geneid | 145957 |
---|---|
ensemblid | ENSG00000169752.17 |
hgncid | 29862 |
symbol | NRG4 |
name | neuregulin 4 |
refseq_nuc | NM_138573.4 |
refseq_prot | NP_612640.1 |
ensembl_nuc | ENST00000394907.8 |
ensembl_prot | ENSP00000378367.3 |
mane_status | MANE Select |
chr | chr15 |
start | 75940936 |
end | 76012424 |
strand | - |
ver | v1.2 |
region | chr15:75940936-76012424 |
region5000 | chr15:75935936-76017424 |
regionname0 | NRG4_chr15_75940936_76012424 |
regionname5000 | NRG4_chr15_75935936_76017424 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 115 | 362 | 77 | 60 | 173 | 14 | 36 | 135 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0002 | 0/0 | 115 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0003 | 0/0 | 115 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 348 | 362 | 77 | 60 | 173 | 14 | 36 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
c0002 | 0/0 | 348 | 5 | 5 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
c0003 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2869 | 104 | 11 | 20 | 52 | 5 | 16 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0002 | 0/1 | 2868 | 64 | 15 | 4 | 34 | 4 | 6 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0003 | 0/0 | 2867 | 57 | 6 | 8 | 31 | 4 | 8 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0004 | 0/0 | 2868 | 30 | 0 | 3 | 26 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0005 | 0/0 | 2870 | 22 | 4 | 3 | 13 | 0 | 2 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0006 | 0/0 | 2868 | 12 | 0 | 8 | 3 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0007 | 0/0 | 2865 | 7 | 5 | 1 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0008 | 0/0 | 2869 | 6 | 0 | 3 | 3 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0009 | 0/0 | 2866 | 6 | 5 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0010 | 0/0 | 2848 | 4 | 4 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0011 | 0/0 | 2868 | 4 | 4 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0012 | 0/0 | 2865 | 3 | 0 | 3 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0013 | 0/0 | 2871 | 3 | 3 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0014 | 0/0 | 2865 | 3 | 1 | 1 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0015 | 0/0 | 2869 | 3 | 1 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0016 | 0/0 | 2847 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0017 | 0/0 | 2869 | 2 | 0 | 2 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0018 | 0/0 | 2870 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0019 | 0/0 | 2871 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0020 | 0/0 | 2869 | 2 | 0 | 1 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0021 | 0/0 | 2868 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0022 | 0/0 | 2866 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0023 | 0/0 | 2869 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0024 | 0/0 | 2869 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0025 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0026 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0027 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0028 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0029 | 0/0 | 2869 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0030 | 0/0 | 2870 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0031 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0032 | 0/0 | 2866 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0033 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0034 | 0/0 | 2868 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0035 | 0/0 | 2869 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0036 | 0/0 | 2869 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0037 | 0/0 | 2869 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0038 | 0/0 | 2870 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0039 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0040 | 0/0 | 2870 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0041 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0042 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0043 | 0/0 | 2867 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0044 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0045 | 1/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0046 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0047 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0048 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
t0049 | 0/0 | 2868 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0003 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0305 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 348 | 362 | 77 | 60 | 173 | 14 | 36 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0002c0002 | 0/0 | 348 | 5 | 5 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0003c0003 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3216 | 104 | 11 | 20 | 52 | 5 | 16 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0002 | 0/1 | 3215 | 63 | 15 | 4 | 33 | 4 | 6 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0003 | 0/0 | 3214 | 57 | 6 | 8 | 31 | 4 | 8 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0004 | 0/0 | 3215 | 30 | 0 | 3 | 26 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0005 | 0/0 | 3217 | 22 | 4 | 3 | 13 | 0 | 2 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0006 | 0/0 | 3215 | 12 | 0 | 8 | 3 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0007 | 0/0 | 3212 | 7 | 5 | 1 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0008 | 0/0 | 3216 | 6 | 0 | 3 | 3 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0009 | 0/0 | 3213 | 3 | 2 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0010 | 0/0 | 3195 | 4 | 4 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0011 | 0/0 | 3215 | 4 | 4 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0012 | 0/0 | 3212 | 3 | 0 | 3 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0013 | 0/0 | 3218 | 3 | 3 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0014 | 0/0 | 3212 | 3 | 1 | 1 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0015 | 0/0 | 3216 | 3 | 1 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0016 | 0/0 | 3194 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0017 | 0/0 | 3216 | 2 | 0 | 2 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0018 | 0/0 | 3217 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0019 | 0/0 | 3218 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0020 | 0/0 | 3216 | 2 | 0 | 1 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0021 | 0/0 | 3215 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0022 | 0/0 | 3213 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0023 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0024 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0025 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0026 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0027 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0028 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0029 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0030 | 0/0 | 3217 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0031 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0032 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0033 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0034 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0035 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0036 | 0/0 | 3216 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0037 | 0/0 | 3216 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0038 | 0/0 | 3217 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0039 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0040 | 0/0 | 3217 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0043 | 0/0 | 3214 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0044 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0045 | 1/0 | 3212 | 1 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0046 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0047 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0048 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0001c0001t0049 | 0/0 | 3215 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0002c0002t0009 | 0/0 | 3213 | 3 | 3 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0002c0002t0041 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0002c0002t0042 | 0/0 | 3212 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
a0003c0003t0002 | 0/0 | 3215 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | copy fasta | chr15 | 75935936 | 76017424 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0003 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0008g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0008g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0008g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0008g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0012g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0012g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0013g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0013g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0014g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0014g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0015g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0015g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0016g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0017g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0018g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0018g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0019g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0019g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0020g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0020g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0021g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0021g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0022g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0023g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0024g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0025g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0026g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0027g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0028g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0029g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0030g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0031g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0032g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0033g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0034g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0035g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0036g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0037g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0038g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0039g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0040g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0043g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0044g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0045g0305 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0046g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0047g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0048g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0001c0001t0049g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0002c0002t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0002c0002t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0002c0002t0041g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0002c0002t0042g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
a0003c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0075 | EUR | GBR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0045 | EUR | GBR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0342 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00544 | hp1 | a0001 | c0001 | t0015 | g0249 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00642 | hp2 | a0001 | c0001 | t0012 | g0098 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0268 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01070 | hp2 | a0001 | c0001 | t0017 | g0010 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01071 | hp1 | a0001 | c0001 | t0017 | g0010 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01109 | hp1 | a0001 | c0001 | t0014 | g0165 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0311 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0097 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0132 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0281 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01261 | hp1 | a0001 | c0001 | t0020 | g0291 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01261 | hp2 | a0001 | c0001 | t0012 | g0099 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0320 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01515 | hp1 | a0001 | c0001 | t0014 | g0056 | EUR | IBS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | IBS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | IBS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0325 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0107 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01943 | hp1 | a0001 | c0001 | t0037 | g0108 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0106 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01978 | hp1 | a0001 | c0001 | t0040 | g0170 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0181 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01993 | hp1 | a0001 | c0001 | t0008 | g0105 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0232 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02015 | hp1 | a0001 | c0001 | t0034 | g0331 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02055 | hp1 | a0001 | c0001 | t0047 | g0129 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02129 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CDX | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0196 | EAS | CDX | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | CDX | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | CDX | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02257 | hp1 | a0002 | c0002 | t0041 | g0111 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0318 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02258 | hp2 | a0001 | c0001 | t0044 | g0274 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02273 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0283 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0123 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | PEL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02451 | hp2 | a0001 | c0001 | t0010 | g0172 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | KHV | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02615 | hp2 | a0001 | c0001 | t0016 | g0125 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02622 | hp1 | a0001 | c0001 | t0013 | g0300 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0109 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0135 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02647 | hp2 | a0002 | c0002 | t0042 | g0113 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02717 | hp2 | a0001 | c0001 | t0033 | g0258 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02809 | hp1 | a0001 | c0001 | t0031 | g0134 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02809 | hp2 | a0001 | c0001 | t0010 | g0127 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0317 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02886 | hp1 | a0001 | c0001 | t0021 | g0121 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02895 | hp1 | a0001 | c0001 | t0046 | g0234 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02896 | hp2 | a0001 | c0001 | t0048 | g0128 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0323 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03017 | hp1 | a0001 | c0001 | t0036 | g0193 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03098 | hp1 | a0001 | c0001 | t0014 | g0102 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03098 | hp2 | a0001 | c0001 | t0029 | g0139 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03130 | hp2 | a0001 | c0001 | t0026 | g0133 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03139 | hp1 | a0002 | c0002 | t0009 | g0008 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0240 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03209 | hp1 | a0001 | c0001 | t0021 | g0122 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03209 | hp2 | a0001 | c0001 | t0019 | g0324 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03225 | hp2 | a0001 | c0001 | t0016 | g0124 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0136 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0126 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0316 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03516 | hp2 | a0001 | c0001 | t0030 | g0140 | AFR | ESN | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03540 | hp2 | a0001 | c0001 | t0025 | g0337 | AFR | GWD | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0229 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | BEB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03834 | hp2 | a0001 | c0001 | t0022 | g0100 | SAS | BEB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0104 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18906 | hp1 | a0002 | c0002 | t0009 | g0112 | AFR | YRI | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | YRI | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18940 | hp1 | a0001 | c0001 | t0043 | g0252 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18963 | hp2 | a0001 | c0001 | t0018 | g0332 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18978 | hp1 | a0001 | c0001 | t0020 | g0326 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18982 | hp2 | a0001 | c0001 | t0032 | g0037 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18988 | hp1 | a0001 | c0001 | t0015 | g0237 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19003 | hp1 | a0001 | c0001 | t0027 | g0262 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19003 | hp2 | a0001 | c0001 | t0024 | g0334 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19004 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19004 | hp2 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19006 | hp1 | a0001 | c0001 | t0018 | g0220 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19007 | hp1 | a0001 | c0001 | t0008 | g0333 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | LWK | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19030 | hp2 | a0001 | c0001 | t0011 | g0138 | AFR | LWK | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | LWK | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19043 | hp2 | a0001 | c0001 | t0019 | g0322 | AFR | LWK | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19064 | hp2 | a0001 | c0001 | t0008 | g0335 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19072 | hp2 | a0001 | c0001 | t0008 | g0330 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ASW | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0254 | SAS | GIH | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01123 | hp1 | a0001 | c0001 | t0009 | g0114 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02486 | hp2 | a0001 | c0001 | t0049 | g0336 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02559 | hp1 | a0001 | c0001 | t0038 | g0224 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0319 | AFR | ACB | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03471 | hp1 | a0002 | c0002 | t0009 | g0008 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | MSL | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | USA | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0173 | AFR | USA | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA18955 | hp2 | a0001 | c0001 | t0035 | g0226 | EAS | JPT | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20300 | hp1 | a0001 | c0001 | t0028 | g0137 | AFR | USA | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA20300 | hp2 | a0001 | c0001 | t0023 | g0141 | AFR | USA | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA21309 | hp1 | a0001 | c0001 | t0039 | g0030 | AFR | LWK | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | LWK | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0287 | REF | REF | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0045 | g0305 | REF | REF | NRG4_chr15_75935936_76017424 | NRG4 | chr15 | 75935936 | 76017424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:75961879
|
G | A | 1 | a0003 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.200C>T | p.Ala67Val | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/6 | 362/3212 | 200/348 | 67/115 | chr15 | 75961879 | ||
chr15:75961970
|
C | T | 1 | a0002 | 5 | HG02257.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.109G>A | p.Val37Ile | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/6 | 271/3212 | 109/348 | 37/115 | chr15 | 75961970 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:75941029
|
A | C | 1 | a0001c0001t0037 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2609T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2609 | chr15 | 75941029 | |||||
chr15:75941350
|
G | A | 1 | a0001c0001t0036 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2288C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2288 | chr15 | 75941350 | |||||
chr15:75941365
|
A | G | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2273T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2273 | chr15 | 75941365 | |||||
chr15:75941386
|
A | G | 1 | a0001c0001t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2252 | chr15 | 75941386 | |||||
chr15:75941499
|
C | A | 46 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(43): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*2139G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2139 | chr15 | 75941499 | |||||
chr15:75941500
|
G | T | 1 | a0001c0001t0035 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2138C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2138 | chr15 | 75941500 | |||||
chr15:75941510
|
G | T | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2128C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 2128 | chr15 | 75941510 | |||||
chr15:75941731
|
G | A | 4 | a0001c0001t0009a0002c0002t0009a0002c0002t0041others(1): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1907C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1907 | chr15 | 75941731 | |||||
chr15:75941742
|
G | A | 5 | a0001c0001t0008a0001c0001t0018a0001c0001t0024others(2): Show | 11 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1896C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1896 | chr15 | 75941742 | |||||
chr15:75941751
|
A | G | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*1887T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1887 | chr15 | 75941751 | |||||
chr15:75941885
|
A | C | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1753T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1753 | chr15 | 75941885 | |||||
chr15:75941907
|
C | G | 1 | a0001c0001t0033 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1731G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1731 | chr15 | 75941907 | |||||
chr15:75941940
|
C | CA | 4 | a0001c0001t0010a0001c0001t0044a0001c0001t0047others(1): Show | 7 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1697dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1697 | chr15 | 75941940 | |||||
chr15:75941960
|
A | AAAAAC | 8 | a0001c0001t0005a0001c0001t0013a0001c0001t0018others(5): Show | 33 | HG00423.hp2 HG00621.hp1 HG01243.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1678insGTTT others(1): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1677 | chr15 | 75941960 | |||||
chr15:75941960
|
A | AAAAC | 12 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(9): Show | 126 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1678insGTTT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1677 | chr15 | 75941960 | |||||
chr15:75941960
|
A | AAAC | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | 117 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1678insGTT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1677 | chr15 | 75941960 | |||||
chr15:75941960
|
A | AAC | 6 | a0001c0001t0003a0001c0001t0028a0001c0001t0033others(3): Show | 62 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1678insGT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1677 | chr15 | 75941960 | |||||
chr15:75941960
|
A | AC | 4 | a0001c0001t0009a0001c0001t0032a0002c0002t0009others(1): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1678insG | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1677 | chr15 | 75941960 | |||||
chr15:75941960
|
A | C | 2 | a0001c0001t0014a0002c0002t0042 | 4 | HG01109.hp1 HG01515.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1678T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1678 | chr15 | 75941960 | |||||
chr15:75941972
|
C | CT | 4 | a0001c0001t0013a0001c0001t0019a0001c0001t0031others(1): Show | 7 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1665dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1665 | chr15 | 75941972 | |||||
chr15:75941988
|
T | A | 2 | a0001c0001t0026a0001c0001t0039 | 2 | HG03130.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1650A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1650 | chr15 | 75941988 | |||||
chr15:75941989
|
A | T | 5 | a0001c0001t0011a0001c0001t0028a0001c0001t0029others(2): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1649T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1649 | chr15 | 75941989 | |||||
chr15:75941990
|
A | C | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1648T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1648 | chr15 | 75941990 | |||||
chr15:75942021
|
A | G | 1 | a0001c0001t0047 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1617T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1617 | chr15 | 75942021 | |||||
chr15:75942079
|
A | G | 1 | a0001c0001t0025 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1559T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1559 | chr15 | 75942079 | |||||
chr15:75942225
|
T | C | 1 | a0001c0001t0019 | 2 | HG03209.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1413 | chr15 | 75942225 | |||||
chr15:75942294
|
C | T | 1 | a0001c0001t0027 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1344G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1344 | chr15 | 75942294 | |||||
chr15:75942296
|
T | G | 4 | a0001c0001t0009a0002c0002t0009a0002c0002t0041others(1): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1342A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1342 | chr15 | 75942296 | |||||
chr15:75942365
|
G | A | 3 | a0001c0001t0006a0001c0001t0020a0001c0001t0040 | 15 | HG00733.hp1 HG00735.hp2 HG01257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1273C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1273 | chr15 | 75942365 | |||||
chr15:75942406
|
A | G | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1232T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1232 | chr15 | 75942406 | |||||
chr15:75942460
|
C | G | 1 | a0002c0002t0041 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1178 | chr15 | 75942460 | |||||
chr15:75942466
|
A | T | 1 | a0001c0001t0017 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1172T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1172 | chr15 | 75942466 | |||||
chr15:75942616
|
C | A | 46 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(43): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*1022G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 1022 | chr15 | 75942616 | |||||
chr15:75942786
|
TTTTCATA others(11): Show |
T | 4 | a0001c0001t0010a0001c0001t0016a0001c0001t0047others(1): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*834_*851delCTTTAA others(12): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 834 | chr15 | 75942786 | |||||
chr15:75942835
|
T | A | 4 | a0001c0001t0009a0002c0002t0009a0002c0002t0041others(1): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*803A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 803 | chr15 | 75942835 | |||||
chr15:75943005
|
T | G | 3 | a0001c0001t0004a0001c0001t0015a0001c0001t0043 | 34 | HG00544.hp1 HG01358.hp2 HG02027.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*633A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 633 | chr15 | 75943005 | |||||
chr15:75943008
|
C | T | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*630G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 630 | chr15 | 75943008 | |||||
chr15:75943235
|
A | G | 1 | a0001c0001t0024 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*403T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 403 | chr15 | 75943235 | |||||
chr15:75943300
|
A | G | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 338 | chr15 | 75943300 | |||||
chr15:75943393
|
T | C | 1 | a0001c0001t0046 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 245 | chr15 | 75943393 | |||||
chr15:75943445
|
T | C | 1 | a0001c0001t0021 | 2 | HG02886.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 193 | chr15 | 75943445 | |||||
chr15:75943530
|
TTTTA | T | 2 | a0001c0001t0012a0001c0001t0022 | 4 | HG00642.hp2 HG01167.hp2 HG01261.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*107delTAAA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 104 | chr15 | 75943530 | |||||
chr15:75943552
|
T | G | 2 | a0001c0001t0047a0001c0001t0048 | 2 | HG02055.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*86A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 6/6 | 86 | chr15 | 75943552 | |||||
chr15:76011259
|
T | C | 1 | a0001c0001t0049 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/6 | 29 | chr15 | 76011259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:75943697
|
A | G | 1 | a0001c0001t0009g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.332-43T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75943697 | ||||||
chr15:75943770
|
G | GTGA | 6 | a0001c0001t0009g0110a0001c0001t0009g0114a0002c0002t0009g0008others(3): Show | 7 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-119_332-117dup others(3): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75943770 | ||||||
chr15:75943815
|
T | G | 1 | a0001c0001t0038g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.332-161A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75943815 | ||||||
chr15:75943852
|
C | A | 24 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(21): Show | 25 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.332-198G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75943852 | ||||||
chr15:75943912
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0152 | 2 | NA18988.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.332-258G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75943912 | ||||||
chr15:75944069
|
TACCAAGG others(1): Show |
T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-423_332-416del others(8): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944069 | ||||||
chr15:75944281
|
A | C | 1 | a0001c0001t0007g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.332-627T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944281 | ||||||
chr15:75944321
|
C | CAT | 340 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(337): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.332-668_332-667ins others(2): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944321 | ||||||
chr15:75944329
|
T | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332-675A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944329 | ||||||
chr15:75944345
|
A | T | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.332-691T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944345 | ||||||
chr15:75944419
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.332-765T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944419 | ||||||
chr15:75944443
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.332-789T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944443 | ||||||
chr15:75944496
|
G | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(171): Show | 187 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.332-842C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944496 | ||||||
chr15:75944624
|
C | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-970G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944624 | ||||||
chr15:75944652
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.332-998C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944652 | ||||||
chr15:75944728
|
T | C | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-1074A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944728 | ||||||
chr15:75944755
|
TTG | T | 316 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(313): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.332-1103_332-1102d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944755 | ||||||
chr15:75944768
|
T | G | 5 | a0001c0001t0001g0276a0001c0001t0002g0339a0001c0001t0009g0109others(2): Show | 5 | HG02630.hp1 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-1114A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944768 | ||||||
chr15:75944775
|
G | A | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332-1121C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944775 | ||||||
chr15:75944872
|
A | G | 29 | a0001c0001t0004g0001a0001c0001t0004g0014a0001c0001t0004g0024others(26): Show | 34 | HG00544.hp1 HG01358.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.332-1218T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944872 | ||||||
chr15:75944943
|
CT | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0177others(8): Show | 14 | HG01123.hp1 HG02015.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.332-1290delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944943 | ||||||
chr15:75944950
|
T | A | 1 | a0001c0001t0038g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.332-1296A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944950 | ||||||
chr15:75944955
|
C | CT | 10 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0313others(7): Show | 10 | HG01891.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.332-1302dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944955 | ||||||
chr15:75944955
|
C | CTT | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.332-1303_332-1302d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944955 | ||||||
chr15:75944965
|
T | A | 1 | a0001c0001t0005g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.332-1311A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75944965 | ||||||
chr15:75945059
|
GA | G | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-1406delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945059 | ||||||
chr15:75945146
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.332-1492C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945146 | ||||||
chr15:75945198
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-1544A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945198 | ||||||
chr15:75945249
|
A | T | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.332-1595T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945249 | ||||||
chr15:75945250
|
T | TA | 5 | a0001c0001t0002g0288a0001c0001t0013g0323a0001c0001t0013g0325others(2): Show | 5 | HG01891.hp1 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-1597_332-1596i others(3): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945250 | ||||||
chr15:75945273
|
TA | T | 333 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(330): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.332-1620delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945273 | ||||||
chr15:75945274
|
A | T | 9 | a0001c0001t0001g0206a0001c0001t0010g0126a0001c0001t0010g0127others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.332-1620T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945274 | ||||||
chr15:75945276
|
T | A | 7 | a0001c0001t0001g0207a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-1622A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945276 | ||||||
chr15:75945277
|
T | A | 1 | a0001c0001t0003g0296 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.332-1623A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945277 | ||||||
chr15:75945621
|
A | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-1967T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945621 | ||||||
chr15:75945809
|
C | T | 1 | a0001c0001t0004g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.332-2155G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945809 | ||||||
chr15:75945837
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.332-2183T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945837 | ||||||
chr15:75945853
|
CACAG | C | 3 | a0002c0002t0009g0008a0002c0002t0009g0112a0002c0002t0042g0113 | 4 | HG02647.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-2203_332-2200d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945853 | ||||||
chr15:75945986
|
C | T | 343 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(340): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.332-2332G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75945986 | ||||||
chr15:75946035
|
G | T | 5 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-2381C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946035 | ||||||
chr15:75946109
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.332-2455C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946109 | ||||||
chr15:75946164
|
T | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0164others(1): Show | 4 | HG01256.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-2510A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946164 | ||||||
chr15:75946328
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.332-2674T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946328 | ||||||
chr15:75946368
|
G | GT | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-2715dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946368 | ||||||
chr15:75946444
|
G | A | 6 | a0001c0001t0009g0110a0001c0001t0009g0114a0002c0002t0009g0008others(3): Show | 7 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-2790C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946444 | ||||||
chr15:75946510
|
A | C | 5 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0202others(2): Show | 5 | HG00544.hp2 HG00597.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-2856T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946510 | ||||||
chr15:75946518
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-2864A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946518 | ||||||
chr15:75946679
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(138): Show | 149 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.332-3025G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946679 | ||||||
chr15:75946696
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.332-3042G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946696 | ||||||
chr15:75946727
|
A | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(92): Show | 101 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.332-3073T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75946727 | ||||||
chr15:75947008
|
A | G | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.332-3354T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75947008 | ||||||
chr15:75947310
|
A | G | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.332-3656T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75947310 | ||||||
chr15:75947414
|
G | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-3760C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75947414 | ||||||
chr15:75947524
|
T | G | 1 | a0001c0001t0003g0296 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.332-3870A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75947524 | ||||||
chr15:75947629
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.332-3975A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75947629 | ||||||
chr15:75947889
|
C | T | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.332-4235G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75947889 | ||||||
chr15:75948005
|
C | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | NA18943.hp1 NA18990.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-4351G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948005 | ||||||
chr15:75948034
|
G | A | 1 | a0001c0001t0006g0281 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.332-4380C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948034 | ||||||
chr15:75948180
|
A | T | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.332-4526T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948180 | ||||||
chr15:75948305
|
C | CTTTA | 10 | a0001c0001t0001g0212a0001c0001t0003g0292a0001c0001t0003g0311others(7): Show | 11 | HG01109.hp2 HG01123.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.332-4655_332-4652d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948305 | ||||||
chr15:75948305
|
C | CTTTATTT others(1): Show |
3 | a0002c0002t0009g0008a0002c0002t0009g0112a0002c0002t0042g0113 | 4 | HG02647.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-4659_332-4652d others(10): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948305 | ||||||
chr15:75948305
|
CTTTA | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(251): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.332-4655_332-4652d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948305 | ||||||
chr15:75948305
|
CTTTATTT others(5): Show |
C | 2 | a0001c0001t0001g0201a0001c0001t0023g0141 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.332-4663_332-4652d others(14): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948305 | ||||||
chr15:75948366
|
C | T | 5 | a0001c0001t0001g0297a0001c0001t0002g0017a0001c0001t0002g0294others(2): Show | 6 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-4712G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948366 | ||||||
chr15:75948520
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.332-4866G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948520 | ||||||
chr15:75948542
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.332-4888C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948542 | ||||||
chr15:75948568
|
G | A | 1 | a0001c0001t0024g0334 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.332-4914C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948568 | ||||||
chr15:75948577
|
G | C | 1 | a0001c0001t0004g0251 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.332-4923C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948577 | ||||||
chr15:75948589
|
GCGC | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.332-4938_332-4936d others(5): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948589 | ||||||
chr15:75948593
|
C | T | 1 | a0001c0001t0011g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.332-4939G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948593 | ||||||
chr15:75948660
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.332-5006C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948660 | ||||||
chr15:75948703
|
T | C | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.332-5049A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948703 | ||||||
chr15:75948738
|
A | C | 340 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(337): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.332-5084T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948738 | ||||||
chr15:75948784
|
T | G | 1 | a0001c0001t0003g0040 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.332-5130A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948784 | ||||||
chr15:75948828
|
G | T | 340 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(337): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.332-5174C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948828 | ||||||
chr15:75948885
|
CA | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-5232delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948885 | ||||||
chr15:75948916
|
T | C | 3 | a0001c0001t0002g0032a0001c0001t0002g0072a0001c0001t0003g0069 | 3 | NA18949.hp2 NA18969.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.332-5262A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948916 | ||||||
chr15:75948918
|
G | A | 1 | a0001c0001t0005g0009 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.332-5264C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948918 | ||||||
chr15:75948947
|
A | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01358.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.332-5293T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75948947 | ||||||
chr15:75949270
|
G | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332-5616C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949270 | ||||||
chr15:75949392
|
C | CAAAA | 6 | a0001c0001t0009g0110a0001c0001t0009g0114a0002c0002t0009g0008others(3): Show | 7 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-5742_332-5739d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949392 | ||||||
chr15:75949392
|
CAAA | C | 7 | a0001c0001t0002g0065a0001c0001t0004g0155a0001c0001t0004g0250others(4): Show | 7 | HG01928.hp1 HG02451.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-5741_332-5739d others(5): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949392 | ||||||
chr15:75949392
|
CAAAA | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(319): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.332-5742_332-5739d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949392 | ||||||
chr15:75949449
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0014g0102 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.332-5795G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949449 | ||||||
chr15:75949689
|
C | T | 2 | a0001c0001t0003g0292a0001c0001t0003g0311 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.332-6035G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949689 | ||||||
chr15:75949892
|
G | C | 1 | a0001c0001t0006g0316 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.331+6040C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75949892 | ||||||
chr15:75950153
|
T | A | 1 | a0001c0001t0011g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.331+5779A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950153 | ||||||
chr15:75950153
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0096 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.331+5779A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950153 | ||||||
chr15:75950182
|
G | A | 342 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(339): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.331+5750C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950182 | ||||||
chr15:75950226
|
T | G | 1 | a0001c0001t0003g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.331+5706A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950226 | ||||||
chr15:75950277
|
T | C | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+5655A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950277 | ||||||
chr15:75950399
|
A | C | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.331+5533T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950399 | ||||||
chr15:75950401
|
C | T | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.331+5531G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950401 | ||||||
chr15:75950406
|
TGAGCATA others(5): Show |
T | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.331+5514_331+5525d others(14): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950406 | ||||||
chr15:75950437
|
CCT | C | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.331+5493_331+5494d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950437 | ||||||
chr15:75950511
|
ATCC | A | 9 | a0001c0001t0002g0272a0001c0001t0002g0288a0001c0001t0003g0278others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.331+5418_331+5420d others(5): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950511 | ||||||
chr15:75950662
|
T | C | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+5270A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950662 | ||||||
chr15:75950716
|
C | T | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.331+5216G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950716 | ||||||
chr15:75950771
|
C | G | 1 | a0001c0001t0003g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.331+5161G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950771 | ||||||
chr15:75950788
|
T | G | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.331+5144A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950788 | ||||||
chr15:75950996
|
T | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.331+4936A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75950996 | ||||||
chr15:75951119
|
G | A | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.331+4813C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951119 | ||||||
chr15:75951163
|
C | CT | 93 | a0001c0001t0001g0211a0001c0001t0001g0257a0001c0001t0001g0264others(90): Show | 99 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.331+4768dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951163 | ||||||
chr15:75951163
|
C | CTT | 215 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(212): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.331+4767_331+4768d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951163 | ||||||
chr15:75951163
|
C | CTTT | 21 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(18): Show | 21 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.331+4766_331+4768d others(5): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951163 | ||||||
chr15:75951163
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.331+4757_331+4768d others(14): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951163 | ||||||
chr15:75951204
|
G | A | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.331+4728C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951204 | ||||||
chr15:75951772
|
T | C | 5 | a0001c0001t0001g0101a0001c0001t0012g0097a0001c0001t0012g0098others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+4160A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951772 | ||||||
chr15:75951792
|
T | C | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+4140A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951792 | ||||||
chr15:75951824
|
A | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+4108T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75951824 | ||||||
chr15:75952111
|
T | C | 1 | a0001c0001t0004g0236 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.331+3821A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952111 | ||||||
chr15:75952373
|
T | C | 4 | a0001c0001t0003g0023a0001c0001t0003g0038a0001c0001t0003g0040others(1): Show | 4 | NA18956.hp2 NA18978.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+3559A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952373 | ||||||
chr15:75952432
|
G | A | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.331+3500C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952432 | ||||||
chr15:75952560
|
AT | A | 339 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(336): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.331+3371delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952560 | ||||||
chr15:75952592
|
GT | G | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.331+3339delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952592 | ||||||
chr15:75952612
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.331+3320A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952612 | ||||||
chr15:75952638
|
A | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+3294T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952638 | ||||||
chr15:75952711
|
C | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.331+3221G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952711 | ||||||
chr15:75952736
|
A | G | 5 | a0001c0001t0003g0005a0001c0001t0003g0051a0001c0001t0003g0052others(2): Show | 6 | NA18948.hp2 NA19001.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+3196T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952736 | ||||||
chr15:75952739
|
G | A | 1 | a0001c0001t0005g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331+3193C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75952739 | ||||||
chr15:75953274
|
A | G | 1 | a0001c0001t0006g0019 | 2 | HG02129.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.331+2658T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75953274 | ||||||
chr15:75953374
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.331+2558T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75953374 | ||||||
chr15:75953382
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.331+2550T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75953382 | ||||||
chr15:75953813
|
G | A | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+2119C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75953813 | ||||||
chr15:75953830
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.331+2102T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75953830 | ||||||
chr15:75953966
|
C | T | 39 | a0001c0001t0001g0257a0001c0001t0001g0265a0001c0001t0001g0282others(36): Show | 44 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.331+1966G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75953966 | ||||||
chr15:75954257
|
G | T | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+1675C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954257 | ||||||
chr15:75954259
|
T | G | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+1673A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954259 | ||||||
chr15:75954265
|
G | GT | 25 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0164others(22): Show | 26 | HG00140.hp1 HG01123.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.331+1666dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954265 | ||||||
chr15:75954268
|
T | G | 25 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(22): Show | 26 | HG00280.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.331+1664A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954268 | ||||||
chr15:75954279
|
G | T | 1 | a0001c0001t0002g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.331+1653C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954279 | ||||||
chr15:75954311
|
T | C | 1 | a0001c0001t0003g0027 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.331+1621A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954311 | ||||||
chr15:75954323
|
C | T | 5 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+1609G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954323 | ||||||
chr15:75954336
|
T | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.331+1596A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954336 | ||||||
chr15:75954431
|
C | CT | 8 | a0001c0001t0009g0110a0001c0001t0009g0114a0001c0001t0023g0141others(5): Show | 9 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.331+1500dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954431 | ||||||
chr15:75954431
|
CT | C | 158 | a0001c0001t0001g0148a0001c0001t0001g0174a0001c0001t0001g0176others(155): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.331+1500delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954431 | ||||||
chr15:75954431
|
CTT | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 184 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.331+1499_331+1500d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954431 | ||||||
chr15:75954586
|
G | GT | 7 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(4): Show | 7 | HG00642.hp2 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+1345dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954586 | ||||||
chr15:75954586
|
G | T | 1 | a0001c0001t0005g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331+1346C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954586 | ||||||
chr15:75954685
|
A | G | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+1247T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75954685 | ||||||
chr15:75955004
|
G | A | 1 | a0001c0001t0005g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331+928C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75955004 | ||||||
chr15:75955362
|
C | A | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.331+570G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75955362 | ||||||
chr15:75955371
|
T | C | 1 | a0001c0001t0005g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.331+561A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75955371 | ||||||
chr15:75955792
|
C | CA | 19 | a0001c0001t0001g0085a0001c0001t0001g0174a0001c0001t0001g0221others(16): Show | 20 | HG01109.hp1 HG01109.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.331+139dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75955792 | ||||||
chr15:75955792
|
CA | C | 103 | a0001c0001t0001g0204a0001c0001t0001g0257a0001c0001t0001g0264others(100): Show | 115 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.331+139delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75955792 | ||||||
chr15:75955839
|
T | G | 1 | a0001c0001t0011g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331+93A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 5/5 | chr15 | 75955839 | ||||||
chr15:75956086
|
GT | G | 342 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(339): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.252-76delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75956086 | ||||||
chr15:75956307
|
C | T | 1 | a0001c0001t0002g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.252-296G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75956307 | ||||||
chr15:75956314
|
C | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.252-303G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75956314 | ||||||
chr15:75956517
|
TATG | T | 316 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(313): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.252-509_252-507del others(3): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75956517 | ||||||
chr15:75956522
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.252-511A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75956522 | ||||||
chr15:75956559
|
G | A | 342 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(339): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.252-548C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75956559 | ||||||
chr15:75957229
|
C | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.252-1218G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957229 | ||||||
chr15:75957244
|
G | A | 18 | a0001c0001t0001g0282a0001c0001t0001g0285a0001c0001t0002g0016others(15): Show | 20 | HG00597.hp1 HG02071.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.252-1233C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957244 | ||||||
chr15:75957353
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.252-1342T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957353 | ||||||
chr15:75957454
|
C | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(329): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.252-1443G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957454 | ||||||
chr15:75957562
|
C | CTA | 342 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(339): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.252-1552_252-1551i others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957562 | ||||||
chr15:75957807
|
C | A | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.252-1796G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957807 | ||||||
chr15:75957872
|
G | A | 1 | a0001c0001t0005g0132 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.252-1861C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75957872 | ||||||
chr15:75958000
|
TA | T | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-1990delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958000 | ||||||
chr15:75958117
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.252-2106T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958117 | ||||||
chr15:75958158
|
A | G | 1 | a0001c0001t0009g0114 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.252-2147T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958158 | ||||||
chr15:75958159
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.252-2148G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958159 | ||||||
chr15:75958254
|
C | T | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.252-2243G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958254 | ||||||
chr15:75958567
|
C | T | 1 | a0001c0001t0006g0232 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.252-2556G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958567 | ||||||
chr15:75958619
|
T | G | 1 | a0001c0001t0005g0159 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.252-2608A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958619 | ||||||
chr15:75958699
|
T | TTA | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-2690_252-2689d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958699 | ||||||
chr15:75958742
|
C | T | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-2731G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958742 | ||||||
chr15:75958764
|
G | A | 28 | a0001c0001t0004g0001a0001c0001t0004g0014a0001c0001t0004g0024others(25): Show | 33 | HG00544.hp1 HG01358.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.252-2753C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958764 | ||||||
chr15:75958977
|
GTTTA | G | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+2847_251+2850d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75958977 | ||||||
chr15:75959003
|
C | T | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.251+2825G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959003 | ||||||
chr15:75959111
|
A | G | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.251+2717T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959111 | ||||||
chr15:75959151
|
A | T | 1 | a0001c0001t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.251+2677T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959151 | ||||||
chr15:75959190
|
G | A | 9 | a0001c0001t0001g0183a0001c0001t0001g0208a0001c0001t0009g0109others(6): Show | 10 | HG01074.hp1 HG01123.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.251+2638C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959190 | ||||||
chr15:75959335
|
ATATTCT | A | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+2487_251+2492d others(8): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959335 | ||||||
chr15:75959361
|
A | C | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+2467T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959361 | ||||||
chr15:75959410
|
T | A | 1 | a0001c0001t0014g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.251+2418A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959410 | ||||||
chr15:75959460
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.251+2368A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959460 | ||||||
chr15:75959507
|
A | T | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+2321T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959507 | ||||||
chr15:75959619
|
C | T | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.251+2209G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959619 | ||||||
chr15:75959636
|
A | T | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.251+2192T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959636 | ||||||
chr15:75959639
|
T | C | 1 | a0001c0001t0004g0239 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.251+2189A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959639 | ||||||
chr15:75959722
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.251+2106T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959722 | ||||||
chr15:75959842
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+1986C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75959842 | ||||||
chr15:75960024
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.251+1804A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960024 | ||||||
chr15:75960027
|
G | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.251+1801C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960027 | ||||||
chr15:75960029
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.251+1799C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960029 | ||||||
chr15:75960059
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.251+1769T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960059 | ||||||
chr15:75960180
|
A | C | 3 | a0001c0001t0025g0337a0001c0001t0026g0133a0001c0001t0044g0274 | 3 | HG02258.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.251+1648T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960180 | ||||||
chr15:75960209
|
A | G | 3 | a0001c0001t0025g0337a0001c0001t0026g0133a0001c0001t0044g0274 | 3 | HG02258.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.251+1619T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960209 | ||||||
chr15:75960320
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.251+1508C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960320 | ||||||
chr15:75960729
|
T | C | 2 | a0001c0001t0002g0272a0001c0001t0003g0286 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.251+1099A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960729 | ||||||
chr15:75960831
|
A | C | 1 | a0001c0001t0003g0033 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.251+997T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75960831 | ||||||
chr15:75961157
|
G | C | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+671C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961157 | ||||||
chr15:75961192
|
A | G | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.251+636T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961192 | ||||||
chr15:75961208
|
A | C | 19 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(16): Show | 20 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.251+620T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961208 | ||||||
chr15:75961278
|
G | GT | 30 | a0001c0001t0004g0001a0001c0001t0004g0014a0001c0001t0004g0024others(27): Show | 35 | HG00544.hp1 HG01358.hp2 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.251+549dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961278 | ||||||
chr15:75961318
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251+510T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961318 | ||||||
chr15:75961335
|
G | T | 1 | a0001c0001t0002g0260 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.251+493C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961335 | ||||||
chr15:75961466
|
T | G | 1 | a0001c0001t0001g0343 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.251+362A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961466 | ||||||
chr15:75961619
|
A | G | 1 | a0001c0001t0011g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.251+209T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961619 | ||||||
chr15:75961635
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.251+193T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 4/5 | chr15 | 75961635 | ||||||
chr15:75961983
|
T | G | 5 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0202others(2): Show | 5 | HG00544.hp2 HG00597.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.105-9A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75961983 | ||||||
chr15:75962117
|
T | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-143A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962117 | ||||||
chr15:75962128
|
C | A | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-154G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962128 | ||||||
chr15:75962166
|
A | G | 43 | a0001c0001t0001g0257a0001c0001t0001g0265a0001c0001t0001g0276others(40): Show | 48 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.105-192T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962166 | ||||||
chr15:75962432
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.105-458A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962432 | ||||||
chr15:75962554
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.105-580C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962554 | ||||||
chr15:75962610
|
G | A | 1 | a0001c0001t0013g0325 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.105-636C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962610 | ||||||
chr15:75962637
|
C | T | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-663G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962637 | ||||||
chr15:75962698
|
T | C | 1 | a0001c0001t0011g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105-724A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962698 | ||||||
chr15:75962843
|
A | C | 1 | a0001c0001t0002g0061 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.105-869T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75962843 | ||||||
chr15:75963069
|
G | A | 2 | a0001c0001t0003g0292a0001c0001t0003g0311 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.105-1095C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963069 | ||||||
chr15:75963073
|
T | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0198a0001c0001t0001g0216 | 3 | NA18943.hp1 NA18990.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.105-1099A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963073 | ||||||
chr15:75963120
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.105-1146C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963120 | ||||||
chr15:75963136
|
T | A | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-1162A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963136 | ||||||
chr15:75963152
|
G | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-1178C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963152 | ||||||
chr15:75963501
|
C | T | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.105-1527G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963501 | ||||||
chr15:75963710
|
G | A | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.105-1736C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963710 | ||||||
chr15:75963777
|
C | CA | 75 | a0001c0001t0001g0095a0001c0001t0001g0144a0001c0001t0001g0145others(72): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.105-1804dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963777 | ||||||
chr15:75963777
|
C | CAA | 6 | a0001c0001t0001g0223a0001c0001t0010g0126a0001c0001t0010g0127others(3): Show | 6 | HG01928.hp2 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-1805_105-1804d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963777 | ||||||
chr15:75963777
|
CA | C | 13 | a0001c0001t0001g0103a0001c0001t0002g0263a0001c0001t0002g0280others(10): Show | 13 | HG01167.hp2 HG01257.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.105-1804delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963777 | ||||||
chr15:75963777
|
CAA | C | 12 | a0001c0001t0007g0321a0001c0001t0009g0109a0001c0001t0009g0110others(9): Show | 13 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.105-1805_105-1804d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963777 | ||||||
chr15:75963833
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.105-1859G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963833 | ||||||
chr15:75963857
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0177others(2): Show | 7 | HG02015.hp2 HG02132.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.105-1883G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963857 | ||||||
chr15:75963858
|
G | A | 1 | a0001c0001t0005g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.105-1884C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963858 | ||||||
chr15:75963896
|
T | C | 1 | a0001c0001t0005g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.105-1922A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963896 | ||||||
chr15:75963996
|
C | A | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.105-2022G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75963996 | ||||||
chr15:75964073
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.105-2099A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964073 | ||||||
chr15:75964169
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.105-2195C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964169 | ||||||
chr15:75964262
|
G | C | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-2288C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964262 | ||||||
chr15:75964331
|
CTTCT | C | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.105-2361_105-2358d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964331 | ||||||
chr15:75964396
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.105-2422A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964396 | ||||||
chr15:75964647
|
C | G | 2 | a0001c0001t0001g0285a0001c0001t0002g0298 | 2 | NA18951.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.105-2673G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964647 | ||||||
chr15:75964662
|
A | G | 3 | a0001c0001t0025g0337a0001c0001t0026g0133a0001c0001t0044g0274 | 3 | HG02258.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105-2688T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964662 | ||||||
chr15:75964688
|
G | C | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-2714C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964688 | ||||||
chr15:75964760
|
C | T | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.105-2786G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964760 | ||||||
chr15:75964798
|
C | T | 2 | a0001c0001t0004g0243a0001c0001t0023g0141 | 2 | NA18994.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.105-2824G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964798 | ||||||
chr15:75964823
|
G | A | 2 | a0001c0001t0002g0269a0001c0001t0002g0273 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.105-2849C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964823 | ||||||
chr15:75964844
|
T | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0051a0001c0001t0003g0052others(2): Show | 6 | NA18948.hp2 NA19001.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-2870A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964844 | ||||||
chr15:75964917
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.105-2943T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964917 | ||||||
chr15:75964947
|
C | T | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.105-2973G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964947 | ||||||
chr15:75964951
|
C | T | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01358.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.105-2977G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964951 | ||||||
chr15:75964963
|
C | A | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-2989G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964963 | ||||||
chr15:75964997
|
G | A | 1 | a0001c0001t0011g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.105-3023C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75964997 | ||||||
chr15:75965055
|
C | T | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.105-3081G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965055 | ||||||
chr15:75965130
|
C | CT | 6 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0187others(3): Show | 6 | HG00544.hp2 HG00597.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.105-3157_105-3156i others(3): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965130 | ||||||
chr15:75965131
|
A | C | 6 | a0001c0001t0001g0179a0001c0001t0001g0182a0001c0001t0001g0187others(3): Show | 6 | HG00544.hp2 HG00597.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.105-3157T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965131 | ||||||
chr15:75965179
|
C | T | 6 | a0001c0001t0006g0018a0001c0001t0006g0115a0001c0001t0006g0232others(3): Show | 7 | HG00733.hp1 HG00735.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-3205G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965179 | ||||||
chr15:75965193
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 184 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.105-3219G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965193 | ||||||
chr15:75965198
|
T | C | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-3224A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965198 | ||||||
chr15:75965320
|
A | C | 3 | a0001c0001t0025g0337a0001c0001t0026g0133a0001c0001t0044g0274 | 3 | HG02258.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105-3346T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965320 | ||||||
chr15:75965549
|
T | C | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-3575A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965549 | ||||||
chr15:75965664
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105-3690T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965664 | ||||||
chr15:75965758
|
G | A | 1 | a0001c0001t0007g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.105-3784C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75965758 | ||||||
chr15:75966118
|
T | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-4144A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966118 | ||||||
chr15:75966135
|
CA | C | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.105-4162delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966135 | ||||||
chr15:75966137
|
G | T | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.105-4163C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966137 | ||||||
chr15:75966282
|
A | C | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-4308T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966282 | ||||||
chr15:75966621
|
G | A | 1 | a0001c0001t0011g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.105-4647C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966621 | ||||||
chr15:75966724
|
GTCAA | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-4754_105-4751d others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966724 | ||||||
chr15:75966733
|
A | T | 3 | a0001c0001t0023g0141a0001c0001t0026g0133a0001c0001t0044g0274 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-4759T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966733 | ||||||
chr15:75966772
|
C | A | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-4798G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966772 | ||||||
chr15:75966844
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0005g0229 | 2 | HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.105-4870G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966844 | ||||||
chr15:75966948
|
C | T | 1 | a0001c0001t0005g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.105-4974G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966948 | ||||||
chr15:75966952
|
T | A | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-4978A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966952 | ||||||
chr15:75966953
|
G | A | 16 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(13): Show | 17 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.105-4979C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966953 | ||||||
chr15:75966975
|
C | T | 1 | a0001c0001t0016g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.105-5001G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75966975 | ||||||
chr15:75967038
|
C | T | 9 | a0001c0001t0009g0109a0001c0001t0011g0116a0001c0001t0011g0135others(6): Show | 9 | HG02486.hp2 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.105-5064G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967038 | ||||||
chr15:75967112
|
C | CA | 39 | a0001c0001t0001g0088a0001c0001t0001g0174a0001c0001t0001g0178others(36): Show | 41 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.105-5139dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967112 | ||||||
chr15:75967112
|
CA | C | 14 | a0001c0001t0001g0103a0001c0001t0001g0264a0001c0001t0001g0297others(11): Show | 15 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.105-5139delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967112 | ||||||
chr15:75967127
|
A | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0277a0001c0001t0002g0279 | 4 | HG02135.hp1 NA18956.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-5153T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967127 | ||||||
chr15:75967213
|
A | G | 65 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0223others(62): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.105-5239T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967213 | ||||||
chr15:75967228
|
G | C | 2 | a0001c0001t0001g0285a0001c0001t0002g0298 | 2 | NA18951.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.105-5254C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967228 | ||||||
chr15:75967383
|
A | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG02083.hp1 NA18944.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-5409T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967383 | ||||||
chr15:75967396
|
C | A | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-5422G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967396 | ||||||
chr15:75967398
|
T | C | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.105-5424A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967398 | ||||||
chr15:75967456
|
A | AT | 103 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(100): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.105-5483dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967456 | ||||||
chr15:75967456
|
A | ATT | 117 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(114): Show | 125 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.105-5484_105-5483d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967456 | ||||||
chr15:75967456
|
A | ATTT | 28 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0095others(25): Show | 28 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.105-5485_105-5483d others(5): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967456 | ||||||
chr15:75967456
|
AT | A | 12 | a0001c0001t0001g0343a0001c0001t0002g0272a0001c0001t0002g0340others(9): Show | 13 | HG00423.hp2 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.105-5483delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967456 | ||||||
chr15:75967650
|
C | T | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-5676G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967650 | ||||||
chr15:75967775
|
C | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-5801G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967775 | ||||||
chr15:75967970
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02572.hp2 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.105-5996T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967970 | ||||||
chr15:75967978
|
A | G | 17 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0002g0235others(14): Show | 17 | HG01167.hp1 HG01169.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.105-6004T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75967978 | ||||||
chr15:75968021
|
C | T | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.105-6047G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968021 | ||||||
chr15:75968089
|
G | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-6115C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968089 | ||||||
chr15:75968150
|
G | A | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.105-6176C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968150 | ||||||
chr15:75968172
|
A | G | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-6198T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968172 | ||||||
chr15:75968212
|
A | G | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-6238T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968212 | ||||||
chr15:75968233
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-6259G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968233 | ||||||
chr15:75968363
|
G | A | 2 | a0001c0001t0002g0269a0001c0001t0002g0273 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.105-6389C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968363 | ||||||
chr15:75968385
|
C | T | 1 | a0001c0001t0044g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.105-6411G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968385 | ||||||
chr15:75968479
|
TCAGGAGG others(22): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.105-6534_105-6506d others(31): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968479 | ||||||
chr15:75968585
|
T | TA | 75 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0180others(72): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.105-6612dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968585 | ||||||
chr15:75968585
|
TA | T | 7 | a0001c0001t0001g0144a0001c0001t0001g0185a0001c0001t0002g0338others(4): Show | 7 | HG01070.hp1 HG02738.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6612delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968585 | ||||||
chr15:75968585
|
TAA | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-6613_105-6612d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968585 | ||||||
chr15:75968640
|
T | C | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-6666A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968640 | ||||||
chr15:75968742
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 285 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.105-6768C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968742 | ||||||
chr15:75968812
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-6838A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968812 | ||||||
chr15:75968896
|
C | A | 10 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(7): Show | 11 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.105-6922G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75968896 | ||||||
chr15:75969044
|
A | G | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-7070T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969044 | ||||||
chr15:75969083
|
A | G | 1 | a0001c0001t0040g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.105-7109T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969083 | ||||||
chr15:75969406
|
A | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-7432T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969406 | ||||||
chr15:75969588
|
A | G | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-7614T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969588 | ||||||
chr15:75969652
|
C | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 285 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.105-7678G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969652 | ||||||
chr15:75969784
|
T | C | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-7810A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969784 | ||||||
chr15:75969833
|
C | T | 1 | a0001c0001t0011g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.105-7859G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969833 | ||||||
chr15:75969867
|
G | A | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105-7893C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75969867 | ||||||
chr15:75970045
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.105-8071G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970045 | ||||||
chr15:75970443
|
C | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0072a0001c0001t0003g0069 | 3 | NA18949.hp2 NA18969.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.105-8469G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970443 | ||||||
chr15:75970514
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.105-8540G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970514 | ||||||
chr15:75970598
|
G | A | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105-8624C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970598 | ||||||
chr15:75970608
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.105-8634C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970608 | ||||||
chr15:75970609
|
A | G | 2 | a0001c0001t0004g0171a0001c0001t0004g0312 | 2 | HG02080.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.105-8635T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970609 | ||||||
chr15:75970753
|
C | T | 2 | a0001c0001t0005g0013a0001c0001t0005g0302 | 3 | HG02040.hp2 HG02523.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.105-8779G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75970753 | ||||||
chr15:75971020
|
T | C | 3 | a0001c0001t0023g0141a0001c0001t0026g0133a0001c0001t0044g0274 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-9046A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971020 | ||||||
chr15:75971117
|
C | T | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105-9143G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971117 | ||||||
chr15:75971353
|
G | T | 2 | a0001c0001t0003g0292a0001c0001t0003g0311 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.105-9379C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971353 | ||||||
chr15:75971623
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.105-9649G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971623 | ||||||
chr15:75971826
|
C | T | 67 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0001g0265others(64): Show | 72 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.105-9852G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971826 | ||||||
chr15:75971983
|
A | G | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-10009T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971983 | ||||||
chr15:75971989
|
T | C | 2 | a0001c0001t0026g0133a0001c0001t0044g0274 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.105-10015A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75971989 | ||||||
chr15:75972219
|
G | T | 2 | a0001c0001t0010g0172a0001c0001t0010g0173 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.105-10245C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972219 | ||||||
chr15:75972306
|
A | C | 1 | a0001c0001t0002g0074 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.105-10332T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972306 | ||||||
chr15:75972509
|
C | T | 1 | a0001c0001t0005g0009 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.105-10535G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972509 | ||||||
chr15:75972578
|
T | C | 1 | a0001c0001t0004g0306 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.105-10604A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972578 | ||||||
chr15:75972592
|
A | T | 1 | a0001c0001t0020g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.105-10618T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972592 | ||||||
chr15:75972641
|
A | G | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.105-10667T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972641 | ||||||
chr15:75972820
|
G | A | 4 | a0001c0001t0011g0135a0001c0001t0011g0136a0001c0001t0028g0137others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-10846C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75972820 | ||||||
chr15:75973009
|
A | G | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.105-11035T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75973009 | ||||||
chr15:75973016
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.105-11042A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75973016 | ||||||
chr15:75973259
|
A | C | 1 | a0001c0001t0005g0342 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.105-11285T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75973259 | ||||||
chr15:75973377
|
G | T | 1 | a0001c0001t0004g0236 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.105-11403C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75973377 | ||||||
chr15:75973696
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.105-11722G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75973696 | ||||||
chr15:75973900
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.105-11926C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75973900 | ||||||
chr15:75974102
|
G | T | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-12128C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974102 | ||||||
chr15:75974207
|
G | A | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.105-12233C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974207 | ||||||
chr15:75974497
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.105-12523G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974497 | ||||||
chr15:75974576
|
T | C | 1 | a0001c0001t0005g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.105-12602A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974576 | ||||||
chr15:75974620
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0014g0102 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.105-12646C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974620 | ||||||
chr15:75974713
|
G | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-12739C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974713 | ||||||
chr15:75974738
|
T | A | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-12764A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974738 | ||||||
chr15:75974945
|
TG | T | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-12972delC | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974945 | ||||||
chr15:75974962
|
C | T | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.105-12988G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974962 | ||||||
chr15:75974974
|
T | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-13000A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974974 | ||||||
chr15:75974993
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105-13019A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75974993 | ||||||
chr15:75975165
|
A | G | 1 | a0001c0001t0005g0184 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.105-13191T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975165 | ||||||
chr15:75975168
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-13194C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975168 | ||||||
chr15:75975332
|
C | T | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-13358G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975332 | ||||||
chr15:75975385
|
G | A | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.105-13411C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975385 | ||||||
chr15:75975462
|
G | T | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-13488C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975462 | ||||||
chr15:75975593
|
C | A | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-13619G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975593 | ||||||
chr15:75975680
|
G | A | 25 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(22): Show | 26 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.105-13706C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975680 | ||||||
chr15:75975816
|
T | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-13842A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975816 | ||||||
chr15:75975834
|
G | A | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-13860C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975834 | ||||||
chr15:75975915
|
G | A | 4 | a0001c0001t0011g0135a0001c0001t0011g0136a0001c0001t0028g0137others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-13941C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975915 | ||||||
chr15:75975971
|
T | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-13997A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75975971 | ||||||
chr15:75976046
|
T | A | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-14072A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976046 | ||||||
chr15:75976127
|
G | A | 11 | a0001c0001t0008g0105a0001c0001t0008g0106a0001c0001t0008g0107others(8): Show | 11 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.105-14153C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976127 | ||||||
chr15:75976140
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0198a0001c0001t0001g0216 | 3 | NA18943.hp1 NA18990.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.105-14166G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976140 | ||||||
chr15:75976354
|
T | C | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.105-14380A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976354 | ||||||
chr15:75976359
|
C | T | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-14385G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976359 | ||||||
chr15:75976643
|
T | C | 10 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(7): Show | 11 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.105-14669A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976643 | ||||||
chr15:75976655
|
G | A | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-14681C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976655 | ||||||
chr15:75976723
|
C | T | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105-14749G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976723 | ||||||
chr15:75976762
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0017g0010 | 3 | HG00741.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.105-14788C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976762 | ||||||
chr15:75976803
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0003g0075 | 2 | HG00099.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.105-14829C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976803 | ||||||
chr15:75976853
|
G | C | 10 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(7): Show | 11 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.105-14879C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976853 | ||||||
chr15:75976933
|
T | A | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-14959A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75976933 | ||||||
chr15:75977025
|
G | T | 1 | a0001c0001t0002g0055 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.105-15051C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977025 | ||||||
chr15:75977063
|
C | T | 4 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0047g0129others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-15089G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977063 | ||||||
chr15:75977172
|
C | A | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-15198G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977172 | ||||||
chr15:75977313
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-15339G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977313 | ||||||
chr15:75977357
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.105-15383C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977357 | ||||||
chr15:75977485
|
A | G | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-15511T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977485 | ||||||
chr15:75977590
|
T | G | 2 | a0001c0001t0003g0025a0001c0001t0003g0026 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.105-15616A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977590 | ||||||
chr15:75977616
|
G | T | 6 | a0001c0001t0009g0110a0001c0001t0009g0114a0002c0002t0009g0008others(3): Show | 7 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-15642C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977616 | ||||||
chr15:75977630
|
T | A | 1 | a0001c0001t0031g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.105-15656A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977630 | ||||||
chr15:75977650
|
T | C | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-15676A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977650 | ||||||
chr15:75977726
|
G | A | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-15752C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977726 | ||||||
chr15:75977828
|
A | T | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.105-15854T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75977828 | ||||||
chr15:75978097
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 151 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.105-16123T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978097 | ||||||
chr15:75978107
|
G | A | 1 | a0001c0001t0002g0287 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.105-16133C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978107 | ||||||
chr15:75978125
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.105-16151G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978125 | ||||||
chr15:75978137
|
A | T | 1 | a0001c0001t0003g0036 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.105-16163T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978137 | ||||||
chr15:75978248
|
T | A | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-16274A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978248 | ||||||
chr15:75978372
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.105-16398G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978372 | ||||||
chr15:75978553
|
T | A | 1 | a0001c0001t0040g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.105-16579A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978553 | ||||||
chr15:75978581
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-16607A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978581 | ||||||
chr15:75978635
|
G | A | 1 | a0001c0001t0005g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.105-16661C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978635 | ||||||
chr15:75978735
|
A | C | 1 | a0001c0001t0047g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.105-16761T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978735 | ||||||
chr15:75978801
|
C | T | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-16827G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978801 | ||||||
chr15:75978802
|
A | T | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-16828T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978802 | ||||||
chr15:75978830
|
G | A | 1 | a0001c0001t0040g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.105-16856C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978830 | ||||||
chr15:75978892
|
C | T | 8 | a0001c0001t0001g0175a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | NA18943.hp1 NA18982.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.105-16918G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75978892 | ||||||
chr15:75979090
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.105-17116C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979090 | ||||||
chr15:75979103
|
T | C | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105-17129A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979103 | ||||||
chr15:75979292
|
A | ATAGTGTA others(3): Show |
9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-17319_105-1731 others(14): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979292 | ||||||
chr15:75979454
|
C | T | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-17480G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979454 | ||||||
chr15:75979465
|
A | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.105-17491T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979465 | ||||||
chr15:75979756
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.105-17782C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979756 | ||||||
chr15:75979886
|
T | C | 1 | a0001c0001t0002g0071 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.105-17912A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979886 | ||||||
chr15:75979954
|
T | C | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-17980A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75979954 | ||||||
chr15:75980109
|
T | A | 10 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(7): Show | 11 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.105-18135A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980109 | ||||||
chr15:75980115
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.105-18141T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980115 | ||||||
chr15:75980268
|
G | C | 1 | a0001c0001t0005g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.105-18294C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980268 | ||||||
chr15:75980383
|
AT | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.105-18410delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980383 | ||||||
chr15:75980383
|
ATT | A | 10 | a0001c0001t0001g0081a0001c0001t0001g0209a0001c0001t0010g0126others(7): Show | 10 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.105-18411_105-1841 others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980383 | ||||||
chr15:75980391
|
T | G | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.105-18417A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980391 | ||||||
chr15:75980420
|
A | C | 4 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0047g0129others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-18446T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980420 | ||||||
chr15:75980481
|
G | A | 24 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0145others(21): Show | 25 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.105-18507C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980481 | ||||||
chr15:75980566
|
G | A | 6 | a0001c0001t0002g0065a0001c0001t0003g0005a0001c0001t0003g0051others(3): Show | 7 | NA18948.hp2 NA19001.hp1 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-18592C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980566 | ||||||
chr15:75980665
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.105-18691G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980665 | ||||||
chr15:75980833
|
G | GA | 33 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0145others(30): Show | 35 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.105-18860dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980833 | ||||||
chr15:75980833
|
GA | G | 18 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0002g0235others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.105-18860delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980833 | ||||||
chr15:75980965
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.105-18991T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980965 | ||||||
chr15:75980987
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.105-19013T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75980987 | ||||||
chr15:75981099
|
T | A | 1 | a0001c0001t0046g0234 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.105-19125A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981099 | ||||||
chr15:75981114
|
A | T | 24 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(21): Show | 25 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.105-19140T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981114 | ||||||
chr15:75981277
|
A | G | 2 | a0001c0001t0003g0033a0001c0001t0003g0068 | 2 | NA18970.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.105-19303T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981277 | ||||||
chr15:75981607
|
A | G | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.105-19633T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981607 | ||||||
chr15:75981894
|
T | C | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0313 | 3 | NA18941.hp1 NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.105-19920A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981894 | ||||||
chr15:75981920
|
C | T | 24 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(21): Show | 25 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.105-19946G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981920 | ||||||
chr15:75981981
|
A | C | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-20007T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981981 | ||||||
chr15:75981987
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.105-20013T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75981987 | ||||||
chr15:75982171
|
G | A | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.105-20197C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75982171 | ||||||
chr15:75982175
|
C | T | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-20201G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75982175 | ||||||
chr15:75982260
|
T | C | 1 | a0001c0001t0036g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.105-20286A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75982260 | ||||||
chr15:75982643
|
A | G | 2 | a0001c0001t0025g0337a0001c0001t0026g0133 | 2 | HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105-20669T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75982643 | ||||||
chr15:75982903
|
T | A | 4 | a0001c0001t0003g0292a0001c0001t0003g0311a0001c0001t0010g0172others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-20929A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75982903 | ||||||
chr15:75982939
|
A | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02572.hp2 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.105-20965T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75982939 | ||||||
chr15:75983173
|
A | G | 1 | a0001c0001t0011g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105-21199T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983173 | ||||||
chr15:75983236
|
T | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105-21262A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983236 | ||||||
chr15:75983252
|
A | T | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-21278T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983252 | ||||||
chr15:75983300
|
G | T | 2 | a0001c0001t0003g0050a0001c0001t0014g0056 | 2 | HG01515.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.105-21326C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983300 | ||||||
chr15:75983332
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0005g0196a0001c0001t0007g0227 | 3 | HG02129.hp2 HG02155.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.105-21358A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983332 | ||||||
chr15:75983436
|
A | G | 1 | a0001c0001t0002g0315 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.105-21462T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983436 | ||||||
chr15:75983591
|
C | T | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-21617G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983591 | ||||||
chr15:75983809
|
T | A | 17 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(14): Show | 18 | HG00280.hp1 HG00642.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.105-21835A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983809 | ||||||
chr15:75983845
|
T | C | 1 | a0001c0001t0004g0251 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.105-21871A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75983845 | ||||||
chr15:75984039
|
T | C | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-22065A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984039 | ||||||
chr15:75984083
|
A | G | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-22109T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984083 | ||||||
chr15:75984088
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.105-22114C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984088 | ||||||
chr15:75984105
|
T | C | 1 | a0001c0001t0003g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.105-22131A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984105 | ||||||
chr15:75984108
|
T | C | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-22134A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984108 | ||||||
chr15:75984131
|
A | C | 1 | a0001c0001t0005g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.105-22157T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984131 | ||||||
chr15:75984286
|
C | A | 4 | a0001c0001t0003g0292a0001c0001t0003g0311a0001c0001t0010g0172others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-22312G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984286 | ||||||
chr15:75984557
|
T | A | 2 | a0001c0001t0004g0171a0001c0001t0004g0312 | 2 | HG02080.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.105-22583A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984557 | ||||||
chr15:75984646
|
G | A | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.105-22672C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984646 | ||||||
chr15:75984751
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(203): Show | 220 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.105-22777A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984751 | ||||||
chr15:75984777
|
AAAGTAT | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0164others(1): Show | 4 | HG01256.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-22809_105-2280 others(10): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984777 | ||||||
chr15:75984899
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.105-22925G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984899 | ||||||
chr15:75984925
|
A | C | 1 | a0001c0001t0001g0314 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.105-22951T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984925 | ||||||
chr15:75984991
|
C | T | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-23017G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75984991 | ||||||
chr15:75985088
|
G | T | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.105-23114C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985088 | ||||||
chr15:75985188
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.105-23214C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985188 | ||||||
chr15:75985226
|
T | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(335): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.105-23252A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985226 | ||||||
chr15:75985241
|
A | G | 1 | a0001c0001t0002g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.105-23267T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985241 | ||||||
chr15:75985405
|
T | A | 9 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-23431A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985405 | ||||||
chr15:75985487
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.105-23513G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985487 | ||||||
chr15:75985815
|
AACTT | A | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.104+23381_104+2338 others(8): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985815 | ||||||
chr15:75985844
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.104+23356T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75985844 | ||||||
chr15:75986026
|
T | G | 2 | a0001c0001t0020g0291a0001c0001t0040g0170 | 2 | HG01261.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.104+23174A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986026 | ||||||
chr15:75986231
|
T | A | 6 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.104+22969A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986231 | ||||||
chr15:75986265
|
C | A | 1 | a0001c0001t0003g0022 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.104+22935G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986265 | ||||||
chr15:75986307
|
C | G | 2 | a0001c0001t0003g0292a0001c0001t0003g0311 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.104+22893G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986307 | ||||||
chr15:75986379
|
G | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+22821C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986379 | ||||||
chr15:75986406
|
C | A | 3 | a0001c0001t0023g0141a0001c0001t0025g0337a0001c0001t0026g0133 | 3 | HG03130.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.104+22794G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986406 | ||||||
chr15:75986696
|
T | A | 1 | a0001c0001t0015g0249 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.104+22504A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986696 | ||||||
chr15:75986778
|
G | T | 2 | a0001c0001t0001g0167a0001c0001t0005g0197 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.104+22422C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986778 | ||||||
chr15:75986919
|
C | G | 1 | a0001c0001t0003g0033 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.104+22281G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986919 | ||||||
chr15:75986991
|
C | T | 10 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(7): Show | 11 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.104+22209G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75986991 | ||||||
chr15:75987031
|
A | G | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.104+22169T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987031 | ||||||
chr15:75987223
|
C | A | 2 | a0001c0001t0023g0141a0001c0001t0026g0133 | 2 | HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.104+21977G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987223 | ||||||
chr15:75987245
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.104+21955C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987245 | ||||||
chr15:75987489
|
C | A | 15 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(12): Show | 16 | HG01123.hp1 HG02257.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.104+21711G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987489 | ||||||
chr15:75987492
|
G | T | 15 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(12): Show | 16 | HG01123.hp1 HG02257.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.104+21708C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987492 | ||||||
chr15:75987572
|
A | T | 10 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.104+21628T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987572 | ||||||
chr15:75987603
|
G | A | 2 | a0001c0001t0008g0335a0001c0001t0018g0332 | 2 | NA18963.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.104+21597C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987603 | ||||||
chr15:75987715
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+21485A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987715 | ||||||
chr15:75987966
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.104+21234C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987966 | ||||||
chr15:75987988
|
T | G | 1 | a0001c0001t0001g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.104+21212A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75987988 | ||||||
chr15:75988159
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+21041G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988159 | ||||||
chr15:75988160
|
G | A | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.104+21040C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988160 | ||||||
chr15:75988162
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.104+21038G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988162 | ||||||
chr15:75988248
|
C | T | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+20952G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988248 | ||||||
chr15:75988249
|
G | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+20951C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988249 | ||||||
chr15:75988278
|
C | T | 1 | a0001c0001t0014g0056 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.104+20922G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988278 | ||||||
chr15:75988447
|
A | C | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+20753T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988447 | ||||||
chr15:75988462
|
C | T | 15 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(12): Show | 16 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.104+20738G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988462 | ||||||
chr15:75988477
|
A | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+20723T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988477 | ||||||
chr15:75988539
|
T | A | 23 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(20): Show | 24 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.104+20661A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988539 | ||||||
chr15:75988771
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.104+20429G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988771 | ||||||
chr15:75988828
|
ATAGAATC | A | 23 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(20): Show | 24 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.104+20365_104+2037 others(11): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988828 | ||||||
chr15:75988853
|
C | CT | 79 | a0001c0001t0001g0081a0001c0001t0001g0144a0001c0001t0001g0178others(76): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.104+20346dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988853 | ||||||
chr15:75988853
|
C | CTT | 8 | a0001c0001t0003g0051a0001c0001t0009g0110a0001c0001t0009g0114others(5): Show | 9 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.104+20345_104+2034 others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988853 | ||||||
chr15:75988853
|
C | T | 1 | a0001c0001t0004g0242 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.104+20347G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988853 | ||||||
chr15:75988853
|
CT | C | 12 | a0001c0001t0002g0079a0001c0001t0002g0299a0001c0001t0002g0304others(9): Show | 12 | HG00642.hp1 HG01515.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.104+20346delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988853 | ||||||
chr15:75988884
|
G | T | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+20316C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988884 | ||||||
chr15:75988905
|
G | A | 1 | a0001c0001t0036g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.104+20295C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988905 | ||||||
chr15:75988924
|
C | G | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.104+20276G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988924 | ||||||
chr15:75988958
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.104+20242T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75988958 | ||||||
chr15:75989209
|
A | G | 8 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(5): Show | 8 | NA18940.hp2 NA18945.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.104+19991T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989209 | ||||||
chr15:75989338
|
G | A | 1 | a0001c0001t0028g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.104+19862C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989338 | ||||||
chr15:75989434
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0036g0193 | 3 | HG00738.hp2 HG00741.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.104+19766G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989434 | ||||||
chr15:75989510
|
GA | G | 10 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(7): Show | 11 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.104+19689delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989510 | ||||||
chr15:75989578
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.104+19622C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989578 | ||||||
chr15:75989714
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+19486C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989714 | ||||||
chr15:75989822
|
T | C | 1 | a0001c0001t0048g0128 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.104+19378A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989822 | ||||||
chr15:75989904
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+19296C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989904 | ||||||
chr15:75989992
|
C | T | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+19208G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75989992 | ||||||
chr15:75990004
|
C | T | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+19196G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990004 | ||||||
chr15:75990011
|
G | A | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+19189C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990011 | ||||||
chr15:75990043
|
C | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.104+19157G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990043 | ||||||
chr15:75990182
|
T | G | 1 | a0001c0001t0009g0110 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.104+19018A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990182 | ||||||
chr15:75990214
|
T | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0313 | 3 | NA18941.hp1 NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.104+18986A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990214 | ||||||
chr15:75990218
|
T | G | 4 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0047g0129others(1): Show | 4 | HG02055.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+18982A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990218 | ||||||
chr15:75990288
|
A | T | 7 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(4): Show | 7 | NA18940.hp2 NA18945.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+18912T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990288 | ||||||
chr15:75990372
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+18828G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990372 | ||||||
chr15:75990407
|
G | A | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+18793C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990407 | ||||||
chr15:75990461
|
C | T | 1 | a0001c0001t0048g0128 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.104+18739G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990461 | ||||||
chr15:75990559
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+18641G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990559 | ||||||
chr15:75990671
|
G | GT | 140 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(137): Show | 148 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.104+18528dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990671 | ||||||
chr15:75990671
|
G | GTT | 8 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0001g0230others(5): Show | 8 | HG01071.hp2 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.104+18527_104+1852 others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990671 | ||||||
chr15:75990671
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+18514_104+1852 others(19): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990671 | ||||||
chr15:75990679
|
T | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01358.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.104+18521A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990679 | ||||||
chr15:75990684
|
G | GT | 6 | a0001c0001t0002g0046a0001c0001t0002g0055a0001c0001t0002g0266others(3): Show | 6 | HG00621.hp2 HG02738.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.104+18515dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990684 | ||||||
chr15:75990684
|
G | T | 9 | a0001c0001t0005g0189a0001c0001t0011g0116a0001c0001t0011g0135others(6): Show | 9 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.104+18516C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990684 | ||||||
chr15:75990684
|
GTTT | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+18513_104+1851 others(7): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990684 | ||||||
chr15:75990689
|
T | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.104+18511A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990689 | ||||||
chr15:75990690
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.104+18510A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990690 | ||||||
chr15:75990703
|
C | A | 2 | a0001c0001t0009g0110a0001c0001t0009g0114 | 2 | HG01123.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.104+18497G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990703 | ||||||
chr15:75990807
|
T | C | 1 | a0001c0001t0003g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.104+18393A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990807 | ||||||
chr15:75990957
|
C | T | 1 | a0001c0001t0034g0331 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.104+18243G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990957 | ||||||
chr15:75990975
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(92): Show | 101 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.104+18225G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75990975 | ||||||
chr15:75991028
|
T | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+18172A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991028 | ||||||
chr15:75991121
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+18079C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991121 | ||||||
chr15:75991276
|
C | T | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+17924G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991276 | ||||||
chr15:75991290
|
G | T | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.104+17910C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991290 | ||||||
chr15:75991384
|
A | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+17816T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991384 | ||||||
chr15:75991453
|
T | C | 6 | a0001c0001t0009g0110a0001c0001t0009g0114a0002c0002t0009g0008others(3): Show | 7 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+17747A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991453 | ||||||
chr15:75991601
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.104+17599T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991601 | ||||||
chr15:75991628
|
A | AT | 29 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(26): Show | 31 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.104+17571dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991628 | ||||||
chr15:75991643
|
G | A | 1 | a0001c0001t0013g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104+17557C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991643 | ||||||
chr15:75991717
|
C | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.104+17483G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991717 | ||||||
chr15:75991753
|
A | G | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+17447T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991753 | ||||||
chr15:75991852
|
G | T | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+17348C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991852 | ||||||
chr15:75991897
|
G | A | 23 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(20): Show | 24 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.104+17303C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75991897 | ||||||
chr15:75992015
|
C | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+17185G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992015 | ||||||
chr15:75992249
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+16951G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992249 | ||||||
chr15:75992257
|
T | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0223 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.104+16943A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992257 | ||||||
chr15:75992406
|
A | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+16794T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992406 | ||||||
chr15:75992436
|
C | A | 4 | a0001c0001t0003g0292a0001c0001t0003g0311a0001c0001t0010g0172others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.104+16764G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992436 | ||||||
chr15:75992518
|
C | G | 28 | a0001c0001t0003g0248a0001c0001t0004g0001a0001c0001t0004g0014others(25): Show | 33 | HG00544.hp1 HG01358.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.104+16682G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992518 | ||||||
chr15:75992715
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+16485T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992715 | ||||||
chr15:75992727
|
T | C | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+16473A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992727 | ||||||
chr15:75992729
|
T | C | 1 | a0001c0001t0005g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.104+16471A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992729 | ||||||
chr15:75992746
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.104+16454C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992746 | ||||||
chr15:75992916
|
C | CT | 11 | a0001c0001t0001g0083a0001c0001t0001g0180a0001c0001t0003g0044others(8): Show | 11 | HG00423.hp1 HG00438.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.104+16283dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992916 | ||||||
chr15:75992916
|
CT | C | 9 | a0001c0001t0004g0236a0001c0001t0009g0109a0001c0001t0009g0110others(6): Show | 10 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.104+16283delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75992916 | ||||||
chr15:75993008
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.104+16192C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993008 | ||||||
chr15:75993040
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.104+16160T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993040 | ||||||
chr15:75993157
|
C | G | 1 | a0001c0001t0038g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.104+16043G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993157 | ||||||
chr15:75993158
|
T | C | 1 | a0001c0001t0038g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.104+16042A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993158 | ||||||
chr15:75993284
|
A | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG03017.hp2 HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.104+15916T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993284 | ||||||
chr15:75993290
|
GT | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+15909delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993290 | ||||||
chr15:75993298
|
T | C | 1 | a0001c0001t0003g0022 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.104+15902A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993298 | ||||||
chr15:75993324
|
C | T | 4 | a0002c0002t0009g0008a0002c0002t0009g0112a0002c0002t0041g0111others(1): Show | 5 | HG02257.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.104+15876G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993324 | ||||||
chr15:75993342
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.104+15858T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993342 | ||||||
chr15:75993392
|
T | TA | 45 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0147others(42): Show | 47 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.104+15807dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993392 | ||||||
chr15:75993392
|
T | TAA | 6 | a0001c0001t0002g0046a0001c0001t0002g0072a0001c0001t0003g0033others(3): Show | 6 | HG01109.hp1 HG02738.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+15806_104+1580 others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993392 | ||||||
chr15:75993392
|
TA | T | 19 | a0001c0001t0001g0103a0001c0001t0001g0149a0001c0001t0001g0188others(16): Show | 19 | HG00099.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.104+15807delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993392 | ||||||
chr15:75993392
|
TAA | T | 12 | a0001c0001t0002g0263a0001c0001t0009g0110a0001c0001t0009g0114others(9): Show | 13 | HG01123.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.104+15806_104+1580 others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993392 | ||||||
chr15:75993697
|
C | CA | 12 | a0001c0001t0002g0298a0001c0001t0002g0299a0001c0001t0002g0344others(9): Show | 12 | HG00642.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.104+15502dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993697 | ||||||
chr15:75993697
|
C | CAA | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+15501_104+1550 others(6): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993697 | ||||||
chr15:75993923
|
T | A | 1 | a0001c0001t0013g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104+15277A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993923 | ||||||
chr15:75993972
|
A | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.104+15228T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75993972 | ||||||
chr15:75994217
|
A | G | 29 | a0001c0001t0002g0233a0001c0001t0003g0248a0001c0001t0004g0001others(26): Show | 34 | HG00544.hp1 HG01358.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.104+14983T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994217 | ||||||
chr15:75994241
|
G | T | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+14959C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994241 | ||||||
chr15:75994335
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.104+14865G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994335 | ||||||
chr15:75994370
|
T | G | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.104+14830A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994370 | ||||||
chr15:75994375
|
G | T | 4 | a0001c0001t0001g0185a0001c0001t0005g0184a0001c0001t0005g0186others(1): Show | 4 | NA18955.hp2 NA19011.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.104+14825C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994375 | ||||||
chr15:75994672
|
G | A | 6 | a0001c0001t0009g0110a0001c0001t0009g0114a0002c0002t0009g0008others(3): Show | 7 | HG01123.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+14528C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994672 | ||||||
chr15:75994827
|
G | C | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.104+14373C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994827 | ||||||
chr15:75994977
|
T | C | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.104+14223A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75994977 | ||||||
chr15:75995015
|
T | G | 1 | a0001c0001t0002g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.104+14185A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995015 | ||||||
chr15:75995058
|
C | T | 1 | a0001c0001t0003g0049 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.104+14142G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995058 | ||||||
chr15:75995197
|
C | CA | 8 | a0001c0001t0004g0171a0001c0001t0004g0239a0001c0001t0004g0312others(5): Show | 9 | HG01123.hp1 HG02027.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.104+14002dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995197 | ||||||
chr15:75995205
|
A | G | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+13995T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995205 | ||||||
chr15:75995239
|
C | T | 1 | a0001c0001t0007g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.104+13961G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995239 | ||||||
chr15:75995295
|
G | A | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.104+13905C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995295 | ||||||
chr15:75995300
|
C | T | 9 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(6): Show | 9 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.104+13900G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995300 | ||||||
chr15:75995476
|
A | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+13724T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995476 | ||||||
chr15:75995514
|
C | T | 1 | a0001c0001t0004g0241 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.104+13686G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995514 | ||||||
chr15:75995576
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.104+13624G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995576 | ||||||
chr15:75995676
|
A | G | 1 | a0001c0001t0027g0262 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.104+13524T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995676 | ||||||
chr15:75995756
|
T | C | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+13444A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995756 | ||||||
chr15:75995859
|
A | C | 1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+13341T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995859 | ||||||
chr15:75995900
|
A | G | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+13300T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75995900 | ||||||
chr15:75996252
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+12948C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996252 | ||||||
chr15:75996489
|
A | AGACAGTG others(36): Show |
1 | a0001c0001t0001g0080 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.104+12668_104+1271 others(47): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996489 | ||||||
chr15:75996535
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.104+12665T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996535 | ||||||
chr15:75996605
|
G | A | 3 | a0001c0001t0010g0126a0001c0001t0047g0129a0001c0001t0048g0128 | 3 | HG02055.hp1 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.104+12595C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996605 | ||||||
chr15:75996616
|
C | A | 3 | a0001c0001t0010g0126a0001c0001t0047g0129a0001c0001t0048g0128 | 3 | HG02055.hp1 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.104+12584G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996616 | ||||||
chr15:75996626
|
T | C | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+12574A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996626 | ||||||
chr15:75996671
|
A | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+12529T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996671 | ||||||
chr15:75996682
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.104+12518A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996682 | ||||||
chr15:75996747
|
A | T | 3 | a0001c0001t0003g0029a0001c0001t0003g0047a0001c0001t0003g0048 | 3 | HG01169.hp1 HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.104+12453T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996747 | ||||||
chr15:75996930
|
G | C | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.104+12270C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996930 | ||||||
chr15:75996931
|
G | C | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.104+12269C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996931 | ||||||
chr15:75996990
|
A | G | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+12210T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75996990 | ||||||
chr15:75997096
|
A | G | 3 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | NA18940.hp2 NA18971.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.104+12104T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997096 | ||||||
chr15:75997110
|
A | G | 6 | a0001c0001t0002g0046a0001c0001t0003g0003a0001c0001t0003g0004others(3): Show | 8 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+12090T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997110 | ||||||
chr15:75997127
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.104+12073G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997127 | ||||||
chr15:75997303
|
T | C | 2 | a0001c0001t0016g0124a0001c0001t0016g0125 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.104+11897A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997303 | ||||||
chr15:75997419
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.104+11781G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997419 | ||||||
chr15:75997456
|
T | C | 1 | a0001c0001t0020g0326 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.104+11744A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997456 | ||||||
chr15:75997489
|
G | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.104+11711C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997489 | ||||||
chr15:75997582
|
G | A | 2 | a0001c0001t0029g0139a0001c0001t0030g0140 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.104+11618C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997582 | ||||||
chr15:75997701
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(168): Show | 184 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.104+11499C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997701 | ||||||
chr15:75997875
|
T | C | 19 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(16): Show | 20 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.104+11325A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997875 | ||||||
chr15:75997901
|
A | G | 1 | a0001c0001t0033g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.104+11299T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75997901 | ||||||
chr15:75998092
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.104+11108G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75998092 | ||||||
chr15:75998197
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+11003C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75998197 | ||||||
chr15:75998472
|
C | T | 3 | a0001c0001t0010g0126a0001c0001t0047g0129a0001c0001t0048g0128 | 3 | HG02055.hp1 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.104+10728G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75998472 | ||||||
chr15:75998760
|
T | C | 1 | a0001c0001t0003g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.104+10440A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75998760 | ||||||
chr15:75998889
|
T | TAAATTC | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+10310_104+1031 others(10): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75998889 | ||||||
chr15:75999114
|
T | C | 2 | a0001c0001t0047g0129a0001c0001t0048g0128 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.104+10086A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999114 | ||||||
chr15:75999367
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.104+9833A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999367 | ||||||
chr15:75999473
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+9727G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999473 | ||||||
chr15:75999921
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+9279C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999921 | ||||||
chr15:75999925
|
C | T | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+9275G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999925 | ||||||
chr15:75999938
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.104+9262G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999938 | ||||||
chr15:75999994
|
C | T | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+9206G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 75999994 | ||||||
chr15:76000028
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+9172A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000028 | ||||||
chr15:76000120
|
A | G | 16 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(13): Show | 17 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.104+9080T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000120 | ||||||
chr15:76000174
|
G | T | 1 | a0001c0001t0003g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.104+9026C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000174 | ||||||
chr15:76000276
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.104+8924A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000276 | ||||||
chr15:76000284
|
T | C | 1 | a0001c0001t0015g0237 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.104+8916A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000284 | ||||||
chr15:76000326
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.104+8874T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000326 | ||||||
chr15:76000545
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.104+8655C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000545 | ||||||
chr15:76000552
|
A | G | 1 | a0001c0001t0015g0240 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.104+8648T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000552 | ||||||
chr15:76000985
|
A | ATTATTT | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+8209_104+8214d others(8): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76000985 | ||||||
chr15:76001090
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.104+8110T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001090 | ||||||
chr15:76001277
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.104+7923C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001277 | ||||||
chr15:76001294
|
GC | G | 6 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.104+7905delG | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001294 | ||||||
chr15:76001326
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0238 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.104+7874G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001326 | ||||||
chr15:76001368
|
A | G | 1 | a0001c0001t0005g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.104+7832T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001368 | ||||||
chr15:76001480
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104+7720G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001480 | ||||||
chr15:76001524
|
T | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0026 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.104+7676A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001524 | ||||||
chr15:76001630
|
A | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(167): Show | 183 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.104+7570T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001630 | ||||||
chr15:76001661
|
C | T | 9 | a0001c0001t0003g0021a0001c0001t0003g0023a0001c0001t0003g0036others(6): Show | 9 | NA18950.hp2 NA18955.hp1 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.104+7539G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001661 | ||||||
chr15:76001788
|
C | T | 1 | a0001c0001t0009g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+7412G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001788 | ||||||
chr15:76001793
|
T | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+7407A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76001793 | ||||||
chr15:76002165
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.104+7035C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002165 | ||||||
chr15:76002278
|
A | G | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.104+6922T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002278 | ||||||
chr15:76002283
|
G | A | 2 | a0001c0001t0026g0133a0001c0001t0031g0134 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.104+6917C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002283 | ||||||
chr15:76002529
|
C | T | 16 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(13): Show | 17 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.104+6671G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002529 | ||||||
chr15:76002622
|
T | C | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+6578A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002622 | ||||||
chr15:76002686
|
A | C | 1 | a0001c0001t0007g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.104+6514T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002686 | ||||||
chr15:76002722
|
C | A | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+6478G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002722 | ||||||
chr15:76002813
|
A | G | 1 | a0001c0001t0049g0336 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.104+6387T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76002813 | ||||||
chr15:76003016
|
C | A | 1 | a0001c0001t0008g0330 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.104+6184G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76003016 | ||||||
chr15:76003390
|
A | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+5810T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76003390 | ||||||
chr15:76003556
|
A | G | 1 | a0003c0003t0002g0035 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.104+5644T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76003556 | ||||||
chr15:76003978
|
A | G | 1 | a0001c0001t0007g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.104+5222T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76003978 | ||||||
chr15:76004130
|
G | A | 2 | a0001c0001t0026g0133a0001c0001t0031g0134 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.104+5070C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004130 | ||||||
chr15:76004172
|
A | G | 1 | a0001c0001t0004g0239 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.104+5028T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004172 | ||||||
chr15:76004291
|
G | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0238 | 2 | NA18971.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.104+4909C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004291 | ||||||
chr15:76004343
|
G | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+4857C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004343 | ||||||
chr15:76004536
|
T | C | 8 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+4664A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004536 | ||||||
chr15:76004599
|
C | CA | 6 | a0001c0001t0001g0144a0001c0001t0003g0027a0001c0001t0003g0034others(3): Show | 6 | HG00099.hp2 HG01256.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+4600dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004599 | ||||||
chr15:76004599
|
CA | C | 13 | a0001c0001t0001g0080a0001c0001t0001g0179a0001c0001t0001g0180others(10): Show | 13 | HG02055.hp1 HG02273.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.104+4600delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004599 | ||||||
chr15:76004617
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.104+4583T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004617 | ||||||
chr15:76004753
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+4447T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004753 | ||||||
chr15:76004802
|
A | T | 1 | a0001c0001t0004g0236 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.104+4398T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004802 | ||||||
chr15:76004918
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.104+4282T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76004918 | ||||||
chr15:76005243
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+3957C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005243 | ||||||
chr15:76005281
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0177 | 3 | NA18960.hp1 NA18992.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.104+3919G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005281 | ||||||
chr15:76005383
|
T | TA | 69 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(66): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.104+3816dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005383 | ||||||
chr15:76005383
|
TA | T | 18 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(15): Show | 18 | HG01515.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.104+3816delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005383 | ||||||
chr15:76005448
|
GC | G | 343 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(340): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.104+3751delG | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005448 | ||||||
chr15:76005581
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+3619C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005581 | ||||||
chr15:76005615
|
G | A | 1 | a0001c0001t0001g0314 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.104+3585C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005615 | ||||||
chr15:76005637
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0007g0227 | 2 | HG02129.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.104+3563C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005637 | ||||||
chr15:76005679
|
G | GA | 18 | a0001c0001t0001g0096a0001c0001t0001g0228a0001c0001t0001g0230others(15): Show | 18 | HG00597.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.104+3520dupT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005679 | ||||||
chr15:76005679
|
G | GAA | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+3519_104+3520d others(4): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005679 | ||||||
chr15:76005679
|
GA | G | 15 | a0001c0001t0001g0175a0001c0001t0002g0339a0001c0001t0003g0023others(12): Show | 15 | HG01167.hp2 HG01993.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.104+3520delT | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005679 | ||||||
chr15:76005791
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 147 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.104+3409T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005791 | ||||||
chr15:76005960
|
G | A | 1 | a0001c0001t0005g0013 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.104+3240C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76005960 | ||||||
chr15:76006165
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.104+3035T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006165 | ||||||
chr15:76006400
|
A | T | 5 | a0001c0001t0011g0116a0001c0001t0011g0135a0001c0001t0011g0136others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.104+2800T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006400 | ||||||
chr15:76006403
|
A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 147 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.104+2797T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006403 | ||||||
chr15:76006569
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.104+2631G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006569 | ||||||
chr15:76006792
|
C | T | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+2408G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006792 | ||||||
chr15:76006843
|
T | C | 2 | a0001c0001t0026g0133a0001c0001t0031g0134 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.104+2357A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006843 | ||||||
chr15:76006984
|
G | A | 1 | a0001c0001t0004g0312 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.104+2216C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76006984 | ||||||
chr15:76007138
|
T | TAGAAAAT others(3399): Show |
1 | a0001c0001t0031g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.104+2061_104+2062i others(3408): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007138 | ||||||
chr15:76007138
|
T | TAGAAAAT others(3395): Show |
1 | a0001c0001t0026g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+2061_104+2062i others(3404): Show |
NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007138 | ||||||
chr15:76007244
|
A | G | 1 | a0001c0001t0023g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.104+1956T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007244 | ||||||
chr15:76007249
|
C | G | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0172others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+1951G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007249 | ||||||
chr15:76007314
|
T | C | 4 | a0001c0001t0021g0121a0001c0001t0021g0122a0001c0001t0026g0133others(1): Show | 4 | HG02809.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+1886A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007314 | ||||||
chr15:76007427
|
C | CT | 12 | a0001c0001t0001g0144a0001c0001t0001g0166a0001c0001t0001g0167others(9): Show | 12 | HG01978.hp1 HG02080.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.104+1772dupA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007427 | ||||||
chr15:76007427
|
CT | C | 14 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0002g0315others(11): Show | 15 | HG02055.hp1 HG02257.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.104+1772delA | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007427 | ||||||
chr15:76007452
|
C | T | 30 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(27): Show | 32 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.104+1748G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007452 | ||||||
chr15:76007487
|
C | T | 11 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(8): Show | 12 | HG01123.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.104+1713G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007487 | ||||||
chr15:76007556
|
AG | A | 5 | a0001c0001t0007g0317a0001c0001t0007g0318a0001c0001t0007g0319others(2): Show | 5 | HG01346.hp2 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.104+1643delC | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007556 | ||||||
chr15:76007788
|
C | T | 2 | a0001c0001t0026g0133a0001c0001t0031g0134 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.104+1412G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007788 | ||||||
chr15:76007924
|
T | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+1276A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76007924 | ||||||
chr15:76008269
|
A | G | 1 | a0001c0001t0004g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.104+931T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76008269 | ||||||
chr15:76008283
|
G | A | 3 | a0002c0002t0009g0008a0002c0002t0009g0112a0002c0002t0042g0113 | 4 | HG02647.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.104+917C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76008283 | ||||||
chr15:76008555
|
C | T | 1 | a0001c0001t0004g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.104+645G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76008555 | ||||||
chr15:76008591
|
C | A | 4 | a0001c0001t0013g0323a0001c0001t0013g0325a0001c0001t0019g0322others(1): Show | 4 | HG01891.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+609G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76008591 | ||||||
chr15:76008654
|
A | G | 26 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(23): Show | 27 | HG01123.hp1 HG02055.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.104+546T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76008654 | ||||||
chr15:76009182
|
C | T | 2 | a0001c0001t0005g0132a0001c0001t0007g0131 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.104+18G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 3/5 | chr15 | 76009182 | ||||||
chr15:76009310
|
T | A | 1 | a0001c0001t0020g0326 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.11-17A>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009310 | ||||||
chr15:76009483
|
A | T | 1 | a0001c0001t0005g0130 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.11-190T>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009483 | ||||||
chr15:76009564
|
G | A | 5 | a0001c0001t0001g0101a0001c0001t0012g0097a0001c0001t0012g0098others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.11-271C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009564 | ||||||
chr15:76009636
|
G | T | 6 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0016g0124others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.11-343C>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009636 | ||||||
chr15:76009653
|
C | T | 2 | a0001c0001t0021g0121a0001c0001t0021g0122 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.11-360G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009653 | ||||||
chr15:76009721
|
T | C | 2 | a0001c0001t0002g0327a0001c0001t0002g0328 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.11-428A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009721 | ||||||
chr15:76009927
|
G | C | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.11-634C>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009927 | ||||||
chr15:76009987
|
C | G | 1 | a0001c0001t0006g0123 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.11-694G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76009987 | ||||||
chr15:76010232
|
C | G | 2 | a0001c0001t0021g0121a0001c0001t0021g0122 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.11-939G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010232 | ||||||
chr15:76010486
|
T | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.10+735A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010486 | ||||||
chr15:76010552
|
G | A | 1 | a0001c0001t0009g0114 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.10+669C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010552 | ||||||
chr15:76010569
|
C | G | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.10+652G>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010569 | ||||||
chr15:76010669
|
G | A | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.10+552C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010669 | ||||||
chr15:76010758
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.10+463C>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010758 | ||||||
chr15:76010831
|
T | C | 10 | a0001c0001t0008g0105a0001c0001t0008g0106a0001c0001t0008g0107others(7): Show | 10 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.10+390A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76010831 | ||||||
chr15:76011033
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG02083.hp1 NA18944.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.10+188G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 2/5 | chr15 | 76011033 | ||||||
chr15:76011453
|
T | G | 1 | a0001c0001t0025g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-56-167A>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011453 | ||||||
chr15:76011496
|
C | T | 1 | a0001c0001t0011g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-210G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011496 | ||||||
chr15:76011699
|
T | C | 1 | a0001c0001t0002g0338 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-56-413A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011699 | ||||||
chr15:76011816
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-57+503G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011816 | ||||||
chr15:76011884
|
A | C | 7 | a0001c0001t0009g0109a0001c0001t0009g0110a0001c0001t0009g0114others(4): Show | 8 | HG01123.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+435T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011884 | ||||||
chr15:76011926
|
C | T | 4 | a0001c0001t0008g0105a0001c0001t0008g0106a0001c0001t0008g0107others(1): Show | 4 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+393G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011926 | ||||||
chr15:76011987
|
T | C | 1 | a0001c0001t0014g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+332A>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76011987 | ||||||
chr15:76012076
|
A | G | 1 | a0001c0001t0005g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57+243T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76012076 | ||||||
chr15:76012091
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+228T>G | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76012091 | ||||||
chr15:76012162
|
A | G | 25 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(22): Show | 26 | HG00280.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-57+157T>C | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76012162 | ||||||
chr15:76012301
|
C | A | 6 | a0001c0001t0001g0343a0001c0001t0002g0339a0001c0001t0002g0340others(3): Show | 6 | HG00423.hp2 NA18991.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+18G>T | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76012301 | ||||||
chr15:76012301
|
C | T | 62 | a0001c0001t0002g0032a0001c0001t0002g0046a0001c0001t0002g0055others(59): Show | 66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-57+18G>A | NRG4 | ENSG00000169752.17 | transcript | ENST00000394907.8 | protein_coding | 1/5 | chr15 | 76012301 |