geneid | 152518 |
---|---|
ensemblid | ENSG00000170448.12 |
hgncid | 18726 |
symbol | NFXL1 |
name | nuclear transcription factor, X-box binding like 1 |
refseq_nuc | NM_001278624.2 |
refseq_prot | NP_001265553.1 |
ensembl_nuc | ENST00000507489.2 |
ensembl_prot | ENSP00000422037.1 |
mane_status | MANE Select |
chr | chr4 |
start | 47847240 |
end | 47914583 |
strand | - |
ver | v1.2 |
region | chr4:47847240-47914583 |
region5000 | chr4:47842240-47919583 |
regionname0 | NFXL1_chr4_47847240_47914583 |
regionname5000 | NFXL1_chr4_47842240_47919583 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 911 | 205 | 54 | 51 | 66 | 11 | 22 | 52 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002 | 0/1 | 911 | 162 | 30 | 15 | 93 | 5 | 18 | 72 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0003 | 0/0 | 911 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0004 | 0/0 | 911 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0005 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0006 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0007 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0008 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0009 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0010 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2736 | 160 | 30 | 15 | 91 | 5 | 18 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0002 | 1/0 | 2736 | 109 | 24 | 20 | 51 | 4 | 9 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0003 | 0/0 | 2736 | 89 | 30 | 28 | 12 | 7 | 12 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0004 | 0/0 | 2736 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0005 | 0/0 | 2736 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0006 | 0/0 | 2736 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0007 | 0/0 | 2736 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0008 | 0/0 | 2736 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0009 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0010 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0011 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0012 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0013 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0014 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
c0015 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1144 | 256 | 62 | 23 | 141 | 5 | 24 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0002 | 0/0 | 1144 | 64 | 3 | 25 | 16 | 7 | 13 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0003 | 1/0 | 1145 | 34 | 7 | 14 | 3 | 4 | 5 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0004 | 0/0 | 1144 | 7 | 7 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0005 | 0/0 | 1144 | 4 | 4 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0006 | 0/0 | 1145 | 4 | 4 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0007 | 0/0 | 1144 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0008 | 0/0 | 1144 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0009 | 0/0 | 1144 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0010 | 0/0 | 1144 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0011 | 0/0 | 1144 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
t0012 | 0/0 | 1144 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 1 | 13 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0002 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0312 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 2736 | 109 | 24 | 20 | 51 | 4 | 9 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0003 | 0/0 | 2736 | 89 | 30 | 28 | 12 | 7 | 12 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0004 | 0/0 | 2736 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0006 | 0/0 | 2736 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0009 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0001 | 0/1 | 2736 | 160 | 30 | 15 | 91 | 5 | 18 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0008 | 0/0 | 2736 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0003c0005 | 0/0 | 2736 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0004c0007 | 0/0 | 2736 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0005c0015 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0006c0014 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0007c0013 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0008c0010 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0009c0011 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0010c0012 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 3879 | 73 | 13 | 8 | 48 | 0 | 4 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0002t0003 | 1/0 | 3880 | 31 | 7 | 11 | 3 | 4 | 5 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0002t0006 | 0/0 | 3880 | 4 | 4 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0002t0009 | 0/0 | 3879 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0003t0001 | 0/0 | 3879 | 17 | 16 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0003t0002 | 0/0 | 3879 | 59 | 3 | 25 | 12 | 7 | 12 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0003t0004 | 0/0 | 3879 | 7 | 7 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0003t0005 | 0/0 | 3879 | 4 | 4 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0003t0008 | 0/0 | 3879 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0004t0003 | 0/0 | 3880 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0006t0002 | 0/0 | 3879 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0001c0009t0002 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0001t0001 | 0/1 | 3879 | 155 | 28 | 12 | 91 | 5 | 18 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0001t0007 | 0/0 | 3879 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0001t0011 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0001t0012 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0002c0008t0001 | 0/0 | 3879 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0003c0005t0001 | 0/0 | 3879 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0004c0007t0001 | 0/0 | 3879 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0005c0015t0002 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0006c0014t0001 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0007c0013t0010 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0008c0010t0001 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0009c0011t0001 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
a0010c0012t0001 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | copy fasta | chr4 | 47842240 | 47919583 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0312 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0002t0009g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0008g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0003t0008g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0004t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0004t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0004t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0006t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0006t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0006t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0001c0009t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0001 | 0/0 | 15 | 0 | 1 | 13 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0002 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0007g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0001t0012g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0008t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0002c0008t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0003c0005t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0003c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0004c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0004c0007t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0005c0015t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0006c0014t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0007c0013t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0008c0010t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0009c0011t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
a0010c0012t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0159 | EUR | GBR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0114 | EUR | GBR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0273 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00280 | hp2 | a0001 | c0003 | t0002 | g0117 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00323 | hp1 | a0002 | c0001 | t0001 | g0270 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0106 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0243 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00558 | hp1 | a0001 | c0006 | t0002 | g0154 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0295 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00597 | hp2 | a0001 | c0006 | t0002 | g0149 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0207 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0204 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00639 | hp1 | a0001 | c0004 | t0003 | g0175 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00639 | hp2 | a0001 | c0003 | t0008 | g0315 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0177 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00673 | hp2 | a0002 | c0001 | t0001 | g0257 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0098 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00733 | hp2 | a0001 | c0004 | t0003 | g0158 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00735 | hp1 | a0001 | c0003 | t0002 | g0016 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00735 | hp2 | a0001 | c0003 | t0002 | g0054 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00738 | hp1 | a0001 | c0003 | t0002 | g0017 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0109 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0153 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0160 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01070 | hp1 | a0001 | c0003 | t0002 | g0097 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01070 | hp2 | a0002 | c0001 | t0001 | g0258 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01071 | hp1 | a0001 | c0003 | t0002 | g0141 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01071 | hp2 | a0002 | c0001 | t0001 | g0241 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0140 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0277 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0016 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0120 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0180 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0166 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0169 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01109 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0190 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01169 | hp2 | a0001 | c0003 | t0002 | g0017 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0313 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0100 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0146 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0311 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0283 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01255 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01257 | hp1 | a0002 | c0001 | t0001 | g0272 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0147 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0108 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0176 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01346 | hp2 | a0004 | c0007 | t0001 | g0219 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01358 | hp1 | a0001 | c0003 | t0002 | g0134 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01358 | hp2 | a0001 | c0003 | t0002 | g0111 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0163 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0112 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01433 | hp1 | a0001 | c0004 | t0003 | g0178 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0028 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0018 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0019 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0105 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01517 | hp1 | a0001 | c0003 | t0002 | g0110 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01517 | hp2 | a0001 | c0002 | t0003 | g0018 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0222 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01884 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01891 | hp1 | a0003 | c0005 | t0001 | g0024 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0143 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0242 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01934 | hp2 | a0001 | c0003 | t0002 | g0155 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01943 | hp1 | a0004 | c0007 | t0001 | g0218 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01943 | hp2 | a0001 | c0003 | t0002 | g0151 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01952 | hp1 | a0002 | c0001 | t0007 | g0009 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01952 | hp2 | a0001 | c0003 | t0002 | g0142 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0138 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01981 | hp2 | a0002 | c0001 | t0007 | g0009 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0161 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0170 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02055 | hp1 | a0001 | c0003 | t0002 | g0130 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02055 | hp2 | a0003 | c0005 | t0001 | g0192 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0288 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0152 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02071 | hp1 | a0005 | c0015 | t0002 | g0307 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02071 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02080 | hp2 | a0002 | c0001 | t0001 | g0263 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02083 | hp1 | a0002 | c0001 | t0001 | g0200 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02129 | hp1 | a0002 | c0001 | t0001 | g0264 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02129 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0135 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0035 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0202 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02257 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02273 | hp1 | a0002 | c0001 | t0007 | g0009 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02273 | hp2 | a0002 | c0001 | t0001 | g0236 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02280 | hp2 | a0002 | c0001 | t0001 | g0023 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0104 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02300 | hp2 | a0001 | c0002 | t0009 | g0033 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02451 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02451 | hp2 | a0002 | c0001 | t0001 | g0211 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0290 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0224 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02615 | hp2 | a0010 | c0012 | t0001 | g0253 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02622 | hp1 | a0002 | c0001 | t0001 | g0209 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02630 | hp1 | a0002 | c0001 | t0011 | g0291 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02630 | hp2 | a0007 | c0013 | t0010 | g0256 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0310 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0196 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0164 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0274 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02717 | hp1 | a0003 | c0005 | t0001 | g0024 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0162 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02723 | hp1 | a0002 | c0001 | t0001 | g0210 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02735 | hp2 | a0006 | c0014 | t0001 | g0304 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02818 | hp1 | a0002 | c0001 | t0001 | g0213 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02886 | hp1 | a0002 | c0001 | t0001 | g0188 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0185 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02895 | hp2 | a0002 | c0001 | t0001 | g0022 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02897 | hp1 | a0002 | c0001 | t0001 | g0022 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0021 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0179 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0115 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02965 | hp2 | a0009 | c0011 | t0001 | g0215 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02970 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0194 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03017 | hp1 | a0001 | c0009 | t0002 | g0145 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0126 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03041 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0037 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0182 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03130 | hp1 | a0002 | c0001 | t0001 | g0233 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0309 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03209 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03209 | hp2 | a0001 | c0003 | t0005 | g0029 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0216 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03239 | hp1 | a0001 | c0003 | t0002 | g0103 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0282 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03453 | hp2 | a0001 | c0003 | t0004 | g0183 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03486 | hp1 | a0002 | c0001 | t0001 | g0187 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03486 | hp2 | a0001 | c0003 | t0005 | g0029 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03490 | hp1 | a0001 | c0003 | t0002 | g0119 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03490 | hp2 | a0001 | c0003 | t0002 | g0129 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0157 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03491 | hp2 | a0001 | c0003 | t0002 | g0125 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0220 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03579 | hp1 | a0002 | c0001 | t0001 | g0023 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03579 | hp2 | a0001 | c0003 | t0005 | g0299 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03654 | hp1 | a0001 | c0003 | t0002 | g0121 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0008 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03669 | hp1 | a0002 | c0001 | t0001 | g0267 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03669 | hp2 | a0008 | c0010 | t0001 | g0229 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03688 | hp2 | a0002 | c0001 | t0001 | g0252 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03704 | hp1 | a0001 | c0003 | t0002 | g0044 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03704 | hp2 | a0002 | c0001 | t0001 | g0251 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03710 | hp2 | a0002 | c0001 | t0001 | g0191 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0276 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0027 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03834 | hp1 | a0002 | c0001 | t0001 | g0240 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0278 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0116 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03942 | hp2 | a0001 | c0003 | t0002 | g0128 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0223 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0284 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04199 | hp2 | a0001 | c0003 | t0002 | g0144 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04204 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0019 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0132 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0165 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18522 | hp1 | a0002 | c0001 | t0001 | g0193 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18522 | hp2 | a0001 | c0002 | t0006 | g0040 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0249 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18612 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0226 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18906 | hp1 | a0002 | c0001 | t0001 | g0212 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0195 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18939 | hp1 | a0002 | c0008 | t0001 | g0306 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18940 | hp1 | a0002 | c0001 | t0001 | g0287 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0262 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18942 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18944 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18949 | hp1 | a0002 | c0001 | t0001 | g0269 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18949 | hp2 | a0001 | c0003 | t0002 | g0123 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18957 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18961 | hp1 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0189 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18963 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18965 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18967 | hp1 | a0001 | c0003 | t0002 | g0137 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18968 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18968 | hp2 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18969 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18971 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18972 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18972 | hp2 | a0002 | c0001 | t0001 | g0285 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18973 | hp2 | a0001 | c0006 | t0002 | g0148 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18974 | hp2 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18979 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18981 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0292 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18986 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18987 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18992 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0234 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18997 | hp1 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18999 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19001 | hp1 | a0001 | c0003 | t0002 | g0133 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19002 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19004 | hp2 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19005 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0289 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0266 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0199 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0294 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19011 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0286 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19030 | hp1 | a0002 | c0001 | t0001 | g0214 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19043 | hp1 | a0001 | c0003 | t0004 | g0186 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0302 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19055 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19057 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19058 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19062 | hp1 | a0002 | c0001 | t0001 | g0232 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19062 | hp2 | a0002 | c0001 | t0001 | g0260 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19063 | hp2 | a0001 | c0003 | t0002 | g0122 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19064 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19064 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0293 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19068 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19075 | hp1 | a0001 | c0003 | t0002 | g0113 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19076 | hp1 | a0002 | c0008 | t0001 | g0305 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19076 | hp2 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19078 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19080 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19081 | hp2 | a0002 | c0001 | t0001 | g0297 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19082 | hp1 | a0002 | c0001 | t0001 | g0296 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19082 | hp2 | a0001 | c0003 | t0002 | g0101 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19086 | hp2 | a0001 | c0003 | t0002 | g0118 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0298 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19088 | hp2 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19090 | hp1 | a0002 | c0001 | t0001 | g0279 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19090 | hp2 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20129 | hp1 | a0002 | c0001 | t0001 | g0261 | AFR | ASW | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0102 | AFR | ASW | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0259 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0107 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20805 | hp1 | a0002 | c0001 | t0001 | g0275 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0139 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20905 | hp1 | a0001 | c0003 | t0002 | g0127 | SAS | GIH | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0271 | SAS | GIH | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01123 | hp1 | a0001 | c0003 | t0008 | g0316 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0314 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02109 | hp2 | a0002 | c0001 | t0001 | g0198 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0308 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02486 | hp2 | a0002 | c0001 | t0001 | g0197 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0172 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG02559 | hp2 | a0001 | c0003 | t0005 | g0300 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
HG03471 | hp2 | a0001 | c0003 | t0004 | g0184 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | USA | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0150 | AFR | USA | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA21309 | hp1 | a0002 | c0001 | t0012 | g0228 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0156 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0268 | REF | REF | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0312 | REF | REF | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47848180
|
T | C | 1 | a0003 | 3 | HG01891.hp1 HG02055.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.2719A>G | p.Thr907Ala | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 2940/3880 | 2719/2736 | 907/911 | chr4 | 47848180 | ||
chr4:47862904
|
G | C | 1 | a0008 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2258C>G | p.Thr753Arg | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/23 | 2479/3880 | 2258/2736 | 753/911 | chr4 | 47862904 | ||
chr4:47890643
|
T | A | 1 | a0009 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1513A>T | p.Asn505Tyr | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/23 | 1734/3880 | 1513/2736 | 505/911 | chr4 | 47890643 | ||
chr4:47899459
|
G | A | 7 | a0002a0003a0004others(4): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
missense_variant | MODERATE | c.737C>T | p.Pro246Leu | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/23 | 958/3880 | 737/2736 | 246/911 | chr4 | 47899459 | ||
chr4:47903296
|
T | C | 1 | a0010 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.544A>G | p.Ile182Val | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/23 | 765/3880 | 544/2736 | 182/911 | chr4 | 47903296 | ||
chr4:47903310
|
G | A | 1 | a0007 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.530C>T | p.Ser177Leu | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/23 | 751/3880 | 530/2736 | 177/911 | chr4 | 47903310 | ||
chr4:47905303
|
A | T | 1 | a0004 | 2 | HG01346.hp2 HG01943.hp1 |
missense_variant | MODERATE | c.450T>A | p.Asn150Lys | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/23 | 671/3880 | 450/2736 | 150/911 | chr4 | 47905303 | ||
chr4:47914071
|
C | A | 1 | a0006 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.133G>T | p.Val45Phe | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/23 | 354/3880 | 133/2736 | 45/911 | chr4 | 47914071 | ||
chr4:47914193
|
G | A | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.11C>T | p.Ser4Phe | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/23 | 232/3880 | 11/2736 | 4/911 | chr4 | 47914193 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47885519
|
T | C | 13 | a0001c0003a0001c0006a0001c0009others(10): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
synonymous_variant | LOW | c.1803A>G | p.Ala601Ala | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/23 | 2024/3880 | 1803/2736 | 601/911 | chr4 | 47885519 | ||
chr4:47885558
|
T | C | 1 | a0001c0009 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.1764A>G | p.Lys588Lys | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/23 | 1985/3880 | 1764/2736 | 588/911 | chr4 | 47885558 | ||
chr4:47885974
|
G | A | 13 | a0001c0003a0001c0006a0001c0009others(10): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
synonymous_variant | LOW | c.1569C>T | p.Thr523Thr | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 13/23 | 1790/3880 | 1569/2736 | 523/911 | chr4 | 47885974 | ||
chr4:47899071
|
C | T | 1 | a0001c0004 | 3 | HG00639.hp1 HG00733.hp2 HG01433.hp1 |
synonymous_variant | LOW | c.876G>A | p.Lys292Lys | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 7/23 | 1097/3880 | 876/2736 | 292/911 | chr4 | 47899071 | ||
chr4:47903258
|
G | A | 1 | a0001c0006 | 3 | HG00558.hp1 HG00597.hp2 NA18973.hp2 |
synonymous_variant | LOW | c.582C>T | p.Asp194Asp | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/23 | 803/3880 | 582/2736 | 194/911 | chr4 | 47903258 | ||
chr4:47914171
|
G | A | 1 | a0002c0008 | 2 | NA18939.hp1 NA19076.hp1 |
synonymous_variant | LOW | c.33C>T | p.Gly11Gly | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/23 | 254/3880 | 33/2736 | 11/911 | chr4 | 47914171 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47847501
|
G | A | 1 | a0007c0013t0010 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 662 | chr4 | 47847501 | |||||
chr4:47847582
|
T | A | 1 | a0002c0001t0011 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 581 | chr4 | 47847582 | |||||
chr4:47847585
|
G | A | 1 | a0001c0002t0006 | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*578C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 578 | chr4 | 47847585 | |||||
chr4:47847597
|
T | C | 1 | a0002c0001t0007 | 3 | HG01952.hp1 HG01981.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*566A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 566 | chr4 | 47847597 | |||||
chr4:47847616
|
G | A | 1 | a0002c0001t0012 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 547 | chr4 | 47847616 | |||||
chr4:47847659
|
A | G | 1 | a0001c0003t0004 | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*504T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 504 | chr4 | 47847659 | |||||
chr4:47847749
|
T | A | 5 | a0001c0003t0002a0001c0003t0008a0001c0006t0002others(2): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*414A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 414 | chr4 | 47847749 | |||||
chr4:47847814
|
G | C | 1 | a0001c0003t0005 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*349C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 349 | chr4 | 47847814 | |||||
chr4:47847966
|
TA | T | 22 | a0001c0002t0001a0001c0002t0009a0001c0003t0001others(19): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*196delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 196 | chr4 | 47847966 | |||||
chr4:47914445
|
C | T | 1 | a0001c0002t0009 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/23 | 242 | chr4 | 47914445 | |||||
chr4:47914446
|
G | A | 1 | a0001c0003t0008 | 2 | HG00639.hp2 HG01123.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/23 | chr4 | 47914446 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:47848567
|
G | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2563-231C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848567 | ||||||
chr4:47848617
|
C | T | 5 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2563-281G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848617 | ||||||
chr4:47848665
|
G | A | 1 | a0002c0001t0001g0262 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2563-329C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848665 | ||||||
chr4:47848762
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2563-426C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848762 | ||||||
chr4:47848806
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2563-470C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848806 | ||||||
chr4:47848813
|
A | G | 1 | a0002c0001t0001g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2563-477T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848813 | ||||||
chr4:47848845
|
C | T | 1 | a0001c0002t0001g0094 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2563-509G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848845 | ||||||
chr4:47848896
|
T | A | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2563-560A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848896 | ||||||
chr4:47848923
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2563-587C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848923 | ||||||
chr4:47848976
|
A | G | 12 | a0002c0001t0001g0022a0002c0001t0001g0023a0002c0001t0001g0187others(9): Show | 15 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2563-640T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848976 | ||||||
chr4:47849037
|
T | C | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2563-701A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849037 | ||||||
chr4:47849093
|
A | T | 2 | a0001c0003t0008g0315a0001c0003t0008g0316 | 2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2563-757T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849093 | ||||||
chr4:47849149
|
G | T | 1 | a0001c0002t0001g0096 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2563-813C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849149 | ||||||
chr4:47849191
|
T | C | 71 | a0001c0003t0001g0099a0001c0003t0002g0016a0001c0003t0002g0017others(68): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2563-855A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849191 | ||||||
chr4:47849219
|
C | T | 1 | a0002c0001t0001g0280 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2563-883G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849219 | ||||||
chr4:47849334
|
G | C | 1 | a0001c0003t0002g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2563-998C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849334 | ||||||
chr4:47849382
|
T | C | 1 | a0001c0002t0003g0157 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2563-1046A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849382 | ||||||
chr4:47849554
|
A | C | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2563-1218T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849554 | ||||||
chr4:47849624
|
G | A | 1 | a0001c0002t0003g0176 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2563-1288C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849624 | ||||||
chr4:47849927
|
C | T | 64 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(61): Show | 74 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.2562+1168G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849927 | ||||||
chr4:47849952
|
A | AT | 5 | a0001c0002t0001g0010a0001c0002t0001g0038a0001c0002t0001g0041others(2): Show | 6 | HG00642.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2562+1142dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849952 | ||||||
chr4:47849952
|
A | T | 2 | a0001c0002t0003g0176a0001c0002t0003g0180 | 2 | HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2562+1143T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849952 | ||||||
chr4:47849952
|
AT | A | 163 | a0001c0002t0001g0053a0001c0002t0001g0061a0001c0002t0009g0033others(160): Show | 208 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.2562+1142delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849952 | ||||||
chr4:47849955
|
T | A | 55 | a0001c0003t0001g0099a0001c0003t0002g0016a0001c0003t0002g0017others(52): Show | 59 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2562+1140A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849955 | ||||||
chr4:47849956
|
T | A | 160 | a0001c0002t0001g0049a0001c0003t0001g0030a0001c0003t0001g0031others(157): Show | 205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.2562+1139A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849956 | ||||||
chr4:47849957
|
T | A | 2 | a0002c0001t0001g0217a0010c0012t0001g0253 | 2 | HG02040.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2562+1138A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849957 | ||||||
chr4:47849958
|
T | A | 44 | a0001c0003t0002g0016a0001c0003t0002g0017a0001c0003t0002g0044others(41): Show | 46 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2562+1137A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849958 | ||||||
chr4:47850003
|
T | C | 68 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0022others(65): Show | 89 | HG00408.hp1 HG00423.hp2 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.2562+1092A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850003 | ||||||
chr4:47850166
|
A | G | 65 | a0001c0003t0001g0099a0001c0003t0002g0016a0001c0003t0002g0017others(62): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2562+929T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850166 | ||||||
chr4:47850201
|
T | C | 2 | a0001c0002t0001g0064a0001c0002t0001g0065 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2562+894A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850201 | ||||||
chr4:47850276
|
T | A | 1 | a0002c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2562+819A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850276 | ||||||
chr4:47850608
|
T | C | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2562+487A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850608 | ||||||
chr4:47850717
|
T | C | 1 | a0002c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2562+378A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850717 | ||||||
chr4:47850786
|
G | A | 17 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(14): Show | 20 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2562+309C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850786 | ||||||
chr4:47851360
|
T | C | 1 | a0002c0001t0001g0270 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2509-212A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851360 | ||||||
chr4:47851418
|
A | T | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2509-270T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851418 | ||||||
chr4:47851457
|
CTT | C | 2 | a0001c0002t0003g0018a0001c0002t0003g0160 | 3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2509-311_2509-310d others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851457 | ||||||
chr4:47851464
|
T | C | 1 | a0002c0001t0001g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2509-316A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851464 | ||||||
chr4:47851652
|
T | C | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2508+204A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851652 | ||||||
chr4:47851826
|
T | C | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2508+30A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851826 | ||||||
chr4:47852137
|
A | G | 2 | a0002c0001t0001g0026a0002c0001t0001g0225 | 3 | NA18947.hp1 NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2422-195T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852137 | ||||||
chr4:47852355
|
A | G | 1 | a0001c0003t0002g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2422-413T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852355 | ||||||
chr4:47852567
|
T | A | 1 | a0001c0003t0002g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2422-625A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852567 | ||||||
chr4:47852602
|
T | C | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.2422-660A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852602 | ||||||
chr4:47852677
|
G | A | 12 | a0002c0001t0001g0007a0002c0001t0001g0025a0002c0001t0001g0198others(9): Show | 15 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2422-735C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852677 | ||||||
chr4:47852726
|
T | C | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2422-784A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852726 | ||||||
chr4:47852744
|
C | G | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2422-802G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852744 | ||||||
chr4:47852756
|
C | T | 312 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(309): Show | 374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.2422-814G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852756 | ||||||
chr4:47852850
|
T | C | 2 | a0002c0001t0001g0026a0002c0001t0001g0225 | 3 | NA18947.hp1 NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2422-908A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852850 | ||||||
chr4:47852864
|
T | C | 1 | a0002c0001t0001g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2422-922A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852864 | ||||||
chr4:47852965
|
GT | G | 7 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(4): Show | 8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2422-1024delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852965 | ||||||
chr4:47853096
|
G | A | 1 | a0002c0001t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2422-1154C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853096 | ||||||
chr4:47853263
|
T | C | 2 | a0001c0002t0003g0168a0001c0002t0003g0170 | 2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2422-1321A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853263 | ||||||
chr4:47853393
|
C | T | 1 | a0002c0001t0001g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2422-1451G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853393 | ||||||
chr4:47853481
|
C | T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2422-1539G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853481 | ||||||
chr4:47853686
|
G | A | 1 | a0001c0003t0002g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2421+1373C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853686 | ||||||
chr4:47853982
|
T | C | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2421+1077A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853982 | ||||||
chr4:47854720
|
G | A | 1 | a0001c0002t0001g0013 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2421+339C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854720 | ||||||
chr4:47854846
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2421+213G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854846 | ||||||
chr4:47854940
|
C | CA | 12 | a0001c0002t0001g0303a0001c0002t0003g0169a0001c0002t0003g0174others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2421+118dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854940 | ||||||
chr4:47854940
|
CA | C | 15 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(12): Show | 16 | HG00323.hp1 HG00642.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2421+118delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854940 | ||||||
chr4:47855005
|
C | T | 1 | a0002c0001t0001g0247 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2421+54G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47855005 | ||||||
chr4:47855023
|
T | C | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2421+36A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47855023 | ||||||
chr4:47855168
|
A | T | 1 | a0002c0001t0001g0267 | 1 | HG03669.hp1 | splice_region_variant&intron_variant | LOW | c.2317-5T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855168 | ||||||
chr4:47855470
|
T | C | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2317-307A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855470 | ||||||
chr4:47855562
|
G | A | 7 | a0002c0001t0001g0193a0002c0001t0001g0194a0002c0001t0001g0195others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2317-399C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855562 | ||||||
chr4:47855565
|
C | T | 1 | a0002c0001t0001g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2317-402G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855565 | ||||||
chr4:47855600
|
T | C | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2317-437A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855600 | ||||||
chr4:47855669
|
C | T | 281 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(278): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.2317-506G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855669 | ||||||
chr4:47855987
|
G | A | 2 | a0001c0002t0003g0176a0001c0002t0003g0180 | 2 | HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2317-824C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855987 | ||||||
chr4:47856075
|
T | C | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2317-912A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856075 | ||||||
chr4:47856082
|
G | A | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2317-919C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856082 | ||||||
chr4:47856123
|
G | T | 1 | a0002c0001t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2317-960C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856123 | ||||||
chr4:47856142
|
A | G | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2317-979T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856142 | ||||||
chr4:47856213
|
T | C | 1 | a0009c0011t0001g0215 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2317-1050A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856213 | ||||||
chr4:47856342
|
G | C | 1 | a0001c0003t0002g0016 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2317-1179C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856342 | ||||||
chr4:47856457
|
T | G | 1 | a0001c0003t0001g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2317-1294A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856457 | ||||||
chr4:47856501
|
ATAG | A | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2317-1341_2317-133 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856501 | ||||||
chr4:47856564
|
G | C | 1 | a0002c0001t0001g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2317-1401C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856564 | ||||||
chr4:47856866
|
T | C | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2317-1703A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856866 | ||||||
chr4:47857026
|
C | T | 1 | a0002c0001t0001g0262 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2317-1863G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857026 | ||||||
chr4:47857229
|
G | A | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2317-2066C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857229 | ||||||
chr4:47857303
|
A | C | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2317-2140T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857303 | ||||||
chr4:47857324
|
T | G | 12 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(9): Show | 15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2317-2161A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857324 | ||||||
chr4:47857460
|
G | A | 1 | a0001c0002t0003g0020 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2317-2297C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857460 | ||||||
chr4:47857796
|
T | A | 1 | a0002c0001t0001g0275 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2317-2633A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857796 | ||||||
chr4:47857800
|
T | TTAGGTTT others(77): Show |
2 | a0001c0003t0002g0136a0001c0003t0002g0137 | 2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2317-2721_2317-263 others(88): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857800 | ||||||
chr4:47857812
|
T | C | 1 | a0001c0002t0003g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2317-2649A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857812 | ||||||
chr4:47857884
|
G | T | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2317-2721C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857884 | ||||||
chr4:47858288
|
T | C | 1 | a0001c0003t0002g0123 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2317-3125A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858288 | ||||||
chr4:47858375
|
C | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2317-3212G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858375 | ||||||
chr4:47858479
|
C | A | 1 | a0002c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2317-3316G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858479 | ||||||
chr4:47858708
|
A | C | 1 | a0002c0001t0001g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2317-3545T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858708 | ||||||
chr4:47858764
|
G | A | 1 | a0002c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2317-3601C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858764 | ||||||
chr4:47859240
|
A | G | 1 | a0002c0001t0001g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2316+3606T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859240 | ||||||
chr4:47859455
|
G | T | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2316+3391C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859455 | ||||||
chr4:47859715
|
G | A | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2316+3131C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859715 | ||||||
chr4:47859841
|
C | CA | 11 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0003g0156others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2316+3004dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | ||||||
chr4:47859841
|
C | CAAAA | 12 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(9): Show | 16 | HG02083.hp2 HG02132.hp1 NA18952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2316+3001_2316+300 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | ||||||
chr4:47859841
|
C | CAAAAA | 15 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0052others(12): Show | 18 | HG00609.hp2 HG00621.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.2316+3000_2316+300 others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | ||||||
chr4:47859841
|
C | CAAAAAA | 12 | a0001c0002t0001g0014a0001c0002t0001g0050a0001c0002t0001g0057others(9): Show | 13 | HG01433.hp2 HG01934.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2316+2999_2316+300 others(10): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | ||||||
chr4:47859841
|
C | CAAAAAAA others(3): Show |
2 | a0001c0002t0001g0015a0001c0002t0001g0086 | 3 | HG00423.hp1 NA18940.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2316+2995_2316+300 others(14): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | ||||||
chr4:47859841
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0003g0020 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2316+2993_2316+300 others(16): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | ||||||
chr4:47859854
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0003t0002g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2316+2975_2316+299 others(21): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859854 | ||||||
chr4:47859856
|
AAAAAAAA others(8): Show |
A | 2 | a0001c0002t0001g0051a0001c0002t0001g0067 | 2 | NA18987.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(19): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859856 | ||||||
chr4:47859857
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0001g0079 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2316+2975_2316+298 others(18): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859857 | ||||||
chr4:47859858
|
AAAAAAAA others(6): Show |
A | 3 | a0001c0002t0001g0066a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02523.hp1 NA18947.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(17): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859858 | ||||||
chr4:47859861
|
A | C | 1 | a0001c0003t0002g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2316+2985T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859861 | ||||||
chr4:47859861
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0003t0004g0185a0005c0015t0002g0307 | 2 | HG02071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(14): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859861 | ||||||
chr4:47859862
|
AAAAAAAA others(2): Show |
A | 124 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(121): Show | 150 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(13): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859862 | ||||||
chr4:47859863
|
AAAAAAAA others(1): Show |
A | 73 | a0001c0003t0001g0045a0001c0003t0001g0308a0001c0003t0001g0311others(70): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(12): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859863 | ||||||
chr4:47859864
|
AAAAAAAC | A | 16 | a0002c0001t0001g0028a0002c0001t0001g0191a0002c0001t0001g0198others(13): Show | 17 | HG00621.hp1 HG00673.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(11): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859864 | ||||||
chr4:47859867
|
A | C | 1 | a0001c0002t0003g0177 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2316+2979T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859867 | ||||||
chr4:47859871
|
C | A | 45 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(42): Show | 54 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2316+2975G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859871 | ||||||
chr4:47859940
|
G | A | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2316+2906C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859940 | ||||||
chr4:47859960
|
T | C | 1 | a0010c0012t0001g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2316+2886A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859960 | ||||||
chr4:47860230
|
T | G | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2316+2616A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860230 | ||||||
chr4:47860459
|
G | A | 3 | a0002c0001t0001g0203a0002c0001t0001g0245a0002c0001t0001g0249 | 3 | NA18612.hp1 NA19000.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2316+2387C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860459 | ||||||
chr4:47860464
|
T | C | 1 | a0001c0002t0003g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2316+2382A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860464 | ||||||
chr4:47860576
|
C | T | 49 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0004others(46): Show | 67 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.2316+2270G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860576 | ||||||
chr4:47860628
|
A | C | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2316+2218T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860628 | ||||||
chr4:47860672
|
A | G | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2316+2174T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860672 | ||||||
chr4:47860746
|
G | A | 1 | a0001c0003t0002g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2316+2100C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860746 | ||||||
chr4:47860775
|
T | C | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.2316+2071A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860775 | ||||||
chr4:47860858
|
G | GT | 19 | a0001c0003t0002g0131a0001c0003t0004g0021a0001c0003t0004g0182others(16): Show | 23 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2316+1987dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860858 | ||||||
chr4:47860914
|
G | A | 1 | a0001c0003t0002g0117 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2316+1932C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860914 | ||||||
chr4:47861018
|
A | AT | 200 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(197): Show | 246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2316+1827dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861018 | ||||||
chr4:47861080
|
C | T | 1 | a0005c0015t0002g0307 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2316+1766G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861080 | ||||||
chr4:47861283
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2316+1563T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861283 | ||||||
chr4:47861357
|
C | T | 1 | a0001c0006t0002g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2316+1489G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861357 | ||||||
chr4:47861564
|
A | G | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2316+1282T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861564 | ||||||
chr4:47861626
|
AT | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2316+1219delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861626 | ||||||
chr4:47861626
|
ATTTAT | A | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2316+1215_2316+121 others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861626 | ||||||
chr4:47861640
|
G | A | 7 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(4): Show | 8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2316+1206C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861640 | ||||||
chr4:47862431
|
T | G | 7 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(4): Show | 8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2316+415A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862431 | ||||||
chr4:47862437
|
C | T | 1 | a0001c0003t0004g0021 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2316+409G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862437 | ||||||
chr4:47862588
|
T | G | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2316+258A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862588 | ||||||
chr4:47862605
|
A | G | 1 | a0001c0002t0001g0090 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2316+241T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862605 | ||||||
chr4:47862652
|
A | C | 10 | a0002c0001t0001g0003a0002c0001t0001g0201a0002c0001t0001g0263others(7): Show | 14 | HG00408.hp2 HG02071.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2316+194T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862652 | ||||||
chr4:47862725
|
G | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2316+121C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862725 | ||||||
chr4:47862742
|
T | C | 2 | a0001c0003t0002g0108a0001c0003t0002g0109 | 2 | HG00738.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2316+104A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862742 | ||||||
chr4:47863179
|
T | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-264A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863179 | ||||||
chr4:47863202
|
A | C | 2 | a0001c0003t0008g0315a0001c0003t0008g0316 | 2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2247-287T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863202 | ||||||
chr4:47863231
|
TTATCATT others(1): Show |
T | 12 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(9): Show | 15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2247-324_2247-317d others(10): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863231 | ||||||
chr4:47863243
|
T | C | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2247-328A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863243 | ||||||
chr4:47863284
|
A | C | 1 | a0001c0002t0003g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2247-369T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863284 | ||||||
chr4:47863485
|
C | T | 4 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0081others(1): Show | 4 | HG02080.hp1 HG02083.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-570G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863485 | ||||||
chr4:47863697
|
A | G | 1 | a0002c0001t0001g0272 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2247-782T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863697 | ||||||
chr4:47863760
|
T | G | 1 | a0002c0001t0001g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2247-845A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863760 | ||||||
chr4:47863872
|
G | A | 281 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(278): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.2247-957C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863872 | ||||||
chr4:47864148
|
TCACCTCT others(9): Show |
T | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-1249_2247-123 others(20): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864148 | ||||||
chr4:47864283
|
T | C | 1 | a0001c0003t0002g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2247-1368A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864283 | ||||||
chr4:47864298
|
T | A | 1 | a0002c0001t0001g0263 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2247-1383A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864298 | ||||||
chr4:47864676
|
G | A | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-1761C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864676 | ||||||
chr4:47864722
|
G | A | 2 | a0001c0002t0003g0018a0001c0002t0003g0160 | 3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2247-1807C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864722 | ||||||
chr4:47864726
|
C | T | 224 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(221): Show | 274 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.2247-1811G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864726 | ||||||
chr4:47864750
|
G | A | 2 | a0001c0002t0003g0176a0001c0002t0003g0180 | 2 | HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2247-1835C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864750 | ||||||
chr4:47864945
|
G | A | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.2247-2030C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864945 | ||||||
chr4:47865100
|
C | T | 1 | a0001c0002t0001g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2247-2185G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865100 | ||||||
chr4:47865357
|
T | C | 2 | a0002c0008t0001g0305a0002c0008t0001g0306 | 2 | NA18939.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2247-2442A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865357 | ||||||
chr4:47865488
|
G | GA | 103 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(100): Show | 119 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.2247-2574dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865488 | ||||||
chr4:47865488
|
G | GAA | 6 | a0001c0002t0001g0050a0001c0002t0001g0059a0001c0002t0001g0064others(3): Show | 6 | HG02109.hp1 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2247-2575_2247-257 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865488 | ||||||
chr4:47865488
|
GA | G | 71 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(68): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2247-2574delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865488 | ||||||
chr4:47865499
|
AAAC | A | 116 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(113): Show | 156 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2247-2587_2247-258 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865499 | ||||||
chr4:47865500
|
AAC | A | 17 | a0002c0001t0001g0022a0002c0001t0001g0023a0002c0001t0001g0187others(14): Show | 20 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2247-2587_2247-258 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865500 | ||||||
chr4:47865533
|
C | T | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-2618G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865533 | ||||||
chr4:47865571
|
A | G | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2247-2656T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865571 | ||||||
chr4:47865581
|
T | G | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247-2666A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865581 | ||||||
chr4:47865678
|
C | A | 1 | a0001c0003t0002g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2247-2763G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865678 | ||||||
chr4:47865748
|
TCGGAGGC others(17): Show |
T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247-2857_2247-283 others(28): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865748 | ||||||
chr4:47865782
|
A | C | 1 | a0001c0003t0002g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2247-2867T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865782 | ||||||
chr4:47866011
|
T | G | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247-3096A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866011 | ||||||
chr4:47866087
|
C | T | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2247-3172G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866087 | ||||||
chr4:47866096
|
G | A | 1 | a0001c0002t0003g0314 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2247-3181C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866096 | ||||||
chr4:47866255
|
G | A | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2247-3340C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866255 | ||||||
chr4:47866298
|
C | G | 1 | a0001c0002t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2247-3383G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866298 | ||||||
chr4:47866400
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2247-3485C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866400 | ||||||
chr4:47866872
|
G | A | 281 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(278): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.2247-3957C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866872 | ||||||
chr4:47867029
|
G | A | 6 | a0001c0003t0002g0104a0001c0003t0002g0105a0001c0003t0002g0106others(3): Show | 6 | HG00323.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247-4114C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867029 | ||||||
chr4:47867206
|
T | C | 2 | a0002c0001t0001g0230a0002c0001t0001g0234 | 2 | NA18994.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2247-4291A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867206 | ||||||
chr4:47867241
|
G | GA | 71 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(68): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2247-4327dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867241 | ||||||
chr4:47867361
|
G | A | 1 | a0001c0003t0002g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2247-4446C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867361 | ||||||
chr4:47867386
|
A | G | 1 | a0002c0001t0001g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2247-4471T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867386 | ||||||
chr4:47867507
|
G | C | 2 | a0001c0002t0001g0053a0001c0002t0001g0061 | 2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2247-4592C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867507 | ||||||
chr4:47867530
|
A | G | 1 | a0001c0002t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2247-4615T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867530 | ||||||
chr4:47867642
|
T | TGGA | 75 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(72): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.2247-4730_2247-472 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867642 | ||||||
chr4:47867663
|
G | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-4748C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867663 | ||||||
chr4:47867766
|
G | A | 1 | a0001c0003t0002g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2247-4851C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867766 | ||||||
chr4:47867829
|
T | TTA | 4 | a0001c0002t0003g0171a0001c0004t0003g0158a0001c0004t0003g0175others(1): Show | 4 | HG00639.hp1 HG00733.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-4916_2247-491 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867829 | ||||||
chr4:47867888
|
A | G | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2247-4973T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867888 | ||||||
chr4:47867929
|
G | C | 1 | a0002c0001t0001g0240 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2247-5014C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867929 | ||||||
chr4:47867952
|
T | G | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2247-5037A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867952 | ||||||
chr4:47868185
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2247-5270C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868185 | ||||||
chr4:47868211
|
C | T | 11 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(8): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2247-5296G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868211 | ||||||
chr4:47868250
|
C | T | 1 | a0002c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2247-5335G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868250 | ||||||
chr4:47868268
|
G | A | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2247-5353C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868268 | ||||||
chr4:47868294
|
G | A | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2247-5379C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868294 | ||||||
chr4:47868296
|
G | C | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-5381C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868296 | ||||||
chr4:47868334
|
A | G | 4 | a0002c0001t0001g0189a0002c0001t0001g0231a0002c0001t0001g0286others(1): Show | 4 | NA18961.hp2 NA18974.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-5419T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868334 | ||||||
chr4:47868351
|
A | G | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2247-5436T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868351 | ||||||
chr4:47868357
|
C | T | 48 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0004others(45): Show | 66 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.2247-5442G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868357 | ||||||
chr4:47868456
|
C | CAAAAT | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2247-5542_2247-554 others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868456 | ||||||
chr4:47868537
|
G | A | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.2247-5622C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868537 | ||||||
chr4:47868625
|
T | C | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.2247-5710A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868625 | ||||||
chr4:47868835
|
T | C | 7 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(4): Show | 10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2247-5920A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868835 | ||||||
chr4:47868907
|
C | T | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2247-5992G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868907 | ||||||
chr4:47868948
|
T | C | 1 | a0002c0001t0001g0282 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2247-6033A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868948 | ||||||
chr4:47868986
|
T | C | 68 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0022others(65): Show | 89 | HG00408.hp1 HG00423.hp2 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.2247-6071A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868986 | ||||||
chr4:47869147
|
C | A | 3 | a0001c0002t0003g0020a0001c0002t0003g0172a0001c0002t0003g0179 | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246+5980G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869147 | ||||||
chr4:47869359
|
G | A | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2246+5768C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869359 | ||||||
chr4:47869532
|
T | C | 1 | a0002c0001t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2246+5595A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869532 | ||||||
chr4:47869825
|
C | T | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2246+5302G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869825 | ||||||
chr4:47870161
|
A | T | 4 | a0001c0002t0003g0020a0001c0002t0003g0162a0001c0002t0003g0172others(1): Show | 5 | HG02559.hp1 HG02717.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2246+4966T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870161 | ||||||
chr4:47870424
|
T | A | 1 | a0002c0001t0001g0226 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2246+4703A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870424 | ||||||
chr4:47870477
|
TAAAG | T | 65 | a0001c0003t0001g0115a0001c0003t0002g0016a0001c0003t0002g0017others(62): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2246+4646_2246+464 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870477 | ||||||
chr4:47870536
|
A | G | 1 | a0001c0003t0002g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2246+4591T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870536 | ||||||
chr4:47870604
|
GA | G | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2246+4522delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870604 | ||||||
chr4:47870620
|
A | G | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.2246+4507T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870620 | ||||||
chr4:47870734
|
A | G | 3 | a0001c0002t0003g0018a0001c0002t0003g0159a0001c0002t0003g0160 | 4 | HG00099.hp1 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246+4393T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870734 | ||||||
chr4:47870890
|
G | GT | 3 | a0002c0001t0001g0263a0002c0001t0001g0268a0002c0001t0001g0301 | 3 | HG02080.hp2 NA18612.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2246+4236dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870890 | ||||||
chr4:47870948
|
C | T | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2246+4179G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870948 | ||||||
chr4:47870998
|
GGTTGGGA others(11): Show |
G | 5 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(2): Show | 6 | HG00642.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2246+4111_2246+412 others(22): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870998 | ||||||
chr4:47871117
|
G | A | 281 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(278): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.2246+4010C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871117 | ||||||
chr4:47871119
|
G | C | 1 | a0001c0003t0002g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2246+4008C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871119 | ||||||
chr4:47871150
|
A | C | 2 | a0003c0005t0001g0024a0003c0005t0001g0192 | 3 | HG01891.hp1 HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2246+3977T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871150 | ||||||
chr4:47871175
|
C | T | 1 | a0001c0003t0002g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2246+3952G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871175 | ||||||
chr4:47871180
|
C | A | 1 | a0001c0002t0001g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2246+3947G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871180 | ||||||
chr4:47871209
|
T | C | 1 | a0002c0001t0001g0202 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2246+3918A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871209 | ||||||
chr4:47871346
|
G | A | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2246+3781C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871346 | ||||||
chr4:47871350
|
C | CA | 207 | a0001c0002t0001g0075a0001c0003t0001g0030a0001c0003t0001g0031others(204): Show | 256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2246+3776dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871350 | ||||||
chr4:47871350
|
C | CAA | 6 | a0001c0003t0002g0128a0001c0003t0002g0150a0001c0003t0002g0152others(3): Show | 6 | HG02056.hp2 HG03486.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.2246+3775_2246+377 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871350 | ||||||
chr4:47871361
|
A | C | 7 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(4): Show | 8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2246+3766T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871361 | ||||||
chr4:47871365
|
C | A | 2 | a0001c0003t0002g0125a0001c0003t0002g0152 | 2 | HG02056.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2246+3762G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871365 | ||||||
chr4:47871385
|
A | G | 2 | a0002c0001t0001g0258a0002c0001t0001g0259 | 2 | HG01070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2246+3742T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871385 | ||||||
chr4:47871558
|
G | C | 21 | a0001c0003t0002g0016a0001c0003t0002g0044a0001c0003t0002g0101others(18): Show | 22 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2246+3569C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871558 | ||||||
chr4:47871744
|
T | G | 3 | a0001c0002t0001g0055a0001c0002t0001g0076a0001c0002t0009g0033 | 3 | HG02300.hp2 HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2246+3383A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871744 | ||||||
chr4:47871918
|
G | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2246+3209C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871918 | ||||||
chr4:47872131
|
G | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2246+2996C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872131 | ||||||
chr4:47872359
|
G | A | 68 | a0002c0001t0001g0001a0002c0001t0001g0008a0002c0001t0001g0022others(65): Show | 89 | HG00408.hp1 HG00423.hp2 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.2246+2768C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872359 | ||||||
chr4:47872394
|
A | G | 281 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(278): Show | 340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.2246+2733T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872394 | ||||||
chr4:47872461
|
CA | C | 200 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(197): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2246+2665delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872461 | ||||||
chr4:47872461
|
CAA | C | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01070.hp1 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2246+2664_2246+266 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872461 | ||||||
chr4:47872476
|
AAG | A | 7 | a0002c0001t0001g0007a0002c0001t0001g0198a0002c0001t0001g0209others(4): Show | 9 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2246+2649_2246+265 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872476 | ||||||
chr4:47872479
|
A | G | 7 | a0002c0001t0001g0007a0002c0001t0001g0198a0002c0001t0001g0209others(4): Show | 9 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2246+2648T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872479 | ||||||
chr4:47872528
|
G | C | 1 | a0001c0003t0008g0315 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2246+2599C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872528 | ||||||
chr4:47872560
|
G | A | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2246+2567C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872560 | ||||||
chr4:47872622
|
T | C | 1 | a0002c0001t0001g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2246+2505A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872622 | ||||||
chr4:47872883
|
C | T | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2246+2244G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872883 | ||||||
chr4:47872909
|
T | C | 1 | a0002c0001t0001g0246 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2246+2218A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872909 | ||||||
chr4:47873038
|
C | T | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2246+2089G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873038 | ||||||
chr4:47873299
|
T | G | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2246+1828A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873299 | ||||||
chr4:47873337
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2246+1790C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873337 | ||||||
chr4:47873470
|
C | T | 16 | a0001c0003t0002g0017a0001c0003t0002g0054a0001c0003t0002g0097others(13): Show | 17 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2246+1657G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873470 | ||||||
chr4:47873548
|
T | C | 1 | a0001c0002t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2246+1579A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873548 | ||||||
chr4:47873653
|
T | C | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2246+1474A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873653 | ||||||
chr4:47873707
|
G | A | 1 | a0001c0003t0004g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2246+1420C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873707 | ||||||
chr4:47873841
|
CT | C | 7 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(4): Show | 8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2246+1285delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873841 | ||||||
chr4:47873869
|
T | C | 2 | a0001c0003t0002g0097a0001c0003t0002g0141 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2246+1258A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873869 | ||||||
chr4:47874069
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2246+1058A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874069 | ||||||
chr4:47874278
|
T | C | 1 | a0001c0003t0004g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2246+849A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874278 | ||||||
chr4:47874397
|
C | A | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2246+730G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874397 | ||||||
chr4:47874466
|
T | A | 1 | a0002c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2246+661A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874466 | ||||||
chr4:47874687
|
A | T | 1 | a0001c0002t0001g0068 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2246+440T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874687 | ||||||
chr4:47874710
|
A | AAAT | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.2246+416_2246+417i others(5): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874710 | ||||||
chr4:47874744
|
A | T | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2246+383T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874744 | ||||||
chr4:47874791
|
A | C | 6 | a0002c0001t0001g0189a0002c0001t0001g0231a0002c0001t0001g0232others(3): Show | 6 | NA18961.hp2 NA18974.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.2246+336T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874791 | ||||||
chr4:47874906
|
T | C | 3 | a0002c0001t0001g0007a0002c0001t0001g0198a0002c0001t0001g0209 | 5 | HG01255.hp2 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2246+221A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874906 | ||||||
chr4:47875045
|
C | T | 1 | a0001c0003t0002g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2246+82G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47875045 | ||||||
chr4:47875107
|
T | C | 1 | a0001c0003t0002g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2246+20A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47875107 | ||||||
chr4:47875296
|
G | C | 1 | a0001c0002t0003g0162 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.2080-3C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875296 | ||||||
chr4:47875507
|
T | C | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2080-214A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875507 | ||||||
chr4:47875579
|
G | C | 1 | a0002c0001t0001g0272 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2080-286C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875579 | ||||||
chr4:47875642
|
G | A | 1 | a0010c0012t0001g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2080-349C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875642 | ||||||
chr4:47875670
|
G | A | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2080-377C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875670 | ||||||
chr4:47875823
|
C | A | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2080-530G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875823 | ||||||
chr4:47875985
|
G | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2080-692C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875985 | ||||||
chr4:47876120
|
T | C | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2080-827A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876120 | ||||||
chr4:47876254
|
G | A | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2080-961C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876254 | ||||||
chr4:47876288
|
C | T | 123 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(120): Show | 165 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2080-995G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876288 | ||||||
chr4:47876539
|
T | C | 1 | a0002c0001t0001g0285 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2080-1246A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876539 | ||||||
chr4:47876548
|
T | C | 127 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(124): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2080-1255A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876548 | ||||||
chr4:47876665
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2080-1372A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876665 | ||||||
chr4:47876708
|
G | C | 11 | a0002c0001t0001g0203a0002c0001t0001g0243a0002c0001t0001g0244others(8): Show | 11 | HG00423.hp2 HG03688.hp2 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.2080-1415C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876708 | ||||||
chr4:47876785
|
T | C | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2080-1492A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876785 | ||||||
chr4:47876932
|
A | G | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2079+1593T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876932 | ||||||
chr4:47876962
|
C | CAAAT | 127 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(124): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2079+1559_2079+156 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876962 | ||||||
chr4:47877526
|
C | T | 11 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(8): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2079+999G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877526 | ||||||
chr4:47877537
|
C | A | 52 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(49): Show | 61 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2079+988G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877537 | ||||||
chr4:47877693
|
AAAG | A | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2079+829_2079+831d others(5): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877693 | ||||||
chr4:47877987
|
G | A | 1 | a0001c0003t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2079+538C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877987 | ||||||
chr4:47878132
|
T | C | 3 | a0002c0001t0001g0274a0002c0001t0001g0275a0002c0001t0001g0277 | 3 | HG01074.hp2 HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2079+393A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878132 | ||||||
chr4:47878185
|
CAG | C | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2079+338_2079+339d others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878185 | ||||||
chr4:47878397
|
G | T | 1 | a0001c0002t0003g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2079+128C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878397 | ||||||
chr4:47878477
|
G | A | 126 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(123): Show | 169 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2079+48C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878477 | ||||||
chr4:47878725
|
T | C | 4 | a0001c0002t0001g0052a0001c0002t0001g0077a0001c0002t0001g0078others(1): Show | 4 | NA18973.hp1 NA18974.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-60A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 16/22 | chr4 | 47878725 | ||||||
chr4:47878788
|
GAATAAT | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0067a0001c0002t0001g0079 | 3 | NA18987.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1939-129_1939-124d others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 16/22 | chr4 | 47878788 | ||||||
chr4:47879085
|
C | G | 1 | a0001c0003t0002g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1938+11G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 16/22 | chr4 | 47879085 | ||||||
chr4:47879174
|
C | T | 126 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(123): Show | 169 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1917-57G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879174 | ||||||
chr4:47879575
|
T | C | 2 | a0001c0002t0001g0084a0001c0002t0001g0094 | 2 | NA18747.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1917-458A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879575 | ||||||
chr4:47879742
|
G | C | 2 | a0001c0002t0001g0059a0001c0002t0001g0080 | 2 | HG00609.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1917-625C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879742 | ||||||
chr4:47879777
|
T | C | 12 | a0002c0001t0001g0022a0002c0001t0001g0023a0002c0001t0001g0187others(9): Show | 15 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1917-660A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879777 | ||||||
chr4:47879849
|
C | A | 211 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(208): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1917-732G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879849 | ||||||
chr4:47880015
|
A | G | 1 | a0002c0001t0001g0227 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1917-898T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880015 | ||||||
chr4:47880050
|
T | C | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-933A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880050 | ||||||
chr4:47880055
|
G | A | 2 | a0002c0001t0001g0294a0002c0001t0001g0296 | 2 | NA19010.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1917-938C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880055 | ||||||
chr4:47880057
|
C | T | 11 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(8): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1917-940G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880057 | ||||||
chr4:47880082
|
A | C | 279 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(276): Show | 338 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.1917-965T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880082 | ||||||
chr4:47880137
|
T | A | 12 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(9): Show | 15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1917-1020A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880137 | ||||||
chr4:47880151
|
T | C | 2 | a0002c0001t0001g0222a0002c0001t0001g0233 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1917-1034A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880151 | ||||||
chr4:47880304
|
G | C | 2 | a0001c0002t0003g0166a0001c0002t0003g0169 | 2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1917-1187C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880304 | ||||||
chr4:47880426
|
C | CA | 22 | a0001c0002t0001g0010a0001c0002t0001g0038a0001c0002t0001g0039others(19): Show | 23 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1917-1310dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880426 | ||||||
chr4:47880426
|
CA | C | 22 | a0001c0002t0001g0067a0001c0003t0001g0030a0001c0003t0001g0031others(19): Show | 26 | HG01070.hp2 HG01243.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1917-1310delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880426 | ||||||
chr4:47880473
|
G | A | 1 | a0002c0001t0011g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1917-1356C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880473 | ||||||
chr4:47880720
|
G | A | 1 | a0002c0001t0001g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1917-1603C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880720 | ||||||
chr4:47880748
|
G | A | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1917-1631C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880748 | ||||||
chr4:47880807
|
T | TA | 11 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0042others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-1691dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | ||||||
chr4:47880807
|
TA | T | 128 | a0001c0002t0001g0065a0001c0002t0001g0082a0001c0002t0001g0083others(125): Show | 169 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1917-1691delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | ||||||
chr4:47880807
|
TAA | T | 115 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(112): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1917-1692_1917-169 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | ||||||
chr4:47880807
|
TAAA | T | 8 | a0001c0002t0001g0061a0001c0003t0001g0030a0001c0003t0001g0031others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-1693_1917-169 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | ||||||
chr4:47880820
|
A | G | 1 | a0002c0001t0001g0199 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1917-1703T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880820 | ||||||
chr4:47880824
|
A | C | 1 | a0001c0003t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1917-1707T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880824 | ||||||
chr4:47880916
|
T | C | 1 | a0002c0001t0001g0270 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1917-1799A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880916 | ||||||
chr4:47881007
|
T | C | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1917-1890A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881007 | ||||||
chr4:47881066
|
T | C | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1917-1949A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881066 | ||||||
chr4:47881456
|
T | C | 3 | a0002c0001t0001g0004a0002c0001t0001g0262a0002c0001t0001g0281 | 6 | NA18942.hp1 NA18969.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1917-2339A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881456 | ||||||
chr4:47881529
|
T | C | 211 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(208): Show | 259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1917-2412A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881529 | ||||||
chr4:47881736
|
A | G | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1916+2610T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881736 | ||||||
chr4:47881746
|
T | C | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1916+2600A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881746 | ||||||
chr4:47882143
|
ACT | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1916+2201_1916+220 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882143 | ||||||
chr4:47882203
|
A | G | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1916+2143T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882203 | ||||||
chr4:47882208
|
T | C | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1916+2138A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882208 | ||||||
chr4:47882327
|
A | G | 1 | a0001c0002t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1916+2019T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882327 | ||||||
chr4:47882365
|
G | A | 3 | a0001c0002t0003g0020a0001c0002t0003g0172a0001c0002t0003g0179 | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1916+1981C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882365 | ||||||
chr4:47882372
|
T | C | 8 | a0001c0002t0001g0015a0001c0002t0001g0056a0001c0002t0001g0057others(5): Show | 9 | HG00423.hp1 HG01934.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1916+1974A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882372 | ||||||
chr4:47882720
|
ATTGT | A | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1916+1622_1916+162 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882720 | ||||||
chr4:47882775
|
A | C | 1 | a0001c0002t0003g0161 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1916+1571T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882775 | ||||||
chr4:47882819
|
G | A | 1 | a0002c0001t0001g0250 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1916+1527C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882819 | ||||||
chr4:47883068
|
T | G | 6 | a0001c0003t0002g0017a0001c0003t0002g0054a0001c0003t0002g0114others(3): Show | 7 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1916+1278A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883068 | ||||||
chr4:47883128
|
G | C | 1 | a0001c0002t0001g0061 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1916+1218C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883128 | ||||||
chr4:47883336
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1916+1010C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883336 | ||||||
chr4:47883997
|
G | A | 10 | a0002c0001t0001g0258a0002c0001t0001g0259a0002c0001t0001g0271others(7): Show | 10 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1916+349C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883997 | ||||||
chr4:47884087
|
C | T | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1916+259G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884087 | ||||||
chr4:47884088
|
G | A | 1 | a0001c0003t0002g0101 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1916+258C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884088 | ||||||
chr4:47884101
|
A | C | 9 | a0002c0001t0001g0203a0002c0001t0001g0243a0002c0001t0001g0244others(6): Show | 9 | HG00423.hp2 NA18612.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.1916+245T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884101 | ||||||
chr4:47884302
|
A | C | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1916+44T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884302 | ||||||
chr4:47884312
|
G | T | 3 | a0001c0002t0003g0018a0001c0002t0003g0159a0001c0002t0003g0160 | 4 | HG00099.hp1 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1916+34C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884312 | ||||||
chr4:47884722
|
C | G | 64 | a0001c0003t0002g0016a0001c0003t0002g0017a0001c0003t0002g0044others(61): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1825-285G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47884722 | ||||||
chr4:47884898
|
G | A | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1825-461C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47884898 | ||||||
chr4:47885035
|
G | A | 1 | a0001c0003t0002g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1824+463C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885035 | ||||||
chr4:47885049
|
C | G | 68 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(65): Show | 78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1824+449G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885049 | ||||||
chr4:47885050
|
C | T | 1 | a0001c0003t0002g0133 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1824+448G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885050 | ||||||
chr4:47885119
|
C | T | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1824+379G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885119 | ||||||
chr4:47885188
|
T | C | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1824+310A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885188 | ||||||
chr4:47885376
|
C | T | 68 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(65): Show | 78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1824+122G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885376 | ||||||
chr4:47885491
|
C | G | 1 | a0001c0002t0001g0053 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.1824+7G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885491 | ||||||
chr4:47885700
|
T | C | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1665-43A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 13/22 | chr4 | 47885700 | ||||||
chr4:47886024
|
A | G | 1 | a0001c0003t0002g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1544-25T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886024 | ||||||
chr4:47886120
|
T | A | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1544-121A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886120 | ||||||
chr4:47886176
|
T | C | 1 | a0002c0001t0001g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1544-177A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886176 | ||||||
chr4:47886366
|
T | C | 12 | a0002c0001t0001g0007a0002c0001t0001g0025a0002c0001t0001g0198others(9): Show | 15 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1544-367A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886366 | ||||||
chr4:47886508
|
C | G | 12 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(9): Show | 15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1544-509G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886508 | ||||||
chr4:47886640
|
T | A | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1544-641A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886640 | ||||||
chr4:47886641
|
G | T | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1544-642C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886641 | ||||||
chr4:47886647
|
G | A | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1544-648C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886647 | ||||||
chr4:47886798
|
C | T | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1544-799G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886798 | ||||||
chr4:47886875
|
T | C | 68 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(65): Show | 78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1544-876A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886875 | ||||||
chr4:47886928
|
G | T | 1 | a0001c0002t0001g0058 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1544-929C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886928 | ||||||
chr4:47887066
|
C | T | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1544-1067G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887066 | ||||||
chr4:47887234
|
A | G | 1 | a0001c0003t0002g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1544-1235T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887234 | ||||||
chr4:47887340
|
T | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1544-1341A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887340 | ||||||
chr4:47887354
|
G | T | 1 | a0001c0002t0003g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1544-1355C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887354 | ||||||
chr4:47887634
|
G | A | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1544-1635C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887634 | ||||||
chr4:47887725
|
G | A | 2 | a0002c0001t0001g0202a0002c0001t0001g0236 | 2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1544-1726C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887725 | ||||||
chr4:47887867
|
G | A | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1544-1868C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887867 | ||||||
chr4:47887971
|
T | C | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1544-1972A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887971 | ||||||
chr4:47888201
|
G | T | 1 | a0002c0001t0001g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1544-2202C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888201 | ||||||
chr4:47888488
|
T | C | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+2125A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888488 | ||||||
chr4:47888533
|
T | C | 1 | a0001c0003t0002g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1543+2080A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888533 | ||||||
chr4:47888565
|
AC | A | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1543+2047delG | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888565 | ||||||
chr4:47888692
|
AC | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1920delG | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888692 | ||||||
chr4:47888694
|
T | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1919A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888694 | ||||||
chr4:47888696
|
A | T | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1917T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888696 | ||||||
chr4:47888697
|
G | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1916C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888697 | ||||||
chr4:47888699
|
C | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1914G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888699 | ||||||
chr4:47888701
|
C | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1912G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888701 | ||||||
chr4:47888702
|
T | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1911A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888702 | ||||||
chr4:47888703
|
G | A | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1910C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888703 | ||||||
chr4:47888704
|
A | G | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1909T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888704 | ||||||
chr4:47888705
|
G | C | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1908C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888705 | ||||||
chr4:47888708
|
A | C | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1905T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888708 | ||||||
chr4:47888821
|
T | C | 129 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(126): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1543+1792A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888821 | ||||||
chr4:47889051
|
T | A | 2 | a0001c0002t0003g0172a0001c0002t0003g0179 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1543+1562A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889051 | ||||||
chr4:47889083
|
G | A | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1543+1530C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889083 | ||||||
chr4:47889768
|
A | G | 3 | a0001c0002t0003g0018a0001c0002t0003g0159a0001c0002t0003g0160 | 4 | HG00099.hp1 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543+845T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889768 | ||||||
chr4:47889817
|
T | C | 1 | a0001c0003t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1543+796A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889817 | ||||||
chr4:47889936
|
C | T | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1543+677G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889936 | ||||||
chr4:47890013
|
A | G | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+600T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890013 | ||||||
chr4:47890299
|
T | C | 1 | a0001c0003t0002g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1543+314A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890299 | ||||||
chr4:47890318
|
T | C | 2 | a0001c0003t0002g0119a0001c0003t0002g0120 | 2 | HG01081.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1543+295A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890318 | ||||||
chr4:47890467
|
C | T | 1 | a0002c0001t0001g0241 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1543+146G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890467 | ||||||
chr4:47890564
|
A | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1543+49T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890564 | ||||||
chr4:47891114
|
CT | C | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1453-412delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891114 | ||||||
chr4:47891190
|
C | T | 2 | a0001c0002t0001g0042a0001c0002t0001g0043 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1453-487G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891190 | ||||||
chr4:47891278
|
G | A | 1 | a0002c0001t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1453-575C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891278 | ||||||
chr4:47891413
|
C | T | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-710G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891413 | ||||||
chr4:47891416
|
T | C | 1 | a0001c0003t0001g0032 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1453-713A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891416 | ||||||
chr4:47891601
|
A | G | 1 | a0002c0001t0001g0254 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1453-898T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891601 | ||||||
chr4:47891624
|
T | G | 1 | a0002c0001t0001g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1453-921A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891624 | ||||||
chr4:47891801
|
T | C | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453-1098A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891801 | ||||||
chr4:47891807
|
G | A | 1 | a0001c0002t0006g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-1104C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891807 | ||||||
chr4:47891830
|
C | T | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-1127G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891830 | ||||||
chr4:47891831
|
G | A | 2 | a0001c0002t0001g0034a0001c0002t0001g0039 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1453-1128C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891831 | ||||||
chr4:47891918
|
T | C | 1 | a0002c0001t0001g0237 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1453-1215A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891918 | ||||||
chr4:47892390
|
C | T | 65 | a0001c0003t0001g0115a0001c0003t0002g0016a0001c0003t0002g0017others(62): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1453-1687G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892390 | ||||||
chr4:47892427
|
G | A | 1 | a0002c0001t0001g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1453-1724C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892427 | ||||||
chr4:47892660
|
A | T | 1 | a0002c0001t0001g0226 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1452+1520T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892660 | ||||||
chr4:47892662
|
T | C | 1 | a0002c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1452+1518A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892662 | ||||||
chr4:47892667
|
C | T | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1452+1513G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892667 | ||||||
chr4:47892786
|
C | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1452+1394G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892786 | ||||||
chr4:47892868
|
A | T | 1 | a0001c0002t0001g0066 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1452+1312T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892868 | ||||||
chr4:47892932
|
C | A | 1 | a0001c0002t0001g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1452+1248G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892932 | ||||||
chr4:47893018
|
G | A | 1 | a0002c0001t0001g0239 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1452+1162C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893018 | ||||||
chr4:47893116
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+1064A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893116 | ||||||
chr4:47893136
|
G | A | 1 | a0002c0001t0001g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1452+1044C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893136 | ||||||
chr4:47893201
|
T | C | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1452+979A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893201 | ||||||
chr4:47893449
|
A | C | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1452+731T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893449 | ||||||
chr4:47893564
|
G | T | 2 | a0002c0001t0001g0026a0002c0001t0001g0225 | 3 | NA18947.hp1 NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1452+616C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893564 | ||||||
chr4:47893636
|
A | C | 68 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(65): Show | 78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1452+544T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893636 | ||||||
chr4:47893708
|
AAAAAATG others(11): Show |
A | 1 | a0002c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1452+454_1452+471d others(20): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893708 | ||||||
chr4:47893912
|
CAGTGATC others(6): Show |
C | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1452+255_1452+267d others(15): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893912 | ||||||
chr4:47893925
|
T | TAGTC | 84 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(81): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1452+254_1452+255i others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893925 | ||||||
chr4:47893992
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1452+188A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893992 | ||||||
chr4:47894040
|
T | C | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1452+140A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47894040 | ||||||
chr4:47894177
|
A | C | 1 | a0002c0001t0001g0210 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.1452+3T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47894177 | ||||||
chr4:47894309
|
G | A | 7 | a0002c0001t0001g0193a0002c0001t0001g0194a0002c0001t0001g0195others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1330-7C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894309 | ||||||
chr4:47894422
|
C | T | 11 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(8): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1330-120G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894422 | ||||||
chr4:47894461
|
T | C | 2 | a0002c0001t0001g0290a0002c0001t0011g0291 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1330-159A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894461 | ||||||
chr4:47894539
|
T | TA | 78 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(75): Show | 88 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1330-238dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894539 | ||||||
chr4:47894539
|
T | TAA | 6 | a0001c0002t0001g0053a0001c0002t0001g0061a0001c0002t0001g0062others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-239_1330-238d others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894539 | ||||||
chr4:47894539
|
TA | T | 7 | a0001c0002t0003g0176a0001c0003t0001g0045a0001c0003t0001g0046others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-238delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894539 | ||||||
chr4:47894575
|
AT | A | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1330-274delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894575 | ||||||
chr4:47894719
|
T | G | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1330-417A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894719 | ||||||
chr4:47894763
|
C | G | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1330-461G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894763 | ||||||
chr4:47894780
|
C | T | 1 | a0002c0001t0001g0262 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1330-478G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894780 | ||||||
chr4:47894909
|
G | A | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1330-607C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894909 | ||||||
chr4:47894917
|
C | T | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1330-615G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894917 | ||||||
chr4:47894990
|
A | G | 49 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0004others(46): Show | 67 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1330-688T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894990 | ||||||
chr4:47895100
|
G | C | 1 | a0002c0001t0001g0279 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1330-798C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895100 | ||||||
chr4:47895214
|
G | A | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330-912C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895214 | ||||||
chr4:47895238
|
A | T | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1330-936T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895238 | ||||||
chr4:47895454
|
T | C | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1329+1069A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895454 | ||||||
chr4:47895507
|
C | T | 4 | a0001c0002t0006g0035a0001c0002t0006g0036a0001c0002t0006g0037others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+1016G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895507 | ||||||
chr4:47895649
|
G | T | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1329+874C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895649 | ||||||
chr4:47895678
|
C | T | 2 | a0001c0002t0001g0064a0001c0002t0001g0065 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1329+845G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895678 | ||||||
chr4:47895717
|
T | C | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1329+806A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895717 | ||||||
chr4:47895861
|
T | C | 1 | a0002c0001t0001g0240 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1329+662A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895861 | ||||||
chr4:47896059
|
G | A | 11 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(8): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329+464C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896059 | ||||||
chr4:47896092
|
T | C | 48 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0004others(45): Show | 66 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1329+431A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896092 | ||||||
chr4:47896112
|
C | A | 1 | a0001c0006t0002g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1329+411G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896112 | ||||||
chr4:47896129
|
T | C | 1 | a0002c0001t0001g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1329+394A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896129 | ||||||
chr4:47896217
|
G | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1329+306C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896217 | ||||||
chr4:47896309
|
G | A | 1 | a0002c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1329+214C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896309 | ||||||
chr4:47896339
|
T | C | 6 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0308others(3): Show | 8 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+184A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896339 | ||||||
chr4:47896474
|
C | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1329+49G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896474 | ||||||
chr4:47896702
|
A | G | 1 | a0002c0001t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1205-55T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47896702 | ||||||
chr4:47896738
|
C | T | 1 | a0001c0003t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1205-91G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47896738 | ||||||
chr4:47896868
|
C | A | 1 | a0001c0003t0004g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1205-221G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47896868 | ||||||
chr4:47897309
|
C | G | 2 | a0001c0002t0001g0053a0001c0002t0001g0061 | 2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+658G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897309 | ||||||
chr4:47897352
|
G | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1204+615C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897352 | ||||||
chr4:47897502
|
C | T | 1 | a0002c0001t0001g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1204+465G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897502 | ||||||
chr4:47897546
|
C | G | 1 | a0002c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1204+421G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897546 | ||||||
chr4:47897691
|
T | G | 20 | a0001c0003t0002g0017a0001c0003t0002g0054a0001c0003t0002g0097others(17): Show | 21 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1204+276A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897691 | ||||||
chr4:47897775
|
T | A | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1204+192A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897775 | ||||||
chr4:47897780
|
T | C | 1 | a0001c0003t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1204+187A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897780 | ||||||
chr4:47897824
|
G | A | 2 | a0002c0001t0001g0241a0002c0001t0001g0242 | 2 | HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1204+143C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897824 | ||||||
chr4:47897825
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1204+142C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897825 | ||||||
chr4:47897897
|
G | A | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1204+70C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897897 | ||||||
chr4:47898169
|
CAAAT | C | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1090-92_1090-89del others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898169 | ||||||
chr4:47898320
|
A | G | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1090-239T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898320 | ||||||
chr4:47898452
|
A | G | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.1089+305T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898452 | ||||||
chr4:47898459
|
C | T | 5 | a0001c0003t0002g0113a0001c0003t0002g0118a0001c0003t0002g0122others(2): Show | 5 | NA18949.hp2 NA18961.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+298G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898459 | ||||||
chr4:47898498
|
A | G | 1 | a0002c0001t0001g0022 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1089+259T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898498 | ||||||
chr4:47898542
|
A | G | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1089+215T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898542 | ||||||
chr4:47898708
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1089+49C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898708 | ||||||
chr4:47898708
|
G | C | 2 | a0001c0003t0002g0111a0001c0003t0002g0112 | 2 | HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1089+49C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898708 | ||||||
chr4:47899138
|
C | CA | 11 | a0001c0002t0001g0060a0001c0002t0001g0088a0001c0002t0001g0089others(8): Show | 11 | HG00621.hp2 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.827-19dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | ||||||
chr4:47899138
|
CA | C | 8 | a0001c0002t0001g0063a0001c0002t0003g0157a0002c0001t0001g0216others(5): Show | 8 | HG01346.hp2 HG03225.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-19delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | ||||||
chr4:47899138
|
CAA | C | 136 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(133): Show | 182 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.827-20_827-19delTT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | ||||||
chr4:47899138
|
CAAA | C | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.827-21_827-19delTT others(1): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | ||||||
chr4:47899159
|
A | T | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-39T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899159 | ||||||
chr4:47899236
|
C | T | 1 | a0002c0001t0001g0292 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.827-116G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899236 | ||||||
chr4:47899242
|
G | A | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.827-122C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899242 | ||||||
chr4:47899298
|
A | AT | 5 | a0001c0002t0001g0303a0001c0003t0005g0029a0001c0003t0005g0299others(2): Show | 6 | HG02559.hp2 HG02630.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+71dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899298 | ||||||
chr4:47899298
|
AT | A | 13 | a0001c0002t0003g0173a0001c0003t0001g0030a0001c0003t0001g0031others(10): Show | 16 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.826+71delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899298 | ||||||
chr4:47899982
|
T | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.648-434A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47899982 | ||||||
chr4:47900084
|
G | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-536C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900084 | ||||||
chr4:47900204
|
A | G | 2 | a0002c0001t0001g0260a0002c0001t0001g0287 | 2 | NA18940.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.648-656T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900204 | ||||||
chr4:47900272
|
C | T | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.648-724G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900272 | ||||||
chr4:47900358
|
C | T | 12 | a0002c0001t0001g0007a0002c0001t0001g0025a0002c0001t0001g0198others(9): Show | 15 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.648-810G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900358 | ||||||
chr4:47900594
|
C | T | 1 | a0002c0001t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.648-1046G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900594 | ||||||
chr4:47900595
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.648-1047T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900595 | ||||||
chr4:47900600
|
T | C | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.648-1052A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900600 | ||||||
chr4:47900621
|
C | A | 2 | a0002c0001t0001g0282a0002c0001t0001g0283 | 2 | HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.648-1073G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900621 | ||||||
chr4:47900788
|
T | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.648-1240A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900788 | ||||||
chr4:47900791
|
C | T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-1243G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900791 | ||||||
chr4:47900820
|
C | T | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.648-1272G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900820 | ||||||
chr4:47901150
|
T | G | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-1602A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901150 | ||||||
chr4:47901256
|
G | C | 1 | a0001c0002t0006g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.648-1708C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901256 | ||||||
chr4:47901569
|
G | A | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.647+1624C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901569 | ||||||
chr4:47901907
|
C | T | 2 | a0002c0001t0001g0194a0002c0001t0001g0195 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.647+1286G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901907 | ||||||
chr4:47902113
|
C | T | 1 | a0001c0003t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.647+1080G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902113 | ||||||
chr4:47902436
|
C | T | 68 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(65): Show | 78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.647+757G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902436 | ||||||
chr4:47902529
|
T | C | 1 | a0001c0003t0005g0300 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.647+664A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902529 | ||||||
chr4:47902577
|
C | A | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.647+616G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902577 | ||||||
chr4:47902588
|
G | A | 3 | a0001c0003t0002g0098a0001c0003t0002g0146a0001c0003t0002g0147 | 3 | HG00733.hp1 HG01243.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.647+605C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902588 | ||||||
chr4:47902707
|
G | T | 2 | a0002c0001t0001g0258a0002c0001t0001g0259 | 2 | HG01070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.647+486C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902707 | ||||||
chr4:47902930
|
G | A | 11 | a0002c0001t0001g0203a0002c0001t0001g0243a0002c0001t0001g0244others(8): Show | 11 | HG00423.hp2 HG03688.hp2 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.647+263C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902930 | ||||||
chr4:47903141
|
A | G | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.647+52T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47903141 | ||||||
chr4:47903364
|
C | A | 1 | a0001c0002t0003g0174 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-41G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903364 | ||||||
chr4:47903509
|
G | A | 1 | a0001c0003t0002g0101 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.517-186C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903509 | ||||||
chr4:47903548
|
G | T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-225C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903548 | ||||||
chr4:47903654
|
T | C | 65 | a0001c0003t0001g0115a0001c0003t0002g0016a0001c0003t0002g0017others(62): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.517-331A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903654 | ||||||
chr4:47903727
|
G | A | 2 | a0002c0001t0001g0282a0002c0001t0001g0283 | 2 | HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.517-404C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903727 | ||||||
chr4:47903800
|
C | T | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.517-477G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903800 | ||||||
chr4:47903976
|
T | C | 1 | a0002c0001t0001g0254 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.517-653A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903976 | ||||||
chr4:47904026
|
G | A | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-703C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904026 | ||||||
chr4:47904089
|
C | G | 2 | a0001c0003t0002g0104a0001c0003t0002g0106 | 2 | HG00323.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.517-766G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904089 | ||||||
chr4:47904144
|
T | A | 1 | a0002c0001t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-821A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904144 | ||||||
chr4:47904444
|
A | T | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.516+793T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904444 | ||||||
chr4:47904447
|
C | T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+790G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904447 | ||||||
chr4:47904665
|
G | A | 1 | a0001c0004t0003g0175 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516+572C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904665 | ||||||
chr4:47904741
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+496G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904741 | ||||||
chr4:47904795
|
C | A | 117 | a0002c0001t0001g0001a0002c0001t0001g0002a0002c0001t0001g0003others(114): Show | 156 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.516+442G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904795 | ||||||
chr4:47904907
|
C | CAAACCCA others(2): Show |
217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.516+329_516+330ins others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904907 | ||||||
chr4:47905180
|
A | G | 1 | a0001c0003t0002g0098 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.516+57T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47905180 | ||||||
chr4:47905507
|
G | A | 132 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(129): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.407-161C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905507 | ||||||
chr4:47905634
|
G | C | 1 | a0002c0001t0001g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.407-288C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905634 | ||||||
chr4:47905685
|
T | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.407-339A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905685 | ||||||
chr4:47905893
|
T | C | 1 | a0002c0001t0001g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407-547A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905893 | ||||||
chr4:47905933
|
TTC | T | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-589_407-588del others(2): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905933 | ||||||
chr4:47905996
|
T | A | 12 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(9): Show | 15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.407-650A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905996 | ||||||
chr4:47906038
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.407-692C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906038 | ||||||
chr4:47906079
|
T | C | 1 | a0007c0013t0010g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.407-733A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906079 | ||||||
chr4:47906104
|
T | TGAGCAGT others(9): Show |
1 | a0001c0003t0002g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407-774_407-759dup others(16): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906104 | ||||||
chr4:47906359
|
A | G | 1 | a0001c0003t0002g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.407-1013T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906359 | ||||||
chr4:47906429
|
T | A | 1 | a0001c0002t0001g0090 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.407-1083A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906429 | ||||||
chr4:47906511
|
C | A | 6 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(3): Show | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-1165G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906511 | ||||||
chr4:47906587
|
A | T | 216 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(213): Show | 265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.407-1241T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906587 | ||||||
chr4:47906610
|
A | C | 1 | a0001c0003t0002g0120 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.407-1264T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906610 | ||||||
chr4:47906842
|
G | T | 1 | a0002c0001t0001g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.407-1496C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906842 | ||||||
chr4:47906976
|
A | C | 1 | a0001c0003t0002g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.407-1630T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906976 | ||||||
chr4:47907063
|
T | C | 1 | a0001c0003t0004g0021 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.407-1717A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907063 | ||||||
chr4:47907118
|
A | G | 2 | a0001c0003t0008g0315a0001c0003t0008g0316 | 2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.407-1772T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907118 | ||||||
chr4:47907275
|
A | G | 1 | a0002c0001t0001g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407-1929T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907275 | ||||||
chr4:47907418
|
C | T | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.407-2072G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907418 | ||||||
chr4:47907550
|
T | C | 3 | a0001c0003t0004g0182a0001c0003t0004g0185a0001c0003t0004g0186 | 3 | HG02895.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.407-2204A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907550 | ||||||
chr4:47907686
|
A | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0198a0002c0001t0001g0209 | 5 | HG01255.hp2 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-2340T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907686 | ||||||
chr4:47907773
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.407-2427G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907773 | ||||||
chr4:47907788
|
G | T | 1 | a0002c0001t0001g0206 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.407-2442C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907788 | ||||||
chr4:47907818
|
A | T | 1 | a0001c0003t0002g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.407-2472T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907818 | ||||||
chr4:47908114
|
G | A | 1 | a0002c0008t0001g0306 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.406+2710C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908114 | ||||||
chr4:47908166
|
G | A | 1 | a0002c0001t0001g0283 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.406+2658C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908166 | ||||||
chr4:47908302
|
C | T | 1 | a0001c0003t0002g0117 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.406+2522G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908302 | ||||||
chr4:47908310
|
G | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+2514C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908310 | ||||||
chr4:47908422
|
CA | C | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.406+2401delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908422 | ||||||
chr4:47908507
|
T | C | 49 | a0002c0001t0001g0002a0002c0001t0001g0003a0002c0001t0001g0004others(46): Show | 67 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.406+2317A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908507 | ||||||
chr4:47908510
|
TACTA | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.406+2310_406+2313d others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908510 | ||||||
chr4:47908677
|
C | T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+2147G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908677 | ||||||
chr4:47908678
|
T | G | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.406+2146A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908678 | ||||||
chr4:47908727
|
G | A | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+2097C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908727 | ||||||
chr4:47908731
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0091a0001c0002t0001g0092others(1): Show | 6 | NA18944.hp1 NA18952.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+2093C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908731 | ||||||
chr4:47908759
|
T | C | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.406+2065A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908759 | ||||||
chr4:47908880
|
G | A | 1 | a0001c0002t0003g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.406+1944C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908880 | ||||||
chr4:47908926
|
G | A | 139 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(136): Show | 183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.406+1898C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908926 | ||||||
chr4:47908953
|
G | A | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.406+1871C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908953 | ||||||
chr4:47908954
|
C | CA | 87 | a0001c0002t0001g0041a0001c0002t0001g0052a0001c0002t0001g0059others(84): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.406+1869dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908954 | ||||||
chr4:47908954
|
CA | C | 11 | a0002c0001t0001g0007a0002c0001t0001g0025a0002c0001t0001g0198others(8): Show | 14 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.406+1869delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908954 | ||||||
chr4:47909047
|
C | T | 1 | a0001c0003t0002g0103 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.406+1777G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909047 | ||||||
chr4:47909288
|
C | A | 1 | a0002c0001t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.406+1536G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909288 | ||||||
chr4:47909289
|
T | A | 1 | a0002c0001t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.406+1535A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909289 | ||||||
chr4:47909344
|
T | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+1480A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909344 | ||||||
chr4:47909489
|
C | T | 1 | a0001c0002t0003g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406+1335G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909489 | ||||||
chr4:47909558
|
G | A | 1 | a0002c0001t0001g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.406+1266C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909558 | ||||||
chr4:47909559
|
C | T | 3 | a0002c0001t0001g0206a0002c0001t0001g0207a0002c0001t0001g0208 | 3 | HG00609.hp1 NA18975.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.406+1265G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909559 | ||||||
chr4:47909567
|
T | C | 2 | a0002c0001t0001g0290a0002c0001t0011g0291 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.406+1257A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909567 | ||||||
chr4:47909659
|
C | CT | 58 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(55): Show | 67 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.406+1164dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909659 | ||||||
chr4:47909659
|
CT | C | 7 | a0001c0002t0003g0179a0001c0003t0002g0151a0002c0001t0001g0292others(4): Show | 7 | HG00558.hp2 HG01943.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+1164delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909659 | ||||||
chr4:47909941
|
G | A | 64 | a0001c0003t0002g0016a0001c0003t0002g0017a0001c0003t0002g0044others(61): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+883C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909941 | ||||||
chr4:47910148
|
G | A | 66 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.406+676C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910148 | ||||||
chr4:47910229
|
G | T | 1 | a0002c0001t0001g0205 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.406+595C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910229 | ||||||
chr4:47910236
|
A | G | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.406+588T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910236 | ||||||
chr4:47910263
|
A | G | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+561T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910263 | ||||||
chr4:47910313
|
C | T | 1 | a0001c0003t0002g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.406+511G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910313 | ||||||
chr4:47910396
|
A | C | 1 | a0001c0003t0002g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.406+428T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910396 | ||||||
chr4:47910428
|
G | A | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.406+396C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910428 | ||||||
chr4:47910530
|
C | T | 10 | a0001c0003t0002g0103a0001c0003t0002g0104a0001c0003t0002g0105others(7): Show | 10 | HG00323.hp2 HG00738.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+294G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910530 | ||||||
chr4:47910631
|
T | C | 1 | a0002c0001t0001g0204 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.406+193A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910631 | ||||||
chr4:47911110
|
C | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.236-116G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911110 | ||||||
chr4:47911139
|
T | G | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.236-145A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911139 | ||||||
chr4:47911234
|
G | A | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236-240C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911234 | ||||||
chr4:47911459
|
C | T | 8 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(5): Show | 11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.236-465G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911459 | ||||||
chr4:47911663
|
T | C | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.236-669A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911663 | ||||||
chr4:47912324
|
T | C | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1330A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912324 | ||||||
chr4:47912345
|
C | A | 72 | a0001c0003t0001g0099a0001c0003t0001g0115a0001c0003t0002g0016others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.236-1351G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912345 | ||||||
chr4:47912461
|
C | CT | 57 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0011others(54): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.236-1468dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912461 | ||||||
chr4:47912461
|
CT | C | 219 | a0001c0002t0001g0042a0001c0002t0001g0043a0001c0002t0003g0180others(216): Show | 268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.236-1468delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912461 | ||||||
chr4:47912499
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235+1470C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912499 | ||||||
chr4:47912528
|
C | T | 217 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(214): Show | 266 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.235+1441G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912528 | ||||||
chr4:47912607
|
T | C | 285 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(282): Show | 344 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.235+1362A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912607 | ||||||
chr4:47912611
|
A | AC | 18 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0057others(15): Show | 18 | HG00621.hp1 HG01175.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+1357dupG | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912611 | ||||||
chr4:47912612
|
C | T | 1 | a0001c0003t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+1357G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912612 | ||||||
chr4:47912829
|
T | TA | 9 | a0001c0003t0002g0155a0002c0001t0001g0193a0002c0001t0001g0194others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+1139dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912829 | ||||||
chr4:47912830
|
A | G | 1 | a0001c0003t0002g0098 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.235+1139T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912830 | ||||||
chr4:47912880
|
G | A | 68 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(65): Show | 78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.235+1089C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912880 | ||||||
chr4:47912995
|
C | G | 1 | a0001c0002t0001g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.235+974G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912995 | ||||||
chr4:47913011
|
CA | C | 8 | a0001c0002t0001g0034a0001c0003t0001g0045a0001c0003t0002g0152others(5): Show | 8 | HG00558.hp1 HG00741.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+957delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | ||||||
chr4:47913011
|
CAA | C | 191 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(188): Show | 237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.235+956_235+957del others(2): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | ||||||
chr4:47913011
|
CAAA | C | 15 | a0001c0003t0002g0097a0002c0001t0001g0022a0002c0001t0001g0023others(12): Show | 18 | HG01070.hp1 HG01167.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+955_235+957del others(3): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | ||||||
chr4:47913011
|
CAAAAA | C | 52 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0012others(49): Show | 60 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.235+953_235+957del others(5): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | ||||||
chr4:47913011
|
CAAAAAA | C | 5 | a0001c0002t0001g0011a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 6 | HG02132.hp1 NA18974.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+952_235+957del others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | ||||||
chr4:47913047
|
T | C | 3 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+922A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913047 | ||||||
chr4:47913174
|
C | A | 1 | a0002c0001t0001g0301 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.235+795G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913174 | ||||||
chr4:47913311
|
T | C | 139 | a0001c0003t0004g0021a0001c0003t0004g0182a0001c0003t0004g0183others(136): Show | 183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.235+658A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913311 | ||||||
chr4:47913420
|
G | A | 133 | a0001c0003t0005g0029a0001c0003t0005g0299a0001c0003t0005g0300others(130): Show | 176 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.235+549C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913420 | ||||||
chr4:47913532
|
A | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+437T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913532 | ||||||
chr4:47913547
|
C | G | 1 | a0001c0003t0002g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235+422G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913547 | ||||||
chr4:47913658
|
C | A | 1 | a0001c0003t0002g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235+311G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913658 | ||||||
chr4:47913689
|
C | T | 11 | a0001c0002t0001g0010a0001c0002t0001g0034a0001c0002t0001g0038others(8): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+280G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913689 | ||||||
chr4:47913955
|
G | A | 1 | a0001c0002t0001g0303 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+14C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913955 | ||||||
chr4:47914216
|
GA | G | 7 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(4): Show | 10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-12delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/22 | chr4 | 47914216 | ||||||
chr4:47914309
|
G | A | 7 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(4): Show | 10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-3+56C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/22 | chr4 | 47914309 | ||||||
chr4:47914329
|
C | G | 313 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0010others(310): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.-3+36G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/22 | chr4 | 47914329 |