geneid | 84154 |
---|---|
ensemblid | ENSG00000197498.13 |
hgncid | 20870 |
symbol | RPF2 |
name | ribosome production factor 2 homolog |
refseq_nuc | NM_032194.3 |
refseq_prot | NP_115570.1 |
ensembl_nuc | ENST00000441448.7 |
ensembl_prot | ENSP00000402338.2 |
mane_status | MANE Select |
chr | chr6 |
start | 110982038 |
end | 111028263 |
strand | + |
ver | v1.2 |
region | chr6:110982038-111028263 |
region5000 | chr6:110977038-111033263 |
regionname0 | RPF2_chr6_110982038_111028263 |
regionname5000 | RPF2_chr6_110977038_111033263 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 306 | 345 | 63 | 65 | 159 | 10 | 46 | 122 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0002 | 0/0 | 306 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0003 | 0/0 | 306 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0004 | 0/0 | 306 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0005 | 0/0 | 306 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0006 | 0/0 | 306 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0007 | 0/0 | 303 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 921 | 343 | 61 | 65 | 159 | 10 | 46 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0002 | 0/0 | 921 | 6 | 5 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0003 | 0/0 | 921 | 4 | 4 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0004 | 0/0 | 921 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0005 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0006 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0007 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0008 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
c0009 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2751 | 119 | 5 | 26 | 67 | 3 | 18 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0002 | 0/0 | 2751 | 84 | 14 | 9 | 46 | 3 | 12 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0003 | 0/0 | 2756 | 57 | 16 | 8 | 25 | 0 | 8 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0004 | 1/1 | 2751 | 41 | 14 | 15 | 1 | 4 | 5 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0005 | 0/0 | 2751 | 10 | 0 | 0 | 10 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0006 | 0/0 | 2757 | 8 | 1 | 3 | 2 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0007 | 0/0 | 2756 | 7 | 7 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0008 | 0/0 | 2751 | 5 | 5 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0009 | 0/0 | 2751 | 3 | 3 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0010 | 0/0 | 2756 | 3 | 2 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0011 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0012 | 0/0 | 2751 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0013 | 0/0 | 2756 | 2 | 1 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0014 | 0/0 | 2756 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0015 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0016 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0017 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0018 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0019 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0020 | 0/0 | 2752 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0021 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0022 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0023 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0024 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0025 | 0/0 | 2756 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0026 | 0/0 | 2756 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0027 | 0/0 | 2756 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
t0028 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
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 | 5 | 0 | 4 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 921 | 343 | 61 | 65 | 159 | 10 | 46 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0005 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0006 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0002c0002 | 0/0 | 921 | 6 | 5 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0003c0003 | 0/0 | 921 | 4 | 4 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0004c0004 | 0/0 | 921 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0005c0009 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0006c0008 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0007c0007 | 0/0 | 921 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3671 | 118 | 5 | 26 | 66 | 3 | 18 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0002 | 0/0 | 3671 | 82 | 12 | 9 | 46 | 3 | 12 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0003 | 0/0 | 3676 | 55 | 14 | 8 | 25 | 0 | 8 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0004 | 1/1 | 3671 | 38 | 11 | 15 | 1 | 4 | 5 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0005 | 0/0 | 3671 | 10 | 0 | 0 | 10 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0006 | 0/0 | 3677 | 8 | 1 | 3 | 2 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0007 | 0/0 | 3676 | 6 | 6 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0008 | 0/0 | 3671 | 5 | 5 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0011 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0012 | 0/0 | 3671 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0013 | 0/0 | 3676 | 2 | 1 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0014 | 0/0 | 3676 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0015 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0016 | 0/0 | 3671 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0017 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0019 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0020 | 0/0 | 3672 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0021 | 0/0 | 3677 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0022 | 0/0 | 3677 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0023 | 0/0 | 3677 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0024 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0025 | 0/0 | 3676 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0026 | 0/0 | 3676 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0001t0028 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0005t0027 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0001c0006t0004 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0002c0002t0009 | 0/0 | 3671 | 3 | 3 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0002c0002t0010 | 0/0 | 3676 | 3 | 2 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0003c0003t0003 | 0/0 | 3676 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0003c0003t0004 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0004c0004t0002 | 0/0 | 3671 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0005c0009t0001 | 0/0 | 3671 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0006c0008t0007 | 0/0 | 3676 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
a0007c0007t0018 | 0/0 | 3671 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | copy fasta | chr6 | 110977038 | 111033263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0012g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0012g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0013g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0014g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0016g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0017g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0019g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0020g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0021g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0022g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0024g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0025g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0026g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0001t0028g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0005t0027g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0001c0006t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0002c0002t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0002c0002t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0002c0002t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0002c0002t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0002c0002t0010g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0002c0002t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0003c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0003c0003t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0003c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0003c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0004c0004t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0004c0004t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0005c0009t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0006c0008t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
a0007c0007t0018g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0091 | EUR | FIN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | CHS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00741 | hp1 | a0001 | c0001 | t0013 | g0186 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01109 | hp1 | a0001 | c0001 | t0025 | g0165 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01346 | hp1 | a0001 | c0001 | t0016 | g0036 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01433 | hp2 | a0002 | c0002 | t0010 | g0321 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0073 | EUR | IBS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0092 | EUR | IBS | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01884 | hp1 | a0003 | c0003 | t0004 | g0100 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0188 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01952 | hp1 | a0001 | c0001 | t0022 | g0121 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02040 | hp2 | a0005 | c0009 | t0001 | g0071 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02055 | hp1 | a0004 | c0004 | t0002 | g0318 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02083 | hp2 | a0001 | c0001 | t0026 | g0154 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02135 | hp2 | a0001 | c0001 | t0014 | g0254 | EAS | KHV | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02258 | hp1 | a0003 | c0003 | t0003 | g0099 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02258 | hp2 | a0001 | c0006 | t0004 | g0024 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PEL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02280 | hp2 | a0001 | c0001 | t0013 | g0152 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02572 | hp1 | a0003 | c0003 | t0003 | g0185 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02647 | hp2 | a0002 | c0002 | t0009 | g0323 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02683 | hp1 | a0001 | c0001 | t0023 | g0114 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02717 | hp1 | a0001 | c0001 | t0021 | g0026 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0273 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02818 | hp1 | a0004 | c0004 | t0002 | g0286 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02895 | hp1 | a0006 | c0008 | t0007 | g0097 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0284 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0283 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02965 | hp2 | a0002 | c0002 | t0010 | g0320 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03139 | hp1 | a0007 | c0007 | t0018 | g0183 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03195 | hp1 | a0002 | c0002 | t0009 | g0324 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0066 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03486 | hp1 | a0001 | c0005 | t0027 | g0038 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03516 | hp2 | a0003 | c0003 | t0004 | g0098 | AFR | ESN | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0305 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0264 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0030 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0088 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0124 | SAS | BEB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0180 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18522 | hp1 | a0002 | c0002 | t0010 | g0319 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0285 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0333 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | CHB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18940 | hp2 | a0001 | c0001 | t0024 | g0234 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18969 | hp2 | a0001 | c0001 | t0028 | g0244 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18987 | hp1 | a0001 | c0001 | t0012 | g0327 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18998 | hp2 | a0001 | c0001 | t0020 | g0203 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18999 | hp2 | a0001 | c0001 | t0014 | g0298 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | LWK | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19043 | hp2 | a0001 | c0001 | t0015 | g0187 | AFR | LWK | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19067 | hp2 | a0001 | c0001 | t0019 | g0213 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19083 | hp1 | a0001 | c0001 | t0012 | g0311 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | YRI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | ASW | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0314 | EUR | TSI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0331 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02486 | hp1 | a0002 | c0002 | t0009 | g0322 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0330 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | MSL | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | USA | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0076 | REF | REF | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0084 | REF | REF | RPF2_chr6_110977038_111033263 | RPF2 | chr6 | 110977038 | 111033263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110985104
|
C | G | 1 | a0003 | 4 | HG01884.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.122C>G | p.Ala41Gly | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/10 | 191/3671 | 122/921 | 41/306 | chr6 | 110985104 | ||
chr6:110985106
|
A | C | 1 | a0005 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.124A>C | p.Asn42His | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/10 | 193/3671 | 124/921 | 42/306 | chr6 | 110985106 | ||
chr6:110989049
|
G | A | 1 | a0002 | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
missense_variant | MODERATE | c.178G>A | p.Gly60Ser | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/10 | 247/3671 | 178/921 | 60/306 | chr6 | 110989049 | ||
chr6:111015836
|
G | T | 1 | a0004 | 2 | HG02055.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.576G>T | p.Lys192Asn | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/10 | 645/3671 | 576/921 | 192/306 | chr6 | 111015836 | ||
chr6:111025538
|
A | G | 1 | a0006 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.877A>G | p.Thr293Ala | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 946/3671 | 877/921 | 293/306 | chr6 | 111025538 | ||
chr6:111025571
|
A | T | 1 | a0007 | 1 | HG03139.hp1 | stop_gained | HIGH | c.910A>T | p.Lys304* | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 979/3671 | 910/921 | 304/306 | chr6 | 111025571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110985054
|
G | A | 1 | a0001c0005 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.72G>A | p.Pro24Pro | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/10 | 141/3671 | 72/921 | 24/306 | chr6 | 110985054 | ||
chr6:111025498
|
G | A | 1 | a0001c0006 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.837G>A | p.Arg279Arg | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 906/3671 | 837/921 | 279/306 | chr6 | 111025498 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110982051
|
T | C | 2 | a0002c0002t0009a0002c0002t0010 | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-56T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/10 | 56 | chr6 | 110982051 | |||||
chr6:110982059
|
G | T | 1 | a0001c0001t0028 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/10 | 48 | chr6 | 110982059 | |||||
chr6:110982093
|
A | G | 1 | a0001c0001t0015 | 2 | HG01884.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-14A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/10 | 14 | chr6 | 110982093 | |||||
chr6:111025603
|
C | T | 10 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(7): Show | 74 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*21C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 21 | chr6 | 111025603 | |||||
chr6:111025605
|
G | A | 6 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(3): Show | 63 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 23 | chr6 | 111025605 | |||||
chr6:111025640
|
G | A | 6 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(3): Show | 63 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*58G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 58 | chr6 | 111025640 | |||||
chr6:111025808
|
C | T | 1 | a0001c0001t0024 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 226 | chr6 | 111025808 | |||||
chr6:111025921
|
G | A | 1 | a0001c0001t0011 | 2 | HG03041.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*339G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 339 | chr6 | 111025921 | |||||
chr6:111025936
|
G | A | 1 | a0001c0001t0016 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 354 | chr6 | 111025936 | |||||
chr6:111025943
|
C | T | 2 | a0001c0001t0007a0006c0008t0007 | 7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 361 | chr6 | 111025943 | |||||
chr6:111026017
|
A | ACTTTT | 14 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(11): Show | 85 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*440dupCTTTT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 441 | INFO_REALIGN_3_PRIME | chr6 | 111026017 | ||||
chr6:111026192
|
C | T | 2 | a0001c0001t0006a0001c0001t0023 | 9 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 610 | chr6 | 111026192 | |||||
chr6:111026319
|
T | C | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*737T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 737 | chr6 | 111026319 | |||||
chr6:111026371
|
C | CT | 5 | a0001c0001t0006a0001c0001t0020a0001c0001t0021others(2): Show | 12 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*800dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 801 | INFO_REALIGN_3_PRIME | chr6 | 111026371 | ||||
chr6:111026446
|
C | T | 1 | a0001c0001t0019 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*864C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 864 | chr6 | 111026446 | |||||
chr6:111026624
|
G | A | 3 | a0001c0001t0006a0001c0001t0023a0002c0002t0010 | 12 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1042G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1042 | chr6 | 111026624 | |||||
chr6:111026777
|
A | C | 1 | a0001c0001t0008 | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1195A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1195 | chr6 | 111026777 | |||||
chr6:111026819
|
A | T | 14 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(11): Show | 85 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1237A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1237 | chr6 | 111026819 | |||||
chr6:111026843
|
G | A | 1 | a0001c0001t0017 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1261G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1261 | chr6 | 111026843 | |||||
chr6:111026881
|
T | G | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*1299T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1299 | chr6 | 111026881 | |||||
chr6:111026978
|
A | C | 1 | a0001c0001t0005 | 10 | HG00423.hp2 NA18612.hp2 NA18968.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1396A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1396 | chr6 | 111026978 | |||||
chr6:111027035
|
G | A | 3 | a0001c0001t0006a0001c0001t0021a0001c0001t0023 | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1453G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1453 | chr6 | 111027035 | |||||
chr6:111027206
|
G | A | 1 | a0001c0001t0013 | 2 | HG00741.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1624G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1624 | chr6 | 111027206 | |||||
chr6:111027229
|
A | G | 1 | a0001c0001t0026 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1647A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1647 | chr6 | 111027229 | |||||
chr6:111027279
|
C | A | 1 | a0001c0001t0019 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1697C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1697 | chr6 | 111027279 | |||||
chr6:111027280
|
T | G | 1 | a0001c0001t0019 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1698T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1698 | chr6 | 111027280 | |||||
chr6:111027351
|
C | T | 10 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(7): Show | 74 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1769C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1769 | chr6 | 111027351 | |||||
chr6:111027429
|
G | C | 1 | a0001c0001t0012 | 2 | NA18987.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1847G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1847 | chr6 | 111027429 | |||||
chr6:111027460
|
G | A | 1 | a0007c0007t0018 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1878G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1878 | chr6 | 111027460 | |||||
chr6:111027483
|
C | A | 1 | a0001c0001t0025 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1901C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 1901 | chr6 | 111027483 | |||||
chr6:111027590
|
C | T | 1 | a0001c0001t0023 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2008C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2008 | chr6 | 111027590 | |||||
chr6:111027995
|
T | C | 3 | a0001c0001t0006a0001c0001t0021a0001c0001t0023 | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2413T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2413 | chr6 | 111027995 | |||||
chr6:111028112
|
A | T | 1 | a0001c0001t0014 | 2 | HG02135.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2530 | chr6 | 111028112 | |||||
chr6:111028248
|
A | C | 5 | a0001c0001t0002a0001c0001t0008a0002c0002t0009others(2): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2666A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2666 | chr6 | 111028248 | |||||
chr6:111028258
|
A | C | 1 | a0001c0001t0013 | 2 | HG00741.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2676A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 10/10 | 2676 | chr6 | 111028258 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110982276
|
C | G | 1 | a0001c0001t0003g0338 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.23+147C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982276 | ||||||
chr6:110982317
|
A | C | 3 | a0001c0001t0002g0336a0001c0001t0002g0337a0001c0001t0003g0335 | 3 | HG00438.hp1 HG00621.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.23+188A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982317 | ||||||
chr6:110982417
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0003g0020 | 3 | HG00099.hp1 HG01169.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.23+288G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982417 | ||||||
chr6:110982539
|
A | G | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+410A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982539 | ||||||
chr6:110982681
|
C | T | 1 | a0001c0001t0002g0334 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.23+552C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982681 | ||||||
chr6:110982700
|
A | G | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+571A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982700 | ||||||
chr6:110982733
|
C | G | 2 | a0001c0001t0005g0332a0001c0001t0005g0333 | 2 | NA18612.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.23+604C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982733 | ||||||
chr6:110982771
|
A | G | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+642A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982771 | ||||||
chr6:110982868
|
G | A | 3 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG00597.hp1 NA18940.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.23+739G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982868 | ||||||
chr6:110982948
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0004g0022 | 2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.23+819T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982948 | ||||||
chr6:110982957
|
A | G | 2 | a0001c0001t0015g0187a0001c0001t0015g0188 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.23+828A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110982957 | ||||||
chr6:110983055
|
G | T | 1 | a0001c0001t0013g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.23+926G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983055 | ||||||
chr6:110983244
|
A | G | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+1115A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983244 | ||||||
chr6:110983355
|
GT | G | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+1235delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110983355 | |||||
chr6:110983371
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0004g0025others(2): Show | 5 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+1242G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983371 | ||||||
chr6:110983552
|
C | G | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.23+1423C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983552 | ||||||
chr6:110983611
|
T | C | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.24-1395T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983611 | ||||||
chr6:110983764
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.24-1242G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983764 | ||||||
chr6:110983801
|
GGGT | G | 83 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(80): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.24-1202_24-1200del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110983801 | |||||
chr6:110983803
|
GT | G | 45 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(42): Show | 45 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.24-1202delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983803 | ||||||
chr6:110983804
|
T | G | 17 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(14): Show | 17 | HG02027.hp2 HG02071.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.24-1202T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983804 | ||||||
chr6:110983844
|
A | G | 15 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(12): Show | 15 | HG01257.hp2 HG02071.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.24-1162A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983844 | ||||||
chr6:110983856
|
C | T | 1 | a0001c0001t0007g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.24-1150C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983856 | ||||||
chr6:110983902
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0004g0025others(2): Show | 5 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.24-1104G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983902 | ||||||
chr6:110983921
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.24-1085C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983921 | ||||||
chr6:110983983
|
C | T | 1 | a0003c0003t0003g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.24-1023C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110983983 | ||||||
chr6:110984007
|
C | G | 62 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.24-999C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984007 | ||||||
chr6:110984084
|
A | G | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.24-922A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984084 | ||||||
chr6:110984097
|
A | T | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.24-909A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984097 | ||||||
chr6:110984252
|
G | C | 1 | a0001c0001t0003g0338 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.24-754G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984252 | ||||||
chr6:110984331
|
T | TAAAGTTT others(5): Show |
1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.24-671_24-660dupGT others(10): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984331 | |||||
chr6:110984334
|
A | G | 62 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.24-672A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984334 | ||||||
chr6:110984394
|
C | T | 92 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(89): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.24-612C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984394 | ||||||
chr6:110984482
|
T | A | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.24-524T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984482 | ||||||
chr6:110984562
|
C | T | 1 | a0007c0007t0018g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.24-444C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984562 | ||||||
chr6:110984652
|
C | G | 60 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0131others(57): Show | 62 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.24-354C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984652 | ||||||
chr6:110984774
|
A | G | 4 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128others(1): Show | 4 | HG02818.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-232A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984774 | ||||||
chr6:110984789
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.24-217A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984789 | ||||||
chr6:110984841
|
A | AAAAC | 178 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(175): Show | 184 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.24-157_24-154dupCA others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984841 | |||||
chr6:110984849
|
C | CAAACA | 8 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG02129.hp2 HG02738.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.24-154_24-153insCA others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984849 | |||||
chr6:110984881
|
A | AT | 92 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(89): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.24-117dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 110984881 | |||||
chr6:110984890
|
A | T | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.24-116A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984890 | ||||||
chr6:110984958
|
A | T | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.24-48A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 1/9 | chr6 | 110984958 | ||||||
chr6:110985150
|
T | A | 5 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(2): Show | 5 | HG02738.hp2 HG03579.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+12T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985150 | ||||||
chr6:110985245
|
A | G | 1 | a0001c0001t0006g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.156+107A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985245 | ||||||
chr6:110985422
|
A | T | 62 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.156+284A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985422 | ||||||
chr6:110985445
|
A | T | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+307A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985445 | ||||||
chr6:110985472
|
AC | A | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+335delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985472 | ||||||
chr6:110985544
|
G | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0006t0004g0024 | 3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.156+406G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985544 | ||||||
chr6:110985591
|
C | G | 3 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0022g0121 | 3 | HG01952.hp1 HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.156+453C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985591 | ||||||
chr6:110985667
|
C | T | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+529C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985667 | ||||||
chr6:110985678
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.156+540G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985678 | ||||||
chr6:110985767
|
G | A | 15 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(12): Show | 16 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+629G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985767 | ||||||
chr6:110985794
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.156+656C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985794 | ||||||
chr6:110985852
|
C | T | 1 | a0001c0001t0003g0181 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.156+714C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985852 | ||||||
chr6:110985885
|
T | C | 186 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(183): Show | 192 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.156+747T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985885 | ||||||
chr6:110985886
|
C | G | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+748C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985886 | ||||||
chr6:110985886
|
C | T | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.156+748C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985886 | ||||||
chr6:110985887
|
G | A | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+749G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985887 | ||||||
chr6:110985901
|
G | GCA | 187 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(184): Show | 193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.156+764_156+765ins others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985901 | |||||
chr6:110985903
|
T | A | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+765T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985903 | ||||||
chr6:110985934
|
TC | T | 4 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0001t0021g0026others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+797delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110985934 | ||||||
chr6:110985935
|
C | CA | 88 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0131others(85): Show | 92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.156+815dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985935 | |||||
chr6:110985935
|
CA | C | 26 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0240others(23): Show | 26 | HG01433.hp2 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.156+815delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985935 | |||||
chr6:110985935
|
CAA | C | 14 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(11): Show | 15 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.156+814_156+815del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110985935 | |||||
chr6:110986204
|
A | T | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.156+1066A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986204 | ||||||
chr6:110986229
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.156+1091C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986229 | ||||||
chr6:110986235
|
A | G | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1097A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986235 | ||||||
chr6:110986293
|
G | A | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.156+1155G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986293 | ||||||
chr6:110986410
|
A | G | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.156+1272A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986410 | ||||||
chr6:110986424
|
A | G | 4 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+1286A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986424 | ||||||
chr6:110986474
|
C | T | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+1336C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986474 | ||||||
chr6:110986494
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0021g0026 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.156+1356T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986494 | ||||||
chr6:110986531
|
G | A | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1393G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986531 | ||||||
chr6:110986650
|
T | A | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1512T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986650 | ||||||
chr6:110986651
|
A | G | 92 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(89): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.156+1513A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986651 | ||||||
chr6:110986680
|
A | G | 182 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(179): Show | 187 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.156+1542A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986680 | ||||||
chr6:110986720
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.156+1582G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986720 | ||||||
chr6:110986769
|
C | T | 12 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0179others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+1631C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986769 | ||||||
chr6:110986811
|
C | G | 188 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(185): Show | 194 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.156+1673C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986811 | ||||||
chr6:110986858
|
C | A | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1720C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986858 | ||||||
chr6:110986868
|
G | C | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.156+1730G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986868 | ||||||
chr6:110986872
|
G | A | 1 | a0001c0001t0002g0243 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.156+1734G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986872 | ||||||
chr6:110986930
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.156+1792C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986930 | ||||||
chr6:110986971
|
A | G | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+1833A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986971 | ||||||
chr6:110986971
|
A | T | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.156+1833A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110986971 | ||||||
chr6:110987208
|
C | CACCA | 3 | a0001c0001t0002g0015a0001c0001t0002g0253a0001c0001t0014g0254 | 4 | HG02135.hp2 NA18612.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1819_157-1816d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110987208 | |||||
chr6:110987257
|
C | T | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1771C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987257 | ||||||
chr6:110987304
|
C | A | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1724C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987304 | ||||||
chr6:110987305
|
C | G | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1723C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987305 | ||||||
chr6:110987305
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0021g0026 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.157-1723C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987305 | ||||||
chr6:110987402
|
A | G | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1626A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987402 | ||||||
chr6:110987472
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0006t0004g0024 | 3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.157-1556T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987472 | ||||||
chr6:110987530
|
A | G | 149 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(146): Show | 153 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.157-1498A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987530 | ||||||
chr6:110987550
|
A | T | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1478A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987550 | ||||||
chr6:110987553
|
A | G | 1 | a0001c0001t0002g0326 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.157-1475A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987553 | ||||||
chr6:110987663
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.157-1365G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987663 | ||||||
chr6:110987819
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.157-1209T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987819 | ||||||
chr6:110987822
|
T | G | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1206T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987822 | ||||||
chr6:110987831
|
T | G | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1197T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987831 | ||||||
chr6:110987868
|
T | A | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1160T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987868 | ||||||
chr6:110987952
|
T | C | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-1076T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987952 | ||||||
chr6:110987953
|
G | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-1075G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110987953 | ||||||
chr6:110988050
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.157-978C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988050 | ||||||
chr6:110988340
|
A | G | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-688A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988340 | ||||||
chr6:110988370
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.157-658G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988370 | ||||||
chr6:110988388
|
G | A | 321 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.157-640G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988388 | ||||||
chr6:110988434
|
C | CT | 6 | a0001c0001t0001g0008a0001c0001t0001g0079a0001c0001t0001g0080others(3): Show | 7 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-577dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110988434 | |||||
chr6:110988434
|
CTTT | C | 151 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(148): Show | 156 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.157-579_157-577del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 110988434 | |||||
chr6:110988552
|
T | C | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.157-476T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988552 | ||||||
chr6:110988648
|
G | T | 62 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.157-380G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988648 | ||||||
chr6:110988662
|
C | T | 7 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(4): Show | 7 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-366C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988662 | ||||||
chr6:110988836
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.157-192A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 2/9 | chr6 | 110988836 | ||||||
chr6:110989179
|
TAC | T | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.194+116_194+117del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989179 | |||||
chr6:110989182
|
A | C | 3 | a0001c0001t0002g0120a0001c0001t0003g0118a0001c0001t0003g0119 | 3 | HG02922.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.194+117A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989182 | ||||||
chr6:110989201
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.194+136T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989201 | ||||||
chr6:110989202
|
C | CT | 153 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(150): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.194+140dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989202 | |||||
chr6:110989202
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.194+137C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989202 | ||||||
chr6:110989216
|
G | A | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.194+151G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989216 | ||||||
chr6:110989225
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.194+160A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989225 | ||||||
chr6:110989476
|
C | T | 60 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0131others(57): Show | 62 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.194+411C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989476 | ||||||
chr6:110989477
|
G | A | 154 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.194+412G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989477 | ||||||
chr6:110989482
|
C | T | 1 | a0005c0009t0001g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.194+417C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989482 | ||||||
chr6:110989523
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.194+458T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989523 | ||||||
chr6:110989627
|
G | GT | 24 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(21): Show | 24 | HG00438.hp1 HG00544.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.194+579dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989627 | |||||
chr6:110989627
|
GT | G | 32 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(29): Show | 33 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.194+579delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989627 | |||||
chr6:110989666
|
G | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.194+601G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989666 | ||||||
chr6:110989746
|
C | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.194+681C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989746 | ||||||
chr6:110989783
|
C | G | 1 | a0001c0001t0008g0305 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.194+718C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989783 | ||||||
chr6:110989918
|
C | T | 1 | a0001c0001t0011g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.194+853C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989918 | ||||||
chr6:110989945
|
C | CT | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+890dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110989945 | |||||
chr6:110989951
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.194+886T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110989951 | ||||||
chr6:110990007
|
A | G | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194+942A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990007 | ||||||
chr6:110990218
|
G | A | 15 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(12): Show | 16 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+1153G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990218 | ||||||
chr6:110990227
|
C | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0243 | 3 | NA18942.hp2 NA18961.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.194+1162C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990227 | ||||||
chr6:110990233
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.194+1168C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990233 | ||||||
chr6:110990268
|
T | TC | 187 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(184): Show | 193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.194+1204dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990268 | |||||
chr6:110990448
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0021g0026 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.195-1299A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990448 | ||||||
chr6:110990520
|
T | C | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.195-1227T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990520 | ||||||
chr6:110990559
|
A | AC | 63 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0058others(60): Show | 68 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.195-1174dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | |||||
chr6:110990559
|
AC | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(59): Show | 65 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.195-1174delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | |||||
chr6:110990559
|
ACC | A | 45 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0219others(42): Show | 46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.195-1175_195-1174d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | |||||
chr6:110990559
|
ACCC | A | 48 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(45): Show | 51 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.195-1176_195-1174d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990559 | |||||
chr6:110990570
|
C | G | 24 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0109others(21): Show | 25 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.195-1177C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990570 | ||||||
chr6:110990571
|
C | G | 4 | a0001c0001t0001g0027a0001c0001t0002g0107a0001c0001t0006g0106others(1): Show | 4 | HG01952.hp1 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1176C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990571 | ||||||
chr6:110990571
|
CCCA | C | 24 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0109others(21): Show | 25 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.195-1173_195-1171d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990571 | |||||
chr6:110990572
|
C | G | 5 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0001t0004g0122others(2): Show | 5 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-1175C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990572 | ||||||
chr6:110990573
|
CA | C | 5 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0001t0004g0122others(2): Show | 5 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-1173delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990573 | ||||||
chr6:110990576
|
C | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-1171C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990576 | ||||||
chr6:110990730
|
GC | G | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-1014delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110990730 | |||||
chr6:110990749
|
T | A | 1 | a0001c0001t0016g0036 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.195-998T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990749 | ||||||
chr6:110990753
|
A | G | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0125 | 3 | NA18943.hp2 NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.195-994A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990753 | ||||||
chr6:110990941
|
T | C | 1 | a0001c0001t0003g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.195-806T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110990941 | ||||||
chr6:110991121
|
T | A | 187 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(184): Show | 193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.195-626T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991121 | ||||||
chr6:110991353
|
C | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-394C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991353 | ||||||
chr6:110991373
|
A | G | 188 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(185): Show | 194 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.195-374A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991373 | ||||||
chr6:110991398
|
C | CT | 31 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(28): Show | 32 | HG00621.hp2 HG00642.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.195-333dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110991398 | |||||
chr6:110991398
|
CT | C | 6 | a0001c0001t0002g0140a0001c0001t0002g0260a0001c0001t0003g0013others(3): Show | 7 | HG02602.hp1 HG03490.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-333delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 110991398 | |||||
chr6:110991414
|
T | A | 3 | a0001c0001t0017g0285a0004c0004t0002g0286a0004c0004t0002g0318 | 3 | HG02055.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.195-333T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991414 | ||||||
chr6:110991416
|
A | G | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-331A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991416 | ||||||
chr6:110991614
|
G | A | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.195-133G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 3/9 | chr6 | 110991614 | ||||||
chr6:110991801
|
C | A | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.234+15C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991801 | ||||||
chr6:110991869
|
AT | A | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+90delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110991869 | |||||
chr6:110991894
|
C | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+108C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991894 | ||||||
chr6:110991925
|
G | T | 1 | a0001c0001t0012g0327 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.234+139G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991925 | ||||||
chr6:110991952
|
G | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(30): Show | 34 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+166G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991952 | ||||||
chr6:110991986
|
T | C | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.234+200T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110991986 | ||||||
chr6:110992033
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | NA18950.hp1 NA18964.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+247G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992033 | ||||||
chr6:110992034
|
C | T | 81 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.234+248C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992034 | ||||||
chr6:110992088
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+302C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992088 | ||||||
chr6:110992138
|
C | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0153 | 2 | NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.234+352C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992138 | ||||||
chr6:110992179
|
A | G | 1 | a0001c0001t0004g0304 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.234+393A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992179 | ||||||
chr6:110992295
|
G | A | 198 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0101others(195): Show | 204 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.234+509G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992295 | ||||||
chr6:110992436
|
A | C | 92 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(89): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.234+650A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992436 | ||||||
chr6:110992445
|
C | CT | 7 | a0001c0001t0002g0164a0001c0001t0002g0256a0001c0001t0002g0317others(4): Show | 7 | HG02132.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+674dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | |||||
chr6:110992445
|
C | CTTTT | 14 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(11): Show | 14 | HG00642.hp2 HG01361.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+671_234+674dup others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | |||||
chr6:110992445
|
C | CTTTTT | 19 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(16): Show | 20 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+670_234+674dup others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | |||||
chr6:110992445
|
CT | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0170a0001c0001t0001g0175others(8): Show | 11 | HG00639.hp2 HG01071.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+674delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110992445 | |||||
chr6:110992485
|
C | T | 4 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128others(1): Show | 4 | HG02818.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+699C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992485 | ||||||
chr6:110992493
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.234+707G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992493 | ||||||
chr6:110992517
|
A | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 31 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+731A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992517 | ||||||
chr6:110992523
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.234+737C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992523 | ||||||
chr6:110992553
|
C | T | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.234+767C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992553 | ||||||
chr6:110992661
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.234+875T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992661 | ||||||
chr6:110992695
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0055 | 5 | HG01074.hp1 HG01255.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+909C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992695 | ||||||
chr6:110992766
|
T | C | 26 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0204others(23): Show | 26 | HG00438.hp2 HG00597.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.234+980T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992766 | ||||||
chr6:110992815
|
G | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1029G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992815 | ||||||
chr6:110992882
|
G | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1096G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992882 | ||||||
chr6:110992898
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.234+1112G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110992898 | ||||||
chr6:110993108
|
G | A | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.234+1322G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993108 | ||||||
chr6:110993126
|
G | C | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.234+1340G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993126 | ||||||
chr6:110993231
|
C | T | 1 | a0001c0001t0014g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+1445C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993231 | ||||||
chr6:110993232
|
G | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1446G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993232 | ||||||
chr6:110993245
|
A | G | 1 | a0001c0001t0002g0302 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.234+1459A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993245 | ||||||
chr6:110993257
|
TTTG | T | 3 | a0003c0003t0003g0099a0003c0003t0003g0185a0003c0003t0004g0098 | 3 | HG02258.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.234+1480_234+1482d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110993257 | |||||
chr6:110993265
|
TG | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1480delG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993265 | ||||||
chr6:110993300
|
GT | G | 187 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(184): Show | 193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.234+1523delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110993300 | |||||
chr6:110993354
|
A | T | 259 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(256): Show | 267 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.234+1568A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993354 | ||||||
chr6:110993537
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1751A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993537 | ||||||
chr6:110993714
|
A | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+1928A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993714 | ||||||
chr6:110993969
|
T | C | 1 | a0007c0007t0018g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.234+2183T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993969 | ||||||
chr6:110993975
|
C | T | 2 | a0002c0002t0009g0322a0002c0002t0009g0323 | 2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.234+2189C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110993975 | ||||||
chr6:110994003
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+2217A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994003 | ||||||
chr6:110994029
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234+2243C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994029 | ||||||
chr6:110994029
|
C | T | 23 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(20): Show | 24 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.234+2243C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994029 | ||||||
chr6:110994058
|
C | G | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.234+2272C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994058 | ||||||
chr6:110994112
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(5): Show | 8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+2326A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994112 | ||||||
chr6:110994206
|
T | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+2420T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994206 | ||||||
chr6:110994278
|
TA | T | 179 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(176): Show | 184 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.234+2506delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994278 | |||||
chr6:110994412
|
C | T | 2 | a0001c0001t0007g0328a0001c0001t0007g0329 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.234+2626C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994412 | ||||||
chr6:110994540
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.235-2643G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994540 | ||||||
chr6:110994727
|
G | GTATATAT others(5): Show |
38 | a0001c0001t0001g0222a0001c0001t0001g0266a0001c0001t0001g0270others(35): Show | 41 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(7): Show |
74 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(71): Show | 75 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(9): Show |
22 | a0001c0001t0001g0199a0001c0001t0001g0209a0001c0001t0001g0214others(19): Show | 22 | HG00621.hp1 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(11): Show |
9 | a0001c0001t0001g0105a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG01255.hp2 HG02027.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.235-2448_235-2447i others(20): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(13): Show |
3 | a0001c0001t0001g0231a0001c0001t0002g0120a0001c0001t0003g0119 | 3 | HG03098.hp1 HG03486.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(22): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0002g0104 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(24): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0002g0103a0001c0001t0005g0102 | 2 | NA18968.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(26): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(31): Show |
1 | a0002c0002t0010g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(40): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTATATAT others(33): Show |
1 | a0002c0002t0010g0320 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
G | GTT | 4 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0001t0021g0026others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2455_235-2454i others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994727
|
GTA | G | 4 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128others(1): Show | 4 | HG02818.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2449_235-2448d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994727 | |||||
chr6:110994729
|
A | T | 21 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(18): Show | 22 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.235-2454A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994729 | ||||||
chr6:110994730
|
T | TACACACA others(7): Show |
1 | a0001c0001t0003g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235-2452_235-2451i others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994730 | |||||
chr6:110994732
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235-2451T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994732 | ||||||
chr6:110994732
|
T | TACAC | 4 | a0001c0001t0001g0067a0001c0001t0003g0135a0001c0001t0003g0168others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2450_235-2449i others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | |||||
chr6:110994732
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0019a0001c0001t0003g0141a0001c0001t0003g0155others(3): Show | 6 | HG00099.hp1 HG01891.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-2450_235-2449i others(10): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | |||||
chr6:110994732
|
T | TACACACA others(3): Show |
3 | a0001c0001t0003g0133a0001c0001t0003g0163a0003c0003t0004g0098 | 3 | HG02572.hp2 HG03516.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.235-2450_235-2449i others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | |||||
chr6:110994732
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0018 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.235-2450_235-2449i others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994732 | |||||
chr6:110994734
|
T | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0067others(14): Show | 17 | HG00099.hp1 HG01106.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-2449T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994734 | ||||||
chr6:110994734
|
T | TAC | 4 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0011g0042others(1): Show | 5 | HG03041.hp1 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2414_235-2413d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACAC | 19 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0039others(16): Show | 20 | HG00639.hp1 HG00733.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.235-2416_235-2413d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACACAC | 8 | a0001c0001t0001g0160a0001c0001t0003g0056a0001c0001t0003g0174others(5): Show | 8 | HG00544.hp2 HG01109.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-2418_235-2413d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACACACA others(1): Show |
30 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0150others(27): Show | 32 | HG00558.hp2 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.235-2420_235-2413d others(10): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACACACA others(3): Show |
10 | a0001c0001t0001g0037a0001c0001t0001g0131a0001c0001t0003g0134others(7): Show | 10 | HG01346.hp2 HG02109.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-2422_235-2413d others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACACACA others(5): Show |
4 | a0001c0001t0003g0052a0001c0001t0003g0156a0001c0001t0003g0157others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2424_235-2413d others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACACACA others(7): Show |
2 | a0001c0001t0003g0136a0001c0001t0004g0138 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.235-2426_235-2413d others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TACACACA others(9): Show |
1 | a0001c0001t0004g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.235-2428_235-2413d others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATACACA others(3): Show |
1 | a0001c0001t0003g0162 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(13): Show |
1 | a0001c0001t0003g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(22): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(15): Show |
1 | a0002c0002t0009g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(24): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(25): Show |
1 | a0001c0001t0001g0101 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(34): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(33): Show |
1 | a0001c0001t0007g0328 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235-2448_235-2447i others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(33): Show |
2 | a0001c0001t0007g0017a0001c0001t0007g0330 | 3 | HG02559.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(35): Show |
1 | a0001c0001t0007g0329 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(44): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(35): Show |
1 | a0001c0001t0007g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(44): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(35): Show |
2 | a0002c0002t0009g0322a0002c0002t0010g0319 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.235-2448_235-2447i others(44): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
T | TATATATA others(39): Show |
1 | a0002c0002t0009g0324 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.235-2448_235-2447i others(48): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
TAC | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0057others(1): Show | 4 | HG01346.hp1 HG01934.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-2414_235-2413d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
TACAC | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(21): Show | 28 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.235-2416_235-2413d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994734
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0004g0074 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.235-2426_235-2413d others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994734 | |||||
chr6:110994736
|
C | T | 168 | a0001c0001t0001g0027a0001c0001t0001g0105a0001c0001t0001g0109others(165): Show | 173 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-2447C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994736 | ||||||
chr6:110994738
|
C | T | 154 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(151): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.235-2445C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994738 | ||||||
chr6:110994740
|
C | T | 124 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(121): Show | 130 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.235-2443C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994740 | ||||||
chr6:110994742
|
C | T | 61 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(58): Show | 61 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.235-2441C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994742 | ||||||
chr6:110994744
|
C | T | 49 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.235-2439C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994744 | ||||||
chr6:110994747
|
A | ACACT | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0055 | 5 | HG01074.hp1 HG01255.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2433_235-2432i others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110994747 | |||||
chr6:110994759
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-2424A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994759 | ||||||
chr6:110994760
|
C | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-2423C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994760 | ||||||
chr6:110994761
|
A | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-2422A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994761 | ||||||
chr6:110994770
|
C | T | 92 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(89): Show | 94 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.235-2413C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994770 | ||||||
chr6:110994771
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.235-2412G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994771 | ||||||
chr6:110994895
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235-2288A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994895 | ||||||
chr6:110994939
|
C | G | 5 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0002g0278others(2): Show | 5 | NA18953.hp1 NA18975.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-2244C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110994939 | ||||||
chr6:110995017
|
A | G | 1 | a0001c0001t0002g0296 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.235-2166A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995017 | ||||||
chr6:110995068
|
A | AT | 24 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(21): Show | 25 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.235-2107dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110995068 | |||||
chr6:110995144
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235-2039A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995144 | ||||||
chr6:110995159
|
C | T | 62 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.235-2024C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995159 | ||||||
chr6:110995270
|
C | G | 1 | a0001c0001t0004g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.235-1913C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995270 | ||||||
chr6:110995283
|
G | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1900G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995283 | ||||||
chr6:110995416
|
C | G | 81 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.235-1767C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995416 | ||||||
chr6:110995492
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.235-1691A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995492 | ||||||
chr6:110995543
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.235-1640T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995543 | ||||||
chr6:110995587
|
G | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1596G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995587 | ||||||
chr6:110995682
|
C | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1501C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995682 | ||||||
chr6:110995803
|
A | G | 1 | a0001c0001t0003g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.235-1380A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995803 | ||||||
chr6:110995841
|
C | T | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.235-1342C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995841 | ||||||
chr6:110995868
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1315A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995868 | ||||||
chr6:110995878
|
G | A | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-1305G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995878 | ||||||
chr6:110995908
|
T | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1275T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995908 | ||||||
chr6:110995915
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.235-1268C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110995915 | ||||||
chr6:110996018
|
A | G | 1 | a0001c0001t0017g0285 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235-1165A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996018 | ||||||
chr6:110996069
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.235-1114C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996069 | ||||||
chr6:110996092
|
A | G | 1 | a0001c0001t0011g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.235-1091A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996092 | ||||||
chr6:110996093
|
C | T | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-1090C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996093 | ||||||
chr6:110996098
|
G | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1085G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996098 | ||||||
chr6:110996123
|
AGTT | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1059_235-1057d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996123 | ||||||
chr6:110996124
|
G | GT | 12 | a0001c0001t0001g0069a0001c0001t0001g0131a0001c0001t0001g0150others(9): Show | 12 | HG01346.hp2 HG01433.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-1042dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110996124 | |||||
chr6:110996124
|
GT | G | 139 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(136): Show | 144 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.235-1042delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110996124 | |||||
chr6:110996127
|
T | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-1056T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996127 | ||||||
chr6:110996265
|
G | A | 62 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(59): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.235-918G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996265 | ||||||
chr6:110996290
|
T | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-893T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996290 | ||||||
chr6:110996359
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.235-824A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996359 | ||||||
chr6:110996595
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0064others(1): Show | 4 | HG00639.hp1 HG01106.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-588C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996595 | ||||||
chr6:110996605
|
G | A | 12 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0179others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-578G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996605 | ||||||
chr6:110996660
|
C | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-523C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996660 | ||||||
chr6:110996785
|
T | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-398T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996785 | ||||||
chr6:110996786
|
TAG | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-394_235-393del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 110996786 | |||||
chr6:110996788
|
G | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-395G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996788 | ||||||
chr6:110996790
|
G | A | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.235-393G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996790 | ||||||
chr6:110996912
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | NA18961.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.235-271G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996912 | ||||||
chr6:110996990
|
T | C | 187 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(184): Show | 193 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.235-193T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110996990 | ||||||
chr6:110997091
|
G | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.235-92G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110997091 | ||||||
chr6:110997179
|
A | T | 3 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0006t0004g0024 | 3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
splice_region_variant&intron_variant | LOW | c.235-4A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 4/9 | chr6 | 110997179 | ||||||
chr6:110997385
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+121A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997385 | ||||||
chr6:110997526
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(5): Show | 8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+262A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997526 | ||||||
chr6:110997610
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.316+346G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997610 | ||||||
chr6:110997684
|
C | A | 1 | a0001c0001t0002g0336 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.316+420C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997684 | ||||||
chr6:110997719
|
GA | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+464delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110997719 | |||||
chr6:110997771
|
G | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+507G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997771 | ||||||
chr6:110997775
|
T | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+511T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997775 | ||||||
chr6:110997806
|
T | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+542T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997806 | ||||||
chr6:110997883
|
T | C | 2 | a0004c0004t0002g0286a0004c0004t0002g0318 | 2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.316+619T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997883 | ||||||
chr6:110997899
|
CT | C | 83 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(80): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.316+650delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110997899 | |||||
chr6:110997997
|
C | T | 2 | a0001c0001t0004g0089a0001c0001t0004g0095 | 2 | HG01070.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.316+733C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110997997 | ||||||
chr6:110998030
|
G | A | 1 | a0001c0001t0003g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316+766G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998030 | ||||||
chr6:110998173
|
G | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+909G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998173 | ||||||
chr6:110998383
|
C | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.316+1119C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998383 | ||||||
chr6:110998463
|
C | G | 1 | a0001c0001t0004g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.316+1199C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998463 | ||||||
chr6:110998484
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0020g0203 | 2 | NA18992.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.316+1220C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998484 | ||||||
chr6:110998531
|
A | G | 17 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(14): Show | 18 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.317-1180A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998531 | ||||||
chr6:110998637
|
T | C | 160 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0193others(157): Show | 165 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.317-1074T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998637 | ||||||
chr6:110998690
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.317-1021C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998690 | ||||||
chr6:110998710
|
A | G | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.317-1001A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998710 | ||||||
chr6:110998944
|
C | CA | 13 | a0001c0001t0001g0005a0001c0001t0001g0238a0001c0001t0002g0310others(10): Show | 15 | HG01175.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.317-748dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | |||||
chr6:110998944
|
CA | C | 6 | a0001c0001t0001g0248a0001c0001t0002g0260a0001c0001t0002g0263others(3): Show | 6 | HG01099.hp1 HG03239.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-748delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | |||||
chr6:110998944
|
CAA | C | 6 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(3): Show | 6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-749_317-748del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | |||||
chr6:110998944
|
CAAA | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.317-750_317-748del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 110998944 | |||||
chr6:110998963
|
A | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.317-748A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998963 | ||||||
chr6:110998980
|
A | G | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.317-731A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110998980 | ||||||
chr6:110999105
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | HG02738.hp2 NA18968.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-606G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999105 | ||||||
chr6:110999139
|
C | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0225others(1): Show | 4 | HG00438.hp2 HG02040.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-572C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999139 | ||||||
chr6:110999238
|
C | T | 160 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0193others(157): Show | 165 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.317-473C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999238 | ||||||
chr6:110999348
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.317-363A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999348 | ||||||
chr6:110999467
|
C | T | 4 | a0001c0001t0002g0261a0001c0001t0002g0265a0001c0001t0002g0282others(1): Show | 4 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-244C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999467 | ||||||
chr6:110999493
|
A | G | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.317-218A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999493 | ||||||
chr6:110999494
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.317-217G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999494 | ||||||
chr6:110999532
|
C | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(23): Show | 27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.317-179C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999532 | ||||||
chr6:110999591
|
G | A | 86 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(83): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.317-120G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 5/9 | chr6 | 110999591 | ||||||
chr6:110999831
|
T | A | 1 | a0001c0001t0002g0291 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.393+44T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 110999831 | ||||||
chr6:110999834
|
A | G | 186 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(183): Show | 192 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.393+47A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 110999834 | ||||||
chr6:111000046
|
G | GTTTA | 188 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0105others(185): Show | 194 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.393+262_393+263ins others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111000046 | |||||
chr6:111000111
|
G | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(23): Show | 27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+324G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000111 | ||||||
chr6:111000132
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.393+345G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000132 | ||||||
chr6:111000134
|
C | T | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+347C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000134 | ||||||
chr6:111000231
|
A | G | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.393+444A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000231 | ||||||
chr6:111000246
|
AG | A | 3 | a0001c0001t0004g0122a0001c0001t0004g0123a0001c0001t0022g0121 | 3 | HG01952.hp1 HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.393+461delG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111000246 | |||||
chr6:111000495
|
A | G | 1 | a0001c0001t0003g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.393+708A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000495 | ||||||
chr6:111000724
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.393+937A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000724 | ||||||
chr6:111000771
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | NA18961.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.393+984G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000771 | ||||||
chr6:111000801
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.393+1014G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000801 | ||||||
chr6:111000868
|
A | ATAT | 26 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(23): Show | 27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1082_393+1083i others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111000868 | |||||
chr6:111000965
|
A | C | 1 | a0001c0001t0001g0044 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.393+1178A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111000965 | ||||||
chr6:111001218
|
C | T | 26 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(23): Show | 27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1431C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001218 | ||||||
chr6:111001232
|
A | G | 26 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(23): Show | 27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1445A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001232 | ||||||
chr6:111001240
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.393+1453A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001240 | ||||||
chr6:111001258
|
A | T | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+1471A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001258 | ||||||
chr6:111001310
|
C | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(23): Show | 27 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+1523C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001310 | ||||||
chr6:111001311
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+1524G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001311 | ||||||
chr6:111001430
|
C | T | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+1643C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001430 | ||||||
chr6:111001440
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.393+1653C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001440 | ||||||
chr6:111001626
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.393+1839G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001626 | ||||||
chr6:111001646
|
A | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.393+1859A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001646 | ||||||
chr6:111001647
|
C | G | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+1860C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001647 | ||||||
chr6:111001667
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.393+1880T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001667 | ||||||
chr6:111001692
|
C | A | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.393+1905C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001692 | ||||||
chr6:111001756
|
A | T | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+1969A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001756 | ||||||
chr6:111001817
|
C | G | 1 | a0001c0001t0004g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.393+2030C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001817 | ||||||
chr6:111001881
|
T | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0002g0107others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.393+2094T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001881 | ||||||
chr6:111001953
|
G | C | 88 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0308others(85): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.393+2166G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001953 | ||||||
chr6:111001963
|
G | T | 2 | a0001c0001t0002g0103a0001c0001t0005g0102 | 2 | NA18968.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.393+2176G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001963 | ||||||
chr6:111001984
|
G | A | 2 | a0001c0001t0004g0009a0001c0001t0004g0091 | 3 | HG00280.hp2 HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.393+2197G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111001984 | ||||||
chr6:111002018
|
G | A | 1 | a0001c0001t0002g0334 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.393+2231G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002018 | ||||||
chr6:111002022
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.393+2235G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002022 | ||||||
chr6:111002064
|
G | T | 25 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0002g0107others(22): Show | 26 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.393+2277G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002064 | ||||||
chr6:111002085
|
A | G | 192 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(189): Show | 198 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.393+2298A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002085 | ||||||
chr6:111002295
|
A | AAATAAT | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+2510_393+2511i others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002295 | |||||
chr6:111002375
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+2588C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002375 | ||||||
chr6:111002533
|
A | G | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.393+2746A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002533 | ||||||
chr6:111002769
|
C | G | 67 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(64): Show | 72 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.393+2982C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002769 | ||||||
chr6:111002773
|
C | CT | 46 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0001g0316others(43): Show | 50 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.393+2998dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002773 | |||||
chr6:111002773
|
C | CTT | 89 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(86): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.393+2997_393+2998d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002773 | |||||
chr6:111002773
|
CT | C | 45 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0015others(42): Show | 46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.393+2998delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111002773 | |||||
chr6:111002837
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.393+3050C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111002837 | ||||||
chr6:111003009
|
G | A | 2 | a0001c0001t0015g0187a0001c0001t0015g0188 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.393+3222G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003009 | ||||||
chr6:111003046
|
G | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3259G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003046 | ||||||
chr6:111003052
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.393+3265G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003052 | ||||||
chr6:111003079
|
A | AC | 41 | a0001c0001t0001g0308a0001c0001t0002g0015a0001c0001t0002g0184others(38): Show | 42 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.393+3302dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111003079 | |||||
chr6:111003079
|
ACC | A | 88 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(85): Show | 89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.393+3301_393+3302d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111003079 | |||||
chr6:111003081
|
C | G | 1 | a0001c0001t0008g0305 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+3294C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003081 | ||||||
chr6:111003082
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0150 | 2 | HG01346.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.393+3295C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003082 | ||||||
chr6:111003090
|
T | C | 3 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0287 | 3 | HG01081.hp2 HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.393+3303T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003090 | ||||||
chr6:111003171
|
T | C | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.393+3384T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003171 | ||||||
chr6:111003292
|
T | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3505T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003292 | ||||||
chr6:111003351
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.393+3564C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003351 | ||||||
chr6:111003354
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3567G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003354 | ||||||
chr6:111003376
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0002g0309 | 2 | NA19058.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.393+3589C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003376 | ||||||
chr6:111003447
|
T | C | 190 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(187): Show | 196 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.393+3660T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003447 | ||||||
chr6:111003474
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.393+3687G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003474 | ||||||
chr6:111003546
|
A | G | 2 | a0001c0001t0002g0296a0001c0001t0002g0334 | 2 | NA18953.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.393+3759A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003546 | ||||||
chr6:111003552
|
G | C | 9 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(6): Show | 9 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+3765G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003552 | ||||||
chr6:111003604
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3817T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003604 | ||||||
chr6:111003608
|
A | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+3821A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003608 | ||||||
chr6:111003615
|
GAAGT | G | 5 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0002g0278others(2): Show | 5 | NA18953.hp1 NA18975.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+3832_393+3835d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111003615 | |||||
chr6:111003651
|
G | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(9): Show | 13 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+3864G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003651 | ||||||
chr6:111003694
|
T | C | 25 | a0001c0001t0001g0049a0001c0001t0001g0166a0001c0001t0001g0182others(22): Show | 25 | HG01257.hp2 HG02074.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.393+3907T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003694 | ||||||
chr6:111003858
|
A | G | 109 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(106): Show | 111 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.393+4071A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003858 | ||||||
chr6:111003874
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+4087G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003874 | ||||||
chr6:111003935
|
T | C | 90 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(87): Show | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.394-4103T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111003935 | ||||||
chr6:111004011
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-4027T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004011 | ||||||
chr6:111004032
|
C | T | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-4006C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004032 | ||||||
chr6:111004033
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-4005A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004033 | ||||||
chr6:111004268
|
C | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0224a0001c0001t0001g0230others(1): Show | 4 | NA18959.hp2 NA18973.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-3770C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004268 | ||||||
chr6:111004284
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3754G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004284 | ||||||
chr6:111004306
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-3732C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004306 | ||||||
chr6:111004333
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-3705C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004333 | ||||||
chr6:111004398
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3640A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004398 | ||||||
chr6:111004429
|
A | C | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.394-3609A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004429 | ||||||
chr6:111004430
|
C | A | 1 | a0001c0001t0002g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.394-3608C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004430 | ||||||
chr6:111004476
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.394-3562C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004476 | ||||||
chr6:111004481
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3557C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004481 | ||||||
chr6:111004549
|
G | GT | 7 | a0001c0001t0001g0069a0001c0001t0002g0015a0001c0001t0002g0103others(4): Show | 8 | HG02055.hp1 HG03831.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-3476dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111004549 | |||||
chr6:111004549
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.394-3489G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004549 | ||||||
chr6:111004549
|
GT | G | 89 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(86): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.394-3476delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111004549 | |||||
chr6:111004605
|
G | A | 81 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0001g0316others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.394-3433G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004605 | ||||||
chr6:111004907
|
A | G | 1 | a0001c0001t0005g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.394-3131A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004907 | ||||||
chr6:111004917
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-3121T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111004917 | ||||||
chr6:111005060
|
C | T | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.394-2978C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005060 | ||||||
chr6:111005069
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2969T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005069 | ||||||
chr6:111005134
|
T | G | 2 | a0001c0001t0001g0037a0001c0005t0027g0038 | 2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.394-2904T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005134 | ||||||
chr6:111005176
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.394-2862C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005176 | ||||||
chr6:111005246
|
C | T | 2 | a0001c0001t0011g0042a0001c0001t0011g0066 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.394-2792C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005246 | ||||||
chr6:111005521
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2517A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005521 | ||||||
chr6:111005533
|
G | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2505G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005533 | ||||||
chr6:111005582
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2456A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005582 | ||||||
chr6:111005720
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0139 | 2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.394-2318C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005720 | ||||||
chr6:111005723
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-2315T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005723 | ||||||
chr6:111005884
|
T | G | 69 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(66): Show | 69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.394-2154T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111005884 | ||||||
chr6:111006130
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394-1908C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006130 | ||||||
chr6:111006140
|
A | G | 111 | a0001c0001t0001g0037a0001c0001t0001g0101a0001c0001t0001g0105others(108): Show | 116 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.394-1898A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006140 | ||||||
chr6:111006169
|
G | A | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.394-1869G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006169 | ||||||
chr6:111006194
|
G | C | 72 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(69): Show | 72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.394-1844G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006194 | ||||||
chr6:111006241
|
A | ATT | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1788_394-1787d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111006241 | |||||
chr6:111006267
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.394-1771C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006267 | ||||||
chr6:111006304
|
G | A | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-1734G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006304 | ||||||
chr6:111006479
|
GC | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1555delC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111006479 | |||||
chr6:111006558
|
C | A | 1 | a0001c0001t0002g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.394-1480C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006558 | ||||||
chr6:111006559
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394-1479T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006559 | ||||||
chr6:111006562
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.394-1476T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006562 | ||||||
chr6:111006685
|
G | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1353G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006685 | ||||||
chr6:111006732
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | NA19057.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.394-1306G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006732 | ||||||
chr6:111006765
|
C | G | 81 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0001g0316others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.394-1273C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006765 | ||||||
chr6:111006782
|
A | G | 14 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(11): Show | 15 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-1256A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006782 | ||||||
chr6:111006802
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1236A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006802 | ||||||
chr6:111006845
|
G | A | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-1193G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006845 | ||||||
chr6:111006878
|
G | A | 192 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(189): Show | 198 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.394-1160G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006878 | ||||||
chr6:111006903
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1135A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006903 | ||||||
chr6:111006924
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-1114T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006924 | ||||||
chr6:111006933
|
C | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-1105C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111006933 | ||||||
chr6:111007123
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-915T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007123 | ||||||
chr6:111007169
|
C | T | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-869C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007169 | ||||||
chr6:111007308
|
C | T | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.394-730C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007308 | ||||||
chr6:111007442
|
C | T | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.394-596C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007442 | ||||||
chr6:111007470
|
T | G | 6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-568T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007470 | ||||||
chr6:111007475
|
G | T | 1 | a0001c0001t0003g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394-563G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007475 | ||||||
chr6:111007604
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.394-434A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007604 | ||||||
chr6:111007632
|
G | A | 2 | a0001c0001t0003g0156a0001c0001t0003g0273 | 2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.394-406G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007632 | ||||||
chr6:111007701
|
T | C | 1 | a0001c0001t0004g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.394-337T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007701 | ||||||
chr6:111007813
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.394-225G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007813 | ||||||
chr6:111007861
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.394-177T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007861 | ||||||
chr6:111007909
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-129T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | chr6 | 111007909 | ||||||
chr6:111008018
|
C | CT | 6 | a0001c0001t0001g0033a0001c0001t0002g0258a0001c0001t0002g0272others(3): Show | 6 | HG02135.hp2 HG02717.hp1 NA19067.hp1 others(3): Show |
splice_acceptor_variant&intron_variant | HIGH | c.394-3dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111008018 | |||||
chr6:111008018
|
CT | C | 89 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0029others(86): Show | 90 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
splice_region_variant&intron_variant | LOW | c.394-3delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 111008018 | |||||
chr6:111008167
|
G | T | 3 | a0001c0001t0006g0012a0001c0001t0006g0113a0001c0001t0023g0114 | 4 | HG01168.hp2 HG01192.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+30G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008167 | ||||||
chr6:111008306
|
C | T | 13 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(10): Show | 14 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+169C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008306 | ||||||
chr6:111008420
|
T | TC | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+286dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008420 | |||||
chr6:111008557
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+420A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008557 | ||||||
chr6:111008624
|
T | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+487T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008624 | ||||||
chr6:111008799
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.493+662A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008799 | ||||||
chr6:111008810
|
G | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+673G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008810 | ||||||
chr6:111008898
|
C | CTT | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+778_493+779dup others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(5): Show |
6 | a0002c0002t0009g0322a0002c0002t0009g0323a0002c0002t0009g0324others(3): Show | 6 | HG01433.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+768_493+779dup others(12): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.493+766_493+779dup others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(8): Show |
18 | a0001c0001t0002g0015a0001c0001t0002g0184a0001c0001t0002g0189others(15): Show | 19 | HG00423.hp1 HG00609.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.493+765_493+779dup others(15): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(9): Show |
28 | a0001c0001t0001g0316a0001c0001t0002g0003a0001c0001t0002g0190others(25): Show | 30 | HG00558.hp1 HG00597.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+764_493+779dup others(16): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(10): Show |
18 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0002g0267others(15): Show | 18 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.493+763_493+779dup others(17): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(11): Show |
12 | a0001c0001t0002g0016a0001c0001t0002g0256a0001c0001t0002g0271others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.493+762_493+779dup others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0108a0001c0001t0002g0314a0004c0004t0002g0318 | 3 | HG02055.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.493+779_493+780ins others(19): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(13): Show |
5 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0120others(2): Show | 5 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+779_493+780ins others(20): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.493+779_493+780ins others(24): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
CT | C | 17 | a0001c0001t0001g0045a0001c0001t0003g0126a0001c0001t0003g0127others(14): Show | 17 | HG01515.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.493+779delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008898
|
CTTTTTTT others(1): Show |
C | 90 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(87): Show | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.493+772_493+779del others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111008898 | |||||
chr6:111008923
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+786A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008923 | ||||||
chr6:111008968
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.493+831C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111008968 | ||||||
chr6:111009094
|
C | T | 92 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(89): Show | 93 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.493+957C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009094 | ||||||
chr6:111009296
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(21): Show | 28 | HG00099.hp2 HG00609.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.493+1159C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009296 | ||||||
chr6:111009297
|
A | G | 317 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.493+1160A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009297 | ||||||
chr6:111009306
|
G | A | 81 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0001g0316others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.493+1169G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009306 | ||||||
chr6:111009392
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1255T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009392 | ||||||
chr6:111009408
|
G | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1271G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009408 | ||||||
chr6:111009484
|
C | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0057others(2): Show | 5 | HG01346.hp1 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1347C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009484 | ||||||
chr6:111009524
|
T | G | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+1387T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009524 | ||||||
chr6:111009907
|
T | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1770T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009907 | ||||||
chr6:111009913
|
A | G | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+1776A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009913 | ||||||
chr6:111009976
|
A | G | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.493+1839A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111009976 | ||||||
chr6:111010095
|
T | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1958T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010095 | ||||||
chr6:111010109
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+1972C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010109 | ||||||
chr6:111010128
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.493+1991C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010128 | ||||||
chr6:111010128
|
CTT | C | 87 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(84): Show | 88 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.493+2002_493+2003d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111010128 | |||||
chr6:111010129
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.493+1992T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010129 | ||||||
chr6:111010130
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0004g0122 | 2 | HG03453.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.493+1993T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010130 | ||||||
chr6:111010326
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2189G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010326 | ||||||
chr6:111010352
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.493+2215C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010352 | ||||||
chr6:111010439
|
G | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2302G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010439 | ||||||
chr6:111010547
|
C | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(14): Show | 18 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.493+2410C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010547 | ||||||
chr6:111010554
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2417C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010554 | ||||||
chr6:111010574
|
C | T | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+2437C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010574 | ||||||
chr6:111010652
|
A | C | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.493+2515A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010652 | ||||||
chr6:111010663
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2526C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010663 | ||||||
chr6:111010780
|
A | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2643A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010780 | ||||||
chr6:111010871
|
A | C | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+2734A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010871 | ||||||
chr6:111010915
|
G | C | 13 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(10): Show | 14 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+2778G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010915 | ||||||
chr6:111010918
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.493+2781T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111010918 | ||||||
chr6:111011090
|
G | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(9): Show | 13 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+2953G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011090 | ||||||
chr6:111011105
|
G | A | 13 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0002g0107others(10): Show | 14 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+2968G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011105 | ||||||
chr6:111011276
|
T | TTTTC | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(13): Show | 16 | HG01081.hp1 HG01346.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.493+3171_493+3174d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011276 | |||||
chr6:111011276
|
TTTTC | T | 96 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0270others(93): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.493+3171_493+3174d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011276 | |||||
chr6:111011276
|
TTTTCTTT others(5): Show |
T | 2 | a0001c0001t0002g0295a0001c0001t0003g0139 | 2 | HG01099.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.493+3163_493+3174d others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011276 | |||||
chr6:111011301
|
TTTC | T | 5 | a0001c0001t0001g0235a0001c0001t0004g0122a0001c0001t0004g0123others(2): Show | 5 | HG01952.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+3167_493+3169d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011301 | |||||
chr6:111011302
|
TTC | T | 66 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(63): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.493+3167_493+3168d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011302 | |||||
chr6:111011304
|
C | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(14): Show | 18 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.493+3167C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011304 | ||||||
chr6:111011305
|
TTTC | T | 11 | a0001c0001t0001g0101a0001c0001t0002g0103a0001c0001t0002g0104others(8): Show | 12 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.493+3171_493+3173d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011305 | |||||
chr6:111011308
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3171C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011308 | ||||||
chr6:111011396
|
T | TC | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3260dupC | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111011396 | |||||
chr6:111011448
|
G | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0006t0004g0024 | 3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.493+3311G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011448 | ||||||
chr6:111011493
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3356A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011493 | ||||||
chr6:111011581
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.493+3444G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011581 | ||||||
chr6:111011715
|
T | A | 1 | a0001c0001t0004g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.493+3578T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011715 | ||||||
chr6:111011744
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0004g0025others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+3607T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011744 | ||||||
chr6:111011984
|
A | C | 2 | a0001c0001t0015g0187a0001c0001t0015g0188 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.494-3770A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111011984 | ||||||
chr6:111012057
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3697A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012057 | ||||||
chr6:111012070
|
C | CT | 79 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(76): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.494-3670dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012070 | |||||
chr6:111012070
|
CT | C | 15 | a0001c0001t0001g0039a0001c0001t0001g0101a0001c0001t0001g0105others(12): Show | 16 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-3670delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012070 | |||||
chr6:111012107
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.494-3647T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012107 | ||||||
chr6:111012139
|
T | A | 1 | a0001c0001t0002g0262 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.494-3615T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012139 | ||||||
chr6:111012162
|
A | AT | 21 | a0001c0001t0001g0046a0001c0001t0001g0115a0001c0001t0002g0107others(18): Show | 23 | HG00735.hp2 HG01081.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.494-3577dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | |||||
chr6:111012162
|
A | ATTT | 8 | a0001c0001t0001g0196a0001c0001t0001g0206a0001c0001t0001g0245others(5): Show | 8 | HG00621.hp2 HG02717.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.494-3579_494-3577d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | |||||
chr6:111012162
|
A | ATTTT | 54 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(51): Show | 54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.494-3580_494-3577d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | |||||
chr6:111012162
|
A | ATTTTT | 12 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG02027.hp2 HG02074.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.494-3581_494-3577d others(7): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | |||||
chr6:111012162
|
AT | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0003g0159others(4): Show | 8 | HG02055.hp1 HG02818.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-3577delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111012162 | |||||
chr6:111012178
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3576C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012178 | ||||||
chr6:111012320
|
G | A | 1 | a0003c0003t0004g0098 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.494-3434G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012320 | ||||||
chr6:111012386
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.494-3368G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012386 | ||||||
chr6:111012414
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3340C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012414 | ||||||
chr6:111012418
|
A | G | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.494-3336A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012418 | ||||||
chr6:111012506
|
G | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3248G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012506 | ||||||
chr6:111012690
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-3064A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012690 | ||||||
chr6:111012773
|
G | A | 7 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0008g0264others(4): Show | 7 | HG02615.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-2981G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012773 | ||||||
chr6:111012866
|
C | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-2888C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012866 | ||||||
chr6:111012885
|
G | T | 1 | a0001c0001t0004g0073 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.494-2869G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111012885 | ||||||
chr6:111013614
|
C | T | 2 | a0004c0004t0002g0286a0004c0004t0002g0318 | 2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.494-2140C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111013614 | ||||||
chr6:111013796
|
TATG | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0002g0003 | 5 | NA18954.hp1 NA18964.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-1955_494-1953d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111013796 | |||||
chr6:111013874
|
A | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-1880A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111013874 | ||||||
chr6:111013875
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.494-1879A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111013875 | ||||||
chr6:111014014
|
T | A | 8 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 8 | NA18612.hp2 NA18950.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-1740T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014014 | ||||||
chr6:111014034
|
G | GT | 43 | a0001c0001t0001g0049a0001c0001t0001g0166a0001c0001t0001g0182others(40): Show | 43 | HG00438.hp2 HG00597.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.494-1708dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111014034 | |||||
chr6:111014094
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.494-1660C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014094 | ||||||
chr6:111014113
|
A | C | 100 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0037others(97): Show | 102 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.494-1641A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014113 | ||||||
chr6:111014141
|
G | GT | 16 | a0001c0001t0001g0043a0001c0001t0002g0041a0001c0001t0002g0103others(13): Show | 16 | HG01433.hp2 HG02622.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.494-1600dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 111014141 | |||||
chr6:111014147
|
T | TC | 93 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0037others(90): Show | 94 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.494-1607_494-1606i others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014147 | ||||||
chr6:111014148
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.494-1606T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014148 | ||||||
chr6:111014180
|
A | G | 72 | a0001c0001t0001g0039a0001c0001t0001g0063a0001c0001t0001g0230others(69): Show | 76 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.494-1574A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014180 | ||||||
chr6:111014206
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.494-1548G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014206 | ||||||
chr6:111014345
|
T | G | 100 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0033others(97): Show | 101 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.494-1409T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014345 | ||||||
chr6:111014368
|
A | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.494-1386A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014368 | ||||||
chr6:111014484
|
G | A | 81 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0001g0316others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.494-1270G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014484 | ||||||
chr6:111014485
|
C | T | 320 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.494-1269C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014485 | ||||||
chr6:111014852
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.494-902G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111014852 | ||||||
chr6:111015021
|
G | A | 94 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(91): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-733G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015021 | ||||||
chr6:111015025
|
G | A | 5 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(2): Show | 5 | HG02738.hp2 HG03579.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-729G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015025 | ||||||
chr6:111015051
|
G | T | 94 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(91): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-703G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015051 | ||||||
chr6:111015112
|
A | G | 3 | a0001c0001t0002g0120a0001c0001t0003g0118a0001c0001t0003g0119 | 3 | HG02922.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.494-642A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015112 | ||||||
chr6:111015181
|
AATGCTCT others(11): Show |
A | 1 | a0001c0001t0020g0203 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.494-572_494-555del others(18): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015181 | ||||||
chr6:111015200
|
G | A | 5 | a0001c0001t0022g0121a0002c0002t0009g0324a0002c0002t0010g0319others(2): Show | 5 | HG01433.hp2 HG01952.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-554G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015200 | ||||||
chr6:111015225
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(5): Show | 8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-529A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015225 | ||||||
chr6:111015232
|
A | C | 94 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(91): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-522A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015232 | ||||||
chr6:111015347
|
T | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.494-407T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015347 | ||||||
chr6:111015414
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.494-340G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015414 | ||||||
chr6:111015564
|
C | A | 5 | a0001c0001t0003g0128a0001c0001t0003g0141a0003c0003t0003g0099others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.494-190C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015564 | ||||||
chr6:111015715
|
T | A | 2 | a0001c0001t0012g0311a0001c0001t0012g0327 | 2 | NA18987.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.494-39T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 7/9 | chr6 | 111015715 | ||||||
chr6:111015875
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(21): Show | 26 | HG00099.hp2 HG00609.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.596+19A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111015875 | ||||||
chr6:111015970
|
A | C | 1 | a0001c0001t0002g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.596+114A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111015970 | ||||||
chr6:111016245
|
A | C | 1 | a0001c0001t0004g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.596+389A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016245 | ||||||
chr6:111016302
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+446T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016302 | ||||||
chr6:111016341
|
T | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+485T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016341 | ||||||
chr6:111016565
|
C | G | 6 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(3): Show | 6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+709C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016565 | ||||||
chr6:111016590
|
G | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+734G>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016590 | ||||||
chr6:111016593
|
G | GA | 35 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(32): Show | 36 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.596+743dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016593 | |||||
chr6:111016593
|
G | GAA | 38 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0060others(35): Show | 38 | HG01257.hp2 HG01891.hp1 HG02040.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+742_596+743dup others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016593 | |||||
chr6:111016593
|
G | GAAA | 13 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0001g0215others(10): Show | 13 | HG00438.hp2 HG00597.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.596+741_596+743dup others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016593 | |||||
chr6:111016600
|
C | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+744C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016600 | ||||||
chr6:111016607
|
C | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+751C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016607 | ||||||
chr6:111016610
|
A | AC | 3 | a0001c0001t0004g0138a0001c0001t0004g0142a0001c0001t0021g0026 | 3 | HG02615.hp2 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.596+754_596+755ins others(1): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016610 | ||||||
chr6:111016638
|
T | TAAAGAGT others(3138): Show |
1 | a0001c0001t0020g0203 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.596+796_596+797ins others(3145): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016638 | |||||
chr6:111016670
|
C | CT | 9 | a0001c0001t0001g0035a0001c0001t0022g0121a0002c0002t0009g0324others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.596+826dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016670 | |||||
chr6:111016670
|
CT | C | 96 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(93): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.596+826delT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016670 | |||||
chr6:111016680
|
T | TTTTC | 6 | a0001c0001t0002g0317a0001c0001t0007g0017a0001c0001t0007g0328others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.596+826_596+827ins others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016680 | |||||
chr6:111016681
|
T | TTTC | 81 | a0001c0001t0001g0270a0001c0001t0001g0308a0001c0001t0001g0316others(78): Show | 85 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.596+826_596+827ins others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016681 | |||||
chr6:111016683
|
C | T | 102 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0101others(99): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.596+827C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016683 | ||||||
chr6:111016684
|
T | C | 6 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(3): Show | 6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+828T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016684 | ||||||
chr6:111016684
|
TTTC | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0109a0001c0001t0001g0115others(14): Show | 18 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.596+831_596+833del others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016684 | |||||
chr6:111016685
|
TTC | T | 77 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0050others(74): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.596+831_596+832del others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111016685 | |||||
chr6:111016687
|
C | T | 109 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0101others(106): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.596+831C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016687 | ||||||
chr6:111016688
|
T | C | 1 | a0006c0008t0007g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.596+832T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016688 | ||||||
chr6:111016755
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+899G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016755 | ||||||
chr6:111016828
|
C | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0060others(2): Show | 5 | HG00544.hp1 HG00544.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+972C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016828 | ||||||
chr6:111016891
|
A | G | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1035A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016891 | ||||||
chr6:111016947
|
C | G | 1 | a0001c0001t0012g0311 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.596+1091C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016947 | ||||||
chr6:111016967
|
A | G | 1 | a0001c0001t0006g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.596+1111A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111016967 | ||||||
chr6:111017020
|
C | G | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.596+1164C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017020 | ||||||
chr6:111017077
|
A | C | 77 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(74): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.596+1221A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017077 | ||||||
chr6:111017209
|
A | AT | 5 | a0001c0001t0001g0207a0001c0001t0001g0228a0001c0001t0001g0247others(2): Show | 5 | HG00423.hp2 NA18956.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1353_596+1354i others(3): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017209 | ||||||
chr6:111017210
|
C | CG | 30 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0069others(27): Show | 30 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.596+1358dupG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017210 | |||||
chr6:111017210
|
C | G | 5 | a0001c0001t0001g0207a0001c0001t0001g0228a0001c0001t0001g0247others(2): Show | 5 | HG00423.hp2 NA18956.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1354C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017210 | ||||||
chr6:111017210
|
C | T | 91 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0043others(88): Show | 92 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.596+1354C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017210 | ||||||
chr6:111017221
|
C | G | 1 | a0001c0001t0020g0203 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.596+1365C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017221 | ||||||
chr6:111017255
|
T | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1399T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017255 | ||||||
chr6:111017262
|
G | A | 1 | a0004c0004t0002g0286 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.596+1406G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017262 | ||||||
chr6:111017269
|
T | C | 337 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.596+1413T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017269 | ||||||
chr6:111017276
|
A | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1420A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017276 | ||||||
chr6:111017293
|
G | A | 99 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0270others(96): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.596+1437G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017293 | ||||||
chr6:111017310
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1454G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017310 | ||||||
chr6:111017326
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+1470C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017326 | ||||||
chr6:111017336
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.596+1480G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017336 | ||||||
chr6:111017343
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+1487C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017343 | ||||||
chr6:111017344
|
G | A | 3 | a0001c0001t0004g0138a0001c0001t0004g0142a0001c0001t0004g0143 | 3 | HG02109.hp2 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.596+1488G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017344 | ||||||
chr6:111017347
|
C | T | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1491C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017347 | ||||||
chr6:111017356
|
C | T | 1 | a0002c0002t0009g0322 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.596+1500C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017356 | ||||||
chr6:111017372
|
T | C | 200 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(197): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.596+1516T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017372 | ||||||
chr6:111017389
|
AGGCGGAG others(73): Show |
A | 4 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | NA18950.hp1 NA18964.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1541_596+1620d others(82): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017389 | |||||
chr6:111017391
|
GCGGAGA | G | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0270others(90): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.596+1538_596+1543d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017391 | |||||
chr6:111017392
|
CGGAGACG others(39): Show |
C | 1 | a0001c0001t0002g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.596+1538_596+1583d others(48): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017392 | |||||
chr6:111017398
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.596+1542C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017398 | ||||||
chr6:111017416
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.596+1560C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017416 | ||||||
chr6:111017421
|
C | T | 5 | a0001c0001t0004g0130a0001c0001t0004g0138a0001c0001t0004g0142others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1565C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017421 | ||||||
chr6:111017428
|
C | T | 66 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(63): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.596+1572C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017428 | ||||||
chr6:111017431
|
A | G | 91 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.596+1575A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017431 | ||||||
chr6:111017435
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.596+1579G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017435 | ||||||
chr6:111017469
|
G | A | 91 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(88): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.596+1613G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017469 | ||||||
chr6:111017525
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+1669C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017525 | ||||||
chr6:111017546
|
G | A | 2 | a0001c0001t0015g0187a0001c0001t0015g0188 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.596+1690G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017546 | ||||||
chr6:111017568
|
C | T | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1712C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017568 | ||||||
chr6:111017586
|
G | A | 4 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+1730G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017586 | ||||||
chr6:111017614
|
G | A | 2 | a0001c0001t0005g0332a0001c0001t0005g0333 | 2 | NA18612.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.596+1758G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017614 | ||||||
chr6:111017619
|
G | T | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.596+1763G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017619 | ||||||
chr6:111017632
|
C | T | 2 | a0001c0001t0005g0200a0001c0001t0005g0237 | 2 | NA18982.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.596+1776C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017632 | ||||||
chr6:111017670
|
ACACTCCT others(33): Show |
A | 5 | a0001c0001t0004g0130a0001c0001t0004g0138a0001c0001t0004g0142others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+1816_596+1855d others(42): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017670 | |||||
chr6:111017671
|
C | T | 1 | a0007c0007t0018g0183 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.596+1815C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017671 | ||||||
chr6:111017672
|
A | G | 94 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(91): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.596+1816A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017672 | ||||||
chr6:111017679
|
A | G | 1 | a0001c0001t0002g0334 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.596+1823A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017679 | ||||||
chr6:111017701
|
C | T | 6 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(3): Show | 6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+1845C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017701 | ||||||
chr6:111017767
|
G | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0006t0004g0024 | 3 | HG00642.hp2 HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.596+1911G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017767 | ||||||
chr6:111017774
|
A | G | 194 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(191): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.596+1918A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017774 | ||||||
chr6:111017796
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.596+1940C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017796 | ||||||
chr6:111017805
|
C | CG | 4 | a0001c0001t0001g0063a0001c0001t0001g0202a0001c0001t0001g0247others(1): Show | 4 | HG00621.hp2 HG02027.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1953dupG | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111017805 | |||||
chr6:111017836
|
T | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+1980T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017836 | ||||||
chr6:111017890
|
G | A | 3 | a0001c0001t0017g0285a0004c0004t0002g0286a0004c0004t0002g0318 | 3 | HG02055.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.596+2034G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017890 | ||||||
chr6:111017897
|
C | T | 1 | a0001c0005t0027g0038 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.596+2041C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017897 | ||||||
chr6:111017948
|
C | T | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2092C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017948 | ||||||
chr6:111017973
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.596+2117G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017973 | ||||||
chr6:111017977
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2121G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111017977 | ||||||
chr6:111018043
|
C | T | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2187C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018043 | ||||||
chr6:111018065
|
C | A | 92 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0270others(89): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2209C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018065 | ||||||
chr6:111018074
|
G | A | 5 | a0001c0001t0003g0128a0001c0001t0003g0141a0003c0003t0003g0099others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+2218G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018074 | ||||||
chr6:111018093
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+2237G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018093 | ||||||
chr6:111018127
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.596+2271C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018127 | ||||||
chr6:111018182
|
C | G | 2 | a0001c0001t0006g0012a0001c0001t0006g0113 | 3 | HG01168.hp2 HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.596+2326C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018182 | ||||||
chr6:111018199
|
CGGGGAG | C | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+2358_596+2363d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018199 | |||||
chr6:111018200
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.596+2344G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018200 | ||||||
chr6:111018214
|
G | A | 5 | a0001c0001t0004g0130a0001c0001t0004g0138a0001c0001t0004g0142others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+2358G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018214 | ||||||
chr6:111018214
|
G | GGAGGGAG others(5): Show |
1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.596+2376_596+2387d others(14): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018214 | |||||
chr6:111018214
|
GGAGGGA | G | 4 | a0001c0001t0001g0029a0001c0001t0011g0042a0001c0001t0011g0066others(1): Show | 4 | HG02683.hp1 HG02735.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+2382_596+2387d others(8): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018214 | |||||
chr6:111018245
|
A | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(5): Show | 8 | HG02738.hp2 HG02922.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.596+2389A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018245 | ||||||
chr6:111018253
|
T | A | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.596+2397T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018253 | ||||||
chr6:111018344
|
A | G | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.596+2488A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018344 | ||||||
chr6:111018496
|
T | C | 82 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(79): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.596+2640T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018496 | ||||||
chr6:111018634
|
CAG | C | 72 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(69): Show | 72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.596+2782_596+2783d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111018634 | |||||
chr6:111018891
|
A | C | 1 | a0001c0001t0021g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.596+3035A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018891 | ||||||
chr6:111018938
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+3082G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018938 | ||||||
chr6:111018999
|
C | T | 5 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+3143C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111018999 | ||||||
chr6:111019094
|
A | T | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3238A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019094 | ||||||
chr6:111019115
|
C | G | 1 | a0001c0001t0004g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.596+3259C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019115 | ||||||
chr6:111019169
|
G | A | 6 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(3): Show | 6 | HG02738.hp2 HG03098.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+3313G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019169 | ||||||
chr6:111019175
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+3319C>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019175 | ||||||
chr6:111019248
|
G | A | 72 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(69): Show | 72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.596+3392G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019248 | ||||||
chr6:111019287
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.596+3431G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019287 | ||||||
chr6:111019324
|
C | T | 82 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(79): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.596+3468C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019324 | ||||||
chr6:111019420
|
G | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3564G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019420 | ||||||
chr6:111019455
|
T | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3599T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019455 | ||||||
chr6:111019456
|
T | A | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3600T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019456 | ||||||
chr6:111019551
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0045 | 3 | NA18967.hp1 NA18982.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.596+3695A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019551 | ||||||
chr6:111019590
|
G | A | 201 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(198): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.596+3734G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019590 | ||||||
chr6:111019629
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.596+3773C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019629 | ||||||
chr6:111019754
|
A | G | 100 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031others(97): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.596+3898A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019754 | ||||||
chr6:111019755
|
T | C | 1 | a0003c0003t0004g0098 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.596+3899T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019755 | ||||||
chr6:111019829
|
A | C | 95 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(92): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.596+3973A>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019829 | ||||||
chr6:111019917
|
C | CT | 3 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0252 | 3 | NA18949.hp1 NA18972.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.596+4065dupT | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | |||||
chr6:111019917
|
C | CTT | 79 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0050others(76): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.596+4064_596+4065d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | |||||
chr6:111019917
|
C | CTTT | 16 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0002g0103others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+4063_596+4065d others(5): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | |||||
chr6:111019917
|
C | CTTTT | 4 | a0001c0001t0001g0027a0001c0001t0004g0023a0001c0001t0004g0025others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+4062_596+4065d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111019917 | |||||
chr6:111019922
|
G | T | 102 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0049others(99): Show | 103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.596+4066G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019922 | ||||||
chr6:111019975
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0003g0128others(9): Show | 13 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.596+4119C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111019975 | ||||||
chr6:111020019
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.596+4163A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020019 | ||||||
chr6:111020258
|
C | T | 93 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031others(90): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.597-3925C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020258 | ||||||
chr6:111020269
|
A | G | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0031others(92): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-3914A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020269 | ||||||
chr6:111020319
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.597-3864G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020319 | ||||||
chr6:111020339
|
G | A | 1 | a0001c0001t0006g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.597-3844G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020339 | ||||||
chr6:111020384
|
T | C | 7 | a0001c0001t0007g0017a0001c0001t0007g0328a0001c0001t0007g0329others(4): Show | 8 | HG01952.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-3799T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020384 | ||||||
chr6:111020451
|
T | G | 1 | a0001c0001t0002g0299 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.597-3732T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020451 | ||||||
chr6:111020466
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.597-3717C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020466 | ||||||
chr6:111020491
|
G | A | 75 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(72): Show | 75 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.597-3692G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020491 | ||||||
chr6:111020704
|
T | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.597-3479T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020704 | ||||||
chr6:111020859
|
GA | G | 77 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0014others(74): Show | 82 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.597-3316delA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111020859 | |||||
chr6:111020876
|
T | C | 9 | a0001c0001t0006g0012a0001c0001t0006g0030a0001c0001t0006g0106others(6): Show | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.597-3307T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020876 | ||||||
chr6:111020894
|
C | T | 1 | a0003c0003t0003g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.597-3289C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020894 | ||||||
chr6:111020895
|
G | A | 59 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0014others(56): Show | 63 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.597-3288G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020895 | ||||||
chr6:111020966
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597-3217G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111020966 | ||||||
chr6:111021095
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 38 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.597-3088G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021095 | ||||||
chr6:111021113
|
G | T | 4 | a0001c0005t0027g0038a0002c0002t0010g0319a0002c0002t0010g0320others(1): Show | 4 | HG01433.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-3070G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021113 | ||||||
chr6:111021215
|
T | TAATA | 8 | a0001c0001t0006g0012a0001c0001t0006g0030a0001c0001t0006g0106others(5): Show | 9 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-2967_597-2964d others(6): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111021215 | |||||
chr6:111021268
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.597-2915C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021268 | ||||||
chr6:111021526
|
A | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(99): Show | 106 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.597-2657A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021526 | ||||||
chr6:111021569
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.597-2614C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021569 | ||||||
chr6:111021657
|
C | T | 1 | a0001c0001t0002g0307 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.597-2526C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021657 | ||||||
chr6:111021819
|
A | G | 1 | a0001c0001t0002g0111 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.597-2364A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021819 | ||||||
chr6:111021903
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.597-2280A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021903 | ||||||
chr6:111021987
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.597-2196A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111021987 | ||||||
chr6:111022191
|
T | C | 80 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0014others(77): Show | 85 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.597-1992T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022191 | ||||||
chr6:111022225
|
C | G | 18 | a0001c0001t0002g0015a0001c0001t0002g0087a0001c0001t0002g0140others(15): Show | 19 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.597-1958C>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022225 | ||||||
chr6:111022252
|
G | A | 1 | a0001c0001t0028g0244 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.597-1931G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022252 | ||||||
chr6:111022319
|
A | G | 9 | a0001c0001t0006g0012a0001c0001t0006g0030a0001c0001t0006g0106others(6): Show | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.597-1864A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022319 | ||||||
chr6:111022613
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.597-1570C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022613 | ||||||
chr6:111022616
|
T | TTG | 81 | a0001c0001t0002g0294a0001c0001t0003g0010a0001c0001t0003g0013others(78): Show | 86 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.597-1564_597-1563d others(4): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111022616 | |||||
chr6:111022717
|
G | T | 2 | a0001c0001t0012g0311a0001c0001t0012g0327 | 2 | NA18987.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.597-1466G>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022717 | ||||||
chr6:111022907
|
G | A | 3 | a0002c0002t0010g0319a0002c0002t0010g0320a0002c0002t0010g0321 | 3 | HG01433.hp2 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.597-1276G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022907 | ||||||
chr6:111022967
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.597-1216C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111022967 | ||||||
chr6:111023160
|
A | G | 1 | a0001c0001t0004g0025 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.597-1023A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023160 | ||||||
chr6:111023323
|
T | C | 1 | a0001c0001t0003g0151 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.597-860T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023323 | ||||||
chr6:111023410
|
G | A | 1 | a0001c0001t0006g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.597-773G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023410 | ||||||
chr6:111023494
|
G | A | 1 | a0001c0001t0015g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597-689G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023494 | ||||||
chr6:111023609
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.597-574G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023609 | ||||||
chr6:111023643
|
A | T | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.597-540A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023643 | ||||||
chr6:111023644
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0003g0020 | 2 | HG01169.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.597-539T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023644 | ||||||
chr6:111023880
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.597-303C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023880 | ||||||
chr6:111023982
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.597-201G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111023982 | ||||||
chr6:111023986
|
C | CA | 107 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0027others(104): Show | 112 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.597-184dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 111023986 | |||||
chr6:111024049
|
T | G | 81 | a0001c0001t0001g0037a0001c0001t0003g0010a0001c0001t0003g0013others(78): Show | 86 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.597-134T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111024049 | ||||||
chr6:111024139
|
T | A | 1 | a0001c0001t0002g0302 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.597-44T>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | chr6 | 111024139 | ||||||
chr6:111024400
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.741+73T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024400 | ||||||
chr6:111024479
|
C | T | 100 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0028others(97): Show | 104 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.741+152C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024479 | ||||||
chr6:111024491
|
A | G | 9 | a0001c0001t0006g0012a0001c0001t0006g0030a0001c0001t0006g0106others(6): Show | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+164A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024491 | ||||||
chr6:111024536
|
A | G | 1 | a0001c0001t0002g0271 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.741+209A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024536 | ||||||
chr6:111024611
|
G | A | 1 | a0001c0001t0003g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.741+284G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024611 | ||||||
chr6:111024652
|
G | A | 1 | a0003c0003t0004g0098 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.741+325G>A | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024652 | ||||||
chr6:111024674
|
T | C | 9 | a0001c0001t0006g0012a0001c0001t0006g0030a0001c0001t0006g0106others(6): Show | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+347T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024674 | ||||||
chr6:111024704
|
C | CA | 65 | a0001c0001t0001g0105a0001c0001t0001g0204a0001c0001t0001g0242others(62): Show | 68 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.741+393dupA | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 111024704 | |||||
chr6:111024704
|
C | CAA | 9 | a0001c0001t0003g0136a0001c0001t0003g0151a0001c0001t0006g0012others(6): Show | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+392_741+393dup others(2): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 111024704 | |||||
chr6:111024757
|
T | G | 1 | a0001c0001t0022g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.741+430T>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024757 | ||||||
chr6:111024760
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.741+433A>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024760 | ||||||
chr6:111024870
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.742-533T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111024870 | ||||||
chr6:111025143
|
C | T | 9 | a0001c0001t0006g0012a0001c0001t0006g0030a0001c0001t0006g0106others(6): Show | 10 | HG00621.hp2 HG01168.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.742-260C>T | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111025143 | ||||||
chr6:111025196
|
T | C | 2 | a0001c0001t0013g0152a0001c0001t0013g0186 | 2 | HG00741.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.742-207T>C | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111025196 | ||||||
chr6:111025238
|
A | G | 1 | a0001c0001t0003g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.742-165A>G | RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 9/9 | chr6 | 111025238 |