geneid | 4803 |
---|---|
ensemblid | ENSG00000134259.6 |
hgncid | 7808 |
symbol | NGF |
name | nerve growth factor |
refseq_nuc | NM_002506.3 |
refseq_prot | NP_002497.2 |
ensembl_nuc | ENST00000369512.3 |
ensembl_prot | ENSP00000358525.2 |
mane_status | MANE Select |
chr | chr1 |
start | 115285917 |
end | 115338249 |
strand | - |
ver | v1.2 |
region | chr1:115285917-115338249 |
region5000 | chr1:115280917-115343249 |
regionname0 | NGF_chr1_115285917_115338249 |
regionname5000 | NGF_chr1_115280917_115343249 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 241 | 323 | 84 | 57 | 141 | 5 | 34 | 115 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0002 | 0/0 | 241 | 86 | 11 | 23 | 41 | 1 | 10 | 33 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0003 | 0/0 | 241 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0004 | 0/0 | 241 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0005 | 0/0 | 241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0006 | 0/0 | 241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0007 | 0/0 | 241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0008 | 0/0 | 241 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0009 | 0/0 | 241 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 726 | 308 | 70 | 56 | 141 | 5 | 34 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0002 | 0/0 | 726 | 86 | 11 | 23 | 41 | 1 | 10 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0003 | 0/0 | 726 | 15 | 14 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0004 | 0/0 | 726 | 2 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0005 | 0/0 | 726 | 2 | 0 | 0 | 0 | 0 | 2 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0006 | 0/0 | 726 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0007 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0008 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0009 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
c0010 | 0/0 | 726 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 336 | 417 | 96 | 82 | 184 | 6 | 47 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
t0002 | 0/0 | 336 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
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 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0391 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0392 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0407 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 726 | 308 | 70 | 56 | 141 | 5 | 34 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0001c0003 | 0/0 | 726 | 15 | 14 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0002c0002 | 0/0 | 726 | 86 | 11 | 23 | 41 | 1 | 10 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0003c0004 | 0/0 | 726 | 2 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0004c0005 | 0/0 | 726 | 2 | 0 | 0 | 0 | 0 | 2 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0005c0009 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0006c0007 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0007c0008 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0008c0010 | 0/0 | 726 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0009c0006 | 0/0 | 726 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1061 | 307 | 70 | 56 | 141 | 5 | 33 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0001c0001t0002 | 0/0 | 1061 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0001c0003t0001 | 0/0 | 1061 | 15 | 14 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0002c0002t0001 | 0/0 | 1061 | 86 | 11 | 23 | 41 | 1 | 10 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0003c0004t0001 | 0/0 | 1061 | 2 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0004c0005t0001 | 0/0 | 1061 | 2 | 0 | 0 | 0 | 0 | 2 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0005c0009t0001 | 0/0 | 1061 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0006c0007t0001 | 0/0 | 1061 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0007c0008t0001 | 0/0 | 1061 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0008c0010t0001 | 0/0 | 1061 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
a0009c0006t0001 | 0/0 | 1061 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | copy fasta | chr1 | 115280917 | 115343249 |
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 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0407 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0391 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0003c0004t0001g0392 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0003c0004t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0004c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0004c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0005c0009t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0006c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0007c0008t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0008c0010t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0009c0006t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0379 | EUR | GBR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0375 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0368 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0390 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0328 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0377 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0387 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0381 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0373 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0393 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0385 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01346 | hp1 | a0009 | c0006 | t0001 | g0275 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0394 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0407 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0384 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0398 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0400 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0337 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0369 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0406 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0404 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CDX | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0405 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0388 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0408 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0399 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0376 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0311 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0380 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0277 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0396 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0386 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0285 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0395 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0351 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0370 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0160 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0403 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0401 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0360 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03490 | hp2 | a0004 | c0005 | t0001 | g0089 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03492 | hp1 | a0004 | c0005 | t0001 | g0090 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03516 | hp1 | a0006 | c0007 | t0001 | g0174 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03927 | hp1 | a0003 | c0004 | t0001 | g0392 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0372 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04199 | hp2 | a0008 | c0010 | t0001 | g0294 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0397 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0364 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18987 | hp1 | a0005 | c0009 | t0001 | g0158 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0402 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19074 | hp2 | a0007 | c0008 | t0001 | g0248 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ASW | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0391 | EUR | TSI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | GIH | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0338 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0383 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0359 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0162 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0291 | REF | REF | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0184 | REF | REF | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286474
|
C | T | 1 | a0007 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.322G>A | p.Gly108Ser | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 504/1061 | 322/726 | 108/241 | chr1 | 115286474 | ||
chr1:115286504
|
C | T | 1 | a0004 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.292G>A | p.Ala98Thr | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 474/1061 | 292/726 | 98/241 | chr1 | 115286504 | ||
chr1:115286557
|
C | T | 1 | a0003 | 2 | HG01109.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.239G>A | p.Arg80Gln | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 421/1061 | 239/726 | 80/241 | chr1 | 115286557 | ||
chr1:115286582
|
C | T | 1 | a0006 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.214G>A | p.Val72Met | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 396/1061 | 214/726 | 72/241 | chr1 | 115286582 | ||
chr1:115286623
|
G | A | 1 | a0008 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.173C>T | p.Ala58Val | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 355/1061 | 173/726 | 58/241 | chr1 | 115286623 | ||
chr1:115286641
|
C | A | 1 | a0005 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.155G>T | p.Arg52Leu | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 337/1061 | 155/726 | 52/241 | chr1 | 115286641 | ||
chr1:115286692
|
G | A | 2 | a0002a0008 | 87 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
missense_variant | MODERATE | c.104C>T | p.Ala35Val | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 286/1061 | 104/726 | 35/241 | chr1 | 115286692 | ||
chr1:115286753
|
C | G | 1 | a0009 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.43G>C | p.Gly15Arg | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 225/1061 | 43/726 | 15/241 | chr1 | 115286753 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286742
|
C | T | 1 | a0001c0003 | 15 | HG01433.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
synonymous_variant | LOW | c.54G>A | p.Ala18Ala | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 236/1061 | 54/726 | 18/241 | chr1 | 115286742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286057
|
G | A | 1 | a0001c0001t0002 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 13 | chr1 | 115286057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286925
|
C | G | 2 | a0003c0004t0001g0392a0003c0004t0001g0393 | 2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12-118G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286925 | ||||||
chr1:115286948
|
G | T | 1 | a0002c0002t0001g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-12-141C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286948 | ||||||
chr1:115286962
|
G | T | 1 | a0001c0003t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-12-155C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286962 | ||||||
chr1:115286982
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-12-175G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286982 | ||||||
chr1:115287181
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0076a0001c0001t0001g0307 | 3 | HG00423.hp1 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-12-374C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287181 | ||||||
chr1:115287199
|
T | C | 404 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(401): Show | 414 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.-12-392A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287199 | ||||||
chr1:115287273
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0306others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-466C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287273 | ||||||
chr1:115287294
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0095 | 2 | NA18941.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-12-487A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287294 | ||||||
chr1:115287322
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-12-515G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287322 | ||||||
chr1:115287365
|
C | T | 86 | a0002c0002t0001g0005a0002c0002t0001g0016a0002c0002t0001g0025others(83): Show | 87 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-12-558G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287365 | ||||||
chr1:115287539
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-12-732C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287539 | ||||||
chr1:115287829
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0384 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-12-1022G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287829 | ||||||
chr1:115287840
|
C | G | 30 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0097others(27): Show | 30 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-1033G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287840 | ||||||
chr1:115287849
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12-1042A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287849 | ||||||
chr1:115287916
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-1109G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287916 | ||||||
chr1:115287954
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-12-1147G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287954 | ||||||
chr1:115288005
|
A | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(10): Show | 13 | HG00423.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-1198T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288005 | ||||||
chr1:115288010
|
T | C | 116 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0097others(113): Show | 117 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-1203A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288010 | ||||||
chr1:115288088
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-12-1281G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288088 | ||||||
chr1:115288232
|
C | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(10): Show | 13 | HG00423.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-1425G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288232 | ||||||
chr1:115288270
|
G | C | 1 | a0002c0002t0001g0282 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-12-1463C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288270 | ||||||
chr1:115288290
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(15): Show | 19 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-1483G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288290 | ||||||
chr1:115288370
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0149 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-12-1563C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288370 | ||||||
chr1:115288581
|
G | A | 2 | a0003c0004t0001g0392a0003c0004t0001g0393 | 2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12-1774C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288581 | ||||||
chr1:115288856
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0239 | 3 | HG02055.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-12-2049T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288856 | ||||||
chr1:115288940
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12-2133G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288940 | ||||||
chr1:115289136
|
C | T | 1 | a0001c0001t0001g0401 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-2329G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289136 | ||||||
chr1:115289161
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG00280.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-12-2354C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289161 | ||||||
chr1:115289162
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12-2355G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289162 | ||||||
chr1:115289210
|
C | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0306 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-12-2403G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289210 | ||||||
chr1:115289278
|
A | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0297 | 3 | HG00408.hp2 HG00621.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-12-2471T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289278 | ||||||
chr1:115289372
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12-2565G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289372 | ||||||
chr1:115289374
|
A | G | 1 | a0001c0001t0001g0339 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-12-2567T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289374 | ||||||
chr1:115289382
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0306 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-12-2575T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289382 | ||||||
chr1:115289515
|
G | T | 404 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(401): Show | 414 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.-12-2708C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289515 | ||||||
chr1:115289991
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-12-3184A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289991 | ||||||
chr1:115290261
|
C | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(62): Show | 69 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.-13+3366G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290261 | ||||||
chr1:115290371
|
A | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0371 | 2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-13+3256T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290371 | ||||||
chr1:115290385
|
T | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-13+3242A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290385 | ||||||
chr1:115290386
|
C | CT | 23 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0072others(20): Show | 23 | HG00621.hp2 HG00673.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-13+3240dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | ||||||
chr1:115290386
|
CT | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 164 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.-13+3240delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | ||||||
chr1:115290386
|
CTT | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0049others(82): Show | 87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.-13+3239_-13+3240d others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | ||||||
chr1:115290386
|
CTTT | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0153others(21): Show | 24 | HG01168.hp1 HG01433.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.-13+3238_-13+3240d others(5): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | ||||||
chr1:115290386
|
CTTTTT | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0307others(4): Show | 7 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+3236_-13+3240d others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | ||||||
chr1:115290386
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0220others(3): Show | 6 | HG02451.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+3226_-13+3240d others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | ||||||
chr1:115290405
|
T | C | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-13+3222A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290405 | ||||||
chr1:115290535
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-13+3092T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290535 | ||||||
chr1:115290553
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0239 | 2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-13+3074C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290553 | ||||||
chr1:115290676
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(6): Show | 9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+2951C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290676 | ||||||
chr1:115290796
|
T | C | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-13+2831A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290796 | ||||||
chr1:115290879
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0384 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+2748G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290879 | ||||||
chr1:115290960
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 318 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.-13+2667A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290960 | ||||||
chr1:115290967
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0303 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+2660C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290967 | ||||||
chr1:115291107
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13+2520C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291107 | ||||||
chr1:115291181
|
T | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0201 | 2 | HG01993.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-13+2446A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291181 | ||||||
chr1:115291182
|
A | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(37): Show | 43 | HG00423.hp1 HG00735.hp2 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.-13+2445T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291182 | ||||||
chr1:115291227
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 156 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-13+2400A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291227 | ||||||
chr1:115291231
|
G | GT | 28 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 29 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13+2395dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291231 | ||||||
chr1:115291235
|
A | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 288 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-13+2392T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291235 | ||||||
chr1:115291236
|
A | T | 1 | a0002c0002t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+2391T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291236 | ||||||
chr1:115291246
|
C | A | 1 | a0002c0002t0001g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-13+2381G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291246 | ||||||
chr1:115291570
|
T | G | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+2057A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291570 | ||||||
chr1:115291588
|
G | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 5 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2039C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291588 | ||||||
chr1:115291721
|
C | T | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-13+1906G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291721 | ||||||
chr1:115291801
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0306 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-13+1826T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291801 | ||||||
chr1:115291826
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-13+1801C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291826 | ||||||
chr1:115291901
|
C | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 293 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(290): Show |
intron_variant | MODIFIER | c.-13+1726G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291901 | ||||||
chr1:115291930
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-13+1697A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291930 | ||||||
chr1:115291949
|
G | A | 2 | a0001c0001t0001g0019a0002c0002t0001g0054 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-13+1678C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291949 | ||||||
chr1:115292048
|
G | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 280 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.-13+1579C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292048 | ||||||
chr1:115292099
|
C | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0305others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+1528G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292099 | ||||||
chr1:115292153
|
T | A | 2 | a0004c0005t0001g0089a0004c0005t0001g0090 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-13+1474A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292153 | ||||||
chr1:115292181
|
C | T | 23 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0001g0132others(20): Show | 23 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.-13+1446G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292181 | ||||||
chr1:115292452
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-13+1175A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292452 | ||||||
chr1:115292567
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-13+1060C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292567 | ||||||
chr1:115292632
|
G | A | 3 | a0002c0002t0001g0026a0003c0004t0001g0392a0003c0004t0001g0393 | 3 | HG01109.hp2 HG03927.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-13+995C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292632 | ||||||
chr1:115292777
|
A | G | 6 | a0001c0001t0001g0312a0001c0001t0001g0321a0001c0001t0001g0322others(3): Show | 6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+850T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292777 | ||||||
chr1:115292859
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-13+768A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292859 | ||||||
chr1:115292879
|
T | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 270 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.-13+748A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292879 | ||||||
chr1:115292898
|
C | A | 3 | a0001c0001t0001g0092a0002c0002t0001g0082a0002c0002t0001g0268 | 3 | NA18947.hp1 NA18962.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-13+729G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292898 | ||||||
chr1:115293090
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0303 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+537G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293090 | ||||||
chr1:115293093
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(6): Show | 9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+534C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293093 | ||||||
chr1:115293129
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(6): Show | 9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+498C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293129 | ||||||
chr1:115293135
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0371 | 2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-13+492T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293135 | ||||||
chr1:115293220
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 318 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.-13+407A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293220 | ||||||
chr1:115293290
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0239a0001c0001t0001g0344 | 3 | HG02257.hp2 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-13+337C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293290 | ||||||
chr1:115293308
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-13+319G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293308 | ||||||
chr1:115293341
|
C | T | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(31): Show | 35 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-13+286G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293341 | ||||||
chr1:115293399
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(40): Show | 46 | HG00423.hp1 HG00735.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.-13+228G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293399 | ||||||
chr1:115293442
|
A | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0403 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+185T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293442 | ||||||
chr1:115293482
|
G | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(22): Show | 26 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-13+145C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293482 | ||||||
chr1:115293851
|
G | C | 1 | a0001c0003t0001g0187 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-136-101C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293851 | ||||||
chr1:115293893
|
A | T | 1 | a0002c0002t0001g0285 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-136-143T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293893 | ||||||
chr1:115293916
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-166G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293916 | ||||||
chr1:115293917
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0049a0001c0001t0001g0086others(21): Show | 25 | HG00280.hp2 HG00597.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136-167C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293917 | ||||||
chr1:115293923
|
T | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0305others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-173A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293923 | ||||||
chr1:115293967
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0096a0001c0001t0001g0115 | 4 | NA18944.hp2 NA18974.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136-217C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293967 | ||||||
chr1:115294125
|
C | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 29 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-136-375G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294125 | ||||||
chr1:115294174
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-136-424G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294174 | ||||||
chr1:115294312
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-136-562T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294312 | ||||||
chr1:115294355
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-136-605A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294355 | ||||||
chr1:115294436
|
A | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(308): Show | 321 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.-136-686T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294436 | ||||||
chr1:115294495
|
T | A | 1 | a0001c0001t0001g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-136-745A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294495 | ||||||
chr1:115294661
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-911G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294661 | ||||||
chr1:115294827
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-136-1077C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294827 | ||||||
chr1:115294934
|
C | T | 1 | a0002c0002t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-136-1184G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294934 | ||||||
chr1:115295052
|
C | T | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-1302G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295052 | ||||||
chr1:115295057
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-136-1307T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295057 | ||||||
chr1:115295088
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 289 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(286): Show |
intron_variant | MODIFIER | c.-136-1338T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295088 | ||||||
chr1:115295242
|
A | T | 1 | a0001c0001t0001g0286 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-136-1492T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295242 | ||||||
chr1:115295298
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 148 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.-136-1548G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295298 | ||||||
chr1:115295340
|
C | G | 1 | a0001c0001t0001g0405 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-136-1590G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295340 | ||||||
chr1:115295414
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0305others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-1664G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295414 | ||||||
chr1:115295478
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(15): Show | 19 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-136-1728C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295478 | ||||||
chr1:115295661
|
G | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 187 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.-136-1911C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295661 | ||||||
chr1:115295949
|
T | A | 1 | a0001c0001t0001g0371 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-136-2199A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295949 | ||||||
chr1:115296119
|
TA | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(22): Show | 26 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-136-2370delT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296119 | ||||||
chr1:115296303
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-136-2553G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296303 | ||||||
chr1:115296331
|
C | T | 10 | a0001c0001t0001g0154a0001c0001t0001g0183a0001c0001t0001g0303others(7): Show | 10 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-2581G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296331 | ||||||
chr1:115296434
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-136-2684C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296434 | ||||||
chr1:115296514
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-136-2764G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296514 | ||||||
chr1:115296523
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-136-2773T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296523 | ||||||
chr1:115296575
|
A | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0031others(49): Show | 53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-2825T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296575 | ||||||
chr1:115296646
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(6): Show | 9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-2896A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296646 | ||||||
chr1:115296696
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-136-2946G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296696 | ||||||
chr1:115296703
|
A | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0031others(49): Show | 53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-2953T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296703 | ||||||
chr1:115296837
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-136-3087T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296837 | ||||||
chr1:115296858
|
C | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(3): Show | 6 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-3108G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296858 | ||||||
chr1:115296890
|
G | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0306 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-136-3140C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296890 | ||||||
chr1:115296905
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-136-3155C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296905 | ||||||
chr1:115296974
|
A | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0031others(49): Show | 53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-3224T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296974 | ||||||
chr1:115297027
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-136-3277A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297027 | ||||||
chr1:115297031
|
G | A | 10 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0211others(7): Show | 10 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-3281C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297031 | ||||||
chr1:115297050
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 255 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-136-3300A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297050 | ||||||
chr1:115297059
|
G | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0031others(47): Show | 51 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-136-3309C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297059 | ||||||
chr1:115297065
|
CATGCTTT others(1): Show |
C | 6 | a0002c0002t0001g0313a0002c0002t0001g0337a0002c0002t0001g0375others(3): Show | 6 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-3323_-136-331 others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297065 | ||||||
chr1:115297112
|
T | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(308): Show | 321 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.-136-3362A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297112 | ||||||
chr1:115297147
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136-3397A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297147 | ||||||
chr1:115297151
|
G | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(22): Show | 26 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-136-3401C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297151 | ||||||
chr1:115297157
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 96 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-136-3407A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297157 | ||||||
chr1:115297161
|
A | G | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | HG00621.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-136-3411T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297161 | ||||||
chr1:115297206
|
C | A | 1 | a0001c0001t0001g0013 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-136-3456G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297206 | ||||||
chr1:115297280
|
G | T | 1 | a0002c0002t0001g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-3530C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297280 | ||||||
chr1:115297394
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-136-3644A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297394 | ||||||
chr1:115297411
|
C | T | 2 | a0002c0002t0001g0142a0002c0002t0001g0193 | 2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-136-3661G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297411 | ||||||
chr1:115297749
|
C | G | 2 | a0001c0001t0001g0378a0001c0001t0001g0379 | 2 | HG00099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-136-3999G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297749 | ||||||
chr1:115297792
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136-4042A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297792 | ||||||
chr1:115297817
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-136-4067C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297817 | ||||||
chr1:115297828
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-136-4078G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297828 | ||||||
chr1:115297896
|
C | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0031others(49): Show | 53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-4146G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297896 | ||||||
chr1:115298097
|
T | A | 3 | a0001c0001t0001g0031a0001c0003t0001g0187a0001c0003t0001g0406 | 3 | HG02055.hp1 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-136-4347A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298097 | ||||||
chr1:115298134
|
C | T | 6 | a0001c0001t0001g0312a0001c0001t0001g0321a0001c0001t0001g0322others(3): Show | 6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-4384G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298134 | ||||||
chr1:115298218
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4468G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298218 | ||||||
chr1:115298306
|
AT | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-4557delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298306 | ||||||
chr1:115298466
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-136-4716T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298466 | ||||||
chr1:115298482
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4732T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298482 | ||||||
chr1:115298489
|
T | C | 117 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(114): Show | 119 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-136-4739A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298489 | ||||||
chr1:115298771
|
C | T | 69 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0033others(66): Show | 70 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-136-5021G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298771 | ||||||
chr1:115298831
|
G | T | 1 | a0001c0001t0001g0010 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-136-5081C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298831 | ||||||
chr1:115298882
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0395 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-136-5132C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298882 | ||||||
chr1:115298892
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-136-5142C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298892 | ||||||
chr1:115298956
|
T | G | 60 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0092others(57): Show | 61 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-136-5206A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298956 | ||||||
chr1:115298981
|
C | T | 8 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0071others(5): Show | 8 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-5231G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298981 | ||||||
chr1:115299112
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-136-5362A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299112 | ||||||
chr1:115299399
|
G | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-5649C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299399 | ||||||
chr1:115299661
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-136-5911A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299661 | ||||||
chr1:115299716
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-5966T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299716 | ||||||
chr1:115299768
|
C | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0371a0001c0003t0001g0399others(1): Show | 4 | HG01168.hp1 HG02145.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-6018G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299768 | ||||||
chr1:115299881
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-136-6131C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299881 | ||||||
chr1:115299937
|
T | G | 2 | a0002c0002t0001g0337a0002c0002t0001g0377 | 2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-136-6187A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299937 | ||||||
chr1:115300037
|
G | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0051others(36): Show | 40 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-136-6287C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300037 | ||||||
chr1:115300145
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-136-6395A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300145 | ||||||
chr1:115300189
|
A | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-6439T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300189 | ||||||
chr1:115300277
|
A | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-6527T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300277 | ||||||
chr1:115300286
|
G | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-6536C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300286 | ||||||
chr1:115300405
|
G | A | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | NA19066.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-136-6655C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300405 | ||||||
chr1:115300466
|
T | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(325): Show | 338 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.-136-6716A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300466 | ||||||
chr1:115300537
|
G | A | 27 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(24): Show | 28 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-136-6787C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300537 | ||||||
chr1:115300544
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0071others(5): Show | 8 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-6794C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300544 | ||||||
chr1:115300685
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-6935T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300685 | ||||||
chr1:115300962
|
G | A | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-7212C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300962 | ||||||
chr1:115300969
|
T | C | 3 | a0002c0002t0001g0313a0002c0002t0001g0375a0002c0002t0001g0391 | 3 | HG00639.hp1 HG01243.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-136-7219A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300969 | ||||||
chr1:115301137
|
GAACAA | G | 6 | a0001c0001t0001g0092a0002c0002t0001g0091a0002c0002t0001g0093others(3): Show | 6 | HG00408.hp1 NA18947.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-7392_-136-738 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301137 | ||||||
chr1:115301297
|
C | A | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-7547G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301297 | ||||||
chr1:115301306
|
C | A | 127 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-7556G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301306 | ||||||
chr1:115301419
|
A | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-7669T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301419 | ||||||
chr1:115301549
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-136-7799A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301549 | ||||||
chr1:115301592
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-136-7842G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301592 | ||||||
chr1:115301683
|
T | C | 1 | a0001c0001t0001g0349 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-136-7933A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301683 | ||||||
chr1:115302044
|
G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0403 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-136-8294C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302044 | ||||||
chr1:115302076
|
T | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0384 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-136-8326A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302076 | ||||||
chr1:115302101
|
C | T | 21 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(18): Show | 22 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-136-8351G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302101 | ||||||
chr1:115302425
|
G | A | 79 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(76): Show | 81 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-136-8675C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302425 | ||||||
chr1:115302438
|
C | T | 18 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(15): Show | 19 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-136-8688G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302438 | ||||||
chr1:115302568
|
A | G | 6 | a0001c0001t0001g0080a0001c0001t0001g0218a0001c0001t0001g0221others(3): Show | 6 | NA18940.hp1 NA18959.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-8818T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302568 | ||||||
chr1:115302736
|
G | A | 126 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 128 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-136-8986C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302736 | ||||||
chr1:115302754
|
G | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 38 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-136-9004C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302754 | ||||||
chr1:115302764
|
T | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(315): Show | 328 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.-136-9014A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302764 | ||||||
chr1:115302773
|
C | A | 2 | a0003c0004t0001g0392a0003c0004t0001g0393 | 2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-136-9023G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302773 | ||||||
chr1:115302815
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0371 | 2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-9065G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302815 | ||||||
chr1:115302884
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(23): Show | 27 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-136-9134C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302884 | ||||||
chr1:115302907
|
C | T | 126 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(123): Show | 128 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-136-9157G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302907 | ||||||
chr1:115303074
|
T | TAAGAAAT others(331): Show |
1 | a0001c0003t0001g0399 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-136-9325_-136-932 others(342): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303074 | ||||||
chr1:115303074
|
T | TAAGAAAT others(332): Show |
1 | a0001c0003t0001g0404 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-136-9325_-136-932 others(343): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303074 | ||||||
chr1:115303100
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0384 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-136-9350T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303100 | ||||||
chr1:115303166
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0051others(42): Show | 46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-9416G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303166 | ||||||
chr1:115303350
|
G | C | 45 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0051others(42): Show | 46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-9600C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303350 | ||||||
chr1:115303356
|
C | T | 1 | a0002c0002t0001g0258 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-136-9606G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303356 | ||||||
chr1:115303372
|
A | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0305a0001c0001t0001g0348others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-9622T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303372 | ||||||
chr1:115303524
|
C | T | 121 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(118): Show | 122 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-136-9774G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303524 | ||||||
chr1:115303555
|
C | A | 2 | a0002c0002t0001g0337a0002c0002t0001g0377 | 2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-136-9805G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303555 | ||||||
chr1:115303560
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 325 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.-136-9810A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303560 | ||||||
chr1:115303600
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-9850G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303600 | ||||||
chr1:115303627
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-136-9877T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303627 | ||||||
chr1:115303710
|
CCAT | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0207others(1): Show | 4 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-9963_-136-996 others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303710 | ||||||
chr1:115303812
|
T | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-10062A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303812 | ||||||
chr1:115304019
|
TTTTTC | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0306others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10274_-136-10 others(11): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304019 | ||||||
chr1:115304140
|
C | T | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-10390G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304140 | ||||||
chr1:115304177
|
A | AT | 7 | a0001c0001t0001g0080a0001c0001t0001g0218a0001c0001t0001g0221others(4): Show | 7 | HG01192.hp1 NA18940.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-10428dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304177 | ||||||
chr1:115304210
|
T | G | 10 | a0001c0001t0001g0033a0001c0003t0001g0030a0001c0003t0001g0032others(7): Show | 10 | HG01433.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136-10460A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304210 | ||||||
chr1:115304306
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-136-10556C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304306 | ||||||
chr1:115304309
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-136-10559G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304309 | ||||||
chr1:115304329
|
A | ATTTTTTT others(2): Show |
24 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0033others(21): Show | 24 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-136-10588_-136-10 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(3): Show |
37 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 38 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-136-10589_-136-10 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0072a0002c0002t0001g0026a0002c0002t0001g0058others(1): Show | 4 | HG00621.hp1 HG02027.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10590_-136-10 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(7): Show |
8 | a0001c0001t0001g0121a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 8 | HG01168.hp1 HG02109.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-10593_-136-10 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0274a0001c0001t0001g0303a0001c0001t0001g0305others(1): Show | 4 | HG02071.hp2 HG02976.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10594_-136-10 others(21): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(9): Show |
121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(118): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-136-10595_-136-10 others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(10): Show |
62 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(59): Show | 63 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-136-10580_-136-10 others(23): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(11): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0037others(12): Show | 16 | HG00738.hp2 HG01358.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-136-10580_-136-10 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0208a0001c0001t0001g0269others(1): Show | 4 | HG00544.hp2 HG01928.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10580_-136-10 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304329
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0165 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-136-10580_-136-10 others(27): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | ||||||
chr1:115304340
|
T | TTTTTTTT others(9): Show |
1 | a0001c0003t0001g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-136-10591_-136-10 others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304340 | ||||||
chr1:115304361
|
A | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(310): Show | 323 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.-136-10611T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304361 | ||||||
chr1:115304466
|
G | A | 1 | a0001c0003t0001g0143 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-136-10716C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304466 | ||||||
chr1:115304674
|
T | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(310): Show | 323 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.-136-10924A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304674 | ||||||
chr1:115304771
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 109 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-136-11021G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304771 | ||||||
chr1:115304813
|
C | T | 1 | a0001c0001t0001g0341 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-136-11063G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304813 | ||||||
chr1:115304830
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0389 | 2 | NA18945.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-136-11080G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304830 | ||||||
chr1:115304925
|
G | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 252 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.-136-11175C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304925 | ||||||
chr1:115305032
|
T | C | 10 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(7): Show | 10 | NA18945.hp1 NA18950.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-11282A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305032 | ||||||
chr1:115305061
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-136-11311T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305061 | ||||||
chr1:115305115
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 325 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.-136-11365T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305115 | ||||||
chr1:115305120
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-136-11370A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305120 | ||||||
chr1:115305275
|
T | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0044others(61): Show | 66 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-136-11525A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305275 | ||||||
chr1:115305307
|
C | T | 3 | a0001c0001t0001g0355a0001c0001t0001g0356a0001c0001t0001g0357 | 3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-136-11557G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305307 | ||||||
chr1:115305375
|
G | T | 1 | a0001c0001t0001g0331 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-136-11625C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305375 | ||||||
chr1:115305460
|
C | T | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-11710G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305460 | ||||||
chr1:115305490
|
C | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0347a0001c0001t0001g0401others(2): Show | 5 | HG03195.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-11740G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305490 | ||||||
chr1:115305767
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 83 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-136-12017G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305767 | ||||||
chr1:115305802
|
T | C | 4 | a0002c0002t0001g0016a0002c0002t0001g0055a0002c0002t0001g0353others(1): Show | 4 | NA18966.hp2 NA18967.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-12052A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305802 | ||||||
chr1:115305804
|
C | T | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-12054G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305804 | ||||||
chr1:115305829
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 83 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-136-12079T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305829 | ||||||
chr1:115306089
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0371 | 2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-12339C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306089 | ||||||
chr1:115306399
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0382 | 2 | HG02523.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-136-12649T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306399 | ||||||
chr1:115306457
|
T | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0237a0001c0001t0001g0250others(1): Show | 4 | HG01175.hp1 HG02280.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-12707A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306457 | ||||||
chr1:115306882
|
C | A | 1 | a0001c0001t0001g0242 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-136-13132G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306882 | ||||||
chr1:115306887
|
A | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-13137T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306887 | ||||||
chr1:115306947
|
C | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(26): Show | 30 | HG00544.hp2 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-136-13197G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306947 | ||||||
chr1:115307154
|
T | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-13404A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307154 | ||||||
chr1:115307291
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-136-13541C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307291 | ||||||
chr1:115307317
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0371 | 2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-13567C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307317 | ||||||
chr1:115307347
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-136-13597G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307347 | ||||||
chr1:115307348
|
G | A | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-13598C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307348 | ||||||
chr1:115307385
|
A | C | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-13635T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307385 | ||||||
chr1:115307506
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0306others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-13756G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307506 | ||||||
chr1:115307579
|
A | G | 1 | a0001c0001t0001g0405 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-136-13829T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307579 | ||||||
chr1:115307581
|
G | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(16): Show | 20 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136-13831C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307581 | ||||||
chr1:115307637
|
A | G | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-13887T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307637 | ||||||
chr1:115307747
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-136-13997G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307747 | ||||||
chr1:115307995
|
T | C | 1 | a0002c0002t0001g0296 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-136-14245A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307995 | ||||||
chr1:115308378
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(32): Show | 36 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.-136-14628G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308378 | ||||||
chr1:115308643
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00544.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-136-14893T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308643 | ||||||
chr1:115308847
|
G | A | 2 | a0001c0001t0001g0031a0001c0003t0001g0187 | 2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-136-15097C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308847 | ||||||
chr1:115308870
|
A | G | 139 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(136): Show | 142 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-136-15120T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308870 | ||||||
chr1:115308934
|
T | TTTAGTTT others(2): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0305others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-15185_-136-15 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308934 | ||||||
chr1:115308939
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0305others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-15189T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308939 | ||||||
chr1:115308940
|
A | ATTT | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0305others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-15191_-136-15 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308940 | ||||||
chr1:115309097
|
G | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(3): Show | 6 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-15347C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309097 | ||||||
chr1:115309215
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0051others(42): Show | 46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-15465G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309215 | ||||||
chr1:115309311
|
G | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0260 | 2 | NA18973.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-136-15561C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309311 | ||||||
chr1:115309334
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-136-15584G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309334 | ||||||
chr1:115309383
|
C | T | 130 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(127): Show | 133 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-136-15633G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309383 | ||||||
chr1:115309411
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-136-15661T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309411 | ||||||
chr1:115309632
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-15882C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309632 | ||||||
chr1:115309647
|
C | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(3): Show | 6 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-15897G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309647 | ||||||
chr1:115309753
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(134): Show | 140 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-136-16003G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309753 | ||||||
chr1:115309766
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-136-16016A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309766 | ||||||
chr1:115309803
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-136-16053C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309803 | ||||||
chr1:115309893
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-136-16143G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309893 | ||||||
chr1:115310127
|
T | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-16377A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310127 | ||||||
chr1:115310170
|
T | A | 1 | a0001c0001t0001g0013 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-136-16420A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310170 | ||||||
chr1:115310199
|
T | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(21): Show | 25 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136-16449A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310199 | ||||||
chr1:115310363
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(134): Show | 140 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-136-16613C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310363 | ||||||
chr1:115310463
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 97 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-136-16713A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310463 | ||||||
chr1:115310833
|
G | A | 45 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0051others(42): Show | 46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-17083C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310833 | ||||||
chr1:115310898
|
C | A | 1 | a0001c0001t0001g0002 | 2 | NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-136-17148G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310898 | ||||||
chr1:115311000
|
G | A | 2 | a0001c0001t0001g0018a0001c0003t0001g0023 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-136-17250C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311000 | ||||||
chr1:115311130
|
A | G | 1 | a0001c0001t0001g0349 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-136-17380T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311130 | ||||||
chr1:115311135
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0306others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-17385A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311135 | ||||||
chr1:115311182
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-136-17432C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311182 | ||||||
chr1:115311191
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 327 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.-136-17441A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311191 | ||||||
chr1:115311518
|
G | C | 1 | a0001c0001t0001g0255 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-136-17768C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311518 | ||||||
chr1:115311630
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0306 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-136-17880C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311630 | ||||||
chr1:115311707
|
A | G | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(137): Show | 143 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-136-17957T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311707 | ||||||
chr1:115311814
|
A | G | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(137): Show | 143 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-136-18064T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311814 | ||||||
chr1:115312075
|
G | A | 1 | a0001c0001t0001g0329 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-136-18325C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312075 | ||||||
chr1:115312172
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-136-18422G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312172 | ||||||
chr1:115312247
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-136-18497A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312247 | ||||||
chr1:115312344
|
T | C | 2 | a0001c0003t0001g0399a0001c0003t0001g0404 | 2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-18594A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312344 | ||||||
chr1:115312473
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0306others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-18723A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312473 | ||||||
chr1:115312487
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0367 | 2 | HG00735.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-136-18737G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312487 | ||||||
chr1:115312526
|
G | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 327 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.-136-18776C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312526 | ||||||
chr1:115312609
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0179 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-136-18859C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312609 | ||||||
chr1:115312782
|
C | T | 8 | a0002c0002t0001g0043a0002c0002t0001g0057a0002c0002t0001g0058others(5): Show | 8 | HG00621.hp1 HG02027.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-19032G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312782 | ||||||
chr1:115312803
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-19053C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312803 | ||||||
chr1:115313169
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0283 | 2 | HG01346.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-136-19419A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313169 | ||||||
chr1:115313293
|
G | T | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 327 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.-136-19543C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313293 | ||||||
chr1:115313294
|
T | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 327 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.-136-19544A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313294 | ||||||
chr1:115313366
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0371 | 2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-19616A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313366 | ||||||
chr1:115313390
|
G | T | 1 | a0009c0006t0001g0275 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-136-19640C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313390 | ||||||
chr1:115313457
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(134): Show | 140 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-136-19707G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313457 | ||||||
chr1:115313485
|
G | A | 7 | a0001c0001t0001g0154a0001c0001t0001g0183a0001c0001t0001g0303others(4): Show | 7 | HG02886.hp2 HG03195.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-19735C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313485 | ||||||
chr1:115313539
|
G | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0289a0001c0001t0001g0355others(2): Show | 5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-19789C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313539 | ||||||
chr1:115313574
|
C | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0129a0001c0001t0001g0405others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-19824G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313574 | ||||||
chr1:115313613
|
ATTGT | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-19867_-136-19 others(10): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313613 | ||||||
chr1:115313626
|
T | G | 1 | a0001c0001t0001g0347 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-136-19876A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313626 | ||||||
chr1:115313723
|
A | G | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(137): Show | 143 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-136-19973T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313723 | ||||||
chr1:115313804
|
G | C | 1 | a0002c0002t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-136-20054C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313804 | ||||||
chr1:115314021
|
G | A | 1 | a0002c0002t0001g0268 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-136-20271C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314021 | ||||||
chr1:115314122
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0384 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-136-20372C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314122 | ||||||
chr1:115314129
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-136-20379T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314129 | ||||||
chr1:115314158
|
T | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-20408A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314158 | ||||||
chr1:115314183
|
C | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 317 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.-136-20433G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314183 | ||||||
chr1:115314251
|
A | G | 2 | a0002c0002t0001g0244a0002c0002t0001g0265 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-136-20501T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314251 | ||||||
chr1:115314266
|
G | C | 1 | a0001c0001t0001g0357 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-136-20516C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314266 | ||||||
chr1:115314281
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-136-20531A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314281 | ||||||
chr1:115314500
|
C | A | 1 | a0002c0002t0001g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-20750G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314500 | ||||||
chr1:115314630
|
G | A | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(126): Show | 132 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-136-20880C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314630 | ||||||
chr1:115314717
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0179 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-136-20967C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314717 | ||||||
chr1:115314727
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136-20977A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314727 | ||||||
chr1:115314810
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0177a0001c0001t0001g0179others(1): Show | 4 | HG02486.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136-21060G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314810 | ||||||
chr1:115314850
|
A | G | 1 | a0001c0001t0001g0382 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-136-21100T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314850 | ||||||
chr1:115314937
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0161a0001c0001t0001g0239others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-21187C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314937 | ||||||
chr1:115314987
|
G | A | 1 | a0002c0002t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-136-21237C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314987 | ||||||
chr1:115315027
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0179 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-136-21277C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315027 | ||||||
chr1:115315295
|
G | A | 68 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0056others(65): Show | 68 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-136-21545C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315295 | ||||||
chr1:115315337
|
T | C | 224 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(221): Show | 230 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.-136-21587A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315337 | ||||||
chr1:115315381
|
A | G | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-21631T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315381 | ||||||
chr1:115315387
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00544.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-136-21637G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315387 | ||||||
chr1:115315412
|
A | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0255a0001c0001t0001g0316others(10): Show | 14 | HG02523.hp1 NA18612.hp1 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136-21662T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315412 | ||||||
chr1:115315414
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-136-21664A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315414 | ||||||
chr1:115315469
|
G | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0073others(7): Show | 10 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-21719C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315469 | ||||||
chr1:115315483
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(86): Show | 94 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-136-21733C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315483 | ||||||
chr1:115315803
|
G | A | 1 | a0002c0002t0001g0408 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-136-22053C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315803 | ||||||
chr1:115315910
|
G | A | 1 | a0002c0002t0001g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-22160C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315910 | ||||||
chr1:115315911
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-136-22161G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315911 | ||||||
chr1:115315917
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0049others(24): Show | 28 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-136-22167C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315917 | ||||||
chr1:115315983
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0161a0001c0001t0001g0385others(1): Show | 4 | HG01192.hp2 HG02559.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+22221C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315983 | ||||||
chr1:115316002
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-137+22202A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316002 | ||||||
chr1:115316006
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-137+22198C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316006 | ||||||
chr1:115316117
|
G | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0177a0001c0003t0001g0162others(1): Show | 4 | HG02486.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+22087C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316117 | ||||||
chr1:115316296
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-137+21908C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316296 | ||||||
chr1:115316308
|
G | C | 5 | a0001c0001t0001g0211a0001c0001t0001g0239a0001c0001t0001g0306others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+21896C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316308 | ||||||
chr1:115316485
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+21719T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316485 | ||||||
chr1:115316494
|
A | G | 2 | a0002c0002t0001g0313a0002c0002t0001g0375 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-137+21710T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316494 | ||||||
chr1:115316562
|
C | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+21642G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316562 | ||||||
chr1:115316622
|
T | C | 2 | a0001c0003t0001g0162a0001c0003t0001g0168 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-137+21582A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316622 | ||||||
chr1:115316806
|
T | G | 6 | a0001c0001t0001g0211a0001c0001t0001g0306a0001c0001t0001g0384others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+21398A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316806 | ||||||
chr1:115316827
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-137+21377A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316827 | ||||||
chr1:115316863
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0209 | 2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+21341C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316863 | ||||||
chr1:115317012
|
A | C | 2 | a0002c0002t0001g0193a0002c0002t0001g0403 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-137+21192T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317012 | ||||||
chr1:115317012
|
A | T | 2 | a0002c0002t0001g0048a0002c0002t0001g0079 | 2 | NA18943.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-137+21192T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317012 | ||||||
chr1:115317110
|
TA | T | 13 | a0001c0001t0001g0120a0001c0001t0001g0211a0001c0001t0001g0306others(10): Show | 13 | HG00621.hp1 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-137+21093delT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317110 | ||||||
chr1:115317187
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-137+21017G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317187 | ||||||
chr1:115317352
|
C | T | 10 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036others(7): Show | 10 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+20852G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317352 | ||||||
chr1:115317368
|
T | A | 2 | a0001c0001t0001g0121a0002c0002t0001g0324 | 2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-137+20836A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317368 | ||||||
chr1:115317555
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+20649T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317555 | ||||||
chr1:115317654
|
G | A | 1 | a0002c0002t0001g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+20550C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317654 | ||||||
chr1:115317739
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-137+20465G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317739 | ||||||
chr1:115317741
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+20463A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317741 | ||||||
chr1:115317930
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+20274G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317930 | ||||||
chr1:115318078
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+20126C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318078 | ||||||
chr1:115318180
|
C | A | 22 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0029others(19): Show | 23 | HG01099.hp2 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-137+20024G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318180 | ||||||
chr1:115318197
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+20007G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318197 | ||||||
chr1:115318216
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0303 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-137+19988C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318216 | ||||||
chr1:115318221
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+19983C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318221 | ||||||
chr1:115318252
|
T | A | 3 | a0001c0001t0001g0363a0001c0001t0001g0385a0001c0001t0001g0386 | 3 | HG01192.hp2 HG01261.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-137+19952A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318252 | ||||||
chr1:115318321
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+19883A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318321 | ||||||
chr1:115318342
|
G | C | 1 | a0002c0002t0001g0061 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-137+19862C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318342 | ||||||
chr1:115318400
|
G | A | 1 | a0001c0001t0001g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-137+19804C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318400 | ||||||
chr1:115318638
|
C | T | 1 | a0001c0003t0001g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+19566G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318638 | ||||||
chr1:115318644
|
T | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 161 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-137+19560A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318644 | ||||||
chr1:115318863
|
C | T | 1 | a0002c0002t0001g0376 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-137+19341G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318863 | ||||||
chr1:115318878
|
C | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00544.hp1 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+19326G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318878 | ||||||
chr1:115318906
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+19298C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318906 | ||||||
chr1:115318984
|
G | A | 2 | a0002c0002t0001g0193a0002c0002t0001g0403 | 2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-137+19220C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318984 | ||||||
chr1:115318998
|
A | G | 8 | a0001c0001t0001g0120a0002c0002t0001g0043a0002c0002t0001g0057others(5): Show | 8 | HG00621.hp1 HG02056.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+19206T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318998 | ||||||
chr1:115319258
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-137+18946T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319258 | ||||||
chr1:115319402
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-137+18802A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319402 | ||||||
chr1:115319536
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-137+18668G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319536 | ||||||
chr1:115319613
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+18591T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319613 | ||||||
chr1:115319633
|
A | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.-137+18571T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319633 | ||||||
chr1:115319906
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-137+18298C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319906 | ||||||
chr1:115319946
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-137+18258G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319946 | ||||||
chr1:115319947
|
G | A | 170 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 174 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.-137+18257C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319947 | ||||||
chr1:115319996
|
C | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.-137+18208G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319996 | ||||||
chr1:115320020
|
T | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(316): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.-137+18184A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320020 | ||||||
chr1:115320022
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01243.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-137+18182G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320022 | ||||||
chr1:115320049
|
G | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0029others(19): Show | 23 | HG01099.hp2 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-137+18155C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320049 | ||||||
chr1:115320192
|
T | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | NA18956.hp1 NA18971.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-137+18012A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320192 | ||||||
chr1:115320199
|
T | G | 80 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0105others(77): Show | 82 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-137+18005A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320199 | ||||||
chr1:115320205
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 5 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+17999G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320205 | ||||||
chr1:115320297
|
T | A | 197 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-137+17907A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320297 | ||||||
chr1:115320383
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-137+17821G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320383 | ||||||
chr1:115320441
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+17763G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320441 | ||||||
chr1:115320446
|
A | T | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-137+17758T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320446 | ||||||
chr1:115320758
|
T | C | 3 | a0001c0001t0001g0118a0002c0002t0001g0193a0002c0002t0001g0403 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+17446A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320758 | ||||||
chr1:115320860
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-137+17344G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320860 | ||||||
chr1:115320927
|
C | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-137+17277G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320927 | ||||||
chr1:115321279
|
T | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 202 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-137+16925A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321279 | ||||||
chr1:115321296
|
A | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00544.hp1 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+16908T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321296 | ||||||
chr1:115321301
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG00544.hp1 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+16903C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321301 | ||||||
chr1:115321305
|
A | C | 11 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+16899T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321305 | ||||||
chr1:115321445
|
G | A | 1 | a0001c0003t0001g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+16759C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321445 | ||||||
chr1:115321507
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16697C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321507 | ||||||
chr1:115321508
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16696C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321508 | ||||||
chr1:115321509
|
A | C | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16695T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321509 | ||||||
chr1:115321510
|
C | A | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16694G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321510 | ||||||
chr1:115321512
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16692C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321512 | ||||||
chr1:115321513
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16691G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321513 | ||||||
chr1:115321515
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16689C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321515 | ||||||
chr1:115321517
|
T | TTTTGCCA others(3): Show |
1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16686_-137+16 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321517 | ||||||
chr1:115321518
|
C | A | 1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16686G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321518 | ||||||
chr1:115321551
|
C | T | 1 | a0002c0002t0001g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+16653G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321551 | ||||||
chr1:115321576
|
A | ATG | 25 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0051others(22): Show | 25 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-137+16626_-137+16 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
A | ATGTG | 3 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0151 | 3 | HG03927.hp2 NA18968.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-137+16624_-137+16 others(10): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATG | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0064others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-137+16626_-137+16 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTG | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0044others(50): Show | 55 | HG00280.hp1 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-137+16624_-137+16 others(10): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTG | A | 35 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(32): Show | 36 | HG00280.hp2 HG01123.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-137+16622_-137+16 others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(1): Show |
A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(100): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-137+16620_-137+16 others(14): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(3): Show |
A | 30 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0109others(27): Show | 31 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-137+16618_-137+16 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(5): Show |
A | 11 | a0001c0001t0001g0086a0001c0001t0001g0098a0001c0001t0001g0120others(8): Show | 11 | HG00621.hp1 HG00735.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+16616_-137+16 others(18): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0001g0312a0001c0001t0001g0321a0001c0001t0001g0323 | 3 | HG01069.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-137+16614_-137+16 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+16612_-137+16 others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(11): Show |
A | 14 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0033others(11): Show | 14 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137+16610_-137+16 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(13): Show |
A | 32 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0129others(29): Show | 33 | HG00741.hp2 HG01099.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-137+16608_-137+16 others(26): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(17): Show |
A | 2 | a0001c0001t0001g0161a0001c0001t0001g0347 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-137+16604_-137+16 others(30): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321576
|
ATGTGTGT others(19): Show |
A | 2 | a0001c0001t0001g0015a0001c0001t0001g0121 | 2 | HG02300.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-137+16602_-137+16 others(32): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | ||||||
chr1:115321768
|
C | T | 6 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0199others(3): Show | 6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+16436G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321768 | ||||||
chr1:115321928
|
C | T | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 178 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-137+16276G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321928 | ||||||
chr1:115321966
|
G | A | 1 | a0001c0003t0001g0198 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-137+16238C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321966 | ||||||
chr1:115321982
|
G | A | 1 | a0002c0002t0001g0128 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-137+16222C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321982 | ||||||
chr1:115321983
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-137+16221T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321983 | ||||||
chr1:115321986
|
T | A | 1 | a0002c0002t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-137+16218A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321986 | ||||||
chr1:115322002
|
T | A | 22 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0029others(19): Show | 23 | HG01099.hp2 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-137+16202A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322002 | ||||||
chr1:115322035
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0395 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-137+16169A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322035 | ||||||
chr1:115322068
|
C | T | 3 | a0001c0001t0001g0118a0002c0002t0001g0193a0002c0002t0001g0403 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+16136G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322068 | ||||||
chr1:115322098
|
T | C | 1 | a0002c0002t0001g0353 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-137+16106A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322098 | ||||||
chr1:115322329
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0170 | 2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-137+15875C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322329 | ||||||
chr1:115322486
|
G | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0161a0001c0003t0001g0406 | 3 | HG02055.hp2 HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+15718C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322486 | ||||||
chr1:115322527
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-137+15677G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322527 | ||||||
chr1:115322596
|
A | C | 7 | a0001c0001t0001g0080a0001c0001t0001g0218a0001c0001t0001g0221others(4): Show | 7 | NA18940.hp1 NA18957.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+15608T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322596 | ||||||
chr1:115322610
|
A | G | 1 | a0001c0001t0001g0396 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-137+15594T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322610 | ||||||
chr1:115322698
|
C | A | 1 | a0001c0001t0001g0401 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-137+15506G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322698 | ||||||
chr1:115322771
|
C | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+15433G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322771 | ||||||
chr1:115322865
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-137+15339T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322865 | ||||||
chr1:115322984
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-137+15220G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322984 | ||||||
chr1:115322985
|
A | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0348others(2): Show | 6 | HG01099.hp2 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+15219T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322985 | ||||||
chr1:115323350
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0109a0001c0001t0001g0110others(17): Show | 21 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+14854T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323350 | ||||||
chr1:115323577
|
A | G | 8 | a0001c0001t0001g0120a0002c0002t0001g0043a0002c0002t0001g0057others(5): Show | 8 | HG00621.hp1 HG02056.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+14627T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323577 | ||||||
chr1:115323651
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-137+14553T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323651 | ||||||
chr1:115323848
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+14356T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323848 | ||||||
chr1:115323998
|
C | T | 2 | a0004c0005t0001g0089a0004c0005t0001g0090 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-137+14206G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323998 | ||||||
chr1:115324286
|
G | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0177a0001c0001t0001g0179others(5): Show | 8 | HG02486.hp2 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+13918C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324286 | ||||||
chr1:115324332
|
G | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0306a0001c0001t0001g0384 | 3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+13872C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324332 | ||||||
chr1:115324345
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0306a0001c0001t0001g0384 | 3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+13859C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324345 | ||||||
chr1:115324454
|
C | T | 1 | a0002c0002t0001g0189 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-137+13750G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324454 | ||||||
chr1:115324466
|
T | A | 1 | a0001c0001t0001g0147 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-137+13738A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324466 | ||||||
chr1:115324515
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-137+13689A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324515 | ||||||
chr1:115324549
|
C | A | 1 | a0002c0002t0001g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+13655G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324549 | ||||||
chr1:115324576
|
G | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+13628C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324576 | ||||||
chr1:115324595
|
T | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(81): Show | 88 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-137+13609A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324595 | ||||||
chr1:115324626
|
A | G | 3 | a0001c0001t0001g0325a0001c0001t0001g0330a0001c0001t0001g0366 | 3 | HG03831.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-137+13578T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324626 | ||||||
chr1:115324650
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(303): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.-137+13554C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324650 | ||||||
chr1:115324701
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-137+13503C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324701 | ||||||
chr1:115324713
|
T | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0136a0001c0001t0001g0138others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-137+13491A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324713 | ||||||
chr1:115324950
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+13254G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324950 | ||||||
chr1:115324996
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0037others(83): Show | 87 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-137+13208G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324996 | ||||||
chr1:115325044
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | NA18945.hp1 NA18950.hp2 NA18964.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+13160C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325044 | ||||||
chr1:115325121
|
A | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(78): Show | 85 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137+13083T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325121 | ||||||
chr1:115325185
|
C | T | 4 | a0001c0001t0001g0166a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02155.hp1 NA18990.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+13019G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325185 | ||||||
chr1:115325223
|
G | A | 1 | a0001c0003t0001g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+12981C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325223 | ||||||
chr1:115325264
|
C | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0036others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+12940G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325264 | ||||||
chr1:115325265
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-137+12939C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325265 | ||||||
chr1:115325439
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-137+12765T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325439 | ||||||
chr1:115325527
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+12677T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325527 | ||||||
chr1:115325761
|
A | G | 54 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(51): Show | 55 | HG00621.hp1 HG00741.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-137+12443T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325761 | ||||||
chr1:115325805
|
A | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(41): Show | 45 | HG00621.hp1 HG00741.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.-137+12399T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325805 | ||||||
chr1:115325930
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0314a0001c0001t0001g0315others(6): Show | 9 | NA18954.hp1 NA18957.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.-137+12274G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325930 | ||||||
chr1:115326157
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+12047C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326157 | ||||||
chr1:115326178
|
C | T | 2 | a0003c0004t0001g0392a0003c0004t0001g0393 | 2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-137+12026G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326178 | ||||||
chr1:115326200
|
T | C | 3 | a0001c0001t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02451.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-137+12004A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326200 | ||||||
chr1:115326261
|
A | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(80): Show | 87 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-137+11943T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326261 | ||||||
chr1:115326339
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-137+11865C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326339 | ||||||
chr1:115326468
|
G | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 219 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-137+11736C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326468 | ||||||
chr1:115326471
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(78): Show | 85 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137+11733C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326471 | ||||||
chr1:115326501
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+11703C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326501 | ||||||
chr1:115326520
|
T | A | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-137+11684A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326520 | ||||||
chr1:115326610
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-137+11594A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326610 | ||||||
chr1:115326616
|
A | G | 10 | a0001c0001t0001g0118a0001c0001t0001g0154a0001c0001t0001g0177others(7): Show | 10 | HG02486.hp2 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-137+11588T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326616 | ||||||
chr1:115326676
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+11528A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326676 | ||||||
chr1:115326837
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-137+11367C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326837 | ||||||
chr1:115326878
|
G | A | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-137+11326C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326878 | ||||||
chr1:115327074
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-137+11130A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327074 | ||||||
chr1:115327209
|
G | A | 6 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0199others(3): Show | 6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+10995C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327209 | ||||||
chr1:115327229
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(79): Show | 86 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-137+10975A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327229 | ||||||
chr1:115327306
|
C | T | 7 | a0001c0001t0001g0119a0001c0001t0001g0171a0001c0001t0001g0191others(4): Show | 7 | HG01106.hp1 HG01261.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+10898G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327306 | ||||||
chr1:115327346
|
T | C | 1 | a0001c0001t0001g0400 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-137+10858A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327346 | ||||||
chr1:115327505
|
C | T | 8 | a0001c0001t0001g0120a0002c0002t0001g0043a0002c0002t0001g0057others(5): Show | 8 | HG00621.hp1 HG02056.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+10699G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327505 | ||||||
chr1:115327576
|
G | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0306a0001c0001t0001g0384 | 3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+10628C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327576 | ||||||
chr1:115327689
|
A | G | 49 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(46): Show | 50 | HG00621.hp1 HG00741.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.-137+10515T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327689 | ||||||
chr1:115327708
|
T | C | 2 | a0004c0005t0001g0089a0004c0005t0001g0090 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-137+10496A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327708 | ||||||
chr1:115327854
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+10350G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327854 | ||||||
chr1:115327911
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-137+10293G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327911 | ||||||
chr1:115328165
|
AG | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 243 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.-137+10038delC | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328165 | ||||||
chr1:115328188
|
TG | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(134): Show | 142 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-137+10015delC | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328188 | ||||||
chr1:115328284
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+9920A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328284 | ||||||
chr1:115328525
|
C | T | 3 | a0001c0001t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02451.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-137+9679G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328525 | ||||||
chr1:115328550
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+9654C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328550 | ||||||
chr1:115328568
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-137+9636C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328568 | ||||||
chr1:115328733
|
C | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-137+9471G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328733 | ||||||
chr1:115328795
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-137+9409C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328795 | ||||||
chr1:115328853
|
G | T | 6 | a0001c0001t0001g0295a0001c0001t0001g0297a0001c0001t0001g0298others(3): Show | 6 | HG02056.hp1 HG02071.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+9351C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328853 | ||||||
chr1:115329014
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 83 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-137+9190T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329014 | ||||||
chr1:115329233
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0109a0001c0001t0001g0110others(17): Show | 21 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+8971T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329233 | ||||||
chr1:115329240
|
A | AGTATGTA others(14): Show |
1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+8943_-137+896 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329240 | ||||||
chr1:115329245
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-137+8959C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329245 | ||||||
chr1:115329269
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+8935G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329269 | ||||||
chr1:115329287
|
T | C | 6 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0199others(3): Show | 6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+8917A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329287 | ||||||
chr1:115329414
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-137+8790C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329414 | ||||||
chr1:115329617
|
C | T | 7 | a0002c0002t0001g0043a0002c0002t0001g0057a0002c0002t0001g0058others(4): Show | 7 | HG00621.hp1 HG02056.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+8587G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329617 | ||||||
chr1:115329645
|
T | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 119 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-137+8559A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329645 | ||||||
chr1:115329694
|
A | G | 1 | a0001c0001t0001g0384 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-137+8510T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329694 | ||||||
chr1:115329744
|
C | CT | 15 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0154others(12): Show | 15 | HG02258.hp2 HG02486.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-137+8459dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329744 | ||||||
chr1:115329744
|
CT | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 196 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.-137+8459delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329744 | ||||||
chr1:115329749
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+8455A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329749 | ||||||
chr1:115329751
|
T | C | 1 | a0001c0001t0001g0329 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-137+8453A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329751 | ||||||
chr1:115329803
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0401a0001c0001t0001g0405 | 3 | HG02258.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-137+8401C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329803 | ||||||
chr1:115329907
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 229 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.-137+8297A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329907 | ||||||
chr1:115329933
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+8271A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329933 | ||||||
chr1:115330013
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+8191G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330013 | ||||||
chr1:115330257
|
T | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0247 | 2 | NA18939.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-137+7947A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330257 | ||||||
chr1:115330346
|
G | A | 6 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0199others(3): Show | 6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+7858C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330346 | ||||||
chr1:115330426
|
G | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-137+7778C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330426 | ||||||
chr1:115330431
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-137+7773G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330431 | ||||||
chr1:115330695
|
C | T | 1 | a0001c0003t0001g0406 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+7509G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330695 | ||||||
chr1:115330703
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+7501G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330703 | ||||||
chr1:115330730
|
TCACTC | T | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-137+7469_-137+747 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330730 | ||||||
chr1:115330802
|
A | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0303others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+7402T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330802 | ||||||
chr1:115330847
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-137+7357C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330847 | ||||||
chr1:115330984
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-137+7220G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330984 | ||||||
chr1:115331110
|
A | AG | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(53): Show | 58 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-137+7093dupC | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331110 | ||||||
chr1:115331133
|
T | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0306a0001c0001t0001g0384 | 3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+7071A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331133 | ||||||
chr1:115331298
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-137+6906A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331298 | ||||||
chr1:115331380
|
C | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG01175.hp1 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-137+6824G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331380 | ||||||
chr1:115331453
|
T | G | 1 | a0001c0001t0001g0253 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-137+6751A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331453 | ||||||
chr1:115331829
|
T | G | 2 | a0001c0001t0001g0352a0001c0003t0001g0351 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-137+6375A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331829 | ||||||
chr1:115331891
|
A | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0129others(21): Show | 24 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-137+6313T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331891 | ||||||
chr1:115331978
|
A | G | 2 | a0002c0002t0001g0244a0002c0002t0001g0265 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-137+6226T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331978 | ||||||
chr1:115332082
|
T | A | 1 | a0001c0001t0001g0272 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-137+6122A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332082 | ||||||
chr1:115332133
|
C | T | 2 | a0002c0002t0001g0016a0002c0002t0001g0364 | 2 | NA18967.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-137+6071G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332133 | ||||||
chr1:115332310
|
A | G | 395 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(392): Show | 404 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(401): Show |
intron_variant | MODIFIER | c.-137+5894T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332310 | ||||||
chr1:115332339
|
T | A | 3 | a0001c0001t0001g0390a0003c0004t0001g0392a0003c0004t0001g0393 | 3 | HG00733.hp1 HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-137+5865A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332339 | ||||||
chr1:115332516
|
TA | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.-137+5687delT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332516 | ||||||
chr1:115332573
|
A | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 114 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-137+5631T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332573 | ||||||
chr1:115332588
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-137+5616C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332588 | ||||||
chr1:115332939
|
C | T | 2 | a0001c0001t0001g0239a0001c0003t0001g0406 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-137+5265G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332939 | ||||||
chr1:115333024
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 214 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.-137+5180G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333024 | ||||||
chr1:115333049
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-137+5155A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333049 | ||||||
chr1:115333279
|
A | G | 2 | a0001c0001t0001g0239a0001c0003t0001g0406 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-137+4925T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333279 | ||||||
chr1:115333499
|
T | TA | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(75): Show | 81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-137+4704dupT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | ||||||
chr1:115333499
|
T | TAA | 15 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0024others(12): Show | 16 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-137+4703_-137+470 others(6): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | ||||||
chr1:115333499
|
T | TAAA | 106 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(103): Show | 107 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.-137+4702_-137+470 others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | ||||||
chr1:115333499
|
T | TAAAA | 21 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0132others(18): Show | 21 | HG00544.hp2 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-137+4701_-137+470 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | ||||||
chr1:115333647
|
C | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0037others(87): Show | 91 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-137+4557G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333647 | ||||||
chr1:115333655
|
C | CTCTT | 5 | a0001c0001t0001g0361a0001c0001t0001g0385a0002c0002t0001g0324others(2): Show | 5 | HG01175.hp2 HG01192.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+4545_-137+454 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | ||||||
chr1:115333655
|
CTCTT | C | 19 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0001t0001g0185others(16): Show | 19 | HG00280.hp1 HG00639.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-137+4545_-137+454 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | ||||||
chr1:115333655
|
CTCTTTCT others(1): Show |
C | 24 | a0001c0001t0001g0063a0001c0001t0001g0100a0001c0001t0001g0186others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-137+4541_-137+454 others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | ||||||
chr1:115333655
|
CTCTTTCT others(5): Show |
C | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0044others(11): Show | 16 | HG01358.hp2 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.-137+4537_-137+454 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | ||||||
chr1:115333655
|
CTCTTTCT others(9): Show |
C | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0318others(3): Show | 6 | HG00099.hp1 HG02698.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+4533_-137+454 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | ||||||
chr1:115333655
|
CTCTTTCT others(13): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-137+4529_-137+454 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | ||||||
chr1:115333662
|
T | C | 1 | a0002c0002t0001g0108 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-137+4542A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333662 | ||||||
chr1:115333677
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0001g0341 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-137+4514_-137+452 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333677 | ||||||
chr1:115333677
|
CTTTCTTT others(30): Show |
C | 2 | a0001c0001t0001g0154a0001c0001t0001g0177 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-137+4490_-137+452 others(41): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333677 | ||||||
chr1:115333678
|
TTTCTTTC others(8): Show |
T | 12 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-137+4511_-137+452 others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333678 | ||||||
chr1:115333681
|
CTTTCTTT others(26): Show |
C | 2 | a0001c0003t0001g0162a0001c0003t0001g0168 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-137+4490_-137+452 others(37): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333681 | ||||||
chr1:115333682
|
TTTCTTTC others(4): Show |
T | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0037others(61): Show | 65 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-137+4511_-137+452 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333682 | ||||||
chr1:115333682
|
TTTCTTTC others(8): Show |
T | 2 | a0001c0001t0001g0150a0001c0001t0001g0155 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-137+4507_-137+452 others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333682 | ||||||
chr1:115333686
|
TTTCTTTC | T | 10 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0156others(7): Show | 10 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-137+4511_-137+451 others(11): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333686 | ||||||
chr1:115333689
|
CTTTCTTT others(18): Show |
C | 1 | a0001c0001t0001g0322 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-137+4490_-137+451 others(29): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333689 | ||||||
chr1:115333693
|
CTTTCTTT others(14): Show |
C | 14 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0250others(11): Show | 14 | HG00609.hp1 HG02129.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137+4490_-137+451 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333693 | ||||||
chr1:115333693
|
CTTTCTTT others(15): Show |
C | 1 | a0002c0002t0001g0408 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-137+4489_-137+451 others(26): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333693 | ||||||
chr1:115333697
|
CTTTCTTT others(10): Show |
C | 40 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 42 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-137+4490_-137+450 others(21): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333697 | ||||||
chr1:115333701
|
CTTTCTTT others(6): Show |
C | 48 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(45): Show | 49 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.-137+4490_-137+450 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333701 | ||||||
chr1:115333702
|
TTTCTTTC others(18): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-137+4477_-137+450 others(29): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333702 | ||||||
chr1:115333702
|
TTTCTTTC others(25): Show |
T | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-137+4470_-137+450 others(36): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333702 | ||||||
chr1:115333705
|
CTTTCTTT others(2): Show |
C | 31 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0112others(28): Show | 31 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.-137+4490_-137+449 others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333705 | ||||||
chr1:115333706
|
TTTCTTTC others(14): Show |
T | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-137+4477_-137+449 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333706 | ||||||
chr1:115333706
|
TTTCTTTC others(21): Show |
T | 2 | a0001c0001t0001g0104a0001c0001t0001g0230 | 2 | HG01978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-137+4470_-137+449 others(32): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333706 | ||||||
chr1:115333709
|
CTTTCT | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0110a0001c0001t0001g0111others(18): Show | 21 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+4490_-137+449 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333709 | ||||||
chr1:115333710
|
TTTCTTTT others(17): Show |
T | 15 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0072others(12): Show | 16 | HG00438.hp1 HG01496.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.-137+4470_-137+449 others(28): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333710 | ||||||
chr1:115333713
|
CT | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0076others(18): Show | 21 | HG01123.hp1 HG02056.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+4490delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333713 | ||||||
chr1:115333714
|
TTTTCTTT others(6): Show |
T | 20 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0078others(17): Show | 22 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.-137+4477_-137+448 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333714 | ||||||
chr1:115333714
|
TTTTCTTT others(13): Show |
T | 21 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0070others(18): Show | 22 | HG00423.hp1 HG01243.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.-137+4470_-137+448 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333714 | ||||||
chr1:115333715
|
TTTCTTTC others(4): Show |
T | 1 | a0002c0002t0001g0271 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-137+4478_-137+448 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333715 | ||||||
chr1:115333723
|
TTTCCTTC others(4): Show |
T | 8 | a0001c0001t0001g0013a0001c0001t0001g0077a0001c0001t0001g0122others(5): Show | 8 | HG02080.hp1 HG02080.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+4470_-137+448 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333723 | ||||||
chr1:115333727
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0221 | 2 | NA18949.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-137+4477G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333727 | ||||||
chr1:115333731
|
TTTC | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0046others(19): Show | 24 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+4470_-137+447 others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333731 | ||||||
chr1:115333734
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-137+4470G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333734 | ||||||
chr1:115333738
|
C | T | 3 | a0001c0001t0001g0075a0002c0002t0001g0045a0002c0002t0001g0074 | 3 | NA18941.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-137+4466G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333738 | ||||||
chr1:115333741
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+4463A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333741 | ||||||
chr1:115333747
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+4457A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333747 | ||||||
chr1:115333748
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+4456A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333748 | ||||||
chr1:115333760
|
C | CCT | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(236): Show | 246 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.-137+4442_-137+444 others(6): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333760 | ||||||
chr1:115333760
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+4444G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333760 | ||||||
chr1:115333794
|
C | CTTTCTTT others(13): Show |
1 | a0001c0001t0001g0302 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-137+4409_-137+441 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333794 | ||||||
chr1:115333794
|
CTTTCTTT others(9): Show |
C | 11 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0139others(8): Show | 11 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+4394_-137+440 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333794 | ||||||
chr1:115333804
|
T | C | 1 | a0002c0002t0001g0387 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-137+4400A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333804 | ||||||
chr1:115333804
|
T | TTCTC | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(233): Show | 243 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.-137+4396_-137+439 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333804 | ||||||
chr1:115333810
|
T | C | 3 | a0001c0001t0001g0220a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02723.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-137+4394A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333810 | ||||||
chr1:115333812
|
T | C | 3 | a0001c0001t0001g0220a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02723.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-137+4392A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333812 | ||||||
chr1:115333814
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02723.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-137+4390G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333814 | ||||||
chr1:115333882
|
G | A | 118 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0015others(115): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.-137+4322C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333882 | ||||||
chr1:115333915
|
G | A | 2 | a0001c0001t0001g0115a0002c0002t0001g0099 | 2 | NA18944.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-137+4289C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333915 | ||||||
chr1:115333962
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-137+4242G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333962 | ||||||
chr1:115333997
|
G | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 332 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(329): Show |
intron_variant | MODIFIER | c.-137+4207C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333997 | ||||||
chr1:115334350
|
G | A | 2 | a0002c0002t0001g0107a0002c0002t0001g0108 | 2 | NA18940.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-137+3854C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334350 | ||||||
chr1:115334381
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+3823T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334381 | ||||||
chr1:115334410
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+3794T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334410 | ||||||
chr1:115334455
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-137+3749T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334455 | ||||||
chr1:115334541
|
G | T | 4 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0041others(1): Show | 4 | NA18965.hp2 NA18974.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+3663C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334541 | ||||||
chr1:115334580
|
C | T | 1 | a0002c0002t0001g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+3624G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334580 | ||||||
chr1:115334597
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+3607T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334597 | ||||||
chr1:115334808
|
C | A | 1 | a0001c0003t0001g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-137+3396G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334808 | ||||||
chr1:115334901
|
C | T | 222 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(219): Show | 226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.-137+3303G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334901 | ||||||
chr1:115334906
|
C | T | 3 | a0001c0001t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02451.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-137+3298G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334906 | ||||||
chr1:115334907
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-137+3297C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334907 | ||||||
chr1:115335003
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0037others(89): Show | 93 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.-137+3201C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335003 | ||||||
chr1:115335009
|
A | G | 1 | a0002c0002t0001g0055 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-137+3195T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335009 | ||||||
chr1:115335232
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-137+2972G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335232 | ||||||
chr1:115335592
|
G | A | 2 | a0003c0004t0001g0392a0003c0004t0001g0393 | 2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-137+2612C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335592 | ||||||
chr1:115335621
|
T | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 341 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.-137+2583A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335621 | ||||||
chr1:115335649
|
CT | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 341 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(338): Show |
intron_variant | MODIFIER | c.-137+2554delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335649 | ||||||
chr1:115335685
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-137+2519A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335685 | ||||||
chr1:115335916
|
C | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-137+2288G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335916 | ||||||
chr1:115335954
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-137+2250C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335954 | ||||||
chr1:115336183
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+2021G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336183 | ||||||
chr1:115336184
|
G | A | 4 | a0001c0001t0001g0390a0002c0002t0001g0391a0003c0004t0001g0392others(1): Show | 4 | HG00733.hp1 HG01109.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+2020C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336184 | ||||||
chr1:115336372
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-137+1832G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336372 | ||||||
chr1:115336444
|
A | T | 43 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(40): Show | 44 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.-137+1760T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336444 | ||||||
chr1:115336506
|
G | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0301a0008c0010t0001g0294 | 3 | HG03688.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-137+1698C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336506 | ||||||
chr1:115336605
|
G | C | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-137+1599C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336605 | ||||||
chr1:115336780
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-137+1424C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336780 | ||||||
chr1:115336810
|
G | A | 1 | a0002c0002t0001g0210 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-137+1394C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336810 | ||||||
chr1:115336815
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-137+1389A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336815 | ||||||
chr1:115337176
|
C | T | 1 | a0002c0002t0001g0353 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-137+1028G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337176 | ||||||
chr1:115337200
|
G | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(82): Show | 88 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-137+1004C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337200 | ||||||
chr1:115337250
|
TTTTTTGT others(4): Show |
T | 10 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0342others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+943_-137+953d others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337250 | ||||||
chr1:115337256
|
GTTTTGT | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0179others(1): Show | 4 | HG01081.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+942_-137+947d others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337256 | ||||||
chr1:115337257
|
TTTTGTTT others(3): Show |
T | 3 | a0001c0001t0001g0015a0001c0001t0001g0319a0001c0001t0001g0383 | 3 | HG02109.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-137+937_-137+946d others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337257 | ||||||
chr1:115337267
|
G | GT | 25 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0320others(22): Show | 26 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-137+936dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTT | 8 | a0001c0001t0001g0007a0001c0001t0001g0312a0001c0001t0001g0314others(5): Show | 9 | HG01071.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-137+935_-137+936d others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(10): Show |
1 | a0001c0001t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(13): Show |
1 | a0001c0003t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-137+936_-137+937i others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(14): Show |
1 | a0001c0003t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(23): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(16): Show |
1 | a0001c0001t0001g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(5): Show |
1 | a0001c0001t0001g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(14): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(6): Show |
4 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG03209.hp1 HG03516.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(7): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG03831.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(8): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0170 | 2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(9): Show |
5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 5 | HG01346.hp2 NA18959.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(18): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(10): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0161a0002c0002t0001g0160 | 3 | HG02559.hp1 HG03017.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(11): Show |
4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(1): Show | 4 | HG02083.hp1 HG03491.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(12): Show |
4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(1): Show | 4 | HG02027.hp2 HG02109.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(21): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(13): Show |
1 | a0001c0001t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(14): Show |
3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | NA18961.hp2 NA19072.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(23): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(15): Show |
4 | a0001c0001t0001g0141a0001c0003t0001g0143a0002c0002t0001g0140others(1): Show | 4 | HG03139.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(17): Show |
1 | a0001c0001t0001g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(26): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(18): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG02895.hp2 NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(27): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(19): Show |
1 | a0001c0001t0001g0123 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-137+936_-137+937i others(28): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTGTTT others(22): Show |
1 | a0001c0001t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(31): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-137+926_-137+936d others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0148 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-137+921_-137+936d others(18): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-137+920_-137+936d others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-137+919_-137+936d others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(13): Show |
1 | a0002c0002t0001g0137 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-137+917_-137+936d others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0001g0132 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-137+912_-137+936d others(27): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | GTTTTTTT others(19): Show |
1 | a0001c0001t0001g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-137+911_-137+936d others(28): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
G | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0179a0001c0001t0001g0397others(1): Show | 4 | HG02683.hp2 HG03139.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+937C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTT | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0036others(3): Show | 6 | HG00741.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+935_-137+936d others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTT | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0044others(27): Show | 31 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.-137+934_-137+936d others(5): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTT | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-137+933_-137+936d others(6): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTTT | G | 10 | a0001c0001t0001g0101a0001c0001t0001g0211a0001c0001t0001g0212others(7): Show | 10 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+932_-137+936d others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0002g0388 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-137+927_-137+936d others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0001g0109a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG01175.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-137+926_-137+936d others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTTTTT others(5): Show |
G | 26 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(23): Show | 26 | HG00609.hp1 HG01192.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.-137+925_-137+936d others(14): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTTTTT others(6): Show |
G | 58 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0105others(55): Show | 61 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-137+924_-137+936d others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337267
|
GTTTTTTT others(7): Show |
G | 7 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290others(4): Show | 7 | HG00280.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+923_-137+936d others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | ||||||
chr1:115337269
|
T | TTG | 6 | a0001c0001t0001g0398a0001c0001t0001g0400a0001c0001t0001g0401others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+934_-137+935i others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337269 | ||||||
chr1:115337270
|
T | G | 1 | a0001c0001t0001g0383 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-137+934A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337270 | ||||||
chr1:115337270
|
T | TG | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0003t0001g0404others(1): Show | 4 | HG01981.hp2 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+933_-137+934i others(3): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337270 | ||||||
chr1:115337271
|
T | G | 12 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0194others(9): Show | 12 | HG01884.hp2 HG01978.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-137+933A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337271 | ||||||
chr1:115337272
|
T | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0003t0001g0407 | 3 | HG01109.hp1 HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-137+932A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337272 | ||||||
chr1:115337273
|
T | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0385others(4): Show | 7 | HG00741.hp1 HG01192.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+931A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337273 | ||||||
chr1:115337274
|
T | G | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(22): Show | 25 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.-137+930A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337274 | ||||||
chr1:115337275
|
T | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-137+929A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337275 | ||||||
chr1:115337276
|
T | G | 10 | a0001c0001t0001g0101a0001c0001t0001g0211a0001c0001t0001g0212others(7): Show | 10 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+928A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337276 | ||||||
chr1:115337277
|
T | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0216a0002c0002t0001g0039 | 3 | HG02965.hp1 NA18965.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-137+927A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337277 | ||||||
chr1:115337278
|
T | G | 19 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(16): Show | 19 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.-137+926A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337278 | ||||||
chr1:115337279
|
T | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(64): Show | 70 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-137+925A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337279 | ||||||
chr1:115337280
|
T | G | 5 | a0001c0001t0001g0101a0001c0001t0001g0234a0001c0001t0001g0235others(2): Show | 5 | HG01256.hp1 NA18945.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+924A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337280 | ||||||
chr1:115337281
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-137+923A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337281 | ||||||
chr1:115337282
|
T | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG01175.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-137+922A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337282 | ||||||
chr1:115337283
|
T | G | 34 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0110others(31): Show | 34 | HG00609.hp1 HG00733.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-137+921A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337283 | ||||||
chr1:115337284
|
T | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0105others(55): Show | 61 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-137+920A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337284 | ||||||
chr1:115337285
|
T | G | 7 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG00280.hp2 HG01258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+919A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337285 | ||||||
chr1:115337286
|
T | G | 1 | a0001c0001t0001g0109 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-137+918A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337286 | ||||||
chr1:115337287
|
T | G | 14 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137+917A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337287 | ||||||
chr1:115337288
|
T | G | 14 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(11): Show | 14 | HG01975.hp2 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-137+916A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337288 | ||||||
chr1:115337511
|
G | A | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.-137+693C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337511 | ||||||
chr1:115337575
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-137+629G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337575 | ||||||
chr1:115337710
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-137+494G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337710 | ||||||
chr1:115337754
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-137+450G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337754 | ||||||
chr1:115337776
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-137+428G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337776 | ||||||
chr1:115337972
|
A | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(3): Show | 6 | HG00673.hp1 HG02083.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+232T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337972 | ||||||
chr1:115338054
|
A | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(111): Show | 116 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-137+150T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338054 | ||||||
chr1:115338113
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-137+91T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338113 | ||||||
chr1:115338118
|
T | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0397a0001c0001t0001g0398others(10): Show | 14 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-137+86A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338118 | ||||||
chr1:115338191
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-137+13G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338191 |