geneid | 4683 |
---|---|
ensemblid | ENSG00000104320.15 |
hgncid | 7652 |
symbol | NBN |
name | nibrin |
refseq_nuc | NM_002485.5 |
refseq_prot | NP_002476.2 |
ensembl_nuc | ENST00000265433.8 |
ensembl_prot | ENSP00000265433.4 |
mane_status | MANE Select |
chr | chr8 |
start | 89933331 |
end | 89984667 |
strand | - |
ver | v1.2 |
region | chr8:89933331-89984667 |
region5000 | chr8:89928331-89989667 |
regionname0 | NBN_chr8_89933331_89984667 |
regionname5000 | NBN_chr8_89928331_89989667 |
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 | 1/1 | 754 | 222 | 62 | 33 | 90 | 10 | 25 | 69 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002 | 0/0 | 754 | 149 | 12 | 31 | 83 | 8 | 15 | 63 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0003 | 0/0 | 754 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0004 | 0/0 | 754 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0005 | 0/0 | 754 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0006 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0007 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0008 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0009 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0010 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0011 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0012 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0013 | 0/0 | 754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0014 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0015 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0016 | 0/0 | 754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
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 | 0/0 | 2265 | 147 | 12 | 31 | 81 | 8 | 15 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0002 | 1/1 | 2265 | 126 | 16 | 24 | 55 | 9 | 20 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0003 | 0/0 | 2265 | 86 | 36 | 9 | 35 | 1 | 5 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0004 | 0/0 | 2265 | 10 | 10 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0005 | 0/0 | 2265 | 4 | 4 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0006 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0007 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0008 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0009 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0010 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0011 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0012 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0013 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0014 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0015 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0016 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0017 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0018 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0019 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
c0020 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
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 | 0/0 | 2358 | 133 | 18 | 20 | 68 | 8 | 19 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0002 | 1/1 | 2358 | 107 | 6 | 25 | 51 | 8 | 15 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0003 | 0/0 | 2358 | 44 | 15 | 7 | 19 | 1 | 2 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0004 | 0/0 | 2358 | 42 | 0 | 8 | 32 | 1 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0005 | 0/0 | 2358 | 18 | 15 | 0 | 2 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0006 | 0/0 | 2358 | 10 | 9 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0007 | 0/0 | 2358 | 5 | 4 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0008 | 0/0 | 2358 | 5 | 3 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0009 | 0/0 | 2358 | 4 | 4 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0010 | 0/0 | 2358 | 3 | 0 | 0 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0011 | 0/0 | 2358 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0012 | 0/0 | 2358 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0013 | 0/0 | 2358 | 2 | 1 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0014 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0015 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0016 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0017 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0018 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0019 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0020 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0021 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0022 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0023 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0024 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0025 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
t0026 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
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 | 15 | 2 | 0 | 13 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0002 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0003 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0005 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0008 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0010 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0012 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0013 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0014 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0016 | 1/1 | 4 | 0 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0021 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/1 | 2265 | 126 | 16 | 24 | 55 | 9 | 20 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003 | 0/0 | 2265 | 86 | 36 | 9 | 35 | 1 | 5 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0004 | 0/0 | 2265 | 10 | 10 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001 | 0/0 | 2265 | 147 | 12 | 31 | 81 | 8 | 15 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0009 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0011 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0003c0005 | 0/0 | 2265 | 4 | 4 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0004c0007 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0005c0006 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0006c0019 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0007c0018 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0008c0016 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0009c0015 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0010c0020 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0011c0014 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0012c0017 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0013c0010 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0014c0008 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0015c0012 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0016c0013 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 4622 | 7 | 0 | 0 | 2 | 1 | 4 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0002 | 1/1 | 4622 | 94 | 4 | 23 | 44 | 8 | 13 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0003 | 0/0 | 4622 | 12 | 7 | 0 | 4 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0004 | 0/0 | 4622 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0005 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0009 | 0/0 | 4622 | 4 | 4 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0012 | 0/0 | 4622 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0014 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0021 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0022 | 0/0 | 4622 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0002t0025 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0001 | 0/0 | 4622 | 14 | 9 | 1 | 3 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0002 | 0/0 | 4622 | 6 | 1 | 0 | 3 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0003 | 0/0 | 4622 | 9 | 4 | 1 | 4 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0004 | 0/0 | 4622 | 32 | 0 | 6 | 24 | 1 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0005 | 0/0 | 4622 | 9 | 7 | 0 | 1 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0006 | 0/0 | 4622 | 7 | 7 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0007 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0008 | 0/0 | 4622 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0016 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0017 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0019 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0023 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0003t0026 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0004t0001 | 0/0 | 4622 | 3 | 3 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0004t0005 | 0/0 | 4622 | 6 | 6 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0001c0004t0015 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0001 | 0/0 | 4622 | 101 | 2 | 18 | 60 | 7 | 14 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0002 | 0/0 | 4622 | 6 | 1 | 2 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0003 | 0/0 | 4622 | 19 | 0 | 6 | 11 | 1 | 1 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0004 | 0/0 | 4622 | 5 | 0 | 2 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0005 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0006 | 0/0 | 4622 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0007 | 0/0 | 4622 | 4 | 3 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0008 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0010 | 0/0 | 4622 | 3 | 0 | 0 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0013 | 0/0 | 4622 | 2 | 1 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0020 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0001t0024 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0009t0001 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0002c0011t0001 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0003c0005t0003 | 0/0 | 4622 | 3 | 3 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0003c0005t0011 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0004c0007t0001 | 0/0 | 4622 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0005c0006t0003 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0005c0006t0011 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0006c0019t0004 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0007c0018t0001 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0008c0016t0008 | 0/0 | 4622 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0009c0015t0018 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0010c0020t0002 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0011c0014t0004 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0012c0017t0005 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0013c0010t0001 | 0/0 | 4622 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0014c0008t0001 | 0/0 | 4622 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0015c0012t0001 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
a0016c0013t0004 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | copy fasta | chr8 | 89928331 | 89989667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0001 | 0/0 | 15 | 2 | 0 | 13 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0010 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0016 | 1/1 | 4 | 0 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0021 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0003g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0009g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0012g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0014g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0021g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0022g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0002t0025g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0005 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0006g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0016g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0017g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0019g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0023g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0003t0026g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0001c0004t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0002 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0003 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0006g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0007g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0010g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0013g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0020g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0001t0024g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0002c0011t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0003c0005t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0003c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0003c0005t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0004c0007t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0004c0007t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0005c0006t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0005c0006t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0006c0019t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0007c0018t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0008c0016t0008g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0009c0015t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0010c0020t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0011c0014t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0012c0017t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0013c0010t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0014c0008t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0015c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
a0016c0013t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0092 | EUR | GBR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0044 | EUR | GBR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00140 | hp1 | a0002 | c0001 | t0001 | g0014 | EUR | GBR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0190 | EUR | GBR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0219 | EUR | FIN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00280 | hp2 | a0001 | c0003 | t0004 | g0005 | EUR | FIN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | FIN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00323 | hp2 | a0002 | c0001 | t0001 | g0115 | EUR | FIN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00438 | hp1 | a0011 | c0014 | t0004 | g0163 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0133 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00544 | hp1 | a0001 | c0003 | t0004 | g0254 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0087 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00597 | hp1 | a0001 | c0003 | t0004 | g0149 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00597 | hp2 | a0002 | c0001 | t0001 | g0031 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00609 | hp2 | a0001 | c0003 | t0004 | g0232 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00642 | hp1 | a0002 | c0001 | t0001 | g0083 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00642 | hp2 | a0002 | c0001 | t0003 | g0121 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0080 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00673 | hp2 | a0002 | c0001 | t0003 | g0036 | EAS | CHS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00735 | hp2 | a0002 | c0001 | t0007 | g0018 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0053 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01070 | hp1 | a0001 | c0003 | t0003 | g0264 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01081 | hp1 | a0002 | c0001 | t0003 | g0129 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0024 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01106 | hp2 | a0002 | c0001 | t0003 | g0003 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01109 | hp1 | a0008 | c0016 | t0008 | g0263 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01167 | hp1 | a0002 | c0001 | t0013 | g0039 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01175 | hp1 | a0001 | c0002 | t0022 | g0257 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01175 | hp2 | a0002 | c0001 | t0003 | g0127 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0024 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01243 | hp2 | a0002 | c0001 | t0006 | g0019 | AMR | PUR | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01255 | hp1 | a0002 | c0001 | t0003 | g0130 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01261 | hp1 | a0001 | c0003 | t0008 | g0250 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01358 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01358 | hp2 | a0002 | c0001 | t0004 | g0038 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01361 | hp1 | a0002 | c0001 | t0004 | g0038 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0098 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01496 | hp2 | a0002 | c0001 | t0003 | g0003 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | IBS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0230 | EUR | IBS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0008 | EUR | IBS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0014 | EUR | IBS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0008 | EUR | IBS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0022 | EUR | IBS | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01884 | hp2 | a0001 | c0003 | t0005 | g0172 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01891 | hp1 | a0001 | c0003 | t0023 | g0056 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0144 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01928 | hp1 | a0001 | c0003 | t0004 | g0005 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0116 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01934 | hp1 | a0002 | c0001 | t0002 | g0082 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0211 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01943 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01943 | hp2 | a0001 | c0003 | t0004 | g0158 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01952 | hp2 | a0001 | c0003 | t0004 | g0005 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01975 | hp2 | a0002 | c0001 | t0002 | g0119 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01981 | hp2 | a0001 | c0003 | t0004 | g0005 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02004 | hp1 | a0001 | c0003 | t0004 | g0150 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02015 | hp2 | a0001 | c0002 | t0014 | g0051 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0217 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02027 | hp2 | a0002 | c0001 | t0004 | g0135 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02040 | hp1 | a0001 | c0003 | t0003 | g0161 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02040 | hp2 | a0001 | c0002 | t0004 | g0218 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02055 | hp1 | a0001 | c0002 | t0009 | g0138 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02055 | hp2 | a0001 | c0004 | t0005 | g0064 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0076 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02074 | hp1 | a0001 | c0003 | t0004 | g0143 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02080 | hp1 | a0001 | c0003 | t0004 | g0005 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02080 | hp2 | a0002 | c0001 | t0001 | g0033 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02083 | hp1 | a0002 | c0001 | t0001 | g0099 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02132 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02132 | hp2 | a0001 | c0003 | t0004 | g0164 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0268 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02145 | hp2 | a0001 | c0003 | t0007 | g0178 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | CDX | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02258 | hp1 | a0001 | c0003 | t0003 | g0251 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02258 | hp2 | a0001 | c0002 | t0021 | g0208 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02280 | hp2 | a0002 | c0001 | t0007 | g0018 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02293 | hp1 | a0001 | c0003 | t0004 | g0155 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02293 | hp2 | a0013 | c0010 | t0001 | g0097 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0073 | AMR | PEL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02523 | hp2 | a0002 | c0001 | t0003 | g0036 | EAS | KHV | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02572 | hp1 | a0001 | c0003 | t0003 | g0260 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0265 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0223 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0012 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02615 | hp1 | a0001 | c0003 | t0026 | g0270 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02615 | hp2 | a0001 | c0003 | t0006 | g0055 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02622 | hp1 | a0001 | c0004 | t0005 | g0063 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02622 | hp2 | a0001 | c0003 | t0003 | g0252 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02630 | hp1 | a0004 | c0007 | t0001 | g0184 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0058 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0102 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02717 | hp2 | a0001 | c0003 | t0005 | g0179 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02723 | hp1 | a0001 | c0003 | t0005 | g0170 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02723 | hp2 | a0002 | c0001 | t0006 | g0019 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0214 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02738 | hp2 | a0001 | c0003 | t0005 | g0175 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02809 | hp1 | a0001 | c0004 | t0005 | g0057 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02809 | hp2 | a0002 | c0001 | t0020 | g0078 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02818 | hp1 | a0005 | c0006 | t0011 | g0169 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02818 | hp2 | a0001 | c0003 | t0016 | g0245 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02886 | hp1 | a0001 | c0003 | t0006 | g0017 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02886 | hp2 | a0009 | c0015 | t0018 | g0258 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02895 | hp1 | a0001 | c0004 | t0005 | g0065 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02896 | hp1 | a0001 | c0003 | t0006 | g0253 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02896 | hp2 | a0003 | c0005 | t0003 | g0117 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02897 | hp1 | a0003 | c0005 | t0003 | g0035 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02922 | hp1 | a0002 | c0001 | t0005 | g0125 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02922 | hp2 | a0001 | c0003 | t0005 | g0176 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02965 | hp1 | a0001 | c0004 | t0015 | g0052 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02965 | hp2 | a0001 | c0004 | t0005 | g0062 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02970 | hp1 | a0001 | c0003 | t0008 | g0247 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02970 | hp2 | a0014 | c0008 | t0001 | g0077 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03017 | hp2 | a0002 | c0001 | t0003 | g0003 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0180 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03041 | hp2 | a0002 | c0001 | t0002 | g0067 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03098 | hp1 | a0001 | c0004 | t0001 | g0060 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03098 | hp2 | a0001 | c0003 | t0006 | g0183 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03130 | hp1 | a0001 | c0003 | t0003 | g0261 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03130 | hp2 | a0012 | c0017 | t0005 | g0181 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03139 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03139 | hp2 | a0001 | c0003 | t0017 | g0182 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03195 | hp1 | a0004 | c0007 | t0001 | g0185 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03209 | hp1 | a0003 | c0005 | t0011 | g0118 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03209 | hp2 | a0002 | c0001 | t0001 | g0266 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03225 | hp1 | a0003 | c0005 | t0003 | g0035 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03225 | hp2 | a0002 | c0001 | t0007 | g0018 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0028 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0259 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03453 | hp2 | a0001 | c0003 | t0006 | g0017 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0267 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03486 | hp2 | a0007 | c0018 | t0001 | g0186 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0012 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03490 | hp2 | a0001 | c0003 | t0002 | g0042 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03491 | hp1 | a0002 | c0001 | t0001 | g0027 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03492 | hp1 | a0001 | c0003 | t0002 | g0042 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03492 | hp2 | a0002 | c0001 | t0001 | g0027 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03540 | hp1 | a0005 | c0006 | t0003 | g0246 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03540 | hp2 | a0001 | c0002 | t0009 | g0041 | AFR | GWD | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03579 | hp1 | a0002 | c0001 | t0008 | g0094 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03579 | hp2 | a0002 | c0001 | t0006 | g0019 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0071 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0174 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03669 | hp2 | a0001 | c0002 | t0012 | g0045 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0086 | SAS | STU | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03688 | hp2 | a0001 | c0002 | t0012 | g0045 | SAS | STU | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0012 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0162 | SAS | PJL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0028 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0203 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0088 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0089 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0081 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | BEB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0216 | SAS | STU | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | STU | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | STU | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG04228 | hp2 | a0002 | c0001 | t0001 | g0012 | SAS | STU | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | YRI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | YRI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | CHB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18612 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | CHB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | CHB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0153 | EAS | CHB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18906 | hp1 | a0001 | c0003 | t0005 | g0171 | AFR | YRI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18939 | hp1 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18939 | hp2 | a0001 | c0003 | t0004 | g0009 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18943 | hp2 | a0016 | c0013 | t0004 | g0141 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18944 | hp1 | a0002 | c0001 | t0002 | g0096 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18944 | hp2 | a0002 | c0001 | t0010 | g0032 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18945 | hp1 | a0001 | c0003 | t0004 | g0009 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18945 | hp2 | a0002 | c0001 | t0004 | g0037 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18946 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18948 | hp2 | a0001 | c0003 | t0004 | g0159 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18951 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18952 | hp2 | a0001 | c0003 | t0004 | g0156 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18953 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18953 | hp2 | a0002 | c0001 | t0003 | g0003 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18957 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18959 | hp1 | a0002 | c0001 | t0010 | g0066 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18959 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18961 | hp1 | a0002 | c0001 | t0003 | g0124 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18963 | hp1 | a0006 | c0019 | t0004 | g0148 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18963 | hp2 | a0002 | c0011 | t0001 | g0091 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18964 | hp2 | a0001 | c0003 | t0004 | g0009 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18965 | hp1 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18965 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18966 | hp2 | a0001 | c0003 | t0004 | g0146 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18968 | hp1 | a0002 | c0001 | t0003 | g0003 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18971 | hp2 | a0001 | c0003 | t0004 | g0157 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18975 | hp1 | a0015 | c0012 | t0001 | g0120 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18975 | hp2 | a0002 | c0001 | t0003 | g0123 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18977 | hp2 | a0001 | c0003 | t0003 | g0166 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18978 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18978 | hp2 | a0001 | c0003 | t0004 | g0244 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18983 | hp1 | a0001 | c0003 | t0004 | g0167 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18983 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18984 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18984 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18985 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18988 | hp1 | a0001 | c0003 | t0004 | g0005 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18989 | hp2 | a0002 | c0009 | t0001 | g0084 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18990 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18990 | hp2 | a0010 | c0020 | t0002 | g0239 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18991 | hp2 | a0002 | c0001 | t0003 | g0126 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18993 | hp2 | a0002 | c0001 | t0001 | g0040 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18998 | hp1 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA18999 | hp2 | a0002 | c0001 | t0024 | g0085 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19001 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19001 | hp2 | a0001 | c0002 | t0025 | g0269 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19002 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19003 | hp1 | a0002 | c0001 | t0003 | g0128 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19004 | hp1 | a0001 | c0003 | t0004 | g0020 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19006 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19007 | hp1 | a0001 | c0003 | t0004 | g0020 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19009 | hp1 | a0001 | c0003 | t0005 | g0173 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19030 | hp1 | a0002 | c0001 | t0013 | g0039 | AFR | LWK | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19030 | hp2 | a0001 | c0003 | t0005 | g0177 | AFR | LWK | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19043 | hp1 | a0001 | c0003 | t0006 | g0017 | AFR | LWK | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19043 | hp2 | a0002 | c0001 | t0007 | g0093 | AFR | LWK | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19054 | hp1 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19054 | hp2 | a0001 | c0003 | t0004 | g0009 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19057 | hp1 | a0002 | c0001 | t0003 | g0003 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19057 | hp2 | a0001 | c0003 | t0004 | g0009 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19058 | hp2 | a0002 | c0001 | t0003 | g0003 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19060 | hp1 | a0002 | c0001 | t0004 | g0037 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19060 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19062 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19062 | hp2 | a0001 | c0003 | t0004 | g0020 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19064 | hp1 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19065 | hp2 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19066 | hp2 | a0002 | c0001 | t0010 | g0032 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19067 | hp1 | a0002 | c0001 | t0001 | g0040 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0256 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19070 | hp1 | a0001 | c0003 | t0004 | g0145 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19072 | hp2 | a0002 | c0001 | t0001 | g0101 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19074 | hp2 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19077 | hp2 | a0002 | c0001 | t0001 | g0079 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19082 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19082 | hp2 | a0001 | c0003 | t0004 | g0140 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19084 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19085 | hp1 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19086 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19086 | hp2 | a0001 | c0003 | t0003 | g0152 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19088 | hp1 | a0001 | c0003 | t0004 | g0154 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19088 | hp2 | a0002 | c0001 | t0002 | g0108 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19089 | hp1 | a0002 | c0001 | t0002 | g0105 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19089 | hp2 | a0002 | c0001 | t0003 | g0003 | EAS | JPT | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0262 | AFR | YRI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | TSI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0013 | EUR | TSI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA20805 | hp1 | a0002 | c0001 | t0003 | g0122 | EUR | TSI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0021 | EUR | TSI | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0100 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG01123 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02109 | hp1 | a0001 | c0003 | t0006 | g0017 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02109 | hp2 | a0001 | c0003 | t0008 | g0248 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG02486 | hp2 | a0001 | c0004 | t0005 | g0061 | AFR | ACB | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03471 | hp1 | a0001 | c0003 | t0002 | g0249 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG03471 | hp2 | a0001 | c0002 | t0009 | g0041 | AFR | MSL | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG06807 | hp1 | a0001 | c0002 | t0009 | g0139 | AFR | USA | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0224 | AFR | USA | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | USA | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA20300 | hp2 | a0001 | c0003 | t0005 | g0054 | AFR | USA | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | LWK | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
NA21309 | hp2 | a0001 | c0003 | t0019 | g0235 | AFR | LWK | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0016 | REF | REF | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0016 | REF | REF | NBN_chr8_89928331_89989667 | NBN | chr8 | 89928331 | 89989667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:89943291
|
T | C | 1 | a0005 | 2 | HG02818.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.2146A>G | p.Asn716Asp | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/16 | 2252/4622 | 2146/2265 | 716/754 | chr8 | 89943291 | ||
chr8:89946172
|
C | T | 1 | a0008 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2038G>A | p.Gly680Ser | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/16 | 2144/4622 | 2038/2265 | 680/754 | chr8 | 89946172 | ||
chr8:89947856
|
C | T | 1 | a0009 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1882G>A | p.Glu628Lys | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/16 | 1988/4622 | 1882/2265 | 628/754 | chr8 | 89947856 | ||
chr8:89953280
|
G | T | 1 | a0010 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.1809C>A | p.Phe603Leu | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/16 | 1915/4622 | 1809/2265 | 603/754 | chr8 | 89953280 | ||
chr8:89953312
|
G | C | 1 | a0014 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1777C>G | p.Pro593Ala | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/16 | 1883/4622 | 1777/2265 | 593/754 | chr8 | 89953312 | ||
chr8:89953399
|
C | T | 1 | a0011 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1690G>A | p.Glu564Lys | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/16 | 1796/4622 | 1690/2265 | 564/754 | chr8 | 89953399 | ||
chr8:89953600
|
T | C | 1 | a0003 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.1489A>G | p.Thr497Ala | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/16 | 1595/4622 | 1489/2265 | 497/754 | chr8 | 89953600 | ||
chr8:89955307
|
T | C | 1 | a0013 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1373A>G | p.Tyr458Cys | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/16 | 1479/4622 | 1373/2265 | 458/754 | chr8 | 89955307 | ||
chr8:89955363
|
T | C | 1 | a0012 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1317A>G | p.Ile439Met | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/16 | 1423/4622 | 1317/2265 | 439/754 | chr8 | 89955363 | ||
chr8:89955458
|
T | C | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1222A>G | p.Lys408Glu | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/16 | 1328/4622 | 1222/2265 | 408/754 | chr8 | 89955458 | ||
chr8:89955476
|
T | C | 1 | a0006 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1204A>G | p.Thr402Ala | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/16 | 1310/4622 | 1204/2265 | 402/754 | chr8 | 89955476 | ||
chr8:89970463
|
G | A | 1 | a0004 | 2 | HG02630.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.797C>T | p.Pro266Leu | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/16 | 903/4622 | 797/2265 | 266/754 | chr8 | 89970463 | ||
chr8:89970472
|
A | G | 1 | a0014 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.788T>C | p.Phe263Ser | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/16 | 894/4622 | 788/2265 | 263/754 | chr8 | 89970472 | ||
chr8:89978251
|
C | G | 5 | a0002a0003a0013others(2): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
missense_variant | MODERATE | c.553G>C | p.Glu185Gln | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/16 | 659/4622 | 553/2265 | 185/754 | chr8 | 89978251 | ||
chr8:89978293
|
T | C | 1 | a0015 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.511A>G | p.Ile171Val | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/16 | 617/4622 | 511/2265 | 171/754 | chr8 | 89978293 | ||
chr8:89982788
|
A | C | 1 | a0016 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.105T>G | p.Ile35Met | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/16 | 211/4622 | 105/2265 | 35/754 | chr8 | 89982788 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:89937040
|
A | G | 1 | a0002c0009 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.2220T>C | p.Ala740Ala | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/16 | 2326/4622 | 2220/2265 | 740/754 | chr8 | 89937040 | ||
chr8:89943355
|
A | C | 1 | a0001c0004 | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.2082T>G | p.Pro694Pro | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/16 | 2188/4622 | 2082/2265 | 694/754 | chr8 | 89943355 | ||
chr8:89946194
|
T | C | 7 | a0002c0001a0002c0009a0002c0011others(4): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
synonymous_variant | LOW | c.2016A>G | p.Pro672Pro | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/16 | 2122/4622 | 2016/2265 | 672/754 | chr8 | 89946194 | ||
chr8:89955483
|
A | G | 18 | a0001c0003a0001c0004a0002c0001others(15): Show | 263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
synonymous_variant | LOW | c.1197T>C | p.Asp399Asp | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/16 | 1303/4622 | 1197/2265 | 399/754 | chr8 | 89955483 | ||
chr8:89958814
|
G | A | 1 | a0002c0011 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.1035C>T | p.Gly345Gly | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/16 | 1141/4622 | 1035/2265 | 345/754 | chr8 | 89958814 | ||
chr8:89982791
|
C | T | 8 | a0001c0004a0002c0001a0002c0009others(5): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
synonymous_variant | LOW | c.102G>A | p.Leu34Leu | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/16 | 208/4622 | 102/2265 | 34/754 | chr8 | 89982791 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:89933370
|
C | T | 7 | a0001c0002t0004a0001c0002t0025a0001c0003t0004others(4): Show | 43 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2212G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 2212 | chr8 | 89933370 | |||||
chr8:89933605
|
A | G | 23 | a0001c0002t0003a0001c0002t0004a0001c0002t0005others(20): Show | 119 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1977T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1977 | chr8 | 89933605 | |||||
chr8:89933621
|
A | G | 5 | a0001c0002t0005a0001c0003t0005a0001c0004t0005others(2): Show | 18 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1961T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1961 | chr8 | 89933621 | |||||
chr8:89933759
|
A | G | 1 | a0001c0002t0021 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1823T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1823 | chr8 | 89933759 | |||||
chr8:89933828
|
A | G | 19 | a0001c0002t0001a0001c0003t0001a0001c0003t0007others(16): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1754T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1754 | chr8 | 89933828 | |||||
chr8:89933890
|
T | C | 7 | a0001c0002t0004a0001c0002t0025a0001c0003t0004others(4): Show | 43 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1692A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1692 | chr8 | 89933890 | |||||
chr8:89933999
|
C | T | 1 | a0002c0001t0013 | 2 | HG01167.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1583G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1583 | chr8 | 89933999 | |||||
chr8:89934360
|
T | G | 2 | a0001c0003t0007a0002c0001t0007 | 5 | HG00735.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1222A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1222 | chr8 | 89934360 | |||||
chr8:89934369
|
C | A | 1 | a0001c0002t0022 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1213 | chr8 | 89934369 | |||||
chr8:89934373
|
T | G | 19 | a0001c0002t0001a0001c0003t0001a0001c0003t0007others(16): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1209A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1209 | chr8 | 89934373 | |||||
chr8:89934381
|
C | T | 1 | a0002c0001t0020 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1201G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1201 | chr8 | 89934381 | |||||
chr8:89934417
|
C | T | 1 | a0001c0003t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1165 | chr8 | 89934417 | |||||
chr8:89934550
|
C | G | 1 | a0009c0015t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1032G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1032 | chr8 | 89934550 | |||||
chr8:89934569
|
C | T | 1 | a0001c0002t0012 | 2 | HG03669.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1013G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 1013 | chr8 | 89934569 | |||||
chr8:89934645
|
A | G | 2 | a0001c0003t0006a0002c0001t0006 | 10 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*937T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 937 | chr8 | 89934645 | |||||
chr8:89934779
|
T | C | 1 | a0001c0003t0023 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*803A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 803 | chr8 | 89934779 | |||||
chr8:89934792
|
A | C | 2 | a0001c0003t0006a0002c0001t0006 | 10 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*790T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 790 | chr8 | 89934792 | |||||
chr8:89934825
|
T | C | 5 | a0001c0002t0005a0001c0003t0005a0001c0004t0005others(2): Show | 18 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*757A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 757 | chr8 | 89934825 | |||||
chr8:89935041
|
C | G | 18 | a0001c0002t0001a0001c0003t0001a0001c0003t0007others(15): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*541G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 541 | chr8 | 89935041 | |||||
chr8:89935078
|
T | C | 1 | a0002c0001t0010 | 3 | NA18944.hp2 NA18959.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*504A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 504 | chr8 | 89935078 | |||||
chr8:89935093
|
A | G | 1 | a0001c0003t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*489T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 489 | chr8 | 89935093 | |||||
chr8:89935163
|
G | A | 3 | a0001c0003t0008a0002c0001t0008a0008c0016t0008 | 5 | HG01109.hp1 HG01261.hp1 HG02109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*419C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 419 | chr8 | 89935163 | |||||
chr8:89935232
|
A | G | 1 | a0001c0003t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 350 | chr8 | 89935232 | |||||
chr8:89935266
|
T | C | 1 | a0001c0002t0009 | 4 | HG02055.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*316A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 316 | chr8 | 89935266 | |||||
chr8:89935309
|
C | T | 16 | a0001c0002t0001a0001c0003t0001a0001c0003t0007others(13): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*273G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 273 | chr8 | 89935309 | |||||
chr8:89935517
|
C | T | 1 | a0001c0003t0016 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 65 | chr8 | 89935517 | |||||
chr8:89935525
|
G | A | 1 | a0002c0001t0024 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 16/16 | 57 | chr8 | 89935525 | |||||
chr8:89984562
|
C | A | 1 | a0001c0002t0025 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/16 | 1 | chr8 | 89984562 | |||||
chr8:89984610
|
G | T | 1 | a0001c0004t0015 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/16 | 49 | chr8 | 89984610 | |||||
chr8:89984634
|
C | A | 1 | a0001c0003t0026 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-73G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/16 | 73 | chr8 | 89984634 | |||||
chr8:89984652
|
G | T | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 5_prime_UTR_variant | MODIFIER | c.-91C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/16 | 91 | chr8 | 89984652 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:89935630
|
G | A | 2 | a0001c0003t0004g0157a0001c0003t0004g0167 | 2 | NA18971.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2235-18C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89935630 | ||||||
chr8:89935784
|
G | A | 18 | a0001c0002t0005g0217a0001c0003t0005g0054a0001c0003t0005g0170others(15): Show | 18 | HG01884.hp2 HG02027.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2235-172C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89935784 | ||||||
chr8:89936045
|
C | T | 100 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(97): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2235-433G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936045 | ||||||
chr8:89936087
|
C | CT | 86 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(83): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2235-476dupA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936087 | ||||||
chr8:89936087
|
C | CTT | 16 | a0001c0002t0001g0242a0001c0003t0001g0023a0001c0003t0001g0050others(13): Show | 19 | HG01081.hp2 HG02056.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.2235-477_2235-476d others(4): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936087 | ||||||
chr8:89936087
|
CT | C | 22 | a0001c0002t0002g0204a0001c0002t0002g0210a0001c0002t0005g0217others(19): Show | 22 | HG01884.hp2 HG01943.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.2235-476delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936087 | ||||||
chr8:89936116
|
GTC | G | 2 | a0001c0003t0001g0023a0001c0003t0001g0267 | 4 | HG01081.hp2 HG02486.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2235-506_2235-505d others(4): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936116 | ||||||
chr8:89936138
|
C | T | 1 | a0001c0004t0001g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2235-526G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936138 | ||||||
chr8:89936153
|
C | T | 1 | a0001c0003t0005g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2235-541G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936153 | ||||||
chr8:89936154
|
G | A | 1 | a0001c0003t0004g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2235-542C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936154 | ||||||
chr8:89936158
|
C | A | 1 | a0001c0002t0002g0194 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2235-546G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936158 | ||||||
chr8:89936225
|
T | C | 8 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0260others(5): Show | 9 | HG01070.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2235-613A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936225 | ||||||
chr8:89936226
|
G | A | 8 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0260others(5): Show | 9 | HG01070.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2235-614C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936226 | ||||||
chr8:89936234
|
G | A | 8 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0260others(5): Show | 9 | HG01070.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2235-622C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936234 | ||||||
chr8:89936323
|
C | T | 8 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0260others(5): Show | 9 | HG01070.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2234+703G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936323 | ||||||
chr8:89936422
|
G | A | 1 | a0002c0001t0013g0039 | 2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2234+604C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936422 | ||||||
chr8:89936527
|
GGTTT | G | 103 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(100): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.2234+495_2234+498d others(6): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936527 | ||||||
chr8:89936771
|
C | T | 1 | a0001c0003t0004g0156 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2234+255G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936771 | ||||||
chr8:89936869
|
T | C | 32 | a0001c0002t0004g0218a0001c0002t0004g0241a0001c0002t0025g0269others(29): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2234+157A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936869 | ||||||
chr8:89936938
|
G | C | 29 | a0001c0002t0003g0004a0001c0002t0003g0046a0001c0002t0003g0144others(26): Show | 44 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.2234+88C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 15/15 | chr8 | 89936938 | ||||||
chr8:89937197
|
A | G | 21 | a0001c0002t0003g0004a0001c0002t0003g0046a0001c0002t0003g0144others(18): Show | 35 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.2185-122T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89937197 | ||||||
chr8:89937496
|
C | A | 103 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(100): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.2185-421G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89937496 | ||||||
chr8:89937652
|
A | C | 157 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(154): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2185-577T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89937652 | ||||||
chr8:89937666
|
C | T | 1 | a0002c0001t0001g0074 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2185-591G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89937666 | ||||||
chr8:89937812
|
T | G | 3 | a0003c0005t0011g0118a0005c0006t0003g0246a0005c0006t0011g0169 | 3 | HG02818.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2185-737A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89937812 | ||||||
chr8:89937962
|
C | A | 3 | a0003c0005t0011g0118a0005c0006t0003g0246a0005c0006t0011g0169 | 3 | HG02818.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2185-887G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89937962 | ||||||
chr8:89938033
|
T | A | 9 | a0001c0002t0001g0202a0001c0002t0001g0207a0001c0002t0001g0227others(6): Show | 13 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2185-958A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938033 | ||||||
chr8:89938074
|
T | C | 3 | a0001c0002t0005g0217a0001c0003t0005g0173a0001c0003t0005g0175 | 3 | HG02027.hp1 HG02738.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2185-999A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938074 | ||||||
chr8:89938274
|
T | C | 1 | a0002c0001t0001g0115 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2185-1199A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938274 | ||||||
chr8:89938310
|
T | C | 3 | a0003c0005t0011g0118a0005c0006t0003g0246a0005c0006t0011g0169 | 3 | HG02818.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2185-1235A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938310 | ||||||
chr8:89938373
|
C | T | 1 | a0001c0003t0005g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2185-1298G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938373 | ||||||
chr8:89938458
|
C | A | 2 | a0002c0001t0007g0018a0002c0001t0007g0093 | 4 | HG00735.hp2 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2185-1383G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938458 | ||||||
chr8:89938458
|
C | G | 5 | a0001c0003t0006g0017a0001c0003t0006g0055a0001c0003t0006g0183others(2): Show | 10 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2185-1383G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938458 | ||||||
chr8:89938460
|
C | A | 89 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(86): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2185-1385G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938460 | ||||||
chr8:89938462
|
C | A | 100 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(97): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2185-1387G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938462 | ||||||
chr8:89938464
|
A | C | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2185-1389T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938464 | ||||||
chr8:89938476
|
G | GTA | 5 | a0001c0003t0006g0017a0001c0003t0006g0055a0001c0003t0006g0183others(2): Show | 8 | HG02109.hp1 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2185-1402_2185-140 others(6): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938476 | ||||||
chr8:89938478
|
G | A | 156 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(153): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2185-1403C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938478 | ||||||
chr8:89938674
|
A | G | 1 | a0002c0001t0002g0096 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2185-1599T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938674 | ||||||
chr8:89938702
|
A | G | 2 | a0001c0003t0001g0174a0002c0001t0001g0088 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2185-1627T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938702 | ||||||
chr8:89938825
|
C | A | 48 | a0001c0002t0003g0004a0001c0002t0003g0046a0001c0002t0003g0144others(45): Show | 68 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.2185-1750G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938825 | ||||||
chr8:89938875
|
C | T | 98 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(95): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2185-1800G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89938875 | ||||||
chr8:89939041
|
A | T | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2185-1966T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939041 | ||||||
chr8:89939044
|
C | G | 129 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(126): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2185-1969G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939044 | ||||||
chr8:89939069
|
T | A | 123 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(120): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2185-1994A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939069 | ||||||
chr8:89939160
|
G | T | 108 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(105): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2185-2085C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939160 | ||||||
chr8:89939235
|
G | A | 1 | a0001c0002t0001g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2185-2160C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939235 | ||||||
chr8:89939257
|
CAG | C | 175 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(172): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2185-2184_2185-218 others(6): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939257 | ||||||
chr8:89939308
|
T | C | 55 | a0001c0002t0003g0046a0001c0002t0003g0256a0001c0002t0014g0051others(52): Show | 66 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.2185-2233A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939308 | ||||||
chr8:89939313
|
C | G | 7 | a0001c0003t0001g0050a0001c0003t0001g0180a0001c0004t0001g0058others(4): Show | 8 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2185-2238G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939313 | ||||||
chr8:89939319
|
C | A | 77 | a0001c0002t0003g0004a0001c0002t0003g0046a0001c0002t0003g0144others(74): Show | 101 | HG00673.hp2 HG01070.hp1 HG01081.hp1 others(98): Show |
intron_variant | MODIFIER | c.2185-2244G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939319 | ||||||
chr8:89939351
|
A | G | 1 | a0001c0002t0004g0218 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2185-2276T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939351 | ||||||
chr8:89939439
|
C | CA | 117 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(114): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2185-2365dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939439 | ||||||
chr8:89939589
|
G | A | 1 | a0001c0002t0002g0191 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2185-2514C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939589 | ||||||
chr8:89939590
|
T | A | 1 | a0002c0001t0005g0125 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2185-2515A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939590 | ||||||
chr8:89939657
|
A | G | 21 | a0001c0002t0002g0224a0001c0002t0003g0046a0001c0002t0003g0256others(18): Show | 33 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.2185-2582T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939657 | ||||||
chr8:89939702
|
G | A | 27 | a0001c0002t0004g0218a0001c0002t0025g0269a0001c0003t0001g0151others(24): Show | 38 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2185-2627C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939702 | ||||||
chr8:89939981
|
A | G | 98 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(95): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.2185-2906T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89939981 | ||||||
chr8:89940017
|
G | A | 26 | a0001c0002t0004g0218a0001c0003t0001g0151a0001c0003t0002g0153others(23): Show | 37 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.2185-2942C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940017 | ||||||
chr8:89940045
|
A | G | 2 | a0002c0001t0001g0265a0002c0001t0001g0266 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2185-2970T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940045 | ||||||
chr8:89940111
|
G | C | 3 | a0002c0001t0005g0125a0004c0007t0001g0184a0004c0007t0001g0185 | 3 | HG02630.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2185-3036C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940111 | ||||||
chr8:89940113
|
C | T | 3 | a0002c0001t0005g0125a0004c0007t0001g0184a0004c0007t0001g0185 | 3 | HG02630.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2185-3038G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940113 | ||||||
chr8:89940150
|
A | G | 96 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(93): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2185-3075T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940150 | ||||||
chr8:89940217
|
C | A | 1 | a0001c0002t0002g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2184+3036G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940217 | ||||||
chr8:89940415
|
C | A | 1 | a0001c0002t0002g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2184+2838G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940415 | ||||||
chr8:89940539
|
T | TA | 8 | a0001c0003t0003g0251a0001c0003t0003g0260a0001c0003t0003g0261others(5): Show | 9 | HG01070.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2184+2713dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940539 | ||||||
chr8:89940625
|
G | GA | 117 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(114): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.2184+2627dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940625 | ||||||
chr8:89940626
|
A | G | 8 | a0001c0003t0003g0251a0001c0003t0003g0260a0001c0003t0003g0261others(5): Show | 9 | HG01070.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2184+2627T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940626 | ||||||
chr8:89940678
|
C | T | 1 | a0001c0003t0004g0159 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2184+2575G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940678 | ||||||
chr8:89940763
|
T | C | 1 | a0001c0004t0005g0062 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2184+2490A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940763 | ||||||
chr8:89940856
|
C | T | 1 | a0002c0001t0001g0083 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2184+2397G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940856 | ||||||
chr8:89940980
|
A | G | 6 | a0001c0003t0001g0050a0001c0004t0001g0058a0001c0004t0001g0059others(3): Show | 7 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2184+2273T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89940980 | ||||||
chr8:89941004
|
G | T | 2 | a0002c0001t0001g0109a0002c0001t0001g0110 | 2 | HG02056.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2184+2249C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941004 | ||||||
chr8:89941019
|
T | C | 120 | a0001c0002t0001g0192a0001c0002t0001g0202a0001c0002t0001g0227others(117): Show | 180 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2184+2234A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941019 | ||||||
chr8:89941096
|
T | C | 2 | a0002c0001t0001g0265a0002c0001t0001g0266 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2184+2157A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941096 | ||||||
chr8:89941111
|
G | C | 87 | a0001c0002t0001g0192a0001c0002t0001g0202a0001c0002t0001g0227others(84): Show | 129 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.2184+2142C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941111 | ||||||
chr8:89941165
|
T | C | 6 | a0001c0004t0005g0057a0001c0004t0005g0061a0001c0004t0005g0062others(3): Show | 6 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2184+2088A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941165 | ||||||
chr8:89941220
|
A | G | 1 | a0001c0002t0002g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2184+2033T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941220 | ||||||
chr8:89941344
|
C | T | 37 | a0001c0003t0001g0142a0001c0003t0001g0151a0001c0003t0002g0153others(34): Show | 51 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2184+1909G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941344 | ||||||
chr8:89941469
|
C | T | 1 | a0002c0001t0001g0106 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2184+1784G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941469 | ||||||
chr8:89941669
|
C | T | 2 | a0001c0003t0001g0180a0012c0017t0005g0181 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2184+1584G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941669 | ||||||
chr8:89941830
|
T | A | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184+1423A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941830 | ||||||
chr8:89941915
|
A | G | 1 | a0001c0003t0023g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2184+1338T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89941915 | ||||||
chr8:89942064
|
T | C | 1 | a0001c0003t0026g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2184+1189A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942064 | ||||||
chr8:89942066
|
C | T | 17 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(14): Show | 20 | HG01884.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.2184+1187G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942066 | ||||||
chr8:89942183
|
C | T | 1 | a0002c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2184+1070G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942183 | ||||||
chr8:89942253
|
A | G | 225 | a0001c0002t0001g0190a0001c0002t0001g0202a0001c0002t0001g0207others(222): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2184+1000T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942253 | ||||||
chr8:89942373
|
A | C | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2184+880T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942373 | ||||||
chr8:89942421
|
T | A | 1 | a0007c0018t0001g0186 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2184+832A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942421 | ||||||
chr8:89942507
|
A | C | 34 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(31): Show | 46 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.2184+746T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942507 | ||||||
chr8:89942544
|
G | A | 1 | a0001c0003t0016g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2184+709C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942544 | ||||||
chr8:89942596
|
A | C | 1 | a0001c0003t0005g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2184+657T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942596 | ||||||
chr8:89942668
|
G | C | 1 | a0004c0007t0001g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2184+585C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942668 | ||||||
chr8:89942757
|
G | GA | 55 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(52): Show | 70 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2184+495dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942757 | ||||||
chr8:89942855
|
A | T | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2184+398T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942855 | ||||||
chr8:89942942
|
G | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2184+311C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942942 | ||||||
chr8:89942949
|
C | T | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2184+304G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89942949 | ||||||
chr8:89943025
|
T | G | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.2184+228A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89943025 | ||||||
chr8:89943038
|
C | CT | 103 | a0001c0003t0002g0249a0001c0003t0008g0247a0001c0003t0008g0248others(100): Show | 158 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.2184+214dupA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89943038 | ||||||
chr8:89943038
|
C | CTT | 11 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2184+213_2184+214d others(4): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89943038 | ||||||
chr8:89943038
|
CT | C | 10 | a0001c0002t0002g0213a0001c0003t0001g0050a0001c0003t0001g0259others(7): Show | 11 | HG01070.hp1 HG01109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2184+214delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89943038 | ||||||
chr8:89943068
|
T | C | 1 | a0006c0019t0004g0148 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2184+185A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89943068 | ||||||
chr8:89943130
|
C | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2184+123G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 14/15 | chr8 | 89943130 | ||||||
chr8:89943396
|
T | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2071-30A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89943396 | ||||||
chr8:89943427
|
T | A | 16 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(13): Show | 28 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2071-61A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89943427 | ||||||
chr8:89943582
|
G | A | 1 | a0001c0003t0007g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2071-216C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89943582 | ||||||
chr8:89943740
|
C | T | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2071-374G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89943740 | ||||||
chr8:89944015
|
G | T | 19 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(16): Show | 22 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2071-649C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89944015 | ||||||
chr8:89944091
|
TTTTG | T | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2071-729_2071-726d others(6): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89944091 | ||||||
chr8:89944109
|
A | G | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2071-743T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89944109 | ||||||
chr8:89944150
|
G | A | 3 | a0001c0003t0005g0054a0001c0003t0006g0055a0001c0003t0023g0056 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2071-784C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89944150 | ||||||
chr8:89944618
|
T | C | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2071-1252A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89944618 | ||||||
chr8:89945261
|
G | A | 2 | a0001c0002t0002g0211a0001c0002t0012g0045 | 3 | HG01934.hp2 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2070+879C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89945261 | ||||||
chr8:89945378
|
T | C | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070+762A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89945378 | ||||||
chr8:89945647
|
A | G | 7 | a0002c0001t0001g0015a0002c0001t0001g0033a0002c0001t0001g0103others(4): Show | 11 | HG00408.hp1 HG02074.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.2070+493T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89945647 | ||||||
chr8:89945714
|
A | C | 1 | a0003c0005t0011g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2070+426T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89945714 | ||||||
chr8:89945797
|
A | C | 1 | a0001c0003t0004g0020 | 3 | NA19004.hp1 NA19007.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2070+343T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89945797 | ||||||
chr8:89945928
|
A | T | 2 | a0001c0003t0005g0170a0001c0003t0005g0172 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2070+212T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89945928 | ||||||
chr8:89946107
|
A | G | 3 | a0001c0002t0009g0041a0001c0002t0009g0138a0001c0002t0009g0139 | 4 | HG02055.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2070+33T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 13/15 | chr8 | 89946107 | ||||||
chr8:89946302
|
T | C | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
splice_region_variant&intron_variant | LOW | c.1915-7A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89946302 | ||||||
chr8:89946317
|
T | C | 1 | a0001c0002t0002g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1915-22A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89946317 | ||||||
chr8:89946360
|
T | C | 1 | a0009c0015t0018g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1915-65A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89946360 | ||||||
chr8:89946435
|
G | T | 2 | a0001c0003t0005g0177a0001c0003t0007g0178 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1915-140C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89946435 | ||||||
chr8:89946696
|
A | G | 1 | a0002c0001t0013g0039 | 2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1915-401T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89946696 | ||||||
chr8:89946886
|
G | A | 1 | a0005c0006t0003g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1915-591C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89946886 | ||||||
chr8:89947175
|
A | T | 1 | a0001c0002t0009g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1914+649T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947175 | ||||||
chr8:89947311
|
C | G | 1 | a0001c0003t0005g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1914+513G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947311 | ||||||
chr8:89947401
|
G | A | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1914+423C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947401 | ||||||
chr8:89947448
|
A | G | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+376T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947448 | ||||||
chr8:89947515
|
G | C | 1 | a0002c0001t0003g0036 | 2 | HG00673.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1914+309C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947515 | ||||||
chr8:89947625
|
G | A | 2 | a0001c0002t0009g0041a0001c0002t0009g0139 | 3 | HG03471.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1914+199C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947625 | ||||||
chr8:89947656
|
AAAT | A | 2 | a0001c0002t0002g0048a0001c0002t0004g0241 | 3 | NA18939.hp1 NA18952.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1914+165_1914+167d others(5): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947656 | ||||||
chr8:89947772
|
T | C | 1 | a0002c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1914+52A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947772 | ||||||
chr8:89947814
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1914+10G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947814 | ||||||
chr8:89947815
|
G | A | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1914+9C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 12/15 | chr8 | 89947815 | ||||||
chr8:89947932
|
T | C | 1 | a0001c0003t0004g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1846-40A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89947932 | ||||||
chr8:89948141
|
T | C | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1846-249A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948141 | ||||||
chr8:89948143
|
T | G | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1846-251A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948143 | ||||||
chr8:89948201
|
A | G | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1846-309T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948201 | ||||||
chr8:89948275
|
G | A | 1 | a0001c0002t0002g0044 | 2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1846-383C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948275 | ||||||
chr8:89948282
|
G | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1846-390C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948282 | ||||||
chr8:89948318
|
T | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1846-426A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948318 | ||||||
chr8:89948340
|
G | A | 1 | a0001c0003t0016g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1846-448C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948340 | ||||||
chr8:89948546
|
T | G | 1 | a0001c0002t0002g0188 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1846-654A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948546 | ||||||
chr8:89948570
|
A | AG | 34 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(31): Show | 46 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1846-679_1846-678i others(3): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948570 | ||||||
chr8:89948571
|
A | T | 34 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(31): Show | 46 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1846-679T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948571 | ||||||
chr8:89948572
|
C | A | 34 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(31): Show | 46 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1846-680G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948572 | ||||||
chr8:89948746
|
A | G | 1 | a0002c0001t0002g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1846-854T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948746 | ||||||
chr8:89948808
|
C | G | 2 | a0001c0003t0001g0050a0001c0003t0003g0260 | 3 | HG02572.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1846-916G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948808 | ||||||
chr8:89948910
|
C | G | 2 | a0001c0002t0001g0190a0001c0002t0002g0189 | 2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1846-1018G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89948910 | ||||||
chr8:89949201
|
T | C | 17 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(14): Show | 30 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1846-1309A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949201 | ||||||
chr8:89949284
|
T | C | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1846-1392A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949284 | ||||||
chr8:89949387
|
T | C | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1846-1495A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949387 | ||||||
chr8:89949475
|
G | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1846-1583C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949475 | ||||||
chr8:89949686
|
A | T | 1 | a0002c0001t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1846-1794T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949686 | ||||||
chr8:89949738
|
T | C | 1 | a0002c0001t0003g0036 | 2 | HG00673.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1846-1846A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949738 | ||||||
chr8:89949813
|
G | A | 121 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(118): Show | 176 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1846-1921C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949813 | ||||||
chr8:89949900
|
T | C | 1 | a0002c0001t0001g0132 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1846-2008A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949900 | ||||||
chr8:89949965
|
A | C | 3 | a0001c0003t0005g0054a0001c0003t0006g0055a0001c0003t0023g0056 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1846-2073T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949965 | ||||||
chr8:89949999
|
G | A | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1846-2107C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89949999 | ||||||
chr8:89950109
|
T | C | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1846-2217A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950109 | ||||||
chr8:89950241
|
C | T | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1846-2349G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950241 | ||||||
chr8:89950278
|
A | G | 1 | a0001c0003t0026g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1846-2386T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950278 | ||||||
chr8:89950342
|
C | T | 2 | a0002c0001t0003g0121a0002c0001t0003g0122 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1846-2450G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950342 | ||||||
chr8:89950350
|
C | T | 1 | a0002c0001t0001g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1846-2458G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950350 | ||||||
chr8:89950450
|
AT | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1846-2559delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950450 | ||||||
chr8:89950549
|
C | T | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1846-2657G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950549 | ||||||
chr8:89950617
|
G | T | 2 | a0001c0002t0003g0004a0001c0002t0003g0144 | 7 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1845+2627C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950617 | ||||||
chr8:89950631
|
C | G | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1845+2613G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950631 | ||||||
chr8:89950704
|
C | T | 2 | a0002c0001t0003g0036a0002c0001t0003g0124 | 3 | HG00673.hp2 HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1845+2540G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950704 | ||||||
chr8:89950712
|
G | A | 1 | a0002c0001t0013g0039 | 2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1845+2532C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950712 | ||||||
chr8:89950748
|
GTTTC | G | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1845+2492_1845+249 others(8): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950748 | ||||||
chr8:89950889
|
G | C | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1845+2355C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89950889 | ||||||
chr8:89951184
|
C | T | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1845+2060G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951184 | ||||||
chr8:89951263
|
G | T | 5 | a0002c0001t0001g0029a0002c0001t0001g0030a0002c0001t0001g0072others(2): Show | 7 | HG02083.hp1 NA18946.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.1845+1981C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951263 | ||||||
chr8:89951311
|
C | CA | 49 | a0001c0002t0001g0242a0001c0002t0002g0047a0001c0002t0002g0221others(46): Show | 56 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1845+1932dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951311 | ||||||
chr8:89951311
|
C | CAA | 26 | a0001c0003t0002g0042a0002c0001t0001g0029a0002c0001t0001g0068others(23): Show | 41 | HG00642.hp2 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1845+1931_1845+193 others(6): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951311 | ||||||
chr8:89951311
|
C | CAAA | 70 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(67): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1845+1930_1845+193 others(7): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951311 | ||||||
chr8:89951369
|
A | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845+1875T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951369 | ||||||
chr8:89951549
|
C | T | 1 | a0001c0002t0002g0188 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1845+1695G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951549 | ||||||
chr8:89951748
|
T | A | 19 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(16): Show | 22 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1845+1496A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951748 | ||||||
chr8:89951758
|
T | TA | 110 | a0001c0002t0002g0211a0001c0004t0001g0058a0001c0004t0001g0059others(107): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1845+1485dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951758 | ||||||
chr8:89951789
|
A | G | 1 | a0001c0002t0002g0022 | 3 | HG00323.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1845+1455T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89951789 | ||||||
chr8:89952004
|
G | A | 3 | a0001c0003t0005g0054a0001c0003t0006g0055a0001c0003t0023g0056 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1845+1240C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952004 | ||||||
chr8:89952086
|
T | C | 2 | a0002c0001t0003g0121a0002c0001t0003g0122 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1845+1158A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952086 | ||||||
chr8:89952090
|
C | T | 2 | a0002c0001t0003g0121a0002c0001t0003g0122 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1845+1154G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952090 | ||||||
chr8:89952325
|
T | C | 1 | a0001c0002t0002g0222 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1845+919A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952325 | ||||||
chr8:89952357
|
A | G | 1 | a0001c0002t0002g0198 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1845+887T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952357 | ||||||
chr8:89952363
|
C | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845+881G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952363 | ||||||
chr8:89952392
|
T | A | 18 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(15): Show | 21 | HG01884.hp2 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1845+852A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952392 | ||||||
chr8:89952450
|
G | A | 1 | a0001c0003t0002g0153 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1845+794C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952450 | ||||||
chr8:89952479
|
G | C | 1 | a0001c0003t0007g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1845+765C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952479 | ||||||
chr8:89952555
|
C | T | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1845+689G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952555 | ||||||
chr8:89952560
|
ACTTAATC others(5): Show |
A | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1845+672_1845+683d others(14): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952560 | ||||||
chr8:89952609
|
C | T | 1 | a0001c0002t0002g0240 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1845+635G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952609 | ||||||
chr8:89952825
|
T | C | 27 | a0002c0001t0001g0008a0002c0001t0001g0015a0002c0001t0001g0024others(24): Show | 38 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1845+419A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952825 | ||||||
chr8:89952901
|
A | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845+343T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952901 | ||||||
chr8:89952969
|
A | T | 1 | a0001c0003t0023g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1845+275T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 11/15 | chr8 | 89952969 | ||||||
chr8:89953803
|
G | A | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1398-112C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89953803 | ||||||
chr8:89953914
|
G | C | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-223C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89953914 | ||||||
chr8:89954144
|
A | C | 1 | a0004c0007t0001g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1398-453T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89954144 | ||||||
chr8:89954437
|
T | C | 1 | a0002c0001t0003g0128 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1398-746A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89954437 | ||||||
chr8:89954443
|
G | T | 1 | a0002c0001t0001g0104 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1398-752C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89954443 | ||||||
chr8:89954615
|
C | T | 1 | a0001c0003t0007g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1397+668G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89954615 | ||||||
chr8:89954718
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1397+565G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89954718 | ||||||
chr8:89954979
|
G | A | 13 | a0001c0002t0002g0188a0001c0003t0001g0023a0001c0003t0001g0050others(10): Show | 16 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1397+304C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89954979 | ||||||
chr8:89955126
|
G | C | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1397+157C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89955126 | ||||||
chr8:89955236
|
CT | C | 17 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(14): Show | 30 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1397+46delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89955236 | ||||||
chr8:89955241
|
A | AT | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1397+41dupA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 10/15 | chr8 | 89955241 | ||||||
chr8:89955634
|
G | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1125-79C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89955634 | ||||||
chr8:89955641
|
C | T | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125-86G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89955641 | ||||||
chr8:89955813
|
A | G | 45 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(42): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1125-258T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89955813 | ||||||
chr8:89956075
|
C | G | 12 | a0001c0002t0001g0190a0001c0002t0001g0234a0001c0002t0002g0010others(9): Show | 20 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1125-520G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956075 | ||||||
chr8:89956082
|
T | C | 195 | a0001c0002t0002g0224a0001c0002t0003g0004a0001c0002t0003g0144others(192): Show | 274 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1125-527A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956082 | ||||||
chr8:89956088
|
T | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1125-533A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956088 | ||||||
chr8:89956197
|
G | GA | 130 | a0001c0002t0001g0242a0001c0002t0002g0237a0001c0003t0001g0174others(127): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1125-643dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956197 | ||||||
chr8:89956339
|
T | A | 2 | a0002c0001t0001g0265a0002c0001t0001g0266 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1125-784A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956339 | ||||||
chr8:89956624
|
A | C | 3 | a0001c0002t0002g0137a0001c0002t0002g0212a0001c0002t0002g0213 | 3 | NA18948.hp1 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1125-1069T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956624 | ||||||
chr8:89956831
|
C | A | 1 | a0001c0003t0002g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1125-1276G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956831 | ||||||
chr8:89956856
|
G | T | 1 | a0002c0001t0001g0080 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1125-1301C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956856 | ||||||
chr8:89956979
|
T | C | 1 | a0002c0001t0002g0119 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1125-1424A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89956979 | ||||||
chr8:89957001
|
C | G | 45 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(42): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1125-1446G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957001 | ||||||
chr8:89957111
|
AT | A | 4 | a0001c0003t0002g0249a0001c0003t0008g0247a0001c0003t0008g0248others(1): Show | 4 | HG01261.hp1 HG02109.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125-1557delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957111 | ||||||
chr8:89957125
|
G | T | 1 | a0009c0015t0018g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1125-1570C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957125 | ||||||
chr8:89957256
|
T | C | 1 | a0002c0001t0001g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1124+1469A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957256 | ||||||
chr8:89957307
|
C | A | 79 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(76): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1124+1418G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957307 | ||||||
chr8:89957480
|
G | A | 9 | a0002c0001t0001g0002a0002c0001t0001g0073a0002c0001t0001g0090others(6): Show | 17 | HG01192.hp2 HG01346.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.1124+1245C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957480 | ||||||
chr8:89957559
|
G | A | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1124+1166C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957559 | ||||||
chr8:89957588
|
T | C | 269 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(266): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1124+1137A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957588 | ||||||
chr8:89957609
|
C | G | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1124+1116G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957609 | ||||||
chr8:89957793
|
T | G | 190 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(187): Show | 263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1124+932A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957793 | ||||||
chr8:89957819
|
T | G | 79 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(76): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1124+906A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957819 | ||||||
chr8:89957907
|
T | C | 79 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(76): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1124+818A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89957907 | ||||||
chr8:89958169
|
C | T | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1124+556G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958169 | ||||||
chr8:89958170
|
G | A | 1 | a0001c0003t0004g0143 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1124+555C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958170 | ||||||
chr8:89958214
|
T | C | 2 | a0001c0003t0006g0183a0001c0003t0017g0182 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1124+511A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958214 | ||||||
chr8:89958226
|
C | T | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1124+499G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958226 | ||||||
chr8:89958407
|
A | G | 1 | a0002c0001t0001g0116 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1124+318T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958407 | ||||||
chr8:89958415
|
C | T | 19 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(16): Show | 22 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1124+310G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958415 | ||||||
chr8:89958449
|
A | T | 5 | a0001c0004t0005g0057a0001c0004t0005g0062a0001c0004t0005g0063others(2): Show | 5 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1124+276T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958449 | ||||||
chr8:89958463
|
G | A | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1124+262C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958463 | ||||||
chr8:89958520
|
C | A | 1 | a0002c0001t0003g0128 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1124+205G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958520 | ||||||
chr8:89958634
|
G | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1124+91C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958634 | ||||||
chr8:89958706
|
G | A | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1124+19C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958706 | ||||||
chr8:89958707
|
G | A | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1124+18C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 9/15 | chr8 | 89958707 | ||||||
chr8:89958926
|
T | C | 1 | a0001c0002t0002g0200 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.995-72A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89958926 | ||||||
chr8:89959251
|
A | G | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-397T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89959251 | ||||||
chr8:89959460
|
A | T | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.995-606T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89959460 | ||||||
chr8:89959570
|
C | A | 1 | a0002c0001t0006g0019 | 3 | HG01243.hp2 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.995-716G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89959570 | ||||||
chr8:89959699
|
A | G | 1 | a0002c0001t0001g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.995-845T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89959699 | ||||||
chr8:89960167
|
T | C | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.995-1313A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960167 | ||||||
chr8:89960209
|
T | G | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-1355A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960209 | ||||||
chr8:89960230
|
G | A | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1376C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960230 | ||||||
chr8:89960290
|
T | C | 20 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(17): Show | 23 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.995-1436A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960290 | ||||||
chr8:89960524
|
C | T | 2 | a0001c0002t0003g0004a0001c0002t0003g0144 | 7 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1670G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960524 | ||||||
chr8:89960531
|
A | G | 1 | a0002c0001t0007g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.995-1677T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960531 | ||||||
chr8:89960549
|
G | C | 7 | a0001c0003t0001g0050a0001c0003t0001g0259a0001c0003t0001g0262others(4): Show | 8 | HG01070.hp1 HG01109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.995-1695C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960549 | ||||||
chr8:89960585
|
A | G | 1 | a0009c0015t0018g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995-1731T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960585 | ||||||
chr8:89960718
|
T | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.995-1864A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960718 | ||||||
chr8:89960823
|
G | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.995-1969C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89960823 | ||||||
chr8:89961012
|
C | T | 4 | a0001c0002t0001g0202a0001c0002t0001g0227a0001c0002t0002g0201others(1): Show | 4 | HG03017.hp1 HG03710.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-2158G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961012 | ||||||
chr8:89961127
|
T | C | 1 | a0002c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.995-2273A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961127 | ||||||
chr8:89961157
|
C | T | 1 | a0001c0003t0026g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.995-2303G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961157 | ||||||
chr8:89961377
|
C | T | 2 | a0001c0003t0005g0054a0001c0003t0006g0055 | 2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.995-2523G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961377 | ||||||
chr8:89961436
|
G | A | 37 | a0001c0002t0001g0192a0001c0002t0001g0242a0001c0002t0002g0001others(34): Show | 64 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.995-2582C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961436 | ||||||
chr8:89961510
|
A | G | 1 | a0001c0002t0002g0021 | 3 | HG01256.hp1 HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.995-2656T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961510 | ||||||
chr8:89961574
|
G | A | 17 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(14): Show | 20 | HG01884.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.995-2720C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961574 | ||||||
chr8:89961652
|
T | G | 7 | a0001c0003t0001g0050a0001c0003t0001g0259a0001c0003t0001g0262others(4): Show | 8 | HG01070.hp1 HG01109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.994+2758A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961652 | ||||||
chr8:89961676
|
G | A | 1 | a0002c0001t0001g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.994+2734C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961676 | ||||||
chr8:89961862
|
T | C | 1 | a0001c0003t0001g0050 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.994+2548A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89961862 | ||||||
chr8:89962227
|
G | A | 2 | a0001c0003t0001g0174a0001c0003t0005g0175 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.994+2183C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962227 | ||||||
chr8:89962312
|
T | C | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+2098A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962312 | ||||||
chr8:89962360
|
TTA | T | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+2048_994+2049d others(4): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962360 | ||||||
chr8:89962363
|
T | C | 2 | a0002c0001t0001g0265a0002c0001t0001g0266 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.994+2047A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962363 | ||||||
chr8:89962436
|
C | G | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+1974G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962436 | ||||||
chr8:89962473
|
T | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.994+1937A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962473 | ||||||
chr8:89962692
|
C | T | 1 | a0001c0003t0004g0020 | 3 | NA19004.hp1 NA19007.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.994+1718G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962692 | ||||||
chr8:89962734
|
A | C | 1 | a0002c0001t0003g0123 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.994+1676T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962734 | ||||||
chr8:89962775
|
GA | G | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.994+1634delT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962775 | ||||||
chr8:89962852
|
C | T | 3 | a0001c0002t0002g0198a0001c0002t0002g0199a0001c0002t0002g0200 | 3 | NA18943.hp1 NA18964.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.994+1558G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962852 | ||||||
chr8:89962922
|
G | A | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.994+1488C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962922 | ||||||
chr8:89962992
|
CT | C | 3 | a0002c0001t0007g0018a0002c0001t0007g0093a0002c0001t0008g0094 | 5 | HG00735.hp2 HG02280.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.994+1417delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89962992 | ||||||
chr8:89963031
|
C | A | 1 | a0004c0007t0001g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.994+1379G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963031 | ||||||
chr8:89963036
|
C | T | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.994+1374G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963036 | ||||||
chr8:89963047
|
A | G | 3 | a0001c0002t0009g0041a0001c0002t0009g0138a0001c0002t0009g0139 | 4 | HG02055.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+1363T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963047 | ||||||
chr8:89963073
|
T | C | 3 | a0001c0003t0002g0249a0001c0003t0008g0248a0001c0003t0008g0250 | 3 | HG01261.hp1 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.994+1337A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963073 | ||||||
chr8:89963157
|
A | T | 1 | a0001c0003t0002g0153 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.994+1253T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963157 | ||||||
chr8:89963187
|
CG | C | 79 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(76): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.994+1222delC | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963187 | ||||||
chr8:89963322
|
C | T | 16 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(13): Show | 28 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.994+1088G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963322 | ||||||
chr8:89963556
|
C | T | 1 | a0001c0002t0002g0197 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.994+854G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963556 | ||||||
chr8:89963888
|
C | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.994+522G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89963888 | ||||||
chr8:89964015
|
A | G | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.994+395T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89964015 | ||||||
chr8:89964054
|
C | T | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.994+356G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89964054 | ||||||
chr8:89964129
|
G | A | 1 | a0002c0001t0001g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.994+281C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89964129 | ||||||
chr8:89964138
|
ATG | A | 15 | a0002c0001t0001g0002a0002c0001t0001g0029a0002c0001t0001g0030others(12): Show | 26 | HG00597.hp2 HG01192.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.994+270_994+271del others(2): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89964138 | ||||||
chr8:89964177
|
C | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.994+233G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89964177 | ||||||
chr8:89964324
|
T | C | 1 | a0001c0003t0006g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.994+86A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 8/15 | chr8 | 89964324 | ||||||
chr8:89964571
|
T | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.897-64A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89964571 | ||||||
chr8:89964678
|
G | A | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.897-171C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89964678 | ||||||
chr8:89964834
|
C | T | 3 | a0001c0002t0002g0195a0001c0002t0002g0196a0001c0002t0002g0255 | 3 | HG00741.hp1 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.897-327G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89964834 | ||||||
chr8:89965135
|
A | T | 1 | a0001c0003t0005g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.897-628T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965135 | ||||||
chr8:89965176
|
G | A | 1 | a0001c0003t0006g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.897-669C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965176 | ||||||
chr8:89965227
|
C | T | 1 | a0002c0001t0001g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.897-720G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965227 | ||||||
chr8:89965259
|
A | G | 2 | a0001c0002t0003g0004a0001c0002t0003g0144 | 7 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.897-752T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965259 | ||||||
chr8:89965540
|
G | A | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.897-1033C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965540 | ||||||
chr8:89965653
|
C | A | 1 | a0002c0001t0001g0014 | 4 | HG00140.hp1 HG00741.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-1146G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965653 | ||||||
chr8:89965754
|
T | C | 3 | a0001c0003t0001g0050a0001c0003t0003g0260a0001c0003t0003g0264 | 4 | HG01070.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-1247A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965754 | ||||||
chr8:89965770
|
G | A | 1 | a0001c0003t0001g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.897-1263C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965770 | ||||||
chr8:89965775
|
C | T | 2 | a0001c0002t0002g0237a0001c0002t0002g0238 | 2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.897-1268G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965775 | ||||||
chr8:89965849
|
T | G | 1 | a0002c0001t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.897-1342A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965849 | ||||||
chr8:89965934
|
T | G | 1 | a0001c0002t0009g0041 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.897-1427A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89965934 | ||||||
chr8:89966240
|
G | C | 2 | a0001c0003t0005g0177a0001c0003t0007g0178 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.897-1733C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966240 | ||||||
chr8:89966427
|
T | A | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.897-1920A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966427 | ||||||
chr8:89966602
|
C | T | 17 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(14): Show | 30 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.897-2095G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966602 | ||||||
chr8:89966609
|
C | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.897-2102G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966609 | ||||||
chr8:89966796
|
T | C | 1 | a0002c0001t0003g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.897-2289A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966796 | ||||||
chr8:89966805
|
T | C | 1 | a0004c0007t0001g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.897-2298A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966805 | ||||||
chr8:89966894
|
G | C | 1 | a0002c0001t0001g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.897-2387C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966894 | ||||||
chr8:89966919
|
T | C | 1 | a0001c0003t0004g0150 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.897-2412A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966919 | ||||||
chr8:89966964
|
G | T | 3 | a0001c0003t0001g0050a0001c0003t0003g0260a0001c0003t0003g0264 | 4 | HG01070.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-2457C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89966964 | ||||||
chr8:89967063
|
G | A | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.897-2556C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89967063 | ||||||
chr8:89967098
|
T | G | 2 | a0001c0002t0003g0004a0001c0002t0003g0144 | 7 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.897-2591A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89967098 | ||||||
chr8:89967176
|
G | A | 19 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(16): Show | 22 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.897-2669C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89967176 | ||||||
chr8:89967379
|
G | C | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.897-2872C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89967379 | ||||||
chr8:89967395
|
C | T | 1 | a0007c0018t0001g0186 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.897-2888G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89967395 | ||||||
chr8:89967718
|
G | C | 1 | a0001c0002t0002g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.896+2646C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89967718 | ||||||
chr8:89968111
|
A | G | 6 | a0001c0003t0002g0249a0001c0003t0008g0247a0001c0003t0008g0248others(3): Show | 6 | HG01261.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+2253T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968111 | ||||||
chr8:89968328
|
G | A | 1 | a0001c0002t0002g0238 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.896+2036C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968328 | ||||||
chr8:89968334
|
G | A | 2 | a0001c0002t0002g0237a0001c0002t0002g0238 | 2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.896+2030C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968334 | ||||||
chr8:89968378
|
A | G | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.896+1986T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968378 | ||||||
chr8:89968538
|
G | T | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.896+1826C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968538 | ||||||
chr8:89968576
|
A | G | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.896+1788T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968576 | ||||||
chr8:89968677
|
C | T | 1 | a0002c0001t0001g0103 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.896+1687G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968677 | ||||||
chr8:89968726
|
G | T | 1 | a0009c0015t0018g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.896+1638C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968726 | ||||||
chr8:89968728
|
C | T | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.896+1636G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968728 | ||||||
chr8:89968749
|
T | C | 1 | a0001c0002t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896+1615A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968749 | ||||||
chr8:89968753
|
T | C | 5 | a0001c0003t0001g0050a0001c0003t0001g0259a0001c0003t0003g0260others(2): Show | 6 | HG01070.hp1 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+1611A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968753 | ||||||
chr8:89968926
|
A | G | 16 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(13): Show | 28 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.896+1438T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968926 | ||||||
chr8:89968943
|
G | A | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.896+1421C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89968943 | ||||||
chr8:89969478
|
C | T | 1 | a0002c0001t0020g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.896+886G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89969478 | ||||||
chr8:89969525
|
T | C | 1 | a0001c0003t0005g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.896+839A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89969525 | ||||||
chr8:89969634
|
T | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.896+730A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89969634 | ||||||
chr8:89969674
|
G | A | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.896+690C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89969674 | ||||||
chr8:89969678
|
G | A | 1 | a0001c0003t0004g0164 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.896+686C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89969678 | ||||||
chr8:89970172
|
C | T | 3 | a0002c0001t0001g0074a0002c0001t0001g0075a0002c0001t0001g0136 | 3 | NA18954.hp2 NA18985.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.896+192G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89970172 | ||||||
chr8:89970197
|
C | T | 35 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(32): Show | 47 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.896+167G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89970197 | ||||||
chr8:89970328
|
C | T | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.896+36G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89970328 | ||||||
chr8:89970334
|
G | GT | 13 | a0001c0003t0002g0249a0001c0003t0003g0251a0001c0003t0003g0252others(10): Show | 16 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.896+29dupA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89970334 | ||||||
chr8:89970337
|
T | G | 6 | a0001c0003t0001g0180a0001c0003t0005g0176a0001c0003t0005g0177others(3): Show | 6 | HG02922.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+27A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 7/15 | chr8 | 89970337 | ||||||
chr8:89970575
|
C | T | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.703-18G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89970575 | ||||||
chr8:89970665
|
A | G | 4 | a0002c0001t0003g0121a0002c0001t0003g0122a0002c0001t0003g0129others(1): Show | 4 | HG00642.hp2 HG01081.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-108T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89970665 | ||||||
chr8:89970700
|
G | T | 1 | a0001c0003t0003g0152 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.703-143C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89970700 | ||||||
chr8:89970727
|
C | T | 3 | a0002c0001t0001g0026a0002c0001t0001g0076a0002c0001t0001g0101 | 4 | HG02056.hp1 NA19009.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-170G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89970727 | ||||||
chr8:89970999
|
G | A | 1 | a0001c0002t0025g0269 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.702+174C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89970999 | ||||||
chr8:89971023
|
C | A | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+150G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89971023 | ||||||
chr8:89971024
|
A | G | 4 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0194others(1): Show | 6 | HG00099.hp2 HG01169.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+149T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89971024 | ||||||
chr8:89971157
|
C | G | 1 | a0001c0002t0002g0193 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.702+16G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 6/15 | chr8 | 89971157 | ||||||
chr8:89971371
|
C | T | 12 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0259others(9): Show | 15 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.585-81G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89971371 | ||||||
chr8:89972050
|
T | C | 1 | a0001c0003t0026g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.585-760A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972050 | ||||||
chr8:89972237
|
C | G | 1 | a0007c0018t0001g0186 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.585-947G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972237 | ||||||
chr8:89972328
|
A | G | 18 | a0001c0003t0001g0174a0001c0003t0001g0180a0001c0003t0002g0168others(15): Show | 21 | HG01884.hp2 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.585-1038T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972328 | ||||||
chr8:89972361
|
G | T | 1 | a0001c0002t0001g0192 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.585-1071C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972361 | ||||||
chr8:89972377
|
A | G | 1 | a0001c0002t0002g0191 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.585-1087T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972377 | ||||||
chr8:89972428
|
A | C | 1 | a0001c0003t0001g0151 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.585-1138T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972428 | ||||||
chr8:89972555
|
A | G | 1 | a0001c0002t0002g0189 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.585-1265T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972555 | ||||||
chr8:89972575
|
G | C | 79 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(76): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.585-1285C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89972575 | ||||||
chr8:89973105
|
C | G | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.585-1815G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973105 | ||||||
chr8:89973384
|
A | G | 1 | a0001c0002t0002g0188 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.585-2094T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973384 | ||||||
chr8:89973675
|
T | C | 1 | a0002c0001t0001g0101 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.585-2385A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973675 | ||||||
chr8:89973781
|
C | T | 3 | a0002c0001t0001g0074a0002c0001t0001g0075a0002c0001t0001g0136 | 3 | NA18954.hp2 NA18985.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.585-2491G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973781 | ||||||
chr8:89973837
|
T | C | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.585-2547A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973837 | ||||||
chr8:89973902
|
T | TC | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.585-2613_585-2612i others(3): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973902 | ||||||
chr8:89973903
|
T | C | 269 | a0001c0002t0001g0190a0001c0002t0001g0192a0001c0002t0001g0202others(266): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.585-2613A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89973903 | ||||||
chr8:89974087
|
G | A | 1 | a0002c0001t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.585-2797C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974087 | ||||||
chr8:89974248
|
T | C | 1 | a0001c0003t0005g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.585-2958A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974248 | ||||||
chr8:89974251
|
C | CT | 73 | a0001c0002t0002g0233a0001c0003t0001g0142a0001c0003t0001g0147others(70): Show | 88 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.585-2962dupA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974251 | ||||||
chr8:89974251
|
CT | C | 6 | a0001c0002t0001g0234a0001c0002t0002g0225a0001c0003t0016g0245others(3): Show | 6 | HG02735.hp1 HG02735.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.585-2962delA | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974251 | ||||||
chr8:89974271
|
T | G | 19 | a0002c0001t0001g0015a0002c0001t0001g0025a0002c0001t0001g0033others(16): Show | 25 | HG00408.hp1 HG00609.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.585-2981A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974271 | ||||||
chr8:89974361
|
T | C | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.585-3071A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974361 | ||||||
chr8:89974462
|
C | T | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.585-3172G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974462 | ||||||
chr8:89974465
|
T | C | 1 | a0001c0002t0002g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.585-3175A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974465 | ||||||
chr8:89974475
|
G | C | 2 | a0001c0003t0003g0165a0001c0003t0003g0166 | 2 | NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.585-3185C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974475 | ||||||
chr8:89974607
|
A | C | 1 | a0001c0003t0004g0150 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.585-3317T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974607 | ||||||
chr8:89974614
|
T | C | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585-3324A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974614 | ||||||
chr8:89974623
|
C | T | 3 | a0001c0003t0001g0050a0001c0003t0003g0260a0001c0003t0003g0264 | 4 | HG01070.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-3333G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974623 | ||||||
chr8:89974703
|
G | A | 1 | a0001c0003t0004g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.585-3413C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974703 | ||||||
chr8:89974753
|
C | T | 1 | a0001c0002t0022g0257 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.585-3463G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974753 | ||||||
chr8:89974802
|
T | C | 3 | a0001c0002t0002g0011a0001c0002t0002g0243a0001c0002t0022g0257 | 7 | HG01175.hp1 HG01255.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.584+3418A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89974802 | ||||||
chr8:89975337
|
T | C | 2 | a0002c0001t0003g0129a0002c0001t0003g0130 | 2 | HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.584+2883A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975337 | ||||||
chr8:89975412
|
G | C | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+2808C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975412 | ||||||
chr8:89975428
|
A | C | 1 | a0002c0001t0001g0071 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.584+2792T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975428 | ||||||
chr8:89975487
|
A | G | 1 | a0001c0003t0001g0262 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.584+2733T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975487 | ||||||
chr8:89975573
|
T | C | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.584+2647A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975573 | ||||||
chr8:89975613
|
A | C | 2 | a0002c0001t0001g0024a0002c0001t0001g0053 | 3 | HG00738.hp2 HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.584+2607T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975613 | ||||||
chr8:89975651
|
T | C | 1 | a0001c0002t0001g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.584+2569A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975651 | ||||||
chr8:89975916
|
T | C | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.584+2304A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975916 | ||||||
chr8:89975925
|
T | C | 1 | a0002c0001t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.584+2295A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975925 | ||||||
chr8:89975978
|
G | A | 1 | a0001c0002t0002g0228 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.584+2242C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975978 | ||||||
chr8:89975989
|
T | C | 1 | a0002c0001t0001g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.584+2231A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89975989 | ||||||
chr8:89976003
|
G | C | 1 | a0001c0002t0002g0228 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.584+2217C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976003 | ||||||
chr8:89976054
|
G | A | 1 | a0001c0002t0002g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.584+2166C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976054 | ||||||
chr8:89976225
|
T | C | 4 | a0002c0001t0001g0008a0002c0001t0001g0024a0002c0001t0001g0053others(1): Show | 9 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+1995A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976225 | ||||||
chr8:89976246
|
T | A | 9 | a0001c0003t0002g0249a0001c0003t0005g0054a0001c0003t0006g0055others(6): Show | 9 | HG01261.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+1974A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976246 | ||||||
chr8:89976347
|
A | G | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.584+1873T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976347 | ||||||
chr8:89976454
|
T | C | 4 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0006g0017others(1): Show | 7 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+1766A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976454 | ||||||
chr8:89976512
|
T | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.584+1708A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976512 | ||||||
chr8:89976514
|
G | C | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.584+1706C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976514 | ||||||
chr8:89976569
|
A | G | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+1651T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976569 | ||||||
chr8:89976587
|
T | C | 34 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(31): Show | 46 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.584+1633A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976587 | ||||||
chr8:89976608
|
G | C | 1 | a0001c0002t0002g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.584+1612C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976608 | ||||||
chr8:89976687
|
G | A | 1 | a0001c0002t0002g0231 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.584+1533C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976687 | ||||||
chr8:89976701
|
G | C | 1 | a0002c0001t0006g0019 | 3 | HG01243.hp2 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.584+1519C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976701 | ||||||
chr8:89976765
|
G | C | 1 | a0002c0001t0001g0116 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.584+1455C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976765 | ||||||
chr8:89976839
|
A | G | 2 | a0001c0002t0001g0190a0001c0002t0002g0189 | 2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.584+1381T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89976839 | ||||||
chr8:89977010
|
C | G | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.584+1210G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977010 | ||||||
chr8:89977055
|
T | A | 3 | a0003c0005t0003g0035a0003c0005t0003g0117a0003c0005t0011g0118 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+1165A>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977055 | ||||||
chr8:89977095
|
C | G | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.584+1125G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977095 | ||||||
chr8:89977317
|
G | T | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.584+903C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977317 | ||||||
chr8:89977360
|
G | A | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.584+860C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977360 | ||||||
chr8:89977427
|
T | C | 1 | a0001c0003t0023g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.584+793A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977427 | ||||||
chr8:89977505
|
T | C | 1 | a0002c0001t0002g0119 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.584+715A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977505 | ||||||
chr8:89977688
|
C | G | 1 | a0001c0003t0004g0149 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.584+532G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977688 | ||||||
chr8:89977720
|
C | A | 1 | a0001c0003t0003g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.584+500G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977720 | ||||||
chr8:89977722
|
C | T | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.584+498G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977722 | ||||||
chr8:89977863
|
T | C | 190 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(187): Show | 263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.584+357A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977863 | ||||||
chr8:89977893
|
C | T | 16 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(13): Show | 28 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+327G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977893 | ||||||
chr8:89977970
|
T | G | 1 | a0001c0003t0004g0143 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.584+250A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 5/15 | chr8 | 89977970 | ||||||
chr8:89978482
|
A | T | 4 | a0002c0001t0001g0025a0002c0001t0001g0068a0002c0001t0001g0069others(1): Show | 5 | NA18954.hp1 NA18966.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-159T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978482 | ||||||
chr8:89978625
|
T | C | 3 | a0001c0004t0005g0063a0001c0004t0005g0064a0001c0004t0005g0065 | 3 | HG02055.hp2 HG02622.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.481-302A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978625 | ||||||
chr8:89978653
|
A | G | 1 | a0002c0001t0002g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.481-330T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978653 | ||||||
chr8:89978732
|
C | A | 2 | a0005c0006t0003g0246a0005c0006t0011g0169 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.481-409G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978732 | ||||||
chr8:89978814
|
T | C | 3 | a0001c0003t0005g0054a0001c0003t0006g0055a0001c0003t0023g0056 | 3 | HG01891.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.481-491A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978814 | ||||||
chr8:89978847
|
A | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-524T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978847 | ||||||
chr8:89978878
|
G | C | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481-555C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978878 | ||||||
chr8:89978916
|
A | C | 16 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(13): Show | 28 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.481-593T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89978916 | ||||||
chr8:89979002
|
G | A | 1 | a0001c0003t0003g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.481-679C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979002 | ||||||
chr8:89979006
|
C | T | 2 | a0001c0002t0002g0237a0001c0002t0002g0238 | 2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.481-683G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979006 | ||||||
chr8:89979040
|
T | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.481-717A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979040 | ||||||
chr8:89979134
|
T | C | 1 | a0001c0002t0002g0233 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.481-811A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979134 | ||||||
chr8:89979230
|
C | T | 5 | a0001c0003t0001g0147a0001c0003t0004g0140a0001c0003t0004g0145others(2): Show | 5 | NA18963.hp1 NA18966.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-907G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979230 | ||||||
chr8:89979343
|
G | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.481-1020C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979343 | ||||||
chr8:89979508
|
T | C | 2 | a0004c0007t0001g0184a0004c0007t0001g0185 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.481-1185A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979508 | ||||||
chr8:89979525
|
T | TTTG | 17 | a0002c0001t0003g0003a0002c0001t0003g0036a0002c0001t0003g0121others(14): Show | 30 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.481-1205_481-1203d others(5): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979525 | ||||||
chr8:89979528
|
G | T | 3 | a0001c0003t0005g0170a0001c0003t0005g0171a0001c0003t0005g0172 | 3 | HG01884.hp2 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.481-1205C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979528 | ||||||
chr8:89979546
|
G | GTT | 11 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+1186_480+1187d others(4): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979546 | ||||||
chr8:89979653
|
CA | C | 11 | a0001c0002t0002g0188a0001c0004t0001g0058a0001c0004t0001g0059others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+1080delT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979653 | ||||||
chr8:89979662
|
A | T | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+1072T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979662 | ||||||
chr8:89979793
|
G | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+941C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979793 | ||||||
chr8:89979858
|
T | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+876A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979858 | ||||||
chr8:89979882
|
T | C | 33 | a0001c0003t0001g0142a0001c0003t0001g0147a0001c0003t0001g0151others(30): Show | 45 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.480+852A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979882 | ||||||
chr8:89979893
|
T | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+841A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979893 | ||||||
chr8:89979908
|
A | C | 1 | a0001c0003t0002g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.480+826T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979908 | ||||||
chr8:89979937
|
G | A | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+797C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979937 | ||||||
chr8:89979938
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.480+796G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979938 | ||||||
chr8:89979988
|
T | G | 1 | a0002c0001t0013g0039 | 2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.480+746A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89979988 | ||||||
chr8:89980012
|
C | T | 45 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(42): Show | 60 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.480+722G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980012 | ||||||
chr8:89980100
|
A | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+634T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980100 | ||||||
chr8:89980177
|
G | A | 1 | a0002c0001t0001g0131 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.480+557C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980177 | ||||||
chr8:89980369
|
A | AG | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+364_480+365ins others(1): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980369 | ||||||
chr8:89980442
|
G | C | 189 | a0001c0003t0001g0023a0001c0003t0001g0050a0001c0003t0001g0142others(186): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.480+292C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980442 | ||||||
chr8:89980611
|
T | C | 1 | a0007c0018t0001g0186 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.480+123A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980611 | ||||||
chr8:89980614
|
A | G | 1 | a0001c0002t0002g0236 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.480+120T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 4/15 | chr8 | 89980614 | ||||||
chr8:89980922
|
C | T | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.321-29G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89980922 | ||||||
chr8:89980982
|
A | T | 8 | a0001c0003t0001g0050a0001c0003t0001g0259a0001c0003t0001g0262others(5): Show | 9 | HG01070.hp1 HG01109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.321-89T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89980982 | ||||||
chr8:89980989
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.321-96C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89980989 | ||||||
chr8:89981117
|
A | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.321-224T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89981117 | ||||||
chr8:89981167
|
C | T | 191 | a0001c0002t0003g0004a0001c0002t0003g0144a0001c0003t0001g0023others(188): Show | 269 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.320+208G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89981167 | ||||||
chr8:89981175
|
G | T | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.320+200C>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89981175 | ||||||
chr8:89981291
|
T | C | 2 | a0001c0003t0001g0262a0008c0016t0008g0263 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.320+84A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 3/15 | chr8 | 89981291 | ||||||
chr8:89981589
|
T | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-66A>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89981589 | ||||||
chr8:89981655
|
C | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.172-132G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89981655 | ||||||
chr8:89981801
|
T | C | 3 | a0002c0001t0001g0040a0002c0001t0001g0132a0002c0001t0001g0133 | 4 | HG00438.hp2 NA18991.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-278A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89981801 | ||||||
chr8:89981824
|
GTC | G | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-303_172-302del others(2): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89981824 | ||||||
chr8:89982205
|
G | A | 1 | a0001c0003t0019g0235 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.171+517C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89982205 | ||||||
chr8:89982254
|
A | T | 8 | a0001c0003t0002g0249a0001c0003t0003g0251a0001c0003t0003g0252others(5): Show | 11 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+468T>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89982254 | ||||||
chr8:89982288
|
C | G | 2 | a0001c0003t0001g0142a0001c0003t0004g0143 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.171+434G>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89982288 | ||||||
chr8:89982393
|
G | A | 13 | a0001c0002t0001g0242a0001c0002t0002g0006a0001c0002t0002g0011others(10): Show | 23 | HG00558.hp1 HG01175.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.171+329C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89982393 | ||||||
chr8:89982589
|
T | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+133A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 2/15 | chr8 | 89982589 | ||||||
chr8:89982864
|
A | C | 1 | a0001c0003t0004g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.38-9T>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89982864 | ||||||
chr8:89982929
|
G | A | 1 | a0002c0001t0001g0134 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.38-74C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89982929 | ||||||
chr8:89982960
|
TTAAA | T | 3 | a0001c0002t0009g0041a0001c0002t0009g0138a0001c0002t0009g0139 | 4 | HG02055.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-109_38-106delTT others(2): Show |
NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89982960 | ||||||
chr8:89983024
|
A | G | 1 | a0002c0001t0010g0066 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.38-169T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983024 | ||||||
chr8:89983138
|
C | T | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.38-283G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983138 | ||||||
chr8:89983142
|
T | C | 4 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268others(1): Show | 6 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.38-287A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983142 | ||||||
chr8:89983163
|
T | C | 8 | a0001c0003t0001g0050a0001c0003t0001g0259a0001c0003t0001g0262others(5): Show | 9 | HG01070.hp1 HG01109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-308A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983163 | ||||||
chr8:89983365
|
G | A | 1 | a0005c0006t0003g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.38-510C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983365 | ||||||
chr8:89983381
|
G | C | 13 | a0001c0003t0002g0249a0001c0003t0003g0251a0001c0003t0003g0252others(10): Show | 16 | HG01261.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.38-526C>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983381 | ||||||
chr8:89983396
|
C | T | 1 | a0002c0001t0001g0136 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.38-541G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983396 | ||||||
chr8:89983431
|
C | CA | 7 | a0001c0002t0002g0049a0001c0002t0002g0255a0001c0002t0003g0256others(4): Show | 8 | HG00544.hp1 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.38-577dupT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983431 | ||||||
chr8:89983431
|
CA | C | 101 | a0001c0002t0002g0137a0002c0001t0001g0002a0002c0001t0001g0007others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.38-577delT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983431 | ||||||
chr8:89983431
|
CAA | C | 10 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(7): Show | 10 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.38-578_38-577delTT | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983431 | ||||||
chr8:89983743
|
T | C | 101 | a0002c0001t0001g0002a0002c0001t0001g0007a0002c0001t0001g0008others(98): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.37+782A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983743 | ||||||
chr8:89983964
|
C | A | 1 | a0002c0001t0001g0136 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.37+561G>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89983964 | ||||||
chr8:89984030
|
A | G | 111 | a0001c0004t0001g0058a0001c0004t0001g0059a0001c0004t0001g0060others(108): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.37+495T>C | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89984030 | ||||||
chr8:89984288
|
G | A | 7 | a0001c0003t0001g0050a0001c0003t0001g0259a0001c0003t0001g0262others(4): Show | 8 | HG01070.hp1 HG01109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.37+237C>T | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89984288 | ||||||
chr8:89984495
|
T | C | 2 | a0002c0001t0001g0265a0002c0001t0001g0266 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.37+30A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89984495 | ||||||
chr8:89984514
|
T | C | 3 | a0001c0003t0001g0023a0001c0003t0001g0267a0001c0003t0001g0268 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+11A>G | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89984514 | ||||||
chr8:89984520
|
C | T | 5 | a0001c0003t0005g0054a0001c0003t0006g0055a0001c0003t0023g0056others(2): Show | 6 | HG00738.hp2 HG01099.hp2 HG01192.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.37+5G>A | NBN | ENSG00000104320.15 | transcript | ENST00000265433.8 | protein_coding | 1/15 | chr8 | 89984520 |