Show | 180 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.183+74_183+75insGA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428096 | |||||
chr8:123428096
|
A | G | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.183+73A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428096 | ||||||
chr8:123428289
|
C | T | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(3): Show | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+266C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428289 | ||||||
chr8:123428307
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01109.hp1 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+284C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428307 | ||||||
chr8:123428447
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.183+424C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428447 | ||||||
chr8:123428490
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.183+467G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428490 | ||||||
chr8:123428578
|
G | GT | 124 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(121): Show | 168 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.183+564dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428578 | |||||
chr8:123428697
|
T | TTCAAGTG others(74): Show |
1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.183+708_183+709ins others(81): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428697 | |||||
chr8:123428822
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.183+799G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428822 | ||||||
chr8:123428948
|
T | A | 26 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(23): Show | 29 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.183+925T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428948 | ||||||
chr8:123429046
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.184-937A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429046 | ||||||
chr8:123429048
|
G | A | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.184-935G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429048 | ||||||
chr8:123429128
|
T | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.184-855T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429128 | ||||||
chr8:123429160
|
A | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(282): Show | 356 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.184-823A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429160 | ||||||
chr8:123429192
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.184-791A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429192 | ||||||
chr8:123429264
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 347 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.184-719A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429264 | ||||||
chr8:123429369
|
T | G | 1 | a0002c0002t0002g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-614T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429369 | ||||||
chr8:123429578
|
G | C | 1 | a0002c0002t0002g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.184-405G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429578 | ||||||
chr8:123429593
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.184-390G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429593 | ||||||
chr8:123429602
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0003g0031a0001c0001t0003g0032others(6): Show | 9 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-381C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429602 | ||||||
chr8:123429690
|
C | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.184-293C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429690 | ||||||
chr8:123429696
|
G | A | 1 | a0002c0002t0002g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.184-287G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429696 | ||||||
chr8:123429708
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.184-275C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429708 | ||||||
chr8:123429724
|
T | A | 1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.184-259T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429724 | ||||||
chr8:123429725
|
A | T | 1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.184-258A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429725 | ||||||
chr8:123429768
|
T | A | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.184-215T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429768 | ||||||
chr8:123429769
|
A | T | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.184-214A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429769 | ||||||
chr8:123429792
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.184-191A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429792 | ||||||
chr8:123429874
|
TGTCTCAA others(20): Show |
T | 44 | a0002c0002t0002g0004a0002c0002t0002g0009a0002c0002t0002g0010others(41): Show | 60 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.184-90_184-64delAA others(25): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429874 | |||||
chr8:123429879
|
C | CA | 76 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0072others(73): Show | 104 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.184-86dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429879 | |||||
chr8:123429879
|
C | CAA | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(95): Show | 119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.184-87_184-86dupAA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429879 | |||||
chr8:123429879
|
C | CAAA | 12 | a0001c0001t0001g0206a0001c0001t0001g0217a0001c0001t0001g0221others(9): Show | 12 | HG01109.hp1 HG01433.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-88_184-86dupAA others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429879 | |||||
chr8:123429941
|
T | G | 13 | a0002c0002t0002g0003a0002c0002t0002g0104a0002c0002t0002g0137others(10): Show | 20 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-42T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429941 | ||||||
chr8:123429947
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.184-36A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429947 | ||||||
chr8:123430360
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+327G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430360 | ||||||
chr8:123430362
|
C | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+329C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430362 | ||||||
chr8:123430369
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.234+336C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430369 | ||||||
chr8:123430412
|
T | G | 1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.234+379T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430412 | ||||||
chr8:123430413
|
G | T | 1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.234+380G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430413 | ||||||
chr8:123430462
|
C | T | 1 | a0002c0002t0002g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234+429C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430462 | ||||||
chr8:123430594
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.234+561A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430594 | ||||||
chr8:123430738
|
T | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+705T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430738 | ||||||
chr8:123430787
|
T | C | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+754T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430787 | ||||||
chr8:123430809
|
T | C | 1 | a0002c0002t0002g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.234+776T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430809 | ||||||
chr8:123431024
|
C | A | 1 | a0002c0002t0002g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234+991C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431024 | ||||||
chr8:123431053
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1020T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431053 | ||||||
chr8:123431066
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1033G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431066 | ||||||
chr8:123431179
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.234+1146G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431179 | ||||||
chr8:123431195
|
G | T | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+1162G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431195 | ||||||
chr8:123431241
|
G | A | 9 | a0001c0001t0001g0030a0001c0001t0003g0031a0001c0001t0003g0032others(6): Show | 9 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+1208G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431241 | ||||||
chr8:123431268
|
C | T | 9 | a0001c0001t0001g0030a0001c0001t0003g0031a0001c0001t0003g0032others(6): Show | 9 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+1235C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431268 | ||||||
chr8:123431293
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0073others(23): Show | 29 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+1260C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431293 | ||||||
chr8:123431325
|
G | A | 4 | a0002c0002t0002g0118a0002c0002t0002g0119a0002c0002t0002g0148others(1): Show | 4 | HG02071.hp2 NA18971.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+1292G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431325 | ||||||
chr8:123431337
|
CA | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0074others(3): Show | 6 | HG01099.hp2 HG01175.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+1324delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | |||||
chr8:123431337
|
CAA | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0075others(32): Show | 38 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.234+1323_234+1324d others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | |||||
chr8:123431337
|
CAAA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(91): Show | 115 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.234+1322_234+1324d others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | |||||
chr8:123431337
|
CAAAA | C | 140 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(137): Show | 186 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.234+1321_234+1324d others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | |||||
chr8:123431364
|
T | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1331T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431364 | ||||||
chr8:123431381
|
C | T | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+1348C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431381 | ||||||
chr8:123431419
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1386G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431419 | ||||||
chr8:123431429
|
C | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1396C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431429 | ||||||
chr8:123431439
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.234+1406G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431439 | ||||||
chr8:123431574
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.234+1541C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431574 | ||||||
chr8:123431593
|
T | C | 1 | a0002c0002t0002g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.234+1560T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431593 | ||||||
chr8:123431773
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1740G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431773 | ||||||
chr8:123431774
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+1741C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431774 | ||||||
chr8:123431784
|
G | A | 1 | a0002c0002t0002g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234+1751G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431784 | ||||||
chr8:123431794
|
G | C | 1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.234+1761G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431794 | ||||||
chr8:123431881
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.234+1848G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431881 | ||||||
chr8:123431937
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.234+1904G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431937 | ||||||
chr8:123432237
|
T | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0235a0001c0001t0001g0237others(1): Show | 4 | HG00673.hp1 NA18981.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+2204T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432237 | ||||||
chr8:123432256
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2223A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432256 | ||||||
chr8:123432344
|
C | G | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+2311C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432344 | ||||||
chr8:123432375
|
C | T | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(3): Show | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+2342C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432375 | ||||||
chr8:123432496
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2463G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432496 | ||||||
chr8:123432512
|
G | A | 125 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(122): Show | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2479G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432512 | ||||||
chr8:123432599
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2566T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432599 | ||||||
chr8:123432630
|
A | C | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+2597A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432630 | ||||||
chr8:123432678
|
T | C | 1 | a0002c0002t0002g0121 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.234+2645T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432678 | ||||||
chr8:123432687
|
A | AT | 293 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(290): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.234+2664dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123432687 | |||||
chr8:123432719
|
G | A | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(3): Show | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+2686G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432719 | ||||||
chr8:123432776
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2743G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432776 | ||||||
chr8:123432834
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2801C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432834 | ||||||
chr8:123432876
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.234+2843T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432876 | ||||||
chr8:123432895
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2862A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432895 | ||||||
chr8:123432905
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234+2872C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432905 | ||||||
chr8:123433029
|
C | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.234+2996C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433029 | ||||||
chr8:123433241
|
G | T | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+3208G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433241 | ||||||
chr8:123433493
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.235-2960G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433493 | ||||||
chr8:123433519
|
C | T | 29 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0013others(26): Show | 47 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.235-2934C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433519 | ||||||
chr8:123433557
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0279 | 3 | HG02055.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235-2896C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433557 | ||||||
chr8:123433604
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 347 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
intron_variant | MODIFIER | c.235-2849T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433604 | ||||||
chr8:123433609
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.235-2844G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433609 | ||||||
chr8:123433925
|
A | AT | 24 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0075others(21): Show | 27 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.235-2514dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123433925 | |||||
chr8:123433925
|
A | ATT | 124 | a0001c0001t0001g0072a0001c0001t0001g0074a0002c0002t0002g0002others(121): Show | 167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.235-2515_235-2514d others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123433925 | |||||
chr8:123433925
|
AT | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(115): Show | 141 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.235-2514delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123433925 | |||||
chr8:123434038
|
G | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.235-2415G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434038 | ||||||
chr8:123434129
|
G | GCTCCTGC others(10): Show |
1 | a0001c0001t0001g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.235-2297_235-2281d others(19): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123434129 | |||||
chr8:123434129
|
GCTCCTGC others(10): Show |
G | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0285 | 3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.235-2297_235-2281d others(19): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123434129 | |||||
chr8:123434205
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.235-2248G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434205 | ||||||
chr8:123434316
|
T | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-2137T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434316 | ||||||
chr8:123434352
|
C | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0239 | 2 | HG01123.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.235-2101C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434352 | ||||||
chr8:123434556
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1897T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434556 | ||||||
chr8:123434557
|
G | A | 1 | a0002c0002t0002g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.235-1896G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434557 | ||||||
chr8:123434573
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1880T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434573 | ||||||
chr8:123434579
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.235-1874T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434579 | ||||||
chr8:123434632
|
C | G | 1 | a0002c0002t0002g0145 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.235-1821C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434632 | ||||||
chr8:123434661
|
G | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1792G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434661 | ||||||
chr8:123434690
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1763A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434690 | ||||||
chr8:123434697
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1756G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434697 | ||||||
chr8:123434714
|
G | A | 1 | a0002c0002t0002g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235-1739G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434714 | ||||||
chr8:123434829
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1624T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434829 | ||||||
chr8:123435016
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.235-1437A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435016 | ||||||
chr8:123435068
|
A | G | 1 | a0001c0001t0003g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235-1385A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435068 | ||||||
chr8:123435092
|
T | C | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(3): Show | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-1361T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435092 | ||||||
chr8:123435122
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-1331T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435122 | ||||||
chr8:123435224
|
C | T | 2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.235-1229C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435224 | ||||||
chr8:123435243
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.235-1210C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435243 | ||||||
chr8:123435357
|
CT | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0218a0001c0001t0001g0274others(2): Show | 5 | HG00323.hp1 HG00323.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-1089delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123435357 | |||||
chr8:123435449
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235-1004C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435449 | ||||||
chr8:123435546
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235-907T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435546 | ||||||
chr8:123435559
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-894A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435559 | ||||||
chr8:123435749
|
C | T | 3 | a0001c0001t0001g0243a0001c0001t0001g0277a0001c0001t0001g0288 | 3 | NA18747.hp1 NA18974.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.235-704C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435749 | ||||||
chr8:123435782
|
G | A | 54 | a0002c0002t0002g0004a0002c0002t0002g0009a0002c0002t0002g0010others(51): Show | 70 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.235-671G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435782 | ||||||
chr8:123435870
|
T | A | 1 | a0003c0006t0001g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.235-583T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435870 | ||||||
chr8:123435881
|
T | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-572T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435881 | ||||||
chr8:123435948
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-505G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435948 | ||||||
chr8:123435948
|
G | T | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.235-505G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435948 | ||||||
chr8:123436102
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-351G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436102 | ||||||
chr8:123436123
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235-330C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436123 | ||||||
chr8:123436169
|
C | CA | 46 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0034others(43): Show | 50 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.235-263dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123436169 | |||||
chr8:123436169
|
CA | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0024others(61): Show | 80 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.235-263delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123436169 | |||||
chr8:123436169
|
CAA | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0027others(34): Show | 42 | HG00408.hp1 HG00609.hp1 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.235-264_235-263del others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123436169 | |||||
chr8:123436190
|
A | T | 1 | a0001c0001t0001g0290 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.235-263A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436190 | ||||||
chr8:123436212
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-241A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436212 | ||||||
chr8:123436273
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235-180C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436273 | ||||||
chr8:123436285
|
A | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.235-168A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436285 | ||||||
chr8:123436307
|
G | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(93): Show | 117 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.235-146G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436307 | ||||||
chr8:123436436
|
G | T | 1 | a0002c0002t0002g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.235-17G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436436 | ||||||
chr8:123436449
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 347 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
splice_region_variant&intron_variant | LOW | c.235-4T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436449 | ||||||
chr8:123436667
|
CTT | C | 125 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(122): Show | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.383+76_383+77delTT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 123436667 | |||||
chr8:123436707
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.383+106A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123436707 | ||||||
chr8:123436840
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 359 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.383+239G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123436840 | ||||||
chr8:123436953
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.384-257C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123436953 | ||||||
chr8:123437028
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.384-182G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437028 | ||||||
chr8:123437031
|
G | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.384-179G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437031 | ||||||
chr8:123437095
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.384-115C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437095 | ||||||
chr8:123437103
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-107C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437103 | ||||||
chr8:123437168
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.384-42A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437168 | ||||||
chr8:123437432
|
T | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+98T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437432 | ||||||
chr8:123437472
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+138G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437472 | ||||||
chr8:123437478
|
C | T | 1 | a0001c0001t0003g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.508+144C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437478 | ||||||
chr8:123437502
|
C | G | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+168C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437502 | ||||||
chr8:123437594
|
T | C | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.508+260T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437594 | ||||||
chr8:123437595
|
A | C | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.508+261A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437595 | ||||||
chr8:123437696
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.508+362C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437696 | ||||||
chr8:123437702
|
CA | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(109): Show | 135 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.508+383delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123437702 | |||||
chr8:123437707
|
AAAAAAAA others(4): Show |
A | 122 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.508+380_508+390del others(11): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123437707 | |||||
chr8:123437708
|
AAAAAAAA others(3): Show |
A | 4 | a0002c0002t0002g0133a0002c0002t0002g0147a0002c0002t0002g0148others(1): Show | 4 | HG02071.hp2 HG02738.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+381_508+390del others(10): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123437708 | |||||
chr8:123437711
|
A | C | 41 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0056others(38): Show | 46 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.508+377A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437711 | ||||||
chr8:123437859
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.508+525A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437859 | ||||||
chr8:123437876
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+542C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437876 | ||||||
chr8:123437938
|
C | T | 4 | a0002c0002t0002g0018a0002c0002t0002g0110a0002c0002t0002g0131others(1): Show | 5 | HG01071.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+604C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437938 | ||||||
chr8:123437945
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+611T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437945 | ||||||
chr8:123438023
|
A | T | 1 | a0002c0002t0002g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508+689A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438023 | ||||||
chr8:123438087
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.508+753C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438087 | ||||||
chr8:123438124
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+790G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438124 | ||||||
chr8:123438163
|
T | C | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.508+829T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438163 | ||||||
chr8:123438191
|
A | G | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.508+857A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438191 | ||||||
chr8:123438391
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+1057T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438391 | ||||||
chr8:123438448
|
G | A | 15 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(12): Show | 17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.508+1114G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438448 | ||||||
chr8:123438477
|
G | A | 6 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(3): Show | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+1143G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438477 | ||||||
chr8:123438485
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+1151G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438485 | ||||||
chr8:123438603
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.508+1269C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438603 | ||||||
chr8:123438672
|
C | CA | 226 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(223): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.508+1351dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123438672 | |||||
chr8:123438723
|
T | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.508+1389T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438723 | ||||||
chr8:123438764
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+1430G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438764 | ||||||
chr8:123438789
|
C | G | 1 | a0001c0001t0006g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.508+1455C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438789 | ||||||
chr8:123438842
|
A | C | 1 | a0002c0002t0002g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.508+1508A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438842 | ||||||
chr8:123438905
|
C | T | 4 | a0002c0002t0002g0018a0002c0002t0002g0110a0002c0002t0002g0131others(1): Show | 5 | HG01071.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+1571C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438905 | ||||||
chr8:123439028
|
C | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.508+1694C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439028 | ||||||
chr8:123439113
|
G | A | 1 | a0002c0002t0002g0121 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.508+1779G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439113 | ||||||
chr8:123439158
|
G | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0027others(32): Show | 40 | HG00408.hp1 HG00609.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.508+1824G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439158 | ||||||
chr8:123439271
|
T | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.508+1937T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439271 | ||||||
chr8:123439345
|
G | GT | 113 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0094others(110): Show | 157 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.509-1946dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439345 | |||||
chr8:123439345
|
G | GTT | 10 | a0002c0002t0002g0123a0002c0002t0002g0127a0002c0002t0002g0141others(7): Show | 10 | HG01952.hp1 HG02015.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.509-1947_509-1946d others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439345 | |||||
chr8:123439345
|
GT | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(113): Show | 139 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.509-1946delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439345 | |||||
chr8:123439359
|
T | A | 14 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-1947T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439359 | ||||||
chr8:123439361
|
G | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-1945G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439361 | ||||||
chr8:123439365
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(97): Show | 123 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.509-1941C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439365 | ||||||
chr8:123439428
|
C | T | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.509-1878C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439428 | ||||||
chr8:123439435
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(97): Show | 123 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.509-1871C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439435 | ||||||
chr8:123439536
|
T | TG | 3 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0042 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-1766dupG | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439536 | |||||
chr8:123439547
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-1759C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439547 | ||||||
chr8:123439621
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509-1685C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439621 | ||||||
chr8:123439635
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-1671C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439635 | ||||||
chr8:123439636
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-1670G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439636 | ||||||
chr8:123439698
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(246): Show | 316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.509-1608T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439698 | ||||||
chr8:123439707
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509-1599C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439707 | ||||||
chr8:123439748
|
C | G | 1 | a0002c0007t0002g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.509-1558C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439748 | ||||||
chr8:123440106
|
G | C | 1 | a0002c0002t0002g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509-1200G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440106 | ||||||
chr8:123440127
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509-1179C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440127 | ||||||
chr8:123440146
|
C | CT | 15 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0050others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.509-1133dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
C | CTTT | 15 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0061others(12): Show | 18 | HG00323.hp2 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.509-1135_509-1133d others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
C | CTTTT | 11 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(8): Show | 11 | HG00140.hp1 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-1136_509-1133d others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0003g0093a0001c0001t0006g0070 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509-1143_509-1133d others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.509-1148_509-1133d others(18): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
CTTT | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0257a0001c0001t0001g0266others(6): Show | 11 | HG02015.hp1 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-1135_509-1133d others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
CTTTT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0023others(89): Show | 112 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.509-1136_509-1133d others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440146
|
CTTTTT | C | 120 | a0001c0001t0001g0025a0001c0001t0001g0205a0001c0001t0001g0209others(117): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.509-1137_509-1133d others(7): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | |||||
chr8:123440190
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-1116C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440190 | ||||||
chr8:123440258
|
C | T | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.509-1048C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440258 | ||||||
chr8:123440338
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509-968T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440338 | ||||||
chr8:123440392
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509-914G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440392 | ||||||
chr8:123440463
|
G | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-843G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440463 | ||||||
chr8:123440466
|
T | C | 2 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.509-840T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440466 | ||||||
chr8:123440481
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0285 | 3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.509-825T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440481 | ||||||
chr8:123440502
|
C | CT | 122 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0090others(119): Show | 166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.509-788dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440502 | |||||
chr8:123440504
|
T | TC | 6 | a0002c0002t0002g0039a0002c0002t0002g0044a0002c0002t0002g0106others(3): Show | 6 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.509-802_509-801ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440504 | ||||||
chr8:123440647
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.509-659G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440647 | ||||||
chr8:123440743
|
T | G | 14 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-563T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440743 | ||||||
chr8:123440783
|
G | A | 3 | a0002c0002t0002g0127a0002c0002t0002g0128a0002c0002t0002g0132 | 3 | NA18997.hp1 NA19054.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.509-523G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440783 | ||||||
chr8:123440789
|
A | C | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-517A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440789 | ||||||
chr8:123440836
|
C | T | 8 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(5): Show | 8 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.509-470C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440836 | ||||||
chr8:123440963
|
C | T | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-343C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440963 | ||||||
chr8:123440990
|
TCATGAAG others(8): Show |
T | 1 | a0001c0001t0007g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.509-312_509-298del others(15): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440990 | |||||
chr8:123441040
|
C | CA | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.509-266_509-265ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441040 | ||||||
chr8:123441067
|
G | A | 1 | a0002c0002t0002g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.509-239G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441067 | ||||||
chr8:123441160
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509-146A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441160 | ||||||
chr8:123441303
|
T | A | 126 | a0002c0002t0002g0002a0002c0002t0002g0003a0002c0002t0002g0004others(123): Show | 170 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(167): Show |
splice_region_variant&intron_variant | LOW | c.509-3T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441303 |