geneid | 79707 |
---|---|
ensemblid | ENSG00000162408.11 |
hgncid | 26265 |
symbol | NOL9 |
name | nucleolar protein 9 |
refseq_nuc | NM_024654.5 |
refseq_prot | NP_078930.4 |
ensembl_nuc | ENST00000377705.6 |
ensembl_prot | ENSP00000366934.5 |
mane_status | MANE Select |
chr | chr1 |
start | 6521347 |
end | 6554513 |
strand | - |
ver | v1.2 |
region | chr1:6521347-6554513 |
region5000 | chr1:6516347-6559513 |
regionname0 | NOL9_chr1_6521347_6554513 |
regionname5000 | NOL9_chr1_6516347_6559513 |
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 | 0/1 | 702 | 219 | 40 | 54 | 94 | 8 | 22 | 62 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002 | 0/0 | 702 | 93 | 42 | 9 | 34 | 2 | 6 | 25 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003 | 0/0 | 702 | 7 | 3 | 0 | 2 | 0 | 2 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0004 | 1/0 | 702 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0005 | 0/0 | 702 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0006 | 0/0 | 702 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0007 | 0/0 | 698 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0008 | 0/0 | 702 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0009 | 0/0 | 702 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0010 | 0/0 | 702 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0011 | 0/0 | 702 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
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 | 0/1 | 2109 | 214 | 40 | 54 | 90 | 8 | 21 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0002 | 0/0 | 2109 | 60 | 10 | 8 | 34 | 2 | 6 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0003 | 0/0 | 2109 | 14 | 13 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0004 | 0/0 | 2109 | 13 | 13 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0005 | 0/0 | 2109 | 7 | 3 | 0 | 2 | 0 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0006 | 1/0 | 2109 | 7 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0007 | 0/0 | 2109 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0008 | 0/0 | 2109 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0009 | 0/0 | 2109 | 4 | 0 | 0 | 3 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0010 | 0/0 | 2109 | 3 | 2 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0011 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0012 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0013 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0014 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0015 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0016 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
c0017 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
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 | 0/1 | 4524 | 121 | 17 | 31 | 47 | 5 | 20 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0002 | 0/0 | 4526 | 35 | 4 | 5 | 18 | 2 | 6 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0003 | 0/0 | 4524 | 28 | 0 | 0 | 28 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0004 | 0/0 | 4525 | 17 | 2 | 6 | 9 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0005 | 0/0 | 4524 | 10 | 1 | 4 | 1 | 3 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0006 | 0/0 | 4524 | 9 | 7 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0007 | 0/0 | 4526 | 7 | 7 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0008 | 0/0 | 4525 | 6 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0009 | 0/0 | 4527 | 6 | 2 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0010 | 0/0 | 4528 | 6 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0011 | 0/0 | 4524 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0012 | 0/0 | 4527 | 4 | 1 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0013 | 1/0 | 4519 | 4 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0014 | 0/0 | 4523 | 3 | 0 | 2 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0015 | 0/0 | 4524 | 3 | 0 | 3 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0016 | 0/0 | 4525 | 3 | 1 | 1 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0017 | 0/0 | 4520 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0018 | 0/0 | 4526 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0019 | 0/0 | 4524 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0020 | 0/0 | 4528 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0021 | 0/0 | 4528 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0022 | 0/0 | 4527 | 2 | 1 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0023 | 0/0 | 4524 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0024 | 0/0 | 4521 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0025 | 0/0 | 4528 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0026 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0027 | 0/0 | 4526 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0028 | 0/0 | 4528 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0029 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0030 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0031 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0032 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0033 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0034 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0035 | 0/0 | 4523 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0036 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0037 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0038 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0039 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0040 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0041 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0042 | 0/0 | 4525 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0043 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0044 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0045 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0046 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0047 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0048 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0049 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0050 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0051 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0052 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0053 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0054 | 0/0 | 4525 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0055 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0056 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0057 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0058 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0059 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0060 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0061 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0062 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0063 | 0/0 | 4529 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0064 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0065 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0066 | 0/0 | 4523 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0067 | 0/0 | 4523 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0068 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0069 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0070 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0071 | 0/0 | 4526 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0072 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0073 | 0/0 | 4525 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0074 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
t0075 | 0/0 | 4528 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
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 | 6 | 2 | 2 | 0 | 2 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0003 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2109 | 214 | 40 | 54 | 90 | 8 | 21 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0009 | 0/0 | 2109 | 4 | 0 | 0 | 3 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0015 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002 | 0/0 | 2109 | 60 | 10 | 8 | 34 | 2 | 6 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003 | 0/0 | 2109 | 14 | 13 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004 | 0/0 | 2109 | 13 | 13 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0008 | 0/0 | 2109 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0012 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005 | 0/0 | 2109 | 7 | 3 | 0 | 2 | 0 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0004c0006 | 1/0 | 2109 | 7 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0005c0007 | 0/0 | 2109 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0006c0010 | 0/0 | 2109 | 3 | 2 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0007c0013 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0008c0011 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0009c0017 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0010c0016 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0011c0014 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6632 | 116 | 17 | 31 | 43 | 5 | 19 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0002 | 0/0 | 6634 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0003 | 0/0 | 6632 | 22 | 0 | 0 | 22 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0004 | 0/0 | 6633 | 16 | 1 | 6 | 9 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0005 | 0/0 | 6632 | 9 | 1 | 3 | 1 | 3 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0006 | 0/0 | 6632 | 9 | 7 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0008 | 0/0 | 6633 | 4 | 4 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0011 | 0/0 | 6632 | 5 | 5 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0014 | 0/0 | 6631 | 3 | 0 | 2 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0015 | 0/0 | 6632 | 3 | 0 | 3 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0016 | 0/0 | 6633 | 3 | 1 | 1 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0019 | 0/0 | 6632 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0023 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0029 | 0/0 | 6633 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0030 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0032 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0033 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0035 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0036 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0037 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0039 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0040 | 0/0 | 6633 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0041 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0042 | 0/0 | 6633 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0043 | 0/0 | 6634 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0044 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0045 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0046 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0047 | 0/0 | 6630 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0048 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0049 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0053 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0001t0067 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0009t0001 | 0/0 | 6632 | 3 | 0 | 0 | 2 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0009t0050 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0001c0015t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0002 | 0/0 | 6634 | 33 | 3 | 5 | 18 | 2 | 5 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0005 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0009 | 0/0 | 6635 | 6 | 2 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0012 | 0/0 | 6635 | 4 | 1 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0018 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0023 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0024 | 0/0 | 6629 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0025 | 0/0 | 6636 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0058 | 0/0 | 6635 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0059 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0061 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0062 | 0/0 | 6634 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0063 | 0/0 | 6637 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0064 | 0/0 | 6635 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0065 | 0/0 | 6635 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0066 | 0/0 | 6631 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0002t0068 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003t0007 | 0/0 | 6634 | 7 | 7 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003t0026 | 0/0 | 6635 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003t0027 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003t0069 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003t0070 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0003t0071 | 0/0 | 6634 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004t0008 | 0/0 | 6633 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004t0010 | 0/0 | 6636 | 6 | 6 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004t0028 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004t0072 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004t0073 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0004t0074 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0008t0020 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0008t0021 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0008t0051 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0002c0012t0002 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0031 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0034 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0054 | 0/0 | 6633 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0055 | 0/0 | 6634 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0056 | 0/0 | 6635 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0057 | 0/0 | 6635 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0003c0005t0060 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0004c0006t0013 | 1/0 | 6627 | 4 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0004c0006t0017 | 0/0 | 6628 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0005c0007t0003 | 0/0 | 6632 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0006c0010t0022 | 0/0 | 6635 | 2 | 1 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0006c0010t0052 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0007c0013t0018 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0008c0011t0075 | 0/0 | 6636 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0009c0017t0038 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0010c0016t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
a0011c0014t0004 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | copy fasta | chr1 | 6516347 | 6559513 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 2 | 2 | 0 | 2 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0011g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0011g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0014g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0015g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0015g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0016g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0016g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0019g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0019g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0023g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0029g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0030g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0032g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0033g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0035g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0036g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0037g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0039g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0040g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0041g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0042g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0043g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0044g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0045g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0046g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0047g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0048g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0049g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0053g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0001t0067g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0009t0050g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0001c0015t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0003 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0023g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0024g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0024g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0025g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0025g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0058g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0059g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0061g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0062g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0063g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0064g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0065g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0066g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0002t0068g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0026g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0027g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0027g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0069g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0070g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0003t0071g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0010g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0028g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0028g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0072g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0073g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0004t0074g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0020g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0021g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0021g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0008t0051g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0002c0012t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0031g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0034g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0054g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0055g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0056g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0057g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0003c0005t0060g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0006t0013g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0006t0013g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0006t0013g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0006t0017g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0006t0017g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0004c0006t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0005c0007t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0006c0010t0022g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0006c0010t0022g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0006c0010t0052g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0007c0013t0018g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0008c0011t0075g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0009c0017t0038g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0010c0016t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
a0011c0014t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | GBR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0274 | EUR | GBR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0200 | EUR | FIN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00438 | hp1 | a0002 | c0002 | t0063 | g0071 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00544 | hp1 | a0002 | c0002 | t0062 | g0088 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00544 | hp2 | a0001 | c0001 | t0019 | g0241 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00558 | hp2 | a0002 | c0002 | t0009 | g0075 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00609 | hp1 | a0009 | c0017 | t0038 | g0232 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00609 | hp2 | a0001 | c0001 | t0039 | g0169 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00621 | hp1 | a0010 | c0016 | t0001 | g0245 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00621 | hp2 | a0002 | c0002 | t0064 | g0091 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00642 | hp1 | a0002 | c0002 | t0023 | g0110 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00642 | hp2 | a0001 | c0001 | t0016 | g0155 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00735 | hp1 | a0002 | c0002 | t0012 | g0056 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00735 | hp2 | a0001 | c0001 | t0029 | g0152 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01109 | hp1 | a0002 | c0002 | t0005 | g0059 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01167 | hp1 | a0002 | c0003 | t0071 | g0106 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01168 | hp1 | a0001 | c0001 | t0023 | g0126 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01169 | hp1 | a0001 | c0001 | t0067 | g0125 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01243 | hp1 | a0006 | c0010 | t0022 | g0283 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01257 | hp1 | a0001 | c0001 | t0014 | g0212 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0205 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01433 | hp2 | a0001 | c0001 | t0042 | g0134 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01884 | hp1 | a0001 | c0001 | t0041 | g0208 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01891 | hp1 | a0004 | c0006 | t0013 | g0122 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01891 | hp2 | a0002 | c0003 | t0027 | g0100 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01928 | hp2 | a0001 | c0001 | t0015 | g0031 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01975 | hp1 | a0001 | c0001 | t0035 | g0228 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01978 | hp1 | a0001 | c0001 | t0040 | g0160 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02027 | hp2 | a0001 | c0015 | t0001 | g0157 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02040 | hp1 | a0001 | c0001 | t0030 | g0181 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0099 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02055 | hp2 | a0002 | c0004 | t0073 | g0034 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02074 | hp2 | a0005 | c0007 | t0003 | g0266 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02083 | hp2 | a0001 | c0001 | t0033 | g0186 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02145 | hp1 | a0001 | c0001 | t0032 | g0260 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02145 | hp2 | a0002 | c0004 | t0028 | g0038 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02148 | hp2 | a0001 | c0001 | t0015 | g0161 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02155 | hp2 | a0003 | c0005 | t0054 | g0116 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02165 | hp2 | a0005 | c0007 | t0003 | g0015 | EAS | CDX | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02258 | hp2 | a0003 | c0005 | t0060 | g0114 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02273 | hp1 | a0001 | c0001 | t0015 | g0031 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02280 | hp1 | a0002 | c0003 | t0007 | g0051 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02280 | hp2 | a0002 | c0003 | t0007 | g0046 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02451 | hp2 | a0002 | c0004 | t0008 | g0043 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02572 | hp1 | a0004 | c0006 | t0013 | g0020 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02572 | hp2 | a0002 | c0002 | t0012 | g0096 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02615 | hp1 | a0002 | c0003 | t0007 | g0054 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02622 | hp1 | a0002 | c0002 | t0009 | g0093 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02622 | hp2 | a0002 | c0003 | t0026 | g0053 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02630 | hp2 | a0002 | c0004 | t0074 | g0039 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02647 | hp1 | a0002 | c0008 | t0051 | g0041 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02647 | hp2 | a0008 | c0011 | t0075 | g0033 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02717 | hp1 | a0002 | c0002 | t0018 | g0103 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02723 | hp2 | a0002 | c0004 | t0008 | g0044 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02738 | hp2 | a0002 | c0002 | t0012 | g0072 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02809 | hp1 | a0002 | c0008 | t0021 | g0040 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02818 | hp1 | a0004 | c0006 | t0017 | g0118 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02818 | hp2 | a0002 | c0003 | t0026 | g0049 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02886 | hp1 | a0002 | c0002 | t0061 | g0107 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02886 | hp2 | a0004 | c0006 | t0013 | g0020 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02896 | hp1 | a0002 | c0002 | t0068 | g0105 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02896 | hp2 | a0001 | c0001 | t0053 | g0275 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02897 | hp1 | a0002 | c0004 | t0010 | g0006 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02897 | hp2 | a0002 | c0002 | t0018 | g0104 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02922 | hp1 | a0002 | c0003 | t0027 | g0101 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02965 | hp1 | a0002 | c0004 | t0010 | g0036 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02965 | hp2 | a0003 | c0005 | t0034 | g0115 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02970 | hp1 | a0002 | c0004 | t0010 | g0006 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0129 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03041 | hp2 | a0002 | c0012 | t0002 | g0097 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0150 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03098 | hp2 | a0002 | c0003 | t0069 | g0050 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03130 | hp1 | a0002 | c0004 | t0010 | g0006 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03139 | hp1 | a0007 | c0013 | t0018 | g0123 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03139 | hp2 | a0002 | c0003 | t0007 | g0045 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03195 | hp2 | a0002 | c0004 | t0010 | g0016 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0130 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03209 | hp2 | a0002 | c0003 | t0007 | g0047 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03486 | hp1 | a0002 | c0004 | t0010 | g0016 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | ESN | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | GWD | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03579 | hp2 | a0006 | c0010 | t0052 | g0282 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03688 | hp2 | a0003 | c0005 | t0057 | g0111 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03710 | hp2 | a0003 | c0005 | t0056 | g0112 | SAS | PJL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0193 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03834 | hp2 | a0001 | c0009 | t0001 | g0217 | SAS | BEB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18522 | hp1 | a0004 | c0006 | t0017 | g0119 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18522 | hp2 | a0002 | c0008 | t0020 | g0017 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18747 | hp2 | a0001 | c0009 | t0050 | g0218 | EAS | CHB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0127 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18939 | hp1 | a0002 | c0002 | t0024 | g0079 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18939 | hp2 | a0001 | c0001 | t0049 | g0257 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18948 | hp1 | a0001 | c0001 | t0048 | g0197 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18948 | hp2 | a0001 | c0009 | t0001 | g0224 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18949 | hp2 | a0001 | c0001 | t0046 | g0234 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18956 | hp2 | a0001 | c0001 | t0014 | g0222 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18957 | hp1 | a0002 | c0002 | t0012 | g0063 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18959 | hp1 | a0002 | c0002 | t0024 | g0067 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18960 | hp1 | a0002 | c0002 | t0066 | g0109 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18967 | hp1 | a0005 | c0007 | t0003 | g0265 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18967 | hp2 | a0002 | c0002 | t0025 | g0061 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18968 | hp1 | a0002 | c0002 | t0059 | g0108 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18970 | hp1 | a0001 | c0001 | t0036 | g0219 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18973 | hp2 | a0001 | c0001 | t0045 | g0144 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18975 | hp2 | a0001 | c0001 | t0043 | g0168 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18992 | hp2 | a0001 | c0001 | t0044 | g0163 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18994 | hp2 | a0002 | c0002 | t0009 | g0090 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18997 | hp2 | a0002 | c0002 | t0065 | g0092 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18999 | hp2 | a0003 | c0005 | t0055 | g0117 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19000 | hp2 | a0002 | c0002 | t0009 | g0073 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19007 | hp1 | a0001 | c0001 | t0016 | g0201 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19010 | hp2 | a0005 | c0007 | t0003 | g0015 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19012 | hp2 | a0001 | c0009 | t0001 | g0128 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19030 | hp1 | a0002 | c0003 | t0070 | g0102 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19030 | hp2 | a0006 | c0010 | t0022 | g0281 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19043 | hp1 | a0002 | c0004 | t0072 | g0037 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19043 | hp2 | a0002 | c0008 | t0020 | g0017 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19062 | hp1 | a0002 | c0002 | t0058 | g0086 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19066 | hp1 | a0005 | c0007 | t0003 | g0015 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19066 | hp2 | a0002 | c0002 | t0009 | g0070 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19068 | hp2 | a0001 | c0001 | t0019 | g0243 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19079 | hp1 | a0001 | c0001 | t0047 | g0165 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19085 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19090 | hp2 | a0002 | c0002 | t0025 | g0078 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA19240 | hp2 | a0002 | c0004 | t0028 | g0035 | AFR | YRI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20129 | hp1 | a0002 | c0003 | t0007 | g0052 | AFR | ASW | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20129 | hp2 | a0011 | c0014 | t0004 | g0124 | AFR | ASW | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0057 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0030 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | GIH | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02559 | hp1 | a0003 | c0005 | t0031 | g0113 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG02559 | hp2 | a0002 | c0003 | t0007 | g0048 | AFR | ACB | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA18955 | hp2 | a0005 | c0007 | t0003 | g0141 | EAS | JPT | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20300 | hp1 | a0002 | c0002 | t0009 | g0094 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA20300 | hp2 | a0004 | c0006 | t0017 | g0120 | AFR | USA | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA21309 | hp1 | a0001 | c0001 | t0037 | g0175 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
NA21309 | hp2 | a0002 | c0008 | t0021 | g0042 | AFR | LWK | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
homoSapiens_grch38 | hp1 | a0004 | c0006 | t0013 | g0121 | REF | REF | NOL9_chr1_6516347_6559513 | NOL9 | chr1 | 6516347 | 6559513 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6532574
|
G | A | 1 | a0010 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1424C>T | p.Ala475Val | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1435/6627 | 1424/2109 | 475/702 | chr1 | 6532574 | ||
chr1:6532740
|
T | C | 1 | a0005 | 6 | HG02074.hp2 HG02165.hp2 NA18955.hp2 others(3): Show |
missense_variant | MODERATE | c.1258A>G | p.Ile420Val | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1269/6627 | 1258/2109 | 420/702 | chr1 | 6532740 | ||
chr1:6545166
|
C | A | 1 | a0009 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.759G>T | p.Gln253His | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 4/12 | 770/6627 | 759/2109 | 253/702 | chr1 | 6545166 | ||
chr1:6550612
|
A | G | 1 | a0008 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.400T>C | p.Phe134Leu | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/12 | 411/6627 | 400/2109 | 134/702 | chr1 | 6550612 | ||
chr1:6554264
|
G | A | 1 | a0006 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.239C>T | p.Thr80Ile | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 250/6627 | 239/2109 | 80/702 | chr1 | 6554264 | ||
chr1:6554331
|
A | C | 9 | a0001a0002a0005others(6): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
missense_variant | MODERATE | c.172T>G | p.Ser58Ala | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 183/6627 | 172/2109 | 58/702 | chr1 | 6554331 | ||
chr1:6554355
|
A | G | 10 | a0001a0002a0003others(7): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
missense_variant | MODERATE | c.148T>C | p.Trp50Arg | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 159/6627 | 148/2109 | 50/702 | chr1 | 6554355 | ||
chr1:6554393
|
AGCCGGCG others(5): Show |
A | 1 | a0007 | 1 | HG03139.hp1 | disruptive_inframe_deletion | MODERATE | c.98_109delCCCGCCGCC others(3): Show |
p.Pro33_Arg36del | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 120/6627 | 98/2109 | 33/702 | chr1 | 6554393 | ||
chr1:6554466
|
A | G | 1 | a0011 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.37T>C | p.Cys13Arg | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 48/6627 | 37/2109 | 13/702 | chr1 | 6554466 | ||
chr1:6554475
|
G | A | 6 | a0001a0005a0006others(3): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
missense_variant | MODERATE | c.28C>T | p.Arg10Trp | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 39/6627 | 28/2109 | 10/702 | chr1 | 6554475 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6526750
|
C | T | 1 | a0002c0012 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1905G>A | p.Val635Val | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/12 | 1916/6627 | 1905/2109 | 635/702 | chr1 | 6526750 | ||
chr1:6532570
|
A | G | 1 | a0001c0009 | 4 | HG03834.hp2 NA18747.hp2 NA18948.hp2 others(1): Show |
synonymous_variant | LOW | c.1428T>C | p.Asp476Asp | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1439/6627 | 1428/2109 | 476/702 | chr1 | 6532570 | ||
chr1:6532651
|
A | G | 1 | a0001c0015 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1347T>C | p.Tyr449Tyr | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/12 | 1358/6627 | 1347/2109 | 449/702 | chr1 | 6532651 | ||
chr1:6533305
|
G | A | 1 | a0002c0003 | 14 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(11): Show |
synonymous_variant | LOW | c.1212C>T | p.Ile404Ile | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 7/12 | 1223/6627 | 1212/2109 | 404/702 | chr1 | 6533305 | ||
chr1:6550472
|
G | A | 1 | a0002c0008 | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
synonymous_variant | LOW | c.540C>T | p.His180His | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/12 | 551/6627 | 540/2109 | 180/702 | chr1 | 6550472 | ||
chr1:6554170
|
G | A | 4 | a0002c0002a0002c0003a0002c0012others(1): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
synonymous_variant | LOW | c.333C>T | p.Leu111Leu | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/12 | 344/6627 | 333/2109 | 111/702 | chr1 | 6554170 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6521490
|
T | TGTG | 3 | a0002c0008t0020a0002c0008t0021a0002c0008t0051 | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4361_*4363dupCAC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4363 | chr1 | 6521490 | |||||
chr1:6521659
|
T | A | 3 | a0002c0003t0027a0002c0003t0070a0002c0003t0071 | 4 | HG01167.hp1 HG01891.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4195A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4195 | chr1 | 6521659 | |||||
chr1:6521817
|
G | A | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*4037C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4037 | chr1 | 6521817 | |||||
chr1:6521844
|
A | G | 1 | a0002c0008t0020 | 2 | NA18522.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4010T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4010 | chr1 | 6521844 | |||||
chr1:6521854
|
G | C | 1 | a0002c0002t0065 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4000C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 4000 | chr1 | 6521854 | |||||
chr1:6521870
|
C | T | 2 | a0002c0004t0010a0002c0004t0072 | 7 | HG02897.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3984G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3984 | chr1 | 6521870 | |||||
chr1:6522005
|
A | C | 3 | a0001c0001t0015a0001c0001t0035a0001c0001t0040 | 5 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3849T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3849 | chr1 | 6522005 | |||||
chr1:6522026
|
C | T | 1 | a0001c0001t0042 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3828G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3828 | chr1 | 6522026 | |||||
chr1:6522045
|
C | A | 1 | a0001c0001t0039 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3809G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3809 | chr1 | 6522045 | |||||
chr1:6522084
|
G | A | 1 | a0001c0001t0048 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3770C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3770 | chr1 | 6522084 | |||||
chr1:6522209
|
A | G | 2 | a0001c0001t0011a0002c0002t0061 | 6 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3645T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3645 | chr1 | 6522209 | |||||
chr1:6522623
|
C | A | 1 | a0002c0003t0069 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3231 | chr1 | 6522623 | |||||
chr1:6522712
|
T | C | 2 | a0001c0001t0047a0001c0001t0049 | 2 | NA18939.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3142A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3142 | chr1 | 6522712 | |||||
chr1:6522736
|
T | A | 1 | a0006c0010t0052 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3118A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3118 | chr1 | 6522736 | |||||
chr1:6522745
|
G | A | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(34): Show | 214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*3109C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 3109 | chr1 | 6522745 | |||||
chr1:6522862
|
C | A | 1 | a0001c0001t0044 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2992G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2992 | chr1 | 6522862 | |||||
chr1:6522883
|
C | CAA | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2969_*2970dupTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | |||||
chr1:6522883
|
C | CAAA | 6 | a0001c0001t0016a0001c0001t0040a0001c0001t0043others(3): Show | 8 | HG00642.hp2 HG01978.hp1 HG02155.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2968_*2970dupTTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | |||||
chr1:6522883
|
C | CAAAAA | 23 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(20): Show | 74 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2966_*2970dupTTTT others(1): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | |||||
chr1:6522883
|
C | CAAAAAA | 11 | a0002c0002t0012a0002c0002t0025a0002c0002t0063others(8): Show | 19 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2965_*2970dupTTTT others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2970 | chr1 | 6522883 | |||||
chr1:6522938
|
G | A | 1 | a0003c0005t0057 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2916C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2916 | chr1 | 6522938 | |||||
chr1:6522979
|
G | A | 7 | a0002c0008t0020a0002c0008t0021a0002c0008t0051others(4): Show | 9 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2875C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2875 | chr1 | 6522979 | |||||
chr1:6523123
|
C | T | 22 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(19): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2731G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2731 | chr1 | 6523123 | |||||
chr1:6523148
|
C | T | 2 | a0006c0010t0022a0006c0010t0052 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2706G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2706 | chr1 | 6523148 | |||||
chr1:6523168
|
AAAG | A | 4 | a0002c0008t0020a0002c0008t0021a0002c0008t0051others(1): Show | 6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2683_*2685delCTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2683 | chr1 | 6523168 | |||||
chr1:6523171
|
G | A | 31 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(28): Show | 88 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2683C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2683 | chr1 | 6523171 | |||||
chr1:6523171
|
G | GA | 3 | a0001c0001t0006a0001c0001t0041a0003c0005t0034 | 11 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2682dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2682 | chr1 | 6523171 | |||||
chr1:6523172
|
A | G | 31 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(28): Show | 88 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2682T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2682 | chr1 | 6523172 | |||||
chr1:6523175
|
A | G | 4 | a0002c0008t0020a0002c0008t0021a0002c0008t0051others(1): Show | 6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2679T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2679 | chr1 | 6523175 | |||||
chr1:6523210
|
C | G | 28 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(25): Show | 85 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2644G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2644 | chr1 | 6523210 | |||||
chr1:6523302
|
G | A | 2 | a0006c0010t0022a0006c0010t0052 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2552C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2552 | chr1 | 6523302 | |||||
chr1:6523545
|
C | G | 1 | a0001c0001t0036 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2309 | chr1 | 6523545 | |||||
chr1:6523567
|
G | A | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(34): Show | 214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2287C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2287 | chr1 | 6523567 | |||||
chr1:6523579
|
C | CA | 43 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(40): Show | 217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*2274dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2274 | chr1 | 6523579 | |||||
chr1:6523579
|
C | CAA | 12 | a0001c0001t0004a0001c0001t0029a0001c0001t0042others(9): Show | 29 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274dupTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2274 | chr1 | 6523579 | |||||
chr1:6523579
|
C | CAAA | 2 | a0002c0004t0010a0008c0011t0075 | 7 | HG02647.hp2 HG02897.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2272_*2274dupTTT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2274 | chr1 | 6523579 | |||||
chr1:6523613
|
G | T | 1 | a0001c0001t0033 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2241C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2241 | chr1 | 6523613 | |||||
chr1:6523615
|
C | T | 2 | a0002c0002t0059a0002c0002t0066 | 2 | NA18960.hp1 NA18968.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2239G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2239 | chr1 | 6523615 | |||||
chr1:6523641
|
T | C | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*2213A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2213 | chr1 | 6523641 | |||||
chr1:6523816
|
G | A | 3 | a0002c0004t0010a0002c0004t0028a0002c0004t0072 | 9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2038C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2038 | chr1 | 6523816 | |||||
chr1:6523827
|
A | G | 2 | a0002c0003t0027a0002c0003t0070 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2027T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 2027 | chr1 | 6523827 | |||||
chr1:6523964
|
A | G | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
3_prime_UTR_variant | MODIFIER | c.*1890T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1890 | chr1 | 6523964 | |||||
chr1:6523985
|
C | G | 13 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(10): Show | 55 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1869G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1869 | chr1 | 6523985 | |||||
chr1:6524041
|
A | G | 42 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(39): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1813 | chr1 | 6524041 | |||||
chr1:6524167
|
G | C | 9 | a0001c0001t0003a0001c0001t0019a0001c0001t0044others(6): Show | 36 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1687C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1687 | chr1 | 6524167 | |||||
chr1:6524237
|
G | A | 2 | a0002c0002t0064a0002c0002t0065 | 2 | HG00621.hp2 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1617 | chr1 | 6524237 | |||||
chr1:6524251
|
G | GTA | 83 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(80): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
3_prime_UTR_variant | MODIFIER | c.*1601_*1602dupTA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1602 | chr1 | 6524251 | |||||
chr1:6524259
|
G | GA | 2 | a0001c0001t0008a0002c0004t0008 | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1594_*1595insT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1594 | chr1 | 6524259 | |||||
chr1:6524260
|
T | G | 2 | a0001c0001t0008a0002c0004t0008 | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1594A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1594 | chr1 | 6524260 | |||||
chr1:6524261
|
A | G | 2 | a0001c0001t0008a0002c0004t0008 | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1593T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1593 | chr1 | 6524261 | |||||
chr1:6524360
|
C | A | 28 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(25): Show | 85 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1494G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1494 | chr1 | 6524360 | |||||
chr1:6524410
|
C | T | 3 | a0002c0004t0010a0002c0004t0028a0002c0004t0072 | 9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1444G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1444 | chr1 | 6524410 | |||||
chr1:6524462
|
G | A | 1 | a0001c0001t0019 | 2 | HG00544.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1392C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1392 | chr1 | 6524462 | |||||
chr1:6524483
|
G | A | 1 | a0002c0002t0058 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1371 | chr1 | 6524483 | |||||
chr1:6524484
|
A | G | 1 | a0002c0002t0058 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1370T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1370 | chr1 | 6524484 | |||||
chr1:6524485
|
G | A | 1 | a0002c0002t0058 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1369C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1369 | chr1 | 6524485 | |||||
chr1:6524597
|
T | C | 27 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(24): Show | 84 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1257A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1257 | chr1 | 6524597 | |||||
chr1:6524638
|
C | T | 1 | a0001c0001t0006 | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1216 | chr1 | 6524638 | |||||
chr1:6524741
|
A | AT | 3 | a0002c0002t0058a0003c0005t0056a0003c0005t0057 | 3 | HG03688.hp2 HG03710.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1112dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1112 | chr1 | 6524741 | |||||
chr1:6524741
|
A | T | 6 | a0002c0004t0010a0002c0004t0028a0002c0004t0072others(3): Show | 12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1113T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1113 | chr1 | 6524741 | |||||
chr1:6524743
|
TA | T | 3 | a0001c0001t0067a0002c0002t0066a0002c0002t0068 | 3 | HG01169.hp1 HG02896.hp1 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1110delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1110 | chr1 | 6524743 | |||||
chr1:6524744
|
A | T | 38 | a0001c0001t0002a0001c0001t0023a0002c0002t0002others(35): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1110T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1110 | chr1 | 6524744 | |||||
chr1:6524747
|
T | A | 2 | a0001c0001t0005a0002c0002t0005 | 10 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1107A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 1107 | chr1 | 6524747 | |||||
chr1:6524896
|
C | T | 3 | a0002c0002t0018a0002c0002t0068a0007c0013t0018 | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*958G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 958 | chr1 | 6524896 | |||||
chr1:6524949
|
C | T | 1 | a0003c0005t0031 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 905 | chr1 | 6524949 | |||||
chr1:6524961
|
A | G | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
3_prime_UTR_variant | MODIFIER | c.*893T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 893 | chr1 | 6524961 | |||||
chr1:6524981
|
C | T | 1 | a0001c0001t0030 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 873 | chr1 | 6524981 | |||||
chr1:6525024
|
C | A | 3 | a0001c0001t0047a0001c0001t0048a0001c0001t0049 | 3 | NA18939.hp2 NA18948.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*830G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 830 | chr1 | 6525024 | |||||
chr1:6525099
|
G | A | 1 | a0001c0009t0050 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*755C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 755 | chr1 | 6525099 | |||||
chr1:6525149
|
T | A | 9 | a0002c0002t0018a0002c0002t0068a0002c0003t0007others(6): Show | 18 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*705A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 705 | chr1 | 6525149 | |||||
chr1:6525267
|
A | G | 2 | a0006c0010t0022a0006c0010t0052 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 587 | chr1 | 6525267 | |||||
chr1:6525301
|
C | A | 3 | a0002c0008t0020a0002c0008t0021a0002c0008t0051 | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*553G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 553 | chr1 | 6525301 | |||||
chr1:6525343
|
A | G | 3 | a0001c0001t0006a0003c0005t0054a0003c0005t0055 | 11 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*511T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 511 | chr1 | 6525343 | |||||
chr1:6525403
|
G | T | 6 | a0002c0004t0010a0002c0004t0028a0002c0004t0072others(3): Show | 12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 451 | chr1 | 6525403 | |||||
chr1:6525404
|
AC | A | 8 | a0002c0004t0010a0002c0004t0028a0002c0004t0072others(5): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*449delG | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 449 | chr1 | 6525404 | |||||
chr1:6525479
|
C | T | 44 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(41): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*375G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 375 | chr1 | 6525479 | |||||
chr1:6525591
|
G | A | 1 | a0001c0001t0053 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 263 | chr1 | 6525591 | |||||
chr1:6525744
|
C | T | 46 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(43): Show | 238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 110 | chr1 | 6525744 | |||||
chr1:6525848
|
C | T | 1 | a0001c0001t0029 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 12/12 | 6 | chr1 | 6525848 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:6526010
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
splice_region_variant&intron_variant | LOW | c.1960-7G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526010 | ||||||
chr1:6526029
|
T | C | 1 | a0001c0001t0003g0251 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1960-26A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526029 | ||||||
chr1:6526094
|
A | C | 2 | a0001c0001t0001g0029a0001c0001t0041g0208 | 3 | HG01884.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1960-91T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526094 | ||||||
chr1:6526370
|
C | T | 6 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(3): Show | 9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1959+326G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526370 | ||||||
chr1:6526414
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0016g0150 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1959+282G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526414 | ||||||
chr1:6526461
|
G | C | 2 | a0002c0002t0009g0093a0002c0002t0009g0094 | 2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1959+235C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526461 | ||||||
chr1:6526471
|
G | A | 1 | a0001c0001t0032g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1959+225C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526471 | ||||||
chr1:6526493
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1959+203G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 11/11 | chr1 | 6526493 | ||||||
chr1:6526842
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1826-13G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6526842 | ||||||
chr1:6526934
|
C | T | 8 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(5): Show | 11 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-105G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6526934 | ||||||
chr1:6527012
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1826-183C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527012 | ||||||
chr1:6527120
|
G | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-291C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527120 | ||||||
chr1:6527171
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1826-342G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527171 | ||||||
chr1:6527244
|
CA | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0136others(31): Show | 40 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1826-416delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527244 | ||||||
chr1:6527260
|
AT | A | 2 | a0001c0001t0011g0004a0001c0001t0011g0127 | 5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-432delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527260 | ||||||
chr1:6527263
|
C | T | 2 | a0001c0001t0011g0004a0001c0001t0011g0127 | 5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-434G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527263 | ||||||
chr1:6527263
|
CAA | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(191): Show | 238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1826-436_1826-435d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527263 | ||||||
chr1:6527265
|
A | C | 2 | a0001c0001t0011g0004a0001c0001t0011g0127 | 5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-436T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527265 | ||||||
chr1:6527409
|
G | C | 1 | a0003c0005t0060g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-580C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527409 | ||||||
chr1:6527447
|
G | A | 4 | a0001c0009t0001g0128a0001c0009t0001g0217a0001c0009t0001g0224others(1): Show | 4 | HG03834.hp2 NA18747.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-618C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527447 | ||||||
chr1:6527554
|
C | T | 48 | a0001c0001t0002g0229a0002c0002t0002g0003a0002c0002t0002g0018others(45): Show | 54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1826-725G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527554 | ||||||
chr1:6527625
|
A | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(202): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1826-796T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527625 | ||||||
chr1:6527637
|
AAC | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(187): Show | 234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1826-810_1826-809d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527637 | ||||||
chr1:6527638
|
AC | A | 9 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0023g0126others(6): Show | 12 | HG01168.hp1 HG02129.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1826-810delG | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527638 | ||||||
chr1:6527639
|
CA | C | 3 | a0001c0001t0011g0004a0001c0001t0011g0127a0003c0005t0034g0115 | 6 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-811delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527639 | ||||||
chr1:6527640
|
A | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0249a0002c0004t0073g0034 | 5 | HG01070.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-811T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527640 | ||||||
chr1:6527702
|
G | A | 4 | a0001c0001t0015g0031a0001c0001t0015g0161a0001c0001t0035g0228others(1): Show | 5 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-873C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527702 | ||||||
chr1:6527800
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(202): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1826-971T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527800 | ||||||
chr1:6527827
|
A | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(202): Show | 255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.1826-998T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527827 | ||||||
chr1:6527846
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1826-1017C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527846 | ||||||
chr1:6527942
|
C | A | 3 | a0006c0010t0022g0281a0006c0010t0022g0283a0006c0010t0052g0282 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+1052G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6527942 | ||||||
chr1:6528024
|
A | C | 2 | a0002c0004t0073g0034a0008c0011t0075g0033 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1825+970T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528024 | ||||||
chr1:6528076
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0004g0273 | 2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1825+918C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528076 | ||||||
chr1:6528144
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0199 | 2 | NA18959.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1825+850G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528144 | ||||||
chr1:6528177
|
AG | A | 1 | a0001c0001t0011g0004 | 4 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+816delC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528177 | ||||||
chr1:6528544
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1825+450C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528544 | ||||||
chr1:6528642
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1825+352A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528642 | ||||||
chr1:6528676
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0171a0001c0001t0001g0210others(2): Show | 6 | HG02155.hp2 HG03130.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+318T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528676 | ||||||
chr1:6528779
|
T | C | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1825+215A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528779 | ||||||
chr1:6528811
|
C | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+183G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528811 | ||||||
chr1:6528850
|
C | T | 1 | a0002c0004t0028g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1825+144G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528850 | ||||||
chr1:6528877
|
G | A | 1 | a0001c0001t0053g0275 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1825+117C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528877 | ||||||
chr1:6528895
|
T | G | 1 | a0002c0008t0021g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1825+99A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528895 | ||||||
chr1:6528900
|
T | C | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1825+94A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 10/11 | chr1 | 6528900 | ||||||
chr1:6529329
|
G | A | 4 | a0002c0002t0002g0068a0002c0002t0002g0076a0002c0002t0002g0087others(1): Show | 4 | HG01255.hp2 NA18957.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648-158C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529329 | ||||||
chr1:6529362
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1648-191C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529362 | ||||||
chr1:6529444
|
C | T | 7 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(4): Show | 10 | HG02145.hp2 HG02630.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1648-273G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529444 | ||||||
chr1:6529481
|
G | C | 7 | a0002c0003t0007g0045a0002c0003t0007g0046a0002c0003t0007g0047others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1648-310C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529481 | ||||||
chr1:6529557
|
C | T | 1 | a0009c0017t0038g0232 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1648-386G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529557 | ||||||
chr1:6529581
|
C | T | 72 | a0001c0001t0002g0229a0001c0001t0023g0126a0001c0001t0067g0125others(69): Show | 78 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1648-410G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6529581 | ||||||
chr1:6530053
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(276): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1648-882T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530053 | ||||||
chr1:6530073
|
C | T | 67 | a0001c0001t0002g0229a0002c0002t0002g0003a0002c0002t0002g0018others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1648-902G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530073 | ||||||
chr1:6530093
|
T | G | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648-922A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530093 | ||||||
chr1:6530224
|
G | A | 1 | a0003c0005t0060g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1648-1053C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530224 | ||||||
chr1:6530282
|
G | A | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-1111C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530282 | ||||||
chr1:6530323
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1648-1152T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530323 | ||||||
chr1:6530347
|
G | A | 67 | a0001c0001t0002g0229a0002c0002t0002g0003a0002c0002t0002g0018others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1648-1176C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530347 | ||||||
chr1:6530369
|
G | A | 1 | a0004c0006t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1648-1198C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530369 | ||||||
chr1:6530442
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(188): Show | 238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1648-1271C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530442 | ||||||
chr1:6530670
|
C | G | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1647+1298G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530670 | ||||||
chr1:6530693
|
T | G | 1 | a0001c0001t0016g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1647+1275A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530693 | ||||||
chr1:6530809
|
C | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0239 | 2 | HG02074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1647+1159G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530809 | ||||||
chr1:6530896
|
C | T | 3 | a0006c0010t0022g0281a0006c0010t0022g0283a0006c0010t0052g0282 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1647+1072G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530896 | ||||||
chr1:6530960
|
C | A | 4 | a0002c0002t0018g0103a0002c0002t0018g0104a0002c0002t0068g0105others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647+1008G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6530960 | ||||||
chr1:6531282
|
C | T | 2 | a0002c0004t0073g0034a0008c0011t0075g0033 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1647+686G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531282 | ||||||
chr1:6531310
|
T | C | 1 | a0001c0001t0042g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1647+658A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531310 | ||||||
chr1:6531406
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1647+562C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531406 | ||||||
chr1:6531430
|
G | T | 1 | a0002c0004t0008g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1647+538C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531430 | ||||||
chr1:6531435
|
G | A | 4 | a0001c0001t0001g0210a0001c0001t0003g0013a0001c0001t0003g0164others(1): Show | 6 | HG00408.hp1 HG02080.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+533C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531435 | ||||||
chr1:6531464
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(205): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1647+504A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531464 | ||||||
chr1:6531523
|
A | G | 4 | a0002c0002t0002g0064a0002c0002t0002g0066a0002c0002t0002g0082others(1): Show | 4 | HG00597.hp2 NA18949.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+445T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531523 | ||||||
chr1:6531560
|
G | C | 4 | a0002c0002t0002g0098a0002c0002t0002g0099a0002c0002t0012g0096others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+408C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531560 | ||||||
chr1:6531565
|
C | T | 3 | a0006c0010t0022g0281a0006c0010t0022g0283a0006c0010t0052g0282 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1647+403G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531565 | ||||||
chr1:6531581
|
G | A | 2 | a0002c0004t0028g0035a0002c0004t0028g0038 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1647+387C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531581 | ||||||
chr1:6531877
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1647+91A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 9/11 | chr1 | 6531877 | ||||||
chr1:6532197
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1536-118G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/11 | chr1 | 6532197 | ||||||
chr1:6532317
|
A | G | 67 | a0001c0001t0002g0229a0002c0002t0002g0003a0002c0002t0002g0018others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1535+146T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 8/11 | chr1 | 6532317 | ||||||
chr1:6532808
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1238-48G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 7/11 | chr1 | 6532808 | ||||||
chr1:6533193
|
A | C | 1 | a0001c0001t0043g0168 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1237+87T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 7/11 | chr1 | 6533193 | ||||||
chr1:6533472
|
G | A | 51 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(48): Show | 57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1076-31C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533472 | ||||||
chr1:6533645
|
A | G | 1 | a0001c0001t0001g0023 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1076-204T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533645 | ||||||
chr1:6533681
|
C | T | 1 | a0001c0001t0005g0233 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1076-240G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533681 | ||||||
chr1:6533770
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(200): Show | 253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1076-329G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533770 | ||||||
chr1:6533787
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1076-346A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533787 | ||||||
chr1:6533890
|
C | CT | 11 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(8): Show | 14 | HG02145.hp2 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1076-450dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533890 | ||||||
chr1:6533933
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1076-492C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533933 | ||||||
chr1:6533951
|
G | A | 1 | a0002c0002t0002g0065 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1076-510C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533951 | ||||||
chr1:6533973
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1076-532G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6533973 | ||||||
chr1:6534051
|
C | T | 1 | a0004c0006t0017g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1076-610G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534051 | ||||||
chr1:6534138
|
C | A | 6 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(3): Show | 9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076-697G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534138 | ||||||
chr1:6534245
|
G | A | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1076-804C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534245 | ||||||
chr1:6534324
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1076-883C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534324 | ||||||
chr1:6534501
|
G | A | 66 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(63): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1076-1060C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534501 | ||||||
chr1:6534713
|
A | G | 66 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(63): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1076-1272T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534713 | ||||||
chr1:6534728
|
G | A | 1 | a0001c0001t0003g0242 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1076-1287C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534728 | ||||||
chr1:6534796
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1076-1355A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534796 | ||||||
chr1:6534870
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-1429G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534870 | ||||||
chr1:6534897
|
G | A | 5 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076-1456C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534897 | ||||||
chr1:6534930
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1076-1489T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6534930 | ||||||
chr1:6535099
|
C | T | 4 | a0003c0005t0034g0115a0003c0005t0056g0112a0003c0005t0057g0111others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1658G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535099 | ||||||
chr1:6535106
|
G | T | 1 | a0001c0001t0011g0004 | 4 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1665C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535106 | ||||||
chr1:6535174
|
C | T | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1076-1733G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535174 | ||||||
chr1:6535264
|
G | A | 3 | a0006c0010t0022g0281a0006c0010t0022g0283a0006c0010t0052g0282 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1076-1823C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535264 | ||||||
chr1:6535429
|
A | G | 1 | a0001c0001t0003g0238 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1076-1988T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535429 | ||||||
chr1:6535565
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1076-2124C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535565 | ||||||
chr1:6535630
|
T | C | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1076-2189A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535630 | ||||||
chr1:6535683
|
T | C | 1 | a0001c0001t0004g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1076-2242A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535683 | ||||||
chr1:6535729
|
C | T | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-2288G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535729 | ||||||
chr1:6535842
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-2401A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535842 | ||||||
chr1:6535877
|
G | A | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-2436C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535877 | ||||||
chr1:6535928
|
C | CA | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1076-2488dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535928 | ||||||
chr1:6535948
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-2507C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535948 | ||||||
chr1:6535975
|
G | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076-2534C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6535975 | ||||||
chr1:6536120
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1076-2679T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536120 | ||||||
chr1:6536139
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-2698C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536139 | ||||||
chr1:6536182
|
TAA | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-2743_1076-274 others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536182 | ||||||
chr1:6536190
|
CAA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-2751_1076-275 others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536190 | ||||||
chr1:6536333
|
G | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076-2892C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536333 | ||||||
chr1:6536345
|
CAAATA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-2909_1076-290 others(9): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536345 | ||||||
chr1:6536618
|
C | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-3177G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536618 | ||||||
chr1:6536634
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1076-3193G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536634 | ||||||
chr1:6536735
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0004g0220 | 2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1076-3294A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536735 | ||||||
chr1:6536811
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1076-3370C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536811 | ||||||
chr1:6536874
|
G | A | 1 | a0003c0005t0031g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1076-3433C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536874 | ||||||
chr1:6536962
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1076-3521C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536962 | ||||||
chr1:6536986
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0177a0001c0001t0001g0259others(1): Show | 7 | HG00438.hp2 NA18952.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076-3545C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6536986 | ||||||
chr1:6537027
|
C | T | 4 | a0003c0005t0034g0115a0003c0005t0056g0112a0003c0005t0057g0111others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-3586G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537027 | ||||||
chr1:6537049
|
A | G | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1076-3608T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537049 | ||||||
chr1:6537436
|
C | T | 18 | a0002c0002t0018g0103a0002c0002t0018g0104a0002c0002t0068g0105others(15): Show | 18 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1076-3995G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537436 | ||||||
chr1:6537801
|
T | C | 70 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(67): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1075+4029A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537801 | ||||||
chr1:6537883
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+3947T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537883 | ||||||
chr1:6537919
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+3911A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537919 | ||||||
chr1:6537960
|
C | T | 6 | a0001c0001t0006g0008a0001c0001t0006g0021a0001c0001t0006g0129others(3): Show | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1075+3870G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537960 | ||||||
chr1:6537970
|
C | T | 1 | a0002c0008t0021g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075+3860G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537970 | ||||||
chr1:6537978
|
C | G | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075+3852G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537978 | ||||||
chr1:6537991
|
CA | C | 28 | a0001c0001t0001g0170a0001c0001t0001g0249a0001c0001t0001g0279others(25): Show | 29 | HG00621.hp2 HG01167.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075+3838delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | ||||||
chr1:6537991
|
CAA | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 113 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1075+3837_1075+383 others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | ||||||
chr1:6537991
|
CAAA | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1075+3836_1075+383 others(7): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | ||||||
chr1:6537991
|
CAAAA | C | 10 | a0001c0001t0001g0255a0001c0001t0006g0131a0001c0001t0014g0205others(7): Show | 10 | HG00642.hp1 HG01169.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075+3835_1075+383 others(8): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6537991 | ||||||
chr1:6538394
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1075+3436G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538394 | ||||||
chr1:6538404
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0151others(10): Show | 18 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1075+3426C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538404 | ||||||
chr1:6538507
|
A | T | 4 | a0001c0001t0015g0031a0001c0001t0015g0161a0001c0001t0035g0228others(1): Show | 5 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075+3323T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538507 | ||||||
chr1:6538597
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+3233T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538597 | ||||||
chr1:6538655
|
C | T | 1 | a0001c0001t0001g0023 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1075+3175G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538655 | ||||||
chr1:6538676
|
C | T | 1 | a0002c0002t0002g0069 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1075+3154G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538676 | ||||||
chr1:6538902
|
G | A | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1075+2928C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538902 | ||||||
chr1:6538981
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1075+2849G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6538981 | ||||||
chr1:6539062
|
A | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0136others(20): Show | 29 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1075+2768T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539062 | ||||||
chr1:6539172
|
C | T | 3 | a0002c0003t0007g0051a0002c0003t0007g0054a0002c0003t0069g0050 | 3 | HG02280.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1075+2658G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539172 | ||||||
chr1:6539274
|
T | C | 5 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075+2556A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539274 | ||||||
chr1:6539302
|
T | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1075+2528A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539302 | ||||||
chr1:6539452
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0004g0007a0002c0004t0073g0034others(1): Show | 6 | HG02055.hp2 HG02129.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075+2378A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539452 | ||||||
chr1:6539463
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1075+2367G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539463 | ||||||
chr1:6539478
|
AATT | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1075+2349_1075+235 others(7): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539478 | ||||||
chr1:6539497
|
T | G | 70 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(67): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1075+2333A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539497 | ||||||
chr1:6539498
|
A | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1075+2332T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539498 | ||||||
chr1:6539517
|
G | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+2313C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539517 | ||||||
chr1:6539563
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0004g0190 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1075+2267G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539563 | ||||||
chr1:6539652
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+2178G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539652 | ||||||
chr1:6539659
|
AT | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+2170delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539659 | ||||||
chr1:6539695
|
C | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.1075+2135G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539695 | ||||||
chr1:6539708
|
T | G | 66 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(63): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1075+2122A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539708 | ||||||
chr1:6539872
|
G | A | 2 | a0001c0001t0047g0165a0001c0001t0049g0257 | 2 | NA18939.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1075+1958C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539872 | ||||||
chr1:6539918
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1075+1912T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6539918 | ||||||
chr1:6540014
|
T | C | 1 | a0002c0002t0002g0085 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1075+1816A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540014 | ||||||
chr1:6540033
|
T | C | 1 | a0002c0002t0002g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1075+1797A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540033 | ||||||
chr1:6540088
|
C | T | 1 | a0006c0010t0022g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1075+1742G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540088 | ||||||
chr1:6540124
|
C | CTTTT | 18 | a0001c0001t0001g0198a0001c0001t0001g0255a0002c0004t0010g0006others(15): Show | 22 | HG01243.hp1 HG01256.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1075+1702_1075+170 others(8): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | CTTTTT | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(169): Show | 218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1075+1701_1075+170 others(9): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | CTTTTTT | 8 | a0001c0001t0001g0204a0001c0001t0001g0214a0001c0001t0001g0231others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075+1700_1075+170 others(10): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | CTTTTTTT | 8 | a0002c0002t0002g0085a0002c0002t0018g0103a0002c0002t0018g0104others(5): Show | 8 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075+1699_1075+170 others(11): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | CTTTTTTT others(1): Show |
51 | a0001c0001t0067g0125a0002c0002t0002g0003a0002c0002t0002g0018others(48): Show | 57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+1698_1075+170 others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0023g0126a0002c0002t0002g0055a0002c0002t0009g0073others(7): Show | 10 | HG00642.hp1 HG01168.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+1697_1075+170 others(13): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0002g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1075+1696_1075+170 others(14): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540124
|
C | T | 1 | a0002c0002t0009g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1075+1706G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540124 | ||||||
chr1:6540153
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(198): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1075+1677A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540153 | ||||||
chr1:6540188
|
G | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1075+1642C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540188 | ||||||
chr1:6540343
|
C | T | 9 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(6): Show | 12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+1487G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540343 | ||||||
chr1:6540401
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1075+1429G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540401 | ||||||
chr1:6540547
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(192): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1075+1283G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540547 | ||||||
chr1:6540744
|
C | T | 47 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(44): Show | 53 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1075+1086G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540744 | ||||||
chr1:6540758
|
G | A | 1 | a0002c0002t0002g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1075+1072C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540758 | ||||||
chr1:6540829
|
T | TA | 6 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0008g0032others(3): Show | 7 | HG01109.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075+1000dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540829 | ||||||
chr1:6540829
|
TA | T | 48 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(45): Show | 54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1075+1000delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540829 | ||||||
chr1:6540863
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1075+967G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540863 | ||||||
chr1:6540928
|
G | A | 2 | a0002c0002t0002g0062a0002c0002t0025g0078 | 2 | NA18992.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1075+902C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540928 | ||||||
chr1:6540947
|
T | A | 75 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(72): Show | 81 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1075+883A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6540947 | ||||||
chr1:6541010
|
CGT | C | 26 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0146others(23): Show | 29 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1075+818_1075+819d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541010 | ||||||
chr1:6541010
|
CGTT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(167): Show | 217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1075+817_1075+819d others(5): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541010 | ||||||
chr1:6541010
|
CGTTT | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0223a0003c0005t0031g0113 | 3 | HG02559.hp1 NA18945.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1075+816_1075+819d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541010 | ||||||
chr1:6541011
|
GT | G | 22 | a0002c0002t0002g0062a0002c0002t0002g0064a0002c0002t0002g0065others(19): Show | 23 | HG00597.hp2 HG00735.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1075+818delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541011 | ||||||
chr1:6541011
|
GTT | G | 37 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(34): Show | 43 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1075+817_1075+818d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541011 | ||||||
chr1:6541014
|
T | C | 10 | a0002c0002t0002g0060a0002c0002t0002g0069a0002c0002t0002g0080others(7): Show | 10 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+816A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541014 | ||||||
chr1:6541186
|
T | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1075+644A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541186 | ||||||
chr1:6541187
|
T | G | 1 | a0001c0009t0001g0224 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1075+643A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541187 | ||||||
chr1:6541224
|
G | A | 1 | a0002c0003t0071g0106 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1075+606C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541224 | ||||||
chr1:6541230
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1075+600C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541230 | ||||||
chr1:6541259
|
T | C | 77 | a0001c0001t0006g0021a0001c0001t0023g0126a0001c0001t0048g0197others(74): Show | 84 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1075+571A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541259 | ||||||
chr1:6541276
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1075+554G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541276 | ||||||
chr1:6541315
|
G | A | 2 | a0001c0001t0011g0004a0001c0001t0011g0127 | 5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075+515C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541315 | ||||||
chr1:6541427
|
C | T | 1 | a0001c0001t0033g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1075+403G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541427 | ||||||
chr1:6541547
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(203): Show | 256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.1075+283A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541547 | ||||||
chr1:6541639
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1075+191T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541639 | ||||||
chr1:6541713
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1075+117A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 6/11 | chr1 | 6541713 | ||||||
chr1:6542075
|
T | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG01952.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.978-148A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542075 | ||||||
chr1:6542089
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.978-162G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542089 | ||||||
chr1:6542126
|
G | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-199C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542126 | ||||||
chr1:6542146
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.978-219T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542146 | ||||||
chr1:6542163
|
AT | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(259): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.978-237delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542163 | ||||||
chr1:6542163
|
ATT | A | 7 | a0001c0001t0001g0173a0001c0001t0001g0185a0001c0001t0035g0228others(4): Show | 7 | HG01243.hp1 HG01975.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.978-238_978-237del others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542163 | ||||||
chr1:6542181
|
C | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.978-254G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542181 | ||||||
chr1:6542184
|
T | C | 1 | a0002c0002t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.978-257A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542184 | ||||||
chr1:6542213
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.978-286G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542213 | ||||||
chr1:6542222
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.978-295T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542222 | ||||||
chr1:6542230
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.978-303C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542230 | ||||||
chr1:6542257
|
T | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG01952.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.978-330A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542257 | ||||||
chr1:6542284
|
C | T | 2 | a0001c0001t0016g0201a0002c0002t0009g0093 | 2 | HG02622.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.978-357G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542284 | ||||||
chr1:6542336
|
T | A | 1 | a0003c0005t0056g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.978-409A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542336 | ||||||
chr1:6542343
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.978-416A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542343 | ||||||
chr1:6542410
|
A | T | 2 | a0001c0001t0011g0004a0001c0001t0011g0127 | 5 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.978-483T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542410 | ||||||
chr1:6542465
|
A | AT | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(198): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-539dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542465 | ||||||
chr1:6542526
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.978-599A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542526 | ||||||
chr1:6542604
|
T | C | 1 | a0002c0002t0005g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.978-677A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542604 | ||||||
chr1:6542648
|
G | A | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.978-721C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542648 | ||||||
chr1:6542660
|
T | G | 1 | a0002c0002t0002g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.978-733A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542660 | ||||||
chr1:6542676
|
C | T | 1 | a0003c0005t0034g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.978-749G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542676 | ||||||
chr1:6542695
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.978-768C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542695 | ||||||
chr1:6542745
|
C | A | 1 | a0003c0005t0031g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.978-818G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542745 | ||||||
chr1:6542746
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.978-819G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542746 | ||||||
chr1:6542772
|
A | G | 1 | a0002c0002t0002g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.978-845T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542772 | ||||||
chr1:6542844
|
G | A | 2 | a0002c0002t0018g0104a0002c0002t0068g0105 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.978-917C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542844 | ||||||
chr1:6542886
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.978-959T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542886 | ||||||
chr1:6542940
|
C | T | 4 | a0001c0001t0004g0174a0001c0001t0005g0027a0001c0001t0005g0182others(1): Show | 5 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-1013G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542940 | ||||||
chr1:6542961
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.978-1034T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542961 | ||||||
chr1:6542983
|
T | G | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.978-1056A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6542983 | ||||||
chr1:6543091
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.978-1164T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543091 | ||||||
chr1:6543201
|
C | CT | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(197): Show | 250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.978-1275dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543201 | ||||||
chr1:6543214
|
G | T | 1 | a0006c0010t0022g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1287C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543214 | ||||||
chr1:6543215
|
A | T | 1 | a0006c0010t0022g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1288T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543215 | ||||||
chr1:6543218
|
C | G | 1 | a0006c0010t0022g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1291G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543218 | ||||||
chr1:6543218
|
CAG | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(198): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.978-1293_978-1292d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543218 | ||||||
chr1:6543220
|
G | C | 1 | a0006c0010t0022g0281 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.978-1293C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543220 | ||||||
chr1:6543261
|
T | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-1334A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543261 | ||||||
chr1:6543294
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.978-1367G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543294 | ||||||
chr1:6543347
|
C | T | 2 | a0001c0001t0004g0244a0010c0016t0001g0245 | 2 | HG00423.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.978-1420G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543347 | ||||||
chr1:6543364
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.978-1437C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543364 | ||||||
chr1:6543386
|
G | A | 1 | a0001c0001t0011g0004 | 4 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.977+1440C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543386 | ||||||
chr1:6543462
|
TG | T | 8 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(5): Show | 11 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.977+1363delC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543462 | ||||||
chr1:6543617
|
T | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.977+1209A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543617 | ||||||
chr1:6543712
|
A | G | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.977+1114T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543712 | ||||||
chr1:6543848
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(182): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.977+978C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543848 | ||||||
chr1:6543912
|
G | A | 1 | a0006c0010t0022g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.977+914C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6543912 | ||||||
chr1:6544045
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.977+781C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544045 | ||||||
chr1:6544082
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.977+744A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544082 | ||||||
chr1:6544100
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.977+726A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544100 | ||||||
chr1:6544156
|
T | G | 1 | a0003c0005t0054g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.977+670A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544156 | ||||||
chr1:6544282
|
C | CA | 12 | a0002c0002t0012g0072a0002c0003t0007g0045a0002c0003t0007g0046others(9): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.977+543dupT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544282 | ||||||
chr1:6544282
|
CA | C | 9 | a0001c0001t0001g0185a0001c0001t0023g0126a0001c0001t0053g0275others(6): Show | 9 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.977+543delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544282 | ||||||
chr1:6544300
|
G | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(276): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.977+526C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544300 | ||||||
chr1:6544302
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.977+524C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544302 | ||||||
chr1:6544348
|
C | A | 1 | a0001c0001t0015g0161 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.977+478G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544348 | ||||||
chr1:6544359
|
A | AAAAATAA others(5): Show |
277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.977+466_977+467ins others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544359 | ||||||
chr1:6544521
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.977+305T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544521 | ||||||
chr1:6544525
|
A | ACACGCAC others(1): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0183a0001c0001t0005g0182others(1): Show | 4 | HG00741.hp1 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.977+293_977+300dup others(8): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544525 | ||||||
chr1:6544525
|
A | G | 65 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0025others(62): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.977+301T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544525 | ||||||
chr1:6544537
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.977+289T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544537 | ||||||
chr1:6544543
|
A | AC | 17 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0055others(14): Show | 17 | HG00621.hp2 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.977+282dupG | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544543 | ||||||
chr1:6544543
|
A | ACC | 30 | a0002c0002t0002g0019a0002c0002t0002g0062a0002c0002t0002g0074others(27): Show | 31 | HG00558.hp2 HG00673.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.977+281_977+282dup others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544543 | ||||||
chr1:6544543
|
A | ACCC | 22 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0057others(19): Show | 27 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.977+280_977+282dup others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544543 | ||||||
chr1:6544544
|
C | CGCA | 7 | a0001c0001t0001g0227a0001c0001t0001g0272a0001c0001t0004g0273others(4): Show | 8 | HG01928.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.977+281_977+282ins others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | ||||||
chr1:6544544
|
C | CGCACGCA | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(154): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.977+281_977+282ins others(7): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | ||||||
chr1:6544544
|
C | CGCACGCA others(4): Show |
1 | a0001c0001t0046g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.977+281_977+282ins others(11): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | ||||||
chr1:6544544
|
C | CGCACGCA others(4): Show |
2 | a0006c0010t0022g0283a0006c0010t0052g0282 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.977+281_977+282ins others(11): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544544 | ||||||
chr1:6544545
|
C | A | 34 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0183others(31): Show | 44 | HG00741.hp1 HG00741.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.977+281G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544545 | ||||||
chr1:6544546
|
C | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(164): Show | 207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.977+280G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544546 | ||||||
chr1:6544547
|
C | A | 34 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0183others(31): Show | 44 | HG00741.hp1 HG00741.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.977+279G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544547 | ||||||
chr1:6544548
|
C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(163): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.977+278G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544548 | ||||||
chr1:6544552
|
C | A | 1 | a0001c0001t0046g0234 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.977+274G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544552 | ||||||
chr1:6544553
|
CG | C | 27 | a0001c0001t0002g0229a0001c0001t0003g0250a0001c0001t0006g0008others(24): Show | 37 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.977+272delC | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544553 | ||||||
chr1:6544554
|
G | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(172): Show | 215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.977+272C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544554 | ||||||
chr1:6544555
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.977+271G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544555 | ||||||
chr1:6544556
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(197): Show | 250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.977+270G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544556 | ||||||
chr1:6544561
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.977+265T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544561 | ||||||
chr1:6544623
|
G | C | 1 | a0001c0001t0001g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.977+203C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544623 | ||||||
chr1:6544629
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.977+197C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544629 | ||||||
chr1:6544644
|
G | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0252 | 2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.977+182C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544644 | ||||||
chr1:6544651
|
C | T | 1 | a0001c0001t0030g0181 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.977+175G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 5/11 | chr1 | 6544651 | ||||||
chr1:6545037
|
T | C | 6 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(3): Show | 9 | HG02145.hp2 HG02897.hp1 HG02965.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.880+8A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 4/11 | chr1 | 6545037 | ||||||
chr1:6545581
|
G | A | 1 | a0001c0001t0005g0233 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.745-401C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545581 | ||||||
chr1:6545617
|
G | A | 4 | a0003c0005t0034g0115a0003c0005t0056g0112a0003c0005t0057g0111others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-437C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545617 | ||||||
chr1:6545710
|
G | GCCCATGA others(5): Show |
200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(197): Show | 250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.745-531_745-530ins others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545710 | ||||||
chr1:6545786
|
C | A | 70 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(67): Show | 76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.745-606G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545786 | ||||||
chr1:6545786
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(172): Show | 215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.745-606G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545786 | ||||||
chr1:6545919
|
C | CAA | 15 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0172others(12): Show | 17 | HG00280.hp1 HG01069.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.745-741_745-740dup others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | ||||||
chr1:6545919
|
C | CAAA | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(136): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.745-742_745-740dup others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | ||||||
chr1:6545919
|
C | CAAAA | 85 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0239others(82): Show | 97 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.745-743_745-740dup others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | ||||||
chr1:6545919
|
C | CAAAAA | 15 | a0001c0001t0003g0014a0001c0001t0003g0251a0002c0002t0002g0062others(12): Show | 17 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.745-744_745-740dup others(5): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | ||||||
chr1:6545919
|
CAA | C | 7 | a0002c0003t0007g0045a0002c0003t0007g0046a0002c0003t0007g0047others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-741_745-740del others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | ||||||
chr1:6545919
|
CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0001g0171a0002c0004t0010g0006a0002c0004t0010g0016others(7): Show | 13 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-748_745-740del others(9): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545919 | ||||||
chr1:6545973
|
C | T | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-793G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6545973 | ||||||
chr1:6546024
|
GA | G | 9 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(6): Show | 12 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.745-845delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546024 | ||||||
chr1:6546157
|
T | C | 2 | a0002c0002t0002g0057a0002c0002t0012g0056 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.745-977A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546157 | ||||||
chr1:6546548
|
C | T | 76 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(73): Show | 82 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.745-1368G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546548 | ||||||
chr1:6546893
|
G | A | 1 | a0003c0005t0055g0117 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.745-1713C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546893 | ||||||
chr1:6546931
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0146others(7): Show | 14 | HG00408.hp2 HG00609.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.745-1751G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546931 | ||||||
chr1:6546932
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0270 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.745-1752C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6546932 | ||||||
chr1:6547008
|
G | C | 4 | a0002c0002t0018g0103a0002c0002t0018g0104a0002c0002t0068g0105others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1828C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547008 | ||||||
chr1:6547044
|
T | G | 1 | a0002c0008t0021g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.745-1864A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547044 | ||||||
chr1:6547082
|
C | T | 76 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(73): Show | 82 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.745-1902G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547082 | ||||||
chr1:6547139
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.745-1959A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547139 | ||||||
chr1:6547319
|
T | C | 2 | a0002c0003t0007g0051a0002c0003t0069g0050 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.745-2139A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547319 | ||||||
chr1:6547370
|
T | G | 4 | a0003c0005t0031g0113a0003c0005t0056g0112a0003c0005t0057g0111others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-2190A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547370 | ||||||
chr1:6547375
|
C | A | 2 | a0002c0002t0002g0057a0002c0002t0012g0056 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.745-2195G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547375 | ||||||
chr1:6547376
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.744+2195G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547376 | ||||||
chr1:6547518
|
GA | G | 81 | a0001c0001t0006g0008a0001c0001t0006g0021a0001c0001t0006g0129others(78): Show | 90 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+2052delT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547518 | ||||||
chr1:6547687
|
T | A | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+1884A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547687 | ||||||
chr1:6547711
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.744+1860G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547711 | ||||||
chr1:6547754
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(190): Show | 240 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.744+1817G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547754 | ||||||
chr1:6547822
|
T | C | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.744+1749A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547822 | ||||||
chr1:6547950
|
ATCATAGG others(17): Show |
A | 1 | a0001c0001t0001g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.744+1597_744+1620d others(26): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547950 | ||||||
chr1:6547997
|
G | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(271): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.744+1574C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6547997 | ||||||
chr1:6548097
|
C | A | 1 | a0001c0001t0001g0253 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.744+1474G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548097 | ||||||
chr1:6548129
|
CTTA | C | 16 | a0002c0002t0018g0104a0002c0002t0068g0105a0002c0003t0007g0045others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.744+1439_744+1441d others(5): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548129 | ||||||
chr1:6548138
|
C | CT | 38 | a0001c0001t0001g0133a0001c0001t0001g0143a0001c0001t0001g0146others(35): Show | 39 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.744+1432dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CT | C | 8 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(5): Show | 9 | HG01167.hp1 HG01256.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+1432delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CTT | C | 8 | a0001c0001t0011g0004a0002c0002t0018g0103a0002c0004t0010g0006others(5): Show | 14 | HG02257.hp2 HG02258.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+1431_744+1432d others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CTTTT | C | 9 | a0001c0001t0006g0008a0001c0001t0006g0021a0001c0001t0006g0129others(6): Show | 12 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.744+1429_744+1432d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CTTTTTTT others(3): Show |
C | 12 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0058others(9): Show | 12 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.744+1423_744+1432d others(12): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CTTTTTTT others(4): Show |
C | 62 | a0001c0001t0001g0259a0002c0002t0002g0003a0002c0002t0002g0018others(59): Show | 68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.744+1422_744+1432d others(13): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0004g0258 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.744+1420_744+1432d others(15): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548138
|
CTTTTTTT others(7): Show |
C | 2 | a0002c0004t0028g0035a0002c0004t0028g0038 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.744+1419_744+1432d others(16): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548138 | ||||||
chr1:6548168
|
C | A | 3 | a0006c0010t0022g0281a0006c0010t0022g0283a0006c0010t0052g0282 | 3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.744+1403G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548168 | ||||||
chr1:6548168
|
C | T | 2 | a0001c0001t0011g0004a0002c0003t0071g0106 | 5 | HG01167.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+1403G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548168 | ||||||
chr1:6548218
|
G | C | 4 | a0002c0002t0018g0103a0002c0002t0018g0104a0002c0002t0068g0105others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+1353C>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548218 | ||||||
chr1:6548233
|
CGCCT | C | 50 | a0001c0001t0001g0259a0002c0002t0002g0003a0002c0002t0002g0018others(47): Show | 56 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.744+1334_744+1337d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548233 | ||||||
chr1:6548259
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(190): Show | 240 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.744+1312G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548259 | ||||||
chr1:6548287
|
C | T | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1284G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548287 | ||||||
chr1:6548337
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG01952.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.744+1234C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548337 | ||||||
chr1:6548375
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.744+1196T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548375 | ||||||
chr1:6548439
|
G | A | 1 | a0002c0008t0051g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.744+1132C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548439 | ||||||
chr1:6548443
|
C | T | 69 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(66): Show | 75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.744+1128G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548443 | ||||||
chr1:6548462
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.744+1109A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548462 | ||||||
chr1:6548581
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.744+990T>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548581 | ||||||
chr1:6548660
|
C | T | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+911G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548660 | ||||||
chr1:6548670
|
T | A | 6 | a0001c0001t0006g0008a0001c0001t0006g0021a0001c0001t0006g0129others(3): Show | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+901A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548670 | ||||||
chr1:6548700
|
T | C | 4 | a0002c0002t0018g0103a0002c0002t0018g0104a0002c0002t0068g0105others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+871A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548700 | ||||||
chr1:6548889
|
C | G | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.744+682G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548889 | ||||||
chr1:6548954
|
C | T | 77 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(74): Show | 83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.744+617G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6548954 | ||||||
chr1:6549091
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(272): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.744+480C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549091 | ||||||
chr1:6549113
|
C | T | 5 | a0003c0005t0031g0113a0003c0005t0034g0115a0003c0005t0056g0112others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+458G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549113 | ||||||
chr1:6549150
|
G | A | 4 | a0005c0007t0003g0015a0005c0007t0003g0141a0005c0007t0003g0265others(1): Show | 6 | HG02074.hp2 HG02165.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+421C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549150 | ||||||
chr1:6549265
|
GAACC | G | 41 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(38): Show | 47 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.744+302_744+305del others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549265 | ||||||
chr1:6549266
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.744+305T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549266 | ||||||
chr1:6549405
|
C | T | 1 | a0001c0001t0045g0144 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.744+166G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549405 | ||||||
chr1:6549499
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(179): Show | 228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.744+72G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549499 | ||||||
chr1:6549503
|
CAT | C | 77 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(74): Show | 83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.744+66_744+67delAT | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 3/11 | chr1 | 6549503 | ||||||
chr1:6549732
|
G | GT | 67 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.617-35dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549732 | ||||||
chr1:6549769
|
T | C | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-71A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549769 | ||||||
chr1:6549776
|
G | A | 1 | a0001c0001t0042g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.617-78C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549776 | ||||||
chr1:6549790
|
C | T | 1 | a0001c0001t0042g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.617-92G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549790 | ||||||
chr1:6549791
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(276): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.617-93T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549791 | ||||||
chr1:6549836
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.617-138C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549836 | ||||||
chr1:6549858
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.617-160G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549858 | ||||||
chr1:6549876
|
C | T | 1 | a0001c0009t0001g0128 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.617-178G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549876 | ||||||
chr1:6549898
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.617-200G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549898 | ||||||
chr1:6549989
|
C | T | 67 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.617-291G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6549989 | ||||||
chr1:6550037
|
AT | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(182): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.617-340delA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550037 | ||||||
chr1:6550093
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.616+303C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550093 | ||||||
chr1:6550100
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(197): Show | 250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.616+296G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550100 | ||||||
chr1:6550124
|
C | T | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+272G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550124 | ||||||
chr1:6550134
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.616+262G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550134 | ||||||
chr1:6550135
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.616+261C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550135 | ||||||
chr1:6550157
|
G | A | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.616+239C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550157 | ||||||
chr1:6550174
|
G | A | 1 | a0002c0003t0071g0106 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.616+222C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550174 | ||||||
chr1:6550177
|
G | A | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.616+219C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550177 | ||||||
chr1:6550256
|
C | T | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+140G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550256 | ||||||
chr1:6550277
|
C | T | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.616+119G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550277 | ||||||
chr1:6550278
|
G | A | 7 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0008g0032others(4): Show | 8 | HG01109.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.616+118C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550278 | ||||||
chr1:6550306
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.616+90A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550306 | ||||||
chr1:6550322
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.616+74G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 2/11 | chr1 | 6550322 | ||||||
chr1:6550683
|
C | CT | 178 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(175): Show | 223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.397-69dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550683 | ||||||
chr1:6550683
|
C | CTT | 23 | a0001c0001t0001g0022a0001c0001t0001g0136a0001c0001t0001g0137others(20): Show | 28 | HG01346.hp1 HG01361.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.397-70_397-69dupAA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550683 | ||||||
chr1:6550740
|
A | G | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-125T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550740 | ||||||
chr1:6550761
|
G | A | 1 | a0001c0001t0005g0274 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.397-146C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550761 | ||||||
chr1:6550794
|
C | T | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-179G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550794 | ||||||
chr1:6550858
|
C | T | 2 | a0002c0002t0002g0057a0002c0002t0012g0056 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.397-243G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550858 | ||||||
chr1:6550950
|
T | G | 1 | a0001c0001t0053g0275 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.397-335A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550950 | ||||||
chr1:6550966
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.397-351G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550966 | ||||||
chr1:6550973
|
G | A | 1 | a0003c0005t0060g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.397-358C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6550973 | ||||||
chr1:6551013
|
C | T | 1 | a0002c0004t0074g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.397-398G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551013 | ||||||
chr1:6551021
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.397-406C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551021 | ||||||
chr1:6551236
|
C | T | 1 | a0002c0002t0002g0055 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.397-621G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551236 | ||||||
chr1:6551330
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(274): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.397-715T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551330 | ||||||
chr1:6551340
|
GAGA | G | 5 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0023g0110others(2): Show | 5 | HG00642.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-728_397-726del others(3): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551340 | ||||||
chr1:6551794
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.397-1179C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551794 | ||||||
chr1:6551797
|
C | T | 6 | a0001c0001t0006g0008a0001c0001t0006g0021a0001c0001t0006g0129others(3): Show | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.397-1182G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551797 | ||||||
chr1:6551858
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.397-1243G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551858 | ||||||
chr1:6551921
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.397-1306T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551921 | ||||||
chr1:6551967
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.397-1352C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6551967 | ||||||
chr1:6552022
|
G | A | 18 | a0002c0002t0018g0103a0002c0002t0018g0104a0002c0002t0068g0105others(15): Show | 18 | HG01167.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.397-1407C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552022 | ||||||
chr1:6552048
|
G | A | 2 | a0003c0005t0054g0116a0003c0005t0055g0117 | 2 | HG02155.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.397-1433C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552048 | ||||||
chr1:6552209
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.397-1594G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552209 | ||||||
chr1:6552210
|
T | C | 1 | a0003c0005t0034g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.397-1595A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552210 | ||||||
chr1:6552212
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.397-1597A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552212 | ||||||
chr1:6552267
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(272): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.397-1652C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552267 | ||||||
chr1:6552279
|
G | A | 5 | a0003c0005t0031g0113a0003c0005t0034g0115a0003c0005t0056g0112others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-1664C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552279 | ||||||
chr1:6552292
|
C | T | 1 | a0002c0002t0059g0108 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.397-1677G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552292 | ||||||
chr1:6552317
|
C | T | 5 | a0002c0003t0007g0045a0002c0003t0007g0046a0002c0003t0007g0047others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.397-1702G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552317 | ||||||
chr1:6552322
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(187): Show | 234 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.397-1707C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552322 | ||||||
chr1:6552459
|
T | TTTTA | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+1644_396+1647d others(6): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552459 | ||||||
chr1:6552490
|
T | G | 1 | a0007c0013t0018g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.396+1617A>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552490 | ||||||
chr1:6552516
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(272): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.396+1591T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552516 | ||||||
chr1:6552542
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(179): Show | 228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.396+1565G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552542 | ||||||
chr1:6552591
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.396+1516G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552591 | ||||||
chr1:6552608
|
G | A | 77 | a0001c0001t0023g0126a0001c0001t0067g0125a0002c0002t0002g0003others(74): Show | 83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.396+1499C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552608 | ||||||
chr1:6552722
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(272): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.396+1385T>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552722 | ||||||
chr1:6552834
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.396+1273G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552834 | ||||||
chr1:6552845
|
T | C | 67 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.396+1262A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552845 | ||||||
chr1:6552873
|
G | T | 67 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.396+1234C>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552873 | ||||||
chr1:6552957
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396+1150C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552957 | ||||||
chr1:6552969
|
G | A | 2 | a0004c0006t0013g0020a0004c0006t0013g0122 | 3 | HG01891.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.396+1138C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6552969 | ||||||
chr1:6553130
|
A | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(272): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.396+977T>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553130 | ||||||
chr1:6553147
|
T | C | 4 | a0002c0008t0020g0017a0002c0008t0021g0040a0002c0008t0021g0042others(1): Show | 5 | HG02647.hp1 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.396+960A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553147 | ||||||
chr1:6553314
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.396+793C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553314 | ||||||
chr1:6553322
|
G | A | 1 | a0002c0002t0061g0107 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.396+785C>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553322 | ||||||
chr1:6553524
|
C | CT | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(191): Show | 239 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.396+582dupA | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553524 | ||||||
chr1:6553524
|
C | CTT | 4 | a0001c0001t0004g0007a0001c0001t0011g0004a0001c0001t0011g0127others(1): Show | 9 | HG02257.hp2 HG02258.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.396+581_396+582dup others(2): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553524 | ||||||
chr1:6553646
|
C | T | 67 | a0002c0002t0002g0003a0002c0002t0002g0018a0002c0002t0002g0019others(64): Show | 73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.396+461G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553646 | ||||||
chr1:6553790
|
C | G | 10 | a0002c0003t0007g0045a0002c0003t0007g0046a0002c0003t0007g0047others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.396+317G>C | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553790 | ||||||
chr1:6553798
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.396+309A>G | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553798 | ||||||
chr1:6553828
|
T | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(182): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.396+279A>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553828 | ||||||
chr1:6553849
|
AAAAG | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.396+254_396+257del others(4): Show |
NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553849 | ||||||
chr1:6553939
|
C | T | 8 | a0002c0004t0010g0006a0002c0004t0010g0016a0002c0004t0010g0036others(5): Show | 11 | HG02055.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.396+168G>A | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6553939 | ||||||
chr1:6554096
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.396+11G>T | NOL9 | ENSG00000162408.11 | transcript | ENST00000377705.6 | protein_coding | 1/11 | chr1 | 6554096 |