geneid | 3892 |
---|---|
ensemblid | ENSG00000170442.12 |
hgncid | 6463 |
symbol | KRT86 |
name | keratin 86 |
refseq_nuc | NM_001320198.2 |
refseq_prot | NP_001307127.1 |
ensembl_nuc | ENST00000423955.7 |
ensembl_prot | ENSP00000444533.1 |
mane_status | MANE Select |
chr | chr12 |
start | 52274645 |
end | 52309163 |
strand | + |
ver | v1.2 |
region | chr12:52274645-52309163 |
region5000 | chr12:52269645-52314163 |
regionname0 | KRT86_chr12_52274645_52309163 |
regionname5000 | KRT86_chr12_52269645_52314163 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 486 | 396 | 88 | 79 | 172 | 16 | 40 | 136 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0002 | 0/0 | 486 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0003 | 0/0 | 486 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0004 | 0/0 | 486 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0005 | 0/0 | 486 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0006 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0007 | 0/0 | 486 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0008 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0009 | 0/1 | 486 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0010 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0011 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0012 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
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 | 1/0 | 1461 | 160 | 16 | 40 | 78 | 7 | 18 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0002 | 0/0 | 1461 | 141 | 40 | 21 | 68 | 4 | 8 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0003 | 0/0 | 1461 | 47 | 10 | 7 | 17 | 1 | 12 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0004 | 0/0 | 1461 | 9 | 0 | 5 | 0 | 3 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0005 | 0/0 | 1461 | 8 | 7 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0006 | 0/0 | 1461 | 6 | 4 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0007 | 0/0 | 1461 | 6 | 3 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0008 | 0/0 | 1461 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0009 | 0/0 | 1461 | 4 | 4 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0010 | 0/0 | 1461 | 3 | 0 | 2 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0011 | 0/0 | 1461 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0012 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0013 | 0/0 | 1461 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0014 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0015 | 0/0 | 1461 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0016 | 0/0 | 1461 | 2 | 1 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0017 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0018 | 0/0 | 1461 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0019 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0020 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0021 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0022 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0023 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0024 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0025 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0026 | 0/1 | 1461 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0027 | 0/0 | 1461 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
c0028 | 0/0 | 1461 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 787 | 108 | 7 | 17 | 72 | 4 | 7 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0002 | 1/0 | 787 | 98 | 1 | 28 | 51 | 3 | 14 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0003 | 0/0 | 788 | 60 | 35 | 10 | 8 | 3 | 4 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0004 | 0/0 | 789 | 58 | 20 | 7 | 16 | 1 | 14 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0005 | 0/0 | 789 | 57 | 18 | 13 | 19 | 4 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0006 | 0/0 | 787 | 9 | 6 | 3 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0007 | 0/0 | 787 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0008 | 0/0 | 787 | 3 | 3 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0009 | 0/0 | 789 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0010 | 0/0 | 787 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0011 | 0/0 | 789 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0012 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0013 | 0/0 | 787 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0014 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0015 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0016 | 0/0 | 787 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0017 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0018 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0019 | 0/0 | 789 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0020 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0021 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
t0022 | 0/0 | 787 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
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 | 8 | 0 | 3 | 5 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0003 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0006 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
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 | 1/0 | 1461 | 160 | 16 | 40 | 78 | 7 | 18 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002 | 0/0 | 1461 | 141 | 40 | 21 | 68 | 4 | 8 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0003 | 0/0 | 1461 | 47 | 10 | 7 | 17 | 1 | 12 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0004 | 0/0 | 1461 | 9 | 0 | 5 | 0 | 3 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0005 | 0/0 | 1461 | 8 | 7 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0006 | 0/0 | 1461 | 6 | 4 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0007 | 0/0 | 1461 | 6 | 3 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0008 | 0/0 | 1461 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0010 | 0/0 | 1461 | 3 | 0 | 2 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0014 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0015 | 0/0 | 1461 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0016 | 0/0 | 1461 | 2 | 1 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0017 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0020 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0021 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0023 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0027 | 0/0 | 1461 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0002c0009 | 0/0 | 1461 | 4 | 4 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0003c0011 | 0/0 | 1461 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0004c0012 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0005c0013 | 0/0 | 1461 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0006c0028 | 0/0 | 1461 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0007c0018 | 0/0 | 1461 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0008c0019 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0009c0026 | 0/1 | 1461 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0010c0024 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0011c0022 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0012c0025 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0002 | 1/0 | 2247 | 98 | 1 | 28 | 51 | 3 | 14 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0004 | 0/0 | 2249 | 2 | 1 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0005 | 0/0 | 2249 | 51 | 13 | 12 | 19 | 4 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0007 | 0/0 | 2247 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0009 | 0/0 | 2249 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0011 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0001t0015 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0001 | 0/0 | 2247 | 89 | 1 | 17 | 62 | 4 | 5 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0003 | 0/0 | 2248 | 44 | 32 | 4 | 5 | 0 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0004 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0008 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0011 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0013 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0018 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0020 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0002t0021 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0003t0004 | 0/0 | 2249 | 45 | 10 | 7 | 15 | 1 | 12 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0003t0016 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0003t0019 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0004t0003 | 0/0 | 2248 | 9 | 0 | 5 | 0 | 3 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0005t0004 | 0/0 | 2249 | 5 | 5 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0005t0006 | 0/0 | 2247 | 3 | 2 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0006t0006 | 0/0 | 2247 | 6 | 4 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0007t0003 | 0/0 | 2248 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0007t0005 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0007t0012 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0008t0001 | 0/0 | 2247 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0010t0010 | 0/0 | 2247 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0010t0022 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0014t0008 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0015t0001 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0016t0003 | 0/0 | 2248 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0016t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0017t0004 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0020t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0021t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0023t0001 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0001c0027t0004 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0002c0009t0001 | 0/0 | 2247 | 4 | 4 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0003c0011t0001 | 0/0 | 2247 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0004c0012t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0004c0012t0014 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0005c0013t0001 | 0/0 | 2247 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0006c0028t0004 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0007c0018t0005 | 0/0 | 2249 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0008c0019t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0009c0026t0001 | 0/1 | 2247 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0010c0024t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0011c0022t0017 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
a0012c0025t0001 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | copy fasta | chr12 | 52269645 | 52314163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0011g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0015g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0011g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0018g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0020g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0021g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0016g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0019g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0006 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0008t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0010t0010g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0010t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0010t0022g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0014t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0014t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0015t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0015t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0016t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0016t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0017t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0017t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0020t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0021t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0023t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0027t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0002c0009t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0002c0009t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0002c0009t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0003c0011t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0003c0011t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0003c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0004c0012t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0004c0012t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0005c0013t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0005c0013t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0006c0028t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0007c0018t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0008c0019t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0009c0026t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0010c0024t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0011c0022t0017g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0012c0025t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0004 | g0309 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00099 | hp2 | a0001 | c0010 | t0022 | g0030 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0117 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00140 | hp2 | a0001 | c0004 | t0003 | g0285 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0204 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0192 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00323 | hp2 | a0001 | c0004 | t0003 | g0006 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00408 | hp1 | a0001 | c0008 | t0001 | g0087 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00423 | hp2 | a0001 | c0003 | t0004 | g0287 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0128 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0324 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0109 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00673 | hp2 | a0001 | c0001 | t0015 | g0094 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00733 | hp2 | a0001 | c0003 | t0004 | g0293 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00738 | hp2 | a0001 | c0003 | t0004 | g0258 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00741 | hp2 | a0001 | c0004 | t0003 | g0277 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01069 | hp1 | a0001 | c0004 | t0003 | g0039 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01071 | hp1 | a0001 | c0004 | t0003 | g0039 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01074 | hp1 | a0001 | c0016 | t0003 | g0041 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01099 | hp1 | a0001 | c0003 | t0004 | g0276 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01106 | hp2 | a0001 | c0004 | t0003 | g0278 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01109 | hp2 | a0001 | c0005 | t0006 | g0166 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01167 | hp1 | a0001 | c0006 | t0006 | g0305 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0256 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01169 | hp2 | a0001 | c0006 | t0006 | g0281 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0101 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01255 | hp2 | a0001 | c0003 | t0004 | g0280 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01346 | hp1 | a0007 | c0018 | t0005 | g0025 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01358 | hp1 | a0001 | c0004 | t0003 | g0006 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0124 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01496 | hp2 | a0001 | c0010 | t0010 | g0030 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0026 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0187 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01891 | hp1 | a0001 | c0017 | t0004 | g0130 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0231 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01978 | hp1 | a0001 | c0003 | t0004 | g0286 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02055 | hp1 | a0001 | c0002 | t0008 | g0156 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02071 | hp2 | a0001 | c0003 | t0004 | g0155 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02074 | hp2 | a0001 | c0003 | t0004 | g0317 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02129 | hp2 | a0001 | c0003 | t0004 | g0298 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0332 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02145 | hp2 | a0002 | c0009 | t0001 | g0265 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02148 | hp1 | a0001 | c0003 | t0004 | g0300 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | CDX | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02165 | hp2 | a0001 | c0003 | t0004 | g0288 | EAS | CDX | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02257 | hp1 | a0001 | c0003 | t0004 | g0284 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0250 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02258 | hp1 | a0001 | c0003 | t0004 | g0290 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02258 | hp2 | a0002 | c0009 | t0001 | g0266 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0322 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02293 | hp2 | a0001 | c0010 | t0010 | g0161 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0319 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0162 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02572 | hp1 | a0001 | c0016 | t0005 | g0333 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0282 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02602 | hp2 | a0001 | c0003 | t0004 | g0272 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0310 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02622 | hp1 | a0001 | c0005 | t0006 | g0326 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0342 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02630 | hp2 | a0001 | c0014 | t0008 | g0164 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0274 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02683 | hp1 | a0001 | c0003 | t0004 | g0320 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02683 | hp2 | a0001 | c0004 | t0003 | g0006 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02698 | hp1 | a0001 | c0003 | t0004 | g0291 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02698 | hp2 | a0001 | c0002 | t0003 | g0244 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0337 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0257 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02723 | hp2 | a0008 | c0019 | t0003 | g0252 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0347 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02809 | hp2 | a0001 | c0005 | t0004 | g0151 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02818 | hp1 | a0012 | c0025 | t0001 | g0268 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02818 | hp2 | a0001 | c0007 | t0005 | g0150 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0339 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02895 | hp2 | a0004 | c0012 | t0003 | g0328 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02896 | hp1 | a0002 | c0009 | t0001 | g0031 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02896 | hp2 | a0001 | c0007 | t0005 | g0152 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02897 | hp1 | a0002 | c0009 | t0001 | g0031 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02922 | hp1 | a0001 | c0005 | t0006 | g0139 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02922 | hp2 | a0001 | c0002 | t0018 | g0335 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02965 | hp2 | a0004 | c0012 | t0014 | g0160 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0229 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0270 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0271 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03017 | hp1 | a0005 | c0013 | t0001 | g0185 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0240 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0251 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03041 | hp2 | a0001 | c0006 | t0006 | g0273 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03098 | hp1 | a0001 | c0003 | t0004 | g0279 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03130 | hp1 | a0001 | c0007 | t0012 | g0304 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03130 | hp2 | a0001 | c0020 | t0005 | g0113 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03195 | hp1 | a0001 | c0023 | t0001 | g0338 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0254 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03209 | hp1 | a0001 | c0014 | t0008 | g0163 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03209 | hp2 | a0001 | c0003 | t0004 | g0311 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03225 | hp1 | a0011 | c0022 | t0017 | g0275 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0334 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0249 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03453 | hp2 | a0001 | c0003 | t0004 | g0321 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03486 | hp1 | a0001 | c0006 | t0006 | g0343 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0327 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0295 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0325 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03516 | hp2 | a0001 | c0021 | t0003 | g0261 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03540 | hp1 | a0001 | c0002 | t0021 | g0344 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0312 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03579 | hp1 | a0001 | c0002 | t0011 | g0346 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03669 | hp2 | a0001 | c0003 | t0004 | g0040 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03704 | hp2 | a0001 | c0003 | t0004 | g0308 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0040 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03831 | hp2 | a0001 | c0003 | t0004 | g0323 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03834 | hp1 | a0001 | c0027 | t0004 | g0302 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03834 | hp2 | a0005 | c0013 | t0001 | g0184 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03942 | hp1 | a0001 | c0003 | t0004 | g0007 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04115 | hp1 | a0001 | c0003 | t0004 | g0069 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0114 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0072 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0103 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04228 | hp2 | a0001 | c0003 | t0004 | g0269 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0028 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0158 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | CHB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18906 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18906 | hp2 | a0010 | c0024 | t0005 | g0331 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18947 | hp2 | a0001 | c0003 | t0004 | g0299 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18957 | hp1 | a0001 | c0008 | t0001 | g0037 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18957 | hp2 | a0001 | c0003 | t0004 | g0318 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18963 | hp1 | a0001 | c0003 | t0004 | g0007 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18965 | hp2 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18967 | hp1 | a0001 | c0003 | t0004 | g0262 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18968 | hp1 | a0001 | c0003 | t0004 | g0236 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18968 | hp2 | a0003 | c0011 | t0001 | g0122 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18970 | hp1 | a0001 | c0015 | t0001 | g0077 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18973 | hp2 | a0006 | c0028 | t0004 | g0315 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18974 | hp1 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18977 | hp1 | a0001 | c0002 | t0013 | g0064 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18977 | hp2 | a0001 | c0007 | t0003 | g0067 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18981 | hp1 | a0001 | c0003 | t0004 | g0255 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18982 | hp2 | a0001 | c0007 | t0003 | g0289 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18984 | hp2 | a0003 | c0011 | t0001 | g0132 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18991 | hp2 | a0001 | c0003 | t0016 | g0263 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18994 | hp2 | a0001 | c0015 | t0001 | g0223 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18998 | hp1 | a0001 | c0003 | t0004 | g0242 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18999 | hp2 | a0001 | c0003 | t0019 | g0144 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19002 | hp2 | a0001 | c0008 | t0001 | g0198 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19006 | hp1 | a0001 | c0003 | t0004 | g0007 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19010 | hp1 | a0003 | c0011 | t0001 | g0133 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19030 | hp2 | a0001 | c0006 | t0006 | g0307 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19043 | hp1 | a0001 | c0002 | t0003 | g0329 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19043 | hp2 | a0001 | c0003 | t0004 | g0296 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19056 | hp2 | a0001 | c0008 | t0001 | g0037 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19057 | hp2 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19059 | hp1 | a0001 | c0003 | t0004 | g0316 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19066 | hp2 | a0001 | c0003 | t0004 | g0007 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19074 | hp2 | a0001 | c0007 | t0003 | g0292 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0336 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19240 | hp2 | a0001 | c0005 | t0004 | g0153 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | ASW | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20129 | hp2 | a0001 | c0005 | t0004 | g0028 | AFR | ASW | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0188 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20752 | hp2 | a0001 | c0004 | t0003 | g0006 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0134 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | GIH | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20905 | hp2 | a0001 | c0003 | t0004 | g0154 | SAS | GIH | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02109 | hp2 | a0001 | c0002 | t0020 | g0345 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0248 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02559 | hp2 | a0001 | c0003 | t0004 | g0157 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03471 | hp1 | a0001 | c0003 | t0004 | g0136 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0230 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG06807 | hp1 | a0001 | c0006 | t0006 | g0159 | AFR | USA | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG06807 | hp2 | a0001 | c0003 | t0004 | g0341 | AFR | USA | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA21309 | hp1 | a0001 | c0017 | t0004 | g0297 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
homoSapiens_chm13v2 | hp1 | a0009 | c0026 | t0001 | g0131 | REF | REF | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0176 | REF | REF | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52302071
|
G | A | 1 | a0006 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.155G>A | p.Gly52Glu | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 363/2247 | 155/1461 | 52/486 | chr12 | 52302071 | ||
chr12:52302113
|
G | A | 1 | a0007 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.197G>A | p.Arg66His | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 405/2247 | 197/1461 | 66/486 | chr12 | 52302113 | ||
chr12:52302220
|
G | A | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.304G>A | p.Val102Met | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 512/2247 | 304/1461 | 102/486 | chr12 | 52302220 | ||
chr12:52303146
|
A | C | 1 | a0009 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.416A>C | p.Gln139Pro | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/11 | 624/2247 | 416/1461 | 139/486 | chr12 | 52303146 | ||
chr12:52303217
|
C | T | 1 | a0012 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.487C>T | p.Arg163Trp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/11 | 695/2247 | 487/1461 | 163/486 | chr12 | 52303217 | ||
chr12:52304933
|
A | G | 2 | a0002a0012 | 5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.641A>G | p.Asp214Gly | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 849/2247 | 641/1461 | 214/486 | chr12 | 52304933 | ||
chr12:52305013
|
C | T | 1 | a0003 | 3 | NA18968.hp2 NA18984.hp2 NA19010.hp1 |
missense_variant | MODERATE | c.721C>T | p.Arg241Trp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 929/2247 | 721/1461 | 241/486 | chr12 | 52305013 | ||
chr12:52305024
|
G | C | 1 | a0010 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.732G>C | p.Glu244Asp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 940/2247 | 732/1461 | 244/486 | chr12 | 52305024 | ||
chr12:52305303
|
C | T | 1 | a0005 | 2 | HG03017.hp1 HG03834.hp2 |
missense_variant | MODERATE | c.799C>T | p.Arg267Trp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1007/2247 | 799/1461 | 267/486 | chr12 | 52305303 | ||
chr12:52305366
|
C | G | 1 | a0011 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.862C>G | p.Arg288Gly | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1070/2247 | 862/1461 | 288/486 | chr12 | 52305366 | ||
chr12:52305384
|
G | A | 1 | a0004 | 2 | HG02895.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.880G>A | p.Glu294Lys | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1088/2247 | 880/1461 | 294/486 | chr12 | 52305384 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52301970
|
C | T | 4 | a0001c0003a0001c0017a0001c0027others(1): Show | 51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
synonymous_variant | LOW | c.54C>T | p.Cys18Cys | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 262/2247 | 54/1461 | 18/486 | chr12 | 52301970 | ||
chr12:52301976
|
C | G | 1 | a0001c0016 | 2 | HG01074.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.60C>G | p.Pro20Pro | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 268/2247 | 60/1461 | 20/486 | chr12 | 52301976 | ||
chr12:52302003
|
C | T | 3 | a0001c0003a0001c0017a0006c0028 | 50 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(47): Show |
synonymous_variant | LOW | c.87C>T | p.Ala29Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 295/2247 | 87/1461 | 29/486 | chr12 | 52302003 | ||
chr12:52302117
|
C | T | 1 | a0001c0015 | 2 | NA18970.hp1 NA18994.hp2 |
synonymous_variant | LOW | c.201C>T | p.Ser67Ser | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 409/2247 | 201/1461 | 67/486 | chr12 | 52302117 | ||
chr12:52302204
|
C | T | 1 | a0001c0014 | 2 | HG02630.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.288C>T | p.Asp96Asp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 496/2247 | 288/1461 | 96/486 | chr12 | 52302204 | ||
chr12:52302213
|
G | A | 1 | a0001c0004 | 9 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(6): Show |
synonymous_variant | LOW | c.297G>A | p.Ala99Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 505/2247 | 297/1461 | 99/486 | chr12 | 52302213 | ||
chr12:52302264
|
G | A | 4 | a0001c0003a0001c0020a0001c0027others(1): Show | 50 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(47): Show |
synonymous_variant | LOW | c.348G>A | p.Arg116Arg | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 556/2247 | 348/1461 | 116/486 | chr12 | 52302264 | ||
chr12:52304168
|
G | A | 16 | a0001c0002a0001c0004a0001c0006others(13): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
synonymous_variant | LOW | c.636G>A | p.Lys212Lys | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/11 | 844/2247 | 636/1461 | 212/486 | chr12 | 52304168 | ||
chr12:52304976
|
T | C | 3 | a0001c0005a0001c0006a0001c0021 | 15 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.684T>C | p.Asn228Asn | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 892/2247 | 684/1461 | 228/486 | chr12 | 52304976 | ||
chr12:52305248
|
C | T | 3 | a0001c0008a0002c0009a0012c0025 | 9 | HG00408.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
synonymous_variant | LOW | c.744C>T | p.Arg248Arg | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 952/2247 | 744/1461 | 248/486 | chr12 | 52305248 | ||
chr12:52305275
|
C | G | 1 | a0001c0023 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.771C>G | p.Thr257Thr | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 979/2247 | 771/1461 | 257/486 | chr12 | 52305275 | ||
chr12:52305377
|
T | C | 1 | a0001c0006 | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.873T>C | p.Ala291Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1081/2247 | 873/1461 | 291/486 | chr12 | 52305377 | ||
chr12:52305764
|
T | C | 20 | a0001c0002a0001c0004a0001c0005others(17): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(197): Show |
synonymous_variant | LOW | c.1002T>C | p.Ala334Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/11 | 1210/2247 | 1002/1461 | 334/486 | chr12 | 52305764 | ||
chr12:52306069
|
C | T | 1 | a0001c0014 | 2 | HG02630.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1036C>T | p.Leu346Leu | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/11 | 1244/2247 | 1036/1461 | 346/486 | chr12 | 52306069 | ||
chr12:52306077
|
T | C | 2 | a0001c0005a0001c0010 | 11 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(8): Show |
synonymous_variant | LOW | c.1044T>C | p.Ala348Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/11 | 1252/2247 | 1044/1461 | 348/486 | chr12 | 52306077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52274648
|
C | T | 1 | a0001c0010t0022 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-205C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/11 | chr12 | 52274648 | ||||||
chr12:52274666
|
A | G | 4 | a0001c0001t0011a0001c0002t0011a0001c0002t0020others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-187A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/11 | 27251 | chr12 | 52274666 | |||||
chr12:52274716
|
C | T | 1 | a0001c0003t0019 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/11 | 27201 | chr12 | 52274716 | |||||
chr12:52275841
|
T | C | 1 | a0001c0007t0012 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | 26076 | chr12 | 52275841 | |||||
chr12:52275919
|
G | C | 3 | a0001c0001t0011a0001c0002t0011a0001c0002t0020 | 3 | HG02109.hp2 HG02809.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | 25998 | chr12 | 52275919 | |||||
chr12:52275920
|
G | A | 3 | a0001c0001t0011a0001c0002t0011a0001c0002t0020 | 3 | HG02109.hp2 HG02809.hp1 HG03579.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | chr12 | 52275920 | ||||||
chr12:52275940
|
G | A | 2 | a0001c0001t0007a0001c0002t0013 | 5 | HG02135.hp2 NA18941.hp1 NA18965.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-11G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | 25977 | chr12 | 52275940 | |||||
chr12:52308588
|
G | A | 1 | a0001c0002t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 3 | chr12 | 52308588 | |||||
chr12:52308631
|
A | C | 2 | a0001c0002t0008a0001c0014t0008 | 3 | HG02055.hp1 HG02630.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 46 | chr12 | 52308631 | |||||
chr12:52308679
|
A | G | 13 | a0001c0001t0001a0001c0002t0001a0001c0002t0013others(10): Show | 111 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*94A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 94 | chr12 | 52308679 | |||||
chr12:52308685
|
G | A | 1 | a0004c0012t0014 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 100 | chr12 | 52308685 | |||||
chr12:52308712
|
C | T | 29 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(26): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*127C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 127 | chr12 | 52308712 | |||||
chr12:52308805
|
G | A | 1 | a0001c0001t0015 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 220 | chr12 | 52308805 | |||||
chr12:52308849
|
G | A | 20 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(17): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 264 | chr12 | 52308849 | |||||
chr12:52308856
|
G | GT | 8 | a0001c0002t0003a0001c0004t0003a0001c0007t0003others(5): Show | 61 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*279dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 280 | INFO_REALIGN_3_PRIME | chr12 | 52308856 | ||||
chr12:52308856
|
G | GTT | 20 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(17): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*278_*279dupTT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 280 | INFO_REALIGN_3_PRIME | chr12 | 52308856 | ||||
chr12:52308872
|
A | G | 49 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(46): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*287A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 287 | chr12 | 52308872 | |||||
chr12:52308897
|
C | T | 10 | a0001c0001t0004a0001c0001t0009a0001c0002t0004others(7): Show | 62 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*312C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 312 | chr12 | 52308897 | |||||
chr12:52308943
|
A | G | 2 | a0001c0005t0006a0001c0006t0006 | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*358A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 358 | chr12 | 52308943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52274798
|
A | G | 1 | a0001c0001t0011g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-131+76A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52274798 | ||||||
chr12:52274834
|
A | G | 4 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-131+112A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52274834 | ||||||
chr12:52274932
|
T | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(83): Show | 108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-131+210T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52274932 | ||||||
chr12:52275202
|
T | C | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131+480T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52275202 | ||||||
chr12:52275436
|
AT | A | 41 | a0001c0001t0002g0135a0001c0001t0005g0008a0001c0001t0005g0025others(38): Show | 45 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-130-377delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 52275436 | |||||
chr12:52275627
|
A | G | 4 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130-194A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52275627 | ||||||
chr12:52275628
|
T | A | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130-193T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52275628 | ||||||
chr12:52276029
|
C | A | 1 | a0001c0003t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-5+83C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276029 | ||||||
chr12:52276043
|
T | A | 1 | a0001c0003t0004g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-5+97T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276043 | ||||||
chr12:52276170
|
G | A | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+224G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276170 | ||||||
chr12:52276247
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(82): Show | 107 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-5+301C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276247 | ||||||
chr12:52276394
|
C | T | 2 | a0001c0001t0005g0342a0001c0006t0006g0343 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-5+448C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276394 | ||||||
chr12:52276496
|
T | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(100): Show | 127 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-5+550T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276496 | ||||||
chr12:52276568
|
C | T | 246 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(243): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-5+622C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276568 | ||||||
chr12:52276580
|
AG | A | 99 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(96): Show | 123 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-5+635delG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276580 | ||||||
chr12:52276792
|
A | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(100): Show | 127 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-5+846A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276792 | ||||||
chr12:52276812
|
T | A | 5 | a0001c0001t0002g0011a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 6 | HG02523.hp1 NA18944.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+866T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276812 | ||||||
chr12:52276845
|
T | C | 1 | a0001c0002t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-5+899T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276845 | ||||||
chr12:52276887
|
C | A | 1 | a0001c0005t0006g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5+941C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276887 | ||||||
chr12:52277042
|
G | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(97): Show | 124 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-5+1096G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277042 | ||||||
chr12:52277272
|
A | T | 31 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(28): Show | 33 | HG01168.hp1 HG01891.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.-5+1326A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277272 | ||||||
chr12:52277277
|
G | T | 4 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1331G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277277 | ||||||
chr12:52277319
|
G | A | 1 | a0001c0003t0004g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-5+1373G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277319 | ||||||
chr12:52277343
|
CA | C | 3 | a0001c0014t0008g0163a0001c0014t0008g0164a0002c0009t0001g0031 | 4 | HG02630.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+1400delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52277343 | |||||
chr12:52277470
|
T | G | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(104): Show | 131 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-5+1524T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277470 | ||||||
chr12:52277505
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(83): Show | 108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+1559C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277505 | ||||||
chr12:52277654
|
G | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(83): Show | 108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+1708G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277654 | ||||||
chr12:52277694
|
T | C | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1748T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277694 | ||||||
chr12:52277699
|
G | A | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1753G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277699 | ||||||
chr12:52277768
|
A | C | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1822A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277768 | ||||||
chr12:52277794
|
G | GC | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1849dupC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52277794 | |||||
chr12:52277802
|
C | T | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5+1856C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277802 | ||||||
chr12:52277859
|
C | G | 1 | a0001c0001t0011g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-5+1913C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277859 | ||||||
chr12:52277882
|
T | G | 1 | a0001c0020t0005g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+1936T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277882 | ||||||
chr12:52277982
|
C | T | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+2036C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277982 | ||||||
chr12:52278041
|
C | G | 18 | a0001c0001t0005g0330a0001c0001t0005g0340a0001c0002t0003g0044others(15): Show | 20 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-5+2095C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278041 | ||||||
chr12:52278231
|
TA | T | 5 | a0001c0001t0011g0347a0001c0002t0011g0346a0001c0002t0020g0345others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+2287delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278231 | |||||
chr12:52278252
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-5+2306C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278252 | ||||||
chr12:52278358
|
C | T | 3 | a0001c0002t0001g0225a0001c0002t0001g0226a0001c0002t0001g0227 | 3 | HG01361.hp2 HG01496.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-5+2412C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278358 | ||||||
chr12:52278385
|
A | G | 1 | a0001c0001t0005g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-5+2439A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278385 | ||||||
chr12:52278438
|
G | GT | 58 | a0001c0001t0002g0224a0001c0001t0002g0245a0001c0001t0002g0246others(55): Show | 62 | HG00140.hp1 HG01109.hp2 HG01884.hp1 others(59): Show |
intron_variant | MODIFIER | c.-5+2511dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | |||||
chr12:52278438
|
G | GTT | 110 | a0001c0001t0002g0135a0001c0001t0002g0301a0001c0001t0005g0008others(107): Show | 124 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-5+2510_-5+2511dup others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | |||||
chr12:52278438
|
GT | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0011others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+2511delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | |||||
chr12:52278438
|
GTT | G | 6 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(3): Show | 6 | HG01070.hp2 HG01169.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2510_-5+2511del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | |||||
chr12:52278598
|
G | A | 2 | a0001c0002t0011g0346a0001c0002t0020g0345 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-5+2652G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278598 | ||||||
chr12:52278682
|
T | C | 1 | a0001c0002t0003g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5+2736T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278682 | ||||||
chr12:52278802
|
T | C | 1 | a0001c0003t0004g0269 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-5+2856T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278802 | ||||||
chr12:52278841
|
T | C | 89 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(86): Show | 111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+2895T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278841 | ||||||
chr12:52278852
|
G | C | 160 | a0001c0001t0002g0135a0001c0001t0002g0245a0001c0001t0002g0246others(157): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-5+2906G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278852 | ||||||
chr12:52278873
|
G | A | 42 | a0001c0001t0002g0135a0001c0001t0005g0008a0001c0001t0005g0025others(39): Show | 46 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-5+2927G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278873 | ||||||
chr12:52278909
|
G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+2963G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278909 | ||||||
chr12:52278921
|
C | T | 89 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(86): Show | 111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+2975C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278921 | ||||||
chr12:52278969
|
G | A | 1 | a0001c0002t0003g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+3023G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278969 | ||||||
chr12:52279041
|
G | C | 11 | a0001c0001t0005g0330a0001c0002t0003g0158a0001c0002t0003g0162others(8): Show | 12 | HG00099.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+3095G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279041 | ||||||
chr12:52279087
|
G | GCCGGGCC others(5): Show |
98 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(95): Show | 122 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.-5+3147_-5+3148ins others(12): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52279087 | |||||
chr12:52279102
|
C | T | 77 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0038others(74): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-5+3156C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279102 | ||||||
chr12:52279115
|
C | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0107 | 2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-5+3169C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279115 | ||||||
chr12:52279166
|
C | T | 6 | a0001c0001t0005g0264a0001c0001t0005g0267a0002c0009t0001g0031others(3): Show | 7 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+3220C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279166 | ||||||
chr12:52279206
|
A | C | 1 | a0001c0005t0006g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5+3260A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279206 | ||||||
chr12:52279211
|
T | A | 1 | a0001c0003t0004g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-5+3265T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279211 | ||||||
chr12:52279252
|
A | T | 1 | a0001c0001t0002g0023 | 2 | NA18939.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-5+3306A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279252 | ||||||
chr12:52279305
|
C | T | 89 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(86): Show | 111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+3359C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279305 | ||||||
chr12:52279349
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-5+3403C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279349 | ||||||
chr12:52279409
|
G | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0053 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-5+3463G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279409 | ||||||
chr12:52279461
|
G | A | 88 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+3515G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279461 | ||||||
chr12:52279476
|
C | A | 119 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(116): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-5+3530C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279476 | ||||||
chr12:52279579
|
C | A | 1 | a0001c0001t0005g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-5+3633C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279579 | ||||||
chr12:52279726
|
T | C | 88 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+3780T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279726 | ||||||
chr12:52279765
|
T | G | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-5+3819T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279765 | ||||||
chr12:52279782
|
G | C | 1 | a0001c0001t0005g0055 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-5+3836G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279782 | ||||||
chr12:52279828
|
C | T | 2 | a0001c0002t0011g0346a0001c0002t0020g0345 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-5+3882C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279828 | ||||||
chr12:52279849
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-5+3903C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279849 | ||||||
chr12:52279992
|
G | C | 2 | a0001c0002t0008g0156a0001c0020t0005g0113 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-5+4046G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279992 | ||||||
chr12:52280086
|
C | T | 88 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+4140C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280086 | ||||||
chr12:52280287
|
T | C | 280 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(277): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-5+4341T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280287 | ||||||
chr12:52280304
|
T | C | 1 | a0001c0006t0006g0273 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-5+4358T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280304 | ||||||
chr12:52280472
|
C | T | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+4526C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280472 | ||||||
chr12:52280488
|
C | T | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+4542C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280488 | ||||||
chr12:52280638
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-5+4692C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280638 | ||||||
chr12:52280813
|
A | T | 1 | a0004c0012t0003g0328 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5+4867A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280813 | ||||||
chr12:52280925
|
C | T | 10 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(7): Show | 11 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+4979C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280925 | ||||||
chr12:52280932
|
C | T | 1 | a0001c0001t0005g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-5+4986C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280932 | ||||||
chr12:52280968
|
G | A | 1 | a0001c0001t0007g0056 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-5+5022G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280968 | ||||||
chr12:52281010
|
CT | C | 3 | a0001c0001t0005g0342a0001c0006t0006g0343a0010c0024t0005g0331 | 3 | HG02622.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-5+5067delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52281010 | |||||
chr12:52281241
|
A | G | 17 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(14): Show | 19 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+5295A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281241 | ||||||
chr12:52281250
|
C | T | 88 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+5304C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281250 | ||||||
chr12:52281267
|
A | G | 46 | a0001c0001t0002g0034a0001c0001t0002g0205a0001c0001t0002g0207others(43): Show | 61 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-5+5321A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281267 | ||||||
chr12:52281314
|
T | C | 88 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+5368T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281314 | ||||||
chr12:52281317
|
A | G | 1 | a0001c0001t0005g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-5+5371A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281317 | ||||||
chr12:52281410
|
C | G | 1 | a0001c0001t0002g0102 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-5+5464C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281410 | ||||||
chr12:52281652
|
T | A | 88 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(85): Show | 110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+5706T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281652 | ||||||
chr12:52281661
|
T | G | 86 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(83): Show | 108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+5715T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281661 | ||||||
chr12:52281677
|
C | T | 2 | a0001c0001t0005g0330a0001c0001t0005g0340 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-5+5731C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281677 | ||||||
chr12:52281701
|
C | G | 1 | a0001c0002t0003g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5+5755C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281701 | ||||||
chr12:52281773
|
C | G | 1 | a0001c0002t0003g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-5+5827C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281773 | ||||||
chr12:52281879
|
C | T | 1 | a0001c0001t0002g0107 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-5+5933C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281879 | ||||||
chr12:52281895
|
C | T | 103 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 126 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.-5+5949C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281895 | ||||||
chr12:52281896
|
G | A | 15 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(12): Show | 17 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5+5950G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281896 | ||||||
chr12:52281914
|
A | C | 76 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0038others(73): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+5968A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281914 | ||||||
chr12:52281933
|
G | A | 10 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(7): Show | 11 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+5987G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281933 | ||||||
chr12:52282102
|
G | GAAT | 265 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(262): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-5+6157_-5+6158ins others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52282102 | |||||
chr12:52282118
|
G | A | 15 | a0001c0001t0005g0330a0001c0001t0005g0340a0001c0002t0003g0044others(12): Show | 16 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+6172G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282118 | ||||||
chr12:52282133
|
G | A | 280 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(277): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-5+6187G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282133 | ||||||
chr12:52282151
|
T | A | 1 | a0001c0003t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-5+6205T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282151 | ||||||
chr12:52282215
|
G | A | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6269G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282215 | ||||||
chr12:52282236
|
A | AT | 39 | a0001c0001t0002g0135a0001c0001t0005g0008a0001c0001t0005g0025others(36): Show | 43 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+6304dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52282236 | |||||
chr12:52282236
|
A | ATTT | 83 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(80): Show | 105 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-5+6302_-5+6304dup others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52282236 | |||||
chr12:52282257
|
A | G | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6311A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282257 | ||||||
chr12:52282295
|
C | A | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6349C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282295 | ||||||
chr12:52282323
|
C | T | 14 | a0001c0001t0004g0253a0001c0002t0003g0101a0001c0002t0003g0149others(11): Show | 14 | HG01168.hp1 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-5+6377C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282323 | ||||||
chr12:52282333
|
C | T | 76 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0038others(73): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+6387C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282333 | ||||||
chr12:52282349
|
C | T | 85 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(82): Show | 107 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-5+6403C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282349 | ||||||
chr12:52282417
|
T | C | 6 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(3): Show | 7 | HG02451.hp2 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+6471T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282417 | ||||||
chr12:52282437
|
T | C | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6491T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282437 | ||||||
chr12:52282438
|
G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+6492G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282438 | ||||||
chr12:52282463
|
T | C | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6517T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282463 | ||||||
chr12:52282598
|
C | T | 1 | a0001c0005t0006g0326 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-5+6652C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282598 | ||||||
chr12:52282619
|
A | G | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6673A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282619 | ||||||
chr12:52282635
|
A | G | 1 | a0001c0001t0002g0100 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-5+6689A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282635 | ||||||
chr12:52282694
|
A | G | 15 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(12): Show | 17 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5+6748A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282694 | ||||||
chr12:52282724
|
C | T | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+6778C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282724 | ||||||
chr12:52282741
|
C | T | 87 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(84): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6795C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282741 | ||||||
chr12:52282971
|
C | G | 102 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(99): Show | 125 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-5+7025C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282971 | ||||||
chr12:52283004
|
T | G | 1 | a0001c0005t0004g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-5+7058T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283004 | ||||||
chr12:52283030
|
A | G | 1 | a0001c0001t0005g0325 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+7084A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283030 | ||||||
chr12:52283060
|
C | T | 6 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(3): Show | 7 | HG02451.hp2 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+7114C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283060 | ||||||
chr12:52283134
|
G | A | 3 | a0001c0002t0001g0197a0001c0002t0001g0222a0001c0008t0001g0198 | 3 | NA19000.hp2 NA19002.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-5+7188G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283134 | ||||||
chr12:52283134
|
G | T | 1 | a0001c0001t0005g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-5+7188G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283134 | ||||||
chr12:52283159
|
G | C | 1 | a0011c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-5+7213G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283159 | ||||||
chr12:52283183
|
C | G | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | NA18747.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.-5+7237C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283183 | ||||||
chr12:52283193
|
A | G | 117 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(114): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-5+7247A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283193 | ||||||
chr12:52283205
|
A | C | 86 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(83): Show | 108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+7259A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283205 | ||||||
chr12:52283252
|
G | A | 160 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(157): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-5+7306G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283252 | ||||||
chr12:52283259
|
T | TG | 351 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(348): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.-5+7314dupG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283259 | |||||
chr12:52283275
|
T | C | 279 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(276): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-5+7329T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283275 | ||||||
chr12:52283377
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5+7431G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283377 | ||||||
chr12:52283392
|
C | CA | 56 | a0001c0001t0002g0059a0001c0001t0002g0260a0001c0001t0005g0025others(53): Show | 63 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-5+7470dupA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | |||||
chr12:52283392
|
C | CAA | 27 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(24): Show | 28 | HG00423.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-5+7469_-5+7470dup others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | |||||
chr12:52283392
|
C | CAAA | 13 | a0001c0002t0001g0232a0001c0002t0001g0233a0001c0002t0001g0234others(10): Show | 13 | HG01255.hp1 HG01891.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+7468_-5+7470dup others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | |||||
chr12:52283392
|
CA | C | 76 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(73): Show | 98 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-5+7470delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | |||||
chr12:52283404
|
A | AAAT | 9 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(6): Show | 10 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+7460_-5+7461ins others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283404 | |||||
chr12:52283409
|
A | T | 10 | a0001c0002t0003g0158a0001c0002t0003g0162a0001c0002t0003g0271others(7): Show | 11 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+7463A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283409 | ||||||
chr12:52283425
|
G | T | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+7479G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283425 | ||||||
chr12:52283452
|
T | C | 41 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(38): Show | 43 | HG01109.hp2 HG01168.hp1 HG01255.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+7506T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283452 | ||||||
chr12:52283470
|
A | AT | 11 | a0001c0001t0002g0195a0001c0001t0005g0128a0001c0002t0001g0165others(8): Show | 11 | HG00438.hp1 HG01106.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+7549dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | |||||
chr12:52283470
|
AT | A | 117 | a0001c0001t0002g0034a0001c0001t0002g0135a0001c0001t0002g0205others(114): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-5+7549delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | |||||
chr12:52283470
|
ATT | A | 65 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0038others(62): Show | 73 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-5+7548_-5+7549del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | |||||
chr12:52283470
|
ATTTTTT | A | 14 | a0001c0001t0002g0012a0001c0001t0002g0022a0001c0001t0002g0068others(11): Show | 15 | HG01261.hp1 HG01261.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5+7544_-5+7549del others(6): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | |||||
chr12:52283470
|
ATTTTTTT | A | 74 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(71): Show | 95 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-5+7543_-5+7549del others(7): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | |||||
chr12:52283509
|
G | A | 2 | a0001c0003t0004g0284a0001c0003t0004g0311 | 2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-5+7563G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283509 | ||||||
chr12:52283626
|
A | C | 1 | a0001c0001t0004g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5+7680A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283626 | ||||||
chr12:52283731
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-5+7785C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283731 | ||||||
chr12:52283759
|
C | A | 4 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0014t0008g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+7813C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283759 | ||||||
chr12:52283925
|
T | G | 106 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(103): Show | 131 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.-5+7979T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283925 | ||||||
chr12:52284126
|
A | G | 2 | a0001c0001t0011g0347a0001c0023t0001g0338 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-5+8180A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284126 | ||||||
chr12:52284139
|
T | C | 4 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0014t0008g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8193T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284139 | ||||||
chr12:52284150
|
G | A | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+8204G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284150 | ||||||
chr12:52284167
|
G | A | 1 | a0001c0001t0005g0342 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+8221G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284167 | ||||||
chr12:52284187
|
G | C | 1 | a0001c0020t0005g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+8241G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284187 | ||||||
chr12:52284190
|
T | G | 1 | a0001c0002t0003g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-5+8244T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284190 | ||||||
chr12:52284236
|
C | T | 1 | a0001c0003t0004g0320 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-5+8290C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284236 | ||||||
chr12:52284272
|
G | A | 1 | a0001c0002t0003g0312 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5+8326G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284272 | ||||||
chr12:52284338
|
C | T | 4 | a0001c0001t0005g0042a0001c0001t0005g0283a0001c0001t0005g0310others(1): Show | 5 | HG02615.hp1 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+8392C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284338 | ||||||
chr12:52284343
|
C | A | 1 | a0001c0001t0005g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-5+8397C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284343 | ||||||
chr12:52284343
|
C | T | 1 | a0001c0020t0005g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+8397C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284343 | ||||||
chr12:52284344
|
G | A | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+8398G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284344 | ||||||
chr12:52284351
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-5+8405A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284351 | ||||||
chr12:52284428
|
G | C | 274 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(271): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-5+8482G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284428 | ||||||
chr12:52284440
|
T | G | 15 | a0001c0001t0005g0264a0001c0001t0005g0267a0001c0002t0003g0044others(12): Show | 17 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5+8494T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284440 | ||||||
chr12:52284515
|
T | C | 275 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(272): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-5+8569T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284515 | ||||||
chr12:52284647
|
T | A | 4 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0014t0008g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8701T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284647 | ||||||
chr12:52284654
|
T | C | 4 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0014t0008g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8708T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284654 | ||||||
chr12:52284784
|
C | T | 140 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(137): Show | 167 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+8838C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284784 | ||||||
chr12:52284857
|
T | G | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+8911T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284857 | ||||||
chr12:52284859
|
G | A | 140 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(137): Show | 167 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+8913G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284859 | ||||||
chr12:52285025
|
A | C | 1 | a0001c0003t0004g0309 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-5+9079A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285025 | ||||||
chr12:52285069
|
A | G | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+9123A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285069 | ||||||
chr12:52285116
|
A | G | 128 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(125): Show | 154 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.-5+9170A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285116 | ||||||
chr12:52285134
|
C | G | 1 | a0001c0002t0003g0322 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-5+9188C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285134 | ||||||
chr12:52285240
|
G | A | 133 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(130): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-5+9294G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285240 | ||||||
chr12:52285362
|
TA | T | 265 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(262): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-5+9430delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52285362 | |||||
chr12:52285362
|
TAA | T | 5 | a0001c0001t0002g0021a0001c0001t0005g0125a0001c0001t0005g0147others(2): Show | 6 | HG01099.hp2 HG01256.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+9429_-5+9430del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52285362 | |||||
chr12:52285481
|
C | G | 1 | a0001c0003t0004g0320 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-5+9535C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285481 | ||||||
chr12:52285521
|
T | C | 1 | a0001c0002t0001g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+9575T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285521 | ||||||
chr12:52285548
|
A | G | 2 | a0001c0002t0003g0249a0008c0019t0003g0252 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5+9602A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285548 | ||||||
chr12:52285793
|
G | A | 280 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(277): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-5+9847G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285793 | ||||||
chr12:52285794
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-5+9848G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285794 | ||||||
chr12:52285928
|
T | C | 1 | a0001c0003t0004g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5+9982T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285928 | ||||||
chr12:52285930
|
T | C | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+9984T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285930 | ||||||
chr12:52286119
|
G | T | 2 | a0001c0014t0008g0163a0001c0014t0008g0164 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-5+10173G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286119 | ||||||
chr12:52286153
|
C | G | 138 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(135): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.-5+10207C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286153 | ||||||
chr12:52286224
|
T | C | 130 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(127): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-5+10278T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286224 | ||||||
chr12:52286320
|
C | T | 1 | a0001c0002t0011g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-5+10374C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286320 | ||||||
chr12:52286388
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0005g0267a0001c0023t0001g0338others(4): Show | 8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+10442G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286388 | ||||||
chr12:52286406
|
G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+10460G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286406 | ||||||
chr12:52286409
|
G | A | 1 | a0001c0001t0005g0138 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-5+10463G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286409 | ||||||
chr12:52286426
|
A | G | 1 | a0001c0002t0003g0241 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-5+10480A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286426 | ||||||
chr12:52286619
|
G | A | 1 | a0001c0006t0006g0343 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-5+10673G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286619 | ||||||
chr12:52286634
|
A | C | 1 | a0001c0001t0002g0099 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-5+10688A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286634 | ||||||
chr12:52286643
|
G | A | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+10697G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286643 | ||||||
chr12:52286733
|
T | C | 1 | a0001c0001t0002g0068 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-5+10787T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286733 | ||||||
chr12:52286982
|
G | A | 42 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(39): Show | 44 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5+11036G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286982 | ||||||
chr12:52287005
|
T | C | 3 | a0001c0003t0004g0334a0001c0003t0004g0341a0001c0016t0005g0333 | 3 | HG02572.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-5+11059T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287005 | ||||||
chr12:52287069
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-5+11123G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287069 | ||||||
chr12:52287272
|
C | T | 127 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(124): Show | 153 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.-5+11326C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287272 | ||||||
chr12:52287296
|
G | A | 86 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(83): Show | 109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+11350G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287296 | ||||||
chr12:52287348
|
A | G | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5+11402A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287348 | ||||||
chr12:52287373
|
A | G | 3 | a0001c0002t0001g0179a0001c0002t0001g0191a0001c0002t0001g0196 | 3 | HG01070.hp1 HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-5+11427A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287373 | ||||||
chr12:52287498
|
T | C | 278 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(275): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-5+11552T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287498 | ||||||
chr12:52287632
|
T | C | 139 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+11686T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287632 | ||||||
chr12:52287653
|
A | G | 139 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+11707A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287653 | ||||||
chr12:52287676
|
G | A | 1 | a0001c0003t0004g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-5+11730G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287676 | ||||||
chr12:52287701
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0007t0003g0067 | 5 | NA18947.hp1 NA18965.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+11755C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287701 | ||||||
chr12:52287749
|
T | C | 139 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+11803T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287749 | ||||||
chr12:52287848
|
C | A | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+11902C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287848 | ||||||
chr12:52287930
|
T | C | 338 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(335): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-5+11984T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287930 | ||||||
chr12:52287949
|
A | C | 147 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(144): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-5+12003A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287949 | ||||||
chr12:52287972
|
T | C | 5 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0014t0008g0163others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+12026T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287972 | ||||||
chr12:52288022
|
G | A | 1 | a0001c0003t0004g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-5+12076G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288022 | ||||||
chr12:52288038
|
A | T | 1 | a0009c0026t0001g0131 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-5+12092A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288038 | ||||||
chr12:52288072
|
A | C | 1 | a0001c0008t0001g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-5+12126A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288072 | ||||||
chr12:52288128
|
C | T | 1 | a0001c0001t0005g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-5+12182C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288128 | ||||||
chr12:52288141
|
A | C | 338 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(335): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-5+12195A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288141 | ||||||
chr12:52288184
|
T | C | 349 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(346): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.-5+12238T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288184 | ||||||
chr12:52288310
|
A | T | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+12364A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288310 | ||||||
chr12:52288336
|
T | C | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+12390T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288336 | ||||||
chr12:52288342
|
C | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0007t0003g0067 | 5 | NA18947.hp1 NA18965.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+12396C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288342 | ||||||
chr12:52288346
|
C | T | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+12400C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288346 | ||||||
chr12:52288350
|
T | G | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+12404T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288350 | ||||||
chr12:52288357
|
G | A | 60 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0199others(57): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.-5+12411G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288357 | ||||||
chr12:52288430
|
C | T | 1 | a0001c0001t0015g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-5+12484C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288430 | ||||||
chr12:52288434
|
C | T | 1 | a0001c0002t0004g0029 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-5+12488C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288434 | ||||||
chr12:52288484
|
A | AG | 4 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0006t0006g0343others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+12538_-5+12539i others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288484 | ||||||
chr12:52288591
|
C | T | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+12645C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288591 | ||||||
chr12:52288658
|
G | A | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+12712G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288658 | ||||||
chr12:52288740
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-5+12794C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288740 | ||||||
chr12:52288778
|
A | G | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+12832A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288778 | ||||||
chr12:52288834
|
C | A | 49 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(46): Show | 51 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+12888C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288834 | ||||||
chr12:52288925
|
G | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-5+12979G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288925 | ||||||
chr12:52288934
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12979G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288934 | ||||||
chr12:52288935
|
C | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12978C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288935 | ||||||
chr12:52288940
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12973G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288940 | ||||||
chr12:52288942
|
A | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12971A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288942 | ||||||
chr12:52288944
|
T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12969T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288944 | ||||||
chr12:52288946
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12967G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288946 | ||||||
chr12:52288997
|
C | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12916C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288997 | ||||||
chr12:52289001
|
T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12912T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289001 | ||||||
chr12:52289002
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12911G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289002 | ||||||
chr12:52289007
|
A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12906A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289007 | ||||||
chr12:52289010
|
T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12903T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289010 | ||||||
chr12:52289016
|
C | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12897C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289016 | ||||||
chr12:52289021
|
A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12892A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289021 | ||||||
chr12:52289022
|
GATATTCC others(59): Show |
G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12890_-4-12825d others(68): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289022 | ||||||
chr12:52289032
|
A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12881A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289032 | ||||||
chr12:52289091
|
C | G | 6 | a0001c0003t0004g0318a0001c0005t0004g0028a0001c0005t0004g0151others(3): Show | 7 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-12822C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289091 | ||||||
chr12:52289094
|
A | G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12819A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289094 | ||||||
chr12:52289096
|
C | G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12817C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289096 | ||||||
chr12:52289097
|
C | G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12816C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289097 | ||||||
chr12:52289117
|
T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12796T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289117 | ||||||
chr12:52289118
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12795G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289118 | ||||||
chr12:52289125
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12788G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289125 | ||||||
chr12:52289156
|
G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12757G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289156 | ||||||
chr12:52289161
|
A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12752A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289161 | ||||||
chr12:52289162
|
T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12751T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289162 | ||||||
chr12:52289163
|
C | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12750C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289163 | ||||||
chr12:52289218
|
C | T | 2 | a0001c0002t0003g0145a0001c0002t0020g0345 | 2 | HG00621.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-4-12695C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289218 | ||||||
chr12:52289333
|
C | T | 1 | a0001c0002t0020g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-12580C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289333 | ||||||
chr12:52289361
|
C | G | 46 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(43): Show | 48 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4-12552C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289361 | ||||||
chr12:52289364
|
G | A | 46 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(43): Show | 48 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4-12549G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289364 | ||||||
chr12:52289368
|
A | G | 46 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(43): Show | 48 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4-12545A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289368 | ||||||
chr12:52289419
|
G | C | 9 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0002t0003g0145others(6): Show | 9 | HG00621.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-12494G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289419 | ||||||
chr12:52289422
|
T | G | 9 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0002t0003g0145others(6): Show | 9 | HG00621.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-12491T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289422 | ||||||
chr12:52289426
|
A | G | 9 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0002t0003g0145others(6): Show | 9 | HG00621.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-12487A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289426 | ||||||
chr12:52289634
|
C | G | 7 | a0001c0001t0005g0264a0001c0001t0005g0267a0001c0002t0003g0327others(4): Show | 8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-12279C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289634 | ||||||
chr12:52289685
|
T | C | 12 | a0001c0001t0005g0026a0001c0001t0005g0140a0001c0001t0005g0342others(9): Show | 13 | HG01123.hp2 HG01517.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.-4-12228T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289685 | ||||||
chr12:52289695
|
G | C | 269 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(266): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-4-12218G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289695 | ||||||
chr12:52289798
|
C | T | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-12115C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289798 | ||||||
chr12:52289900
|
C | G | 80 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0042others(77): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-4-12013C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289900 | ||||||
chr12:52290056
|
C | A | 1 | a0001c0001t0002g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-4-11857C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290056 | ||||||
chr12:52290169
|
G | A | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4-11744G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290169 | ||||||
chr12:52290202
|
C | G | 2 | a0001c0001t0005g0330a0001c0001t0005g0340 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-4-11711C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290202 | ||||||
chr12:52290240
|
T | G | 33 | a0001c0001t0002g0135a0001c0001t0005g0008a0001c0001t0005g0025others(30): Show | 37 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-11673T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290240 | ||||||
chr12:52290241
|
G | T | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG01243.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-4-11672G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290241 | ||||||
chr12:52290295
|
C | T | 2 | a0001c0010t0010g0030a0001c0010t0022g0030 | 2 | HG00099.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-4-11618C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290295 | ||||||
chr12:52290296
|
G | A | 2 | a0001c0001t0002g0076a0001c0015t0001g0077 | 2 | NA18970.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-4-11617G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290296 | ||||||
chr12:52290386
|
C | A | 2 | a0001c0002t0008g0156a0001c0003t0004g0341 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4-11527C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290386 | ||||||
chr12:52290534
|
A | AC | 34 | a0001c0001t0002g0210a0001c0001t0002g0212a0001c0001t0002g0217others(31): Show | 43 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-4-11367dupC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290534 | |||||
chr12:52290541
|
C | CCCA | 16 | a0001c0001t0002g0014a0001c0001t0002g0046a0001c0001t0002g0205others(13): Show | 18 | HG00558.hp2 HG01168.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4-11370_-4-11369i others(5): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290541 | |||||
chr12:52290541
|
C | CCCCA | 126 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0011others(123): Show | 150 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4-11369_-4-11368i others(6): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290541 | |||||
chr12:52290541
|
C | CCCCCA | 90 | a0001c0001t0002g0003a0001c0001t0002g0018a0001c0001t0002g0024others(87): Show | 106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-4-11368_-4-11367i others(7): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290541 | |||||
chr12:52290547
|
A | ACCCCCC | 36 | a0001c0001t0002g0012a0001c0001t0002g0019a0001c0001t0002g0135others(33): Show | 37 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.-4-11366_-4-11365i others(8): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290547 | ||||||
chr12:52290547
|
A | C | 244 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(241): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-4-11366A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290547 | ||||||
chr12:52290570
|
G | A | 111 | a0001c0001t0002g0097a0001c0001t0002g0205a0001c0001t0002g0260others(108): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-4-11343G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290570 | ||||||
chr12:52290787
|
G | A | 1 | a0001c0005t0004g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4-11126G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290787 | ||||||
chr12:52290912
|
A | G | 43 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(40): Show | 45 | HG00099.hp2 HG00621.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.-4-11001A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290912 | ||||||
chr12:52290975
|
C | T | 1 | a0003c0011t0001g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-4-10938C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290975 | ||||||
chr12:52290983
|
A | G | 4 | a0001c0001t0005g0038a0001c0005t0004g0274a0001c0005t0006g0166others(1): Show | 5 | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-10930A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290983 | ||||||
chr12:52291027
|
C | T | 4 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0006t0006g0343others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10886C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291027 | ||||||
chr12:52291041
|
G | A | 4 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0006t0006g0343others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10872G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291041 | ||||||
chr12:52291087
|
G | A | 1 | a0001c0002t0003g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-10826G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291087 | ||||||
chr12:52291114
|
C | T | 1 | a0001c0002t0001g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-4-10799C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291114 | ||||||
chr12:52291118
|
C | T | 1 | a0001c0003t0004g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-4-10795C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291118 | ||||||
chr12:52291169
|
C | T | 2 | a0001c0001t0005g0330a0001c0001t0005g0340 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-4-10744C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291169 | ||||||
chr12:52291312
|
C | G | 85 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(82): Show | 108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-4-10601C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291312 | ||||||
chr12:52291332
|
A | G | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-10581A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291332 | ||||||
chr12:52291356
|
C | T | 1 | a0001c0003t0004g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-4-10557C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291356 | ||||||
chr12:52291395
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-4-10518C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291395 | ||||||
chr12:52291404
|
C | T | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-4-10509C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291404 | ||||||
chr12:52291406
|
C | G | 12 | a0001c0001t0002g0017a0001c0001t0002g0065a0001c0001t0002g0068others(9): Show | 14 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-10507C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291406 | ||||||
chr12:52291418
|
C | G | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-4-10495C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291418 | ||||||
chr12:52291429
|
T | G | 43 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0004g0253others(40): Show | 45 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.-4-10484T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291429 | ||||||
chr12:52291465
|
T | G | 1 | a0001c0003t0004g0276 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-4-10448T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291465 | ||||||
chr12:52291585
|
T | G | 4 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0006t0006g0343others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10328T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291585 | ||||||
chr12:52291649
|
C | G | 119 | a0001c0001t0002g0135a0001c0001t0002g0260a0001c0001t0002g0301others(116): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-4-10264C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291649 | ||||||
chr12:52291665
|
G | A | 1 | a0001c0002t0011g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-4-10248G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291665 | ||||||
chr12:52291701
|
T | TAAAAGAT others(307): Show |
3 | a0001c0002t0001g0036a0001c0002t0001g0233a0001c0002t0001g0243 | 4 | NA18966.hp1 NA18969.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(316): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(309): Show |
9 | a0001c0002t0003g0149a0001c0002t0003g0229a0001c0002t0003g0230others(6): Show | 9 | HG01168.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(318): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(310): Show |
1 | a0001c0002t0003g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-4-10194_-4-10193i others(319): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(320): Show |
8 | a0001c0001t0002g0246a0001c0002t0001g0232a0001c0002t0001g0238others(5): Show | 9 | HG03017.hp2 NA18747.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(329): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(321): Show |
7 | a0001c0001t0002g0245a0001c0002t0001g0234a0001c0002t0001g0237others(4): Show | 7 | HG00621.hp1 HG02027.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(330): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(322): Show |
2 | a0001c0002t0001g0235a0001c0003t0004g0255 | 2 | HG02523.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(331): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(327): Show |
2 | a0001c0002t0003g0101a0001c0002t0003g0254 | 2 | HG01255.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(336): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(328): Show |
1 | a0001c0002t0003g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-4-10194_-4-10193i others(337): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(329): Show |
2 | a0001c0002t0003g0247a0001c0002t0003g0282 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(338): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291701
|
T | TAAAAGAT others(330): Show |
1 | a0001c0001t0004g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4-10194_-4-10193i others(339): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | |||||
chr12:52291729
|
G | T | 3 | a0001c0010t0010g0030a0001c0010t0010g0161a0001c0010t0022g0030 | 3 | HG00099.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-4-10184G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291729 | ||||||
chr12:52291761
|
C | T | 33 | a0001c0001t0002g0135a0001c0001t0005g0008a0001c0001t0005g0025others(30): Show | 37 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-10152C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291761 | ||||||
chr12:52292039
|
T | C | 3 | a0001c0002t0003g0162a0001c0002t0003g0271a0001c0002t0003g0337 | 3 | HG02451.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-4-9874T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52292039 | ||||||
chr12:52292666
|
ATTTATT | A | 87 | a0001c0001t0002g0260a0001c0001t0002g0301a0001c0001t0005g0042others(84): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-4-9238_-4-9233del others(6): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52292666 | |||||
chr12:52292982
|
C | T | 1 | a0001c0002t0001g0208 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-4-8931C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52292982 | ||||||
chr12:52293113
|
C | A | 8 | a0001c0002t0003g0044a0001c0002t0003g0257a0001c0002t0003g0329others(5): Show | 9 | HG01884.hp1 HG02145.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-8800C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293113 | ||||||
chr12:52293233
|
C | T | 1 | a0001c0003t0004g0286 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-4-8680C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293233 | ||||||
chr12:52293243
|
C | T | 4 | a0001c0001t0005g0342a0001c0001t0011g0347a0001c0006t0006g0343others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-8670C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293243 | ||||||
chr12:52293262
|
T | C | 1 | a0001c0001t0002g0024 | 2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-8651T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293262 | ||||||
chr12:52293286
|
G | A | 266 | a0001c0001t0002g0034a0001c0001t0002g0060a0001c0001t0002g0205others(263): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-4-8627G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293286 | ||||||
chr12:52293369
|
A | G | 1 | a0001c0005t0004g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-8544A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293369 | ||||||
chr12:52293487
|
T | A | 1 | a0001c0007t0003g0289 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-4-8426T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293487 | ||||||
chr12:52293581
|
C | T | 2 | a0001c0001t0002g0301a0001c0027t0004g0302 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-4-8332C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293581 | ||||||
chr12:52293632
|
A | G | 56 | a0001c0001t0002g0092a0001c0001t0002g0301a0001c0001t0005g0330others(53): Show | 65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-4-8281A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293632 | ||||||
chr12:52293704
|
G | A | 1 | a0001c0002t0020g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-8209G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293704 | ||||||
chr12:52293710
|
C | T | 1 | a0001c0002t0021g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-8203C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293710 | ||||||
chr12:52293847
|
T | C | 1 | a0001c0002t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4-8066T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293847 | ||||||
chr12:52293863
|
G | A | 1 | a0001c0002t0001g0313 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-4-8050G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293863 | ||||||
chr12:52294175
|
G | C | 1 | a0001c0002t0001g0209 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-4-7738G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294175 | ||||||
chr12:52294201
|
C | T | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-7712C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294201 | ||||||
chr12:52294477
|
AAGGGAGG others(17): Show |
A | 1 | a0001c0003t0004g0324 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-4-7416_-4-7393del others(24): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52294477 | |||||
chr12:52294559
|
G | A | 3 | a0001c0007t0005g0150a0001c0007t0005g0152a0001c0007t0012g0304 | 3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-7354G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294559 | ||||||
chr12:52294982
|
C | T | 89 | a0001c0001t0002g0301a0001c0002t0001g0036a0001c0002t0001g0232others(86): Show | 101 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-4-6931C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294982 | ||||||
chr12:52295071
|
C | T | 1 | a0001c0003t0004g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4-6842C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295071 | ||||||
chr12:52295125
|
A | G | 1 | a0001c0002t0001g0188 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-4-6788A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295125 | ||||||
chr12:52295384
|
A | C | 256 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0210others(253): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-4-6529A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295384 | ||||||
chr12:52295498
|
A | T | 1 | a0001c0002t0021g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-6415A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295498 | ||||||
chr12:52295537
|
C | A | 1 | a0001c0001t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4-6376C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295537 | ||||||
chr12:52295693
|
T | C | 1 | a0001c0003t0004g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-4-6220T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295693 | ||||||
chr12:52295755
|
A | G | 1 | a0001c0002t0003g0256 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-4-6158A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295755 | ||||||
chr12:52295977
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-5936G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295977 | ||||||
chr12:52296076
|
G | A | 6 | a0001c0001t0005g0027a0001c0001t0005g0264a0002c0009t0001g0031others(3): Show | 8 | HG00733.hp1 HG01993.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-5837G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296076 | ||||||
chr12:52296112
|
G | C | 1 | a0001c0002t0020g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-5801G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296112 | ||||||
chr12:52296290
|
C | A | 5 | a0001c0001t0005g0264a0002c0009t0001g0031a0002c0009t0001g0265others(2): Show | 6 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-5623C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296290 | ||||||
chr12:52296304
|
G | A | 4 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0016t0005g0333others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-5609G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296304 | ||||||
chr12:52296369
|
C | T | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-5544C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296369 | ||||||
chr12:52296468
|
G | A | 3 | a0001c0007t0005g0150a0001c0007t0005g0152a0001c0007t0012g0304 | 3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-5445G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296468 | ||||||
chr12:52296663
|
G | GC | 160 | a0001c0001t0002g0301a0001c0001t0004g0253a0001c0001t0005g0008others(157): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-4-5249dupC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52296663 | |||||
chr12:52296682
|
C | T | 5 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(2): Show | 6 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-5231C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296682 | ||||||
chr12:52296853
|
G | C | 47 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(44): Show | 52 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-4-5060G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296853 | ||||||
chr12:52296863
|
C | A | 5 | a0001c0001t0005g0264a0002c0009t0001g0031a0002c0009t0001g0265others(2): Show | 6 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-5050C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296863 | ||||||
chr12:52296940
|
C | T | 5 | a0001c0001t0005g0264a0002c0009t0001g0031a0002c0009t0001g0265others(2): Show | 6 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-4973C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296940 | ||||||
chr12:52296941
|
G | A | 2 | a0001c0002t0020g0345a0001c0023t0001g0338 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-4-4972G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296941 | ||||||
chr12:52297026
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-4-4887C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297026 | ||||||
chr12:52297267
|
C | G | 2 | a0001c0001t0002g0073a0001c0001t0002g0098 | 2 | NA18747.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-4-4646C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297267 | ||||||
chr12:52297300
|
C | G | 13 | a0001c0002t0003g0044a0001c0002t0003g0158a0001c0002t0003g0162others(10): Show | 15 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-4-4613C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297300 | ||||||
chr12:52297319
|
T | C | 211 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0210others(208): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-4-4594T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297319 | ||||||
chr12:52297496
|
G | A | 3 | a0001c0001t0005g0038a0001c0001t0005g0330a0001c0001t0005g0340 | 4 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-4417G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297496 | ||||||
chr12:52297500
|
T | C | 2 | a0001c0003t0004g0296a0001c0003t0004g0321 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-4-4413T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297500 | ||||||
chr12:52297536
|
C | T | 3 | a0001c0001t0005g0038a0001c0001t0005g0330a0001c0001t0005g0340 | 4 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-4377C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297536 | ||||||
chr12:52297540
|
G | C | 78 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0210others(75): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-4-4373G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297540 | ||||||
chr12:52297566
|
T | C | 1 | a0001c0002t0003g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-4347T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297566 | ||||||
chr12:52297611
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-4302A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297611 | ||||||
chr12:52297675
|
A | G | 2 | a0001c0002t0011g0346a0001c0016t0005g0333 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-4-4238A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297675 | ||||||
chr12:52298164
|
G | A | 1 | a0001c0016t0005g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-4-3749G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298164 | ||||||
chr12:52298174
|
T | C | 51 | a0001c0002t0001g0036a0001c0002t0001g0232a0001c0002t0001g0233others(48): Show | 59 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-4-3739T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298174 | ||||||
chr12:52298218
|
A | G | 3 | a0001c0007t0005g0150a0001c0007t0005g0152a0001c0007t0012g0304 | 3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-3695A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298218 | ||||||
chr12:52298307
|
C | T | 45 | a0001c0001t0002g0301a0001c0003t0004g0007a0001c0003t0004g0040others(42): Show | 49 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.-4-3606C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298307 | ||||||
chr12:52298423
|
C | T | 5 | a0001c0004t0003g0006a0001c0004t0003g0039a0001c0004t0003g0277others(2): Show | 9 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-3490C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298423 | ||||||
chr12:52298447
|
T | A | 1 | a0001c0001t0005g0125 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-4-3466T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298447 | ||||||
chr12:52298500
|
G | T | 1 | a0001c0002t0021g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-3413G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298500 | ||||||
chr12:52298689
|
G | A | 66 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(63): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-4-3224G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298689 | ||||||
chr12:52298727
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-3186A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298727 | ||||||
chr12:52298729
|
G | A | 2 | a0001c0001t0001g0167a0001c0002t0020g0345 | 2 | HG02040.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-4-3184G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298729 | ||||||
chr12:52298768
|
T | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0034a0001c0001t0002g0062others(6): Show | 11 | HG00609.hp2 NA18965.hp2 NA18979.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-3145T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298768 | ||||||
chr12:52298797
|
A | C | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-4-3116A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298797 | ||||||
chr12:52298810
|
A | T | 274 | a0001c0001t0002g0091a0001c0001t0002g0099a0001c0001t0002g0205others(271): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-4-3103A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298810 | ||||||
chr12:52298886
|
C | G | 252 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0212others(249): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-4-3027C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298886 | ||||||
chr12:52298920
|
C | T | 49 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0212others(46): Show | 63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-4-2993C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298920 | ||||||
chr12:52298921
|
C | T | 10 | a0001c0001t0005g0042a0001c0001t0005g0264a0001c0001t0005g0267others(7): Show | 11 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-2992C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298921 | ||||||
chr12:52298925
|
AC | A | 4 | a0002c0009t0001g0031a0002c0009t0001g0265a0002c0009t0001g0266others(1): Show | 5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-2986delC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52298925 | |||||
chr12:52299015
|
G | A | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-4-2898G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299015 | ||||||
chr12:52299031
|
A | G | 49 | a0001c0003t0004g0007a0001c0003t0004g0040a0001c0003t0004g0069others(46): Show | 53 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-4-2882A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299031 | ||||||
chr12:52299130
|
A | G | 65 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(62): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-4-2783A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299130 | ||||||
chr12:52299176
|
C | T | 1 | a0011c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-2737C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299176 | ||||||
chr12:52299177
|
G | T | 3 | a0001c0007t0005g0150a0001c0007t0005g0152a0001c0007t0012g0304 | 3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-2736G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299177 | ||||||
chr12:52299179
|
A | G | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4-2734A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299179 | ||||||
chr12:52299220
|
A | G | 3 | a0001c0002t0008g0156a0001c0014t0008g0163a0001c0014t0008g0164 | 3 | HG02055.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-4-2693A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299220 | ||||||
chr12:52299392
|
C | T | 42 | a0001c0002t0001g0036a0001c0002t0001g0215a0001c0002t0001g0232others(39): Show | 49 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-4-2521C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299392 | ||||||
chr12:52299529
|
T | C | 3 | a0001c0010t0010g0030a0001c0010t0010g0161a0001c0010t0022g0030 | 3 | HG00099.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-4-2384T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299529 | ||||||
chr12:52299548
|
C | T | 273 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0212others(270): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-4-2365C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299548 | ||||||
chr12:52299723
|
G | T | 3 | a0001c0002t0008g0156a0001c0014t0008g0163a0001c0014t0008g0164 | 3 | HG02055.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-4-2190G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299723 | ||||||
chr12:52299757
|
T | G | 2 | a0005c0013t0001g0184a0005c0013t0001g0185 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-4-2156T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299757 | ||||||
chr12:52299779
|
A | C | 3 | a0001c0002t0001g0206a0001c0002t0001g0214a0001c0002t0001g0219 | 3 | NA18980.hp2 NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-4-2134A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299779 | ||||||
chr12:52299852
|
C | T | 1 | a0001c0003t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-4-2061C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299852 | ||||||
chr12:52300083
|
T | C | 13 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(10): Show | 14 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-1830T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300083 | ||||||
chr12:52300185
|
T | C | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1728T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300185 | ||||||
chr12:52300213
|
G | T | 273 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0212others(270): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-4-1700G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300213 | ||||||
chr12:52300372
|
A | G | 32 | a0001c0002t0003g0015a0001c0002t0003g0041a0001c0002t0003g0101others(29): Show | 37 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-1541A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300372 | ||||||
chr12:52300403
|
G | A | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1510G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300403 | ||||||
chr12:52300509
|
C | A | 117 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(114): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-4-1404C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300509 | ||||||
chr12:52300581
|
A | T | 1 | a0001c0001t0002g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-4-1332A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300581 | ||||||
chr12:52300749
|
G | T | 47 | a0001c0003t0004g0007a0001c0003t0004g0040a0001c0003t0004g0069others(44): Show | 51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-1164G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300749 | ||||||
chr12:52300825
|
G | A | 47 | a0001c0003t0004g0007a0001c0003t0004g0040a0001c0003t0004g0069others(44): Show | 51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-1088G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300825 | ||||||
chr12:52300966
|
A | C | 1 | a0001c0002t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4-947A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300966 | ||||||
chr12:52301165
|
GA | G | 6 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(3): Show | 7 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-747delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301165 | ||||||
chr12:52301166
|
A | G | 1 | a0001c0005t0006g0326 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-4-747A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301166 | ||||||
chr12:52301263
|
G | A | 69 | a0001c0001t0002g0080a0001c0001t0002g0088a0001c0001t0007g0056others(66): Show | 79 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-4-650G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301263 | ||||||
chr12:52301334
|
G | T | 3 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0016t0005g0333 | 3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-4-579G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301334 | ||||||
chr12:52301377
|
C | T | 1 | a0001c0002t0001g0303 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-4-536C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301377 | ||||||
chr12:52301414
|
G | C | 31 | a0001c0002t0003g0015a0001c0002t0003g0041a0001c0002t0003g0101others(28): Show | 36 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.-4-499G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301414 | ||||||
chr12:52301420
|
C | A | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-493C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301420 | ||||||
chr12:52301422
|
A | G | 1 | a0001c0002t0001g0226 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-4-491A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301422 | ||||||
chr12:52301603
|
G | A | 1 | a0001c0002t0001g0211 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-4-310G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301603 | ||||||
chr12:52301654
|
A | T | 1 | a0001c0003t0004g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4-259A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301654 | ||||||
chr12:52301690
|
T | C | 1 | a0001c0002t0001g0215 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-4-223T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301690 | ||||||
chr12:52301832
|
T | C | 1 | a0001c0001t0002g0024 | 2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-81T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301832 | ||||||
chr12:52301846
|
C | T | 47 | a0001c0003t0004g0007a0001c0003t0004g0040a0001c0003t0004g0069others(44): Show | 51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-67C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301846 | ||||||
chr12:52301884
|
C | A | 2 | a0002c0009t0001g0265a0002c0009t0001g0266 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-29C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301884 | ||||||
chr12:52302341
|
C | T | 42 | a0001c0003t0004g0007a0001c0003t0004g0040a0001c0003t0004g0069others(39): Show | 46 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.369+56C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302341 | ||||||
chr12:52302483
|
G | A | 19 | a0001c0002t0003g0043a0001c0002t0003g0044a0001c0002t0003g0158others(16): Show | 22 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.369+198G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302483 | ||||||
chr12:52302629
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.369+344G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302629 | ||||||
chr12:52302732
|
C | T | 1 | a0001c0003t0004g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.370-368C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302732 | ||||||
chr12:52302812
|
T | C | 130 | a0001c0001t0002g0047a0001c0001t0002g0063a0001c0001t0002g0092others(127): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.370-288T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302812 | ||||||
chr12:52302835
|
G | T | 4 | a0001c0001t0002g0207a0001c0002t0001g0180a0001c0015t0001g0077others(1): Show | 4 | HG01934.hp1 HG02293.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-265G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302835 | ||||||
chr12:52302841
|
T | TG | 63 | a0001c0001t0002g0016a0001c0001t0002g0048a0001c0001t0002g0059others(60): Show | 68 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.370-249dupG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 52302841 | |||||
chr12:52302841
|
TG | T | 81 | a0001c0001t0002g0051a0001c0001t0002g0092a0001c0001t0002g0205others(78): Show | 100 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.370-249delG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 52302841 | |||||
chr12:52302841
|
TGG | T | 24 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0121others(21): Show | 26 | HG00280.hp2 HG00639.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.370-250_370-249del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 52302841 | |||||
chr12:52302844
|
G | T | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.370-256G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302844 | ||||||
chr12:52302845
|
G | GA | 16 | a0001c0002t0003g0015a0001c0002t0003g0041a0001c0002t0003g0145others(13): Show | 21 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.370-255_370-254ins others(1): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302845 | ||||||
chr12:52302848
|
G | A | 2 | a0001c0002t0003g0239a0001c0002t0003g0241 | 2 | NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.370-252G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302848 | ||||||
chr12:52302871
|
G | A | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.370-229G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302871 | ||||||
chr12:52303000
|
G | T | 41 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(38): Show | 45 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.370-100G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52303000 | ||||||
chr12:52303091
|
G | A | 4 | a0001c0002t0021g0344a0001c0010t0010g0030a0001c0010t0010g0161others(1): Show | 4 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-9G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52303091 | ||||||
chr12:52303348
|
G | T | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.578+40G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303348 | ||||||
chr12:52303349
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.578+41T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303349 | ||||||
chr12:52303363
|
A | G | 2 | a0001c0002t0003g0229a0001c0002t0003g0230 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.578+55A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303363 | ||||||
chr12:52303486
|
G | C | 12 | a0001c0002t0003g0339a0001c0003t0004g0069a0001c0003t0004g0072others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.578+178G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303486 | ||||||
chr12:52303566
|
G | C | 4 | a0002c0009t0001g0031a0002c0009t0001g0265a0002c0009t0001g0266others(1): Show | 5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+258G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303566 | ||||||
chr12:52303569
|
G | A | 1 | a0001c0017t0004g0297 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.578+261G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303569 | ||||||
chr12:52303691
|
G | C | 180 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(177): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.578+383G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303691 | ||||||
chr12:52303701
|
A | G | 181 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(178): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.578+393A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303701 | ||||||
chr12:52303724
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.579-387C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303724 | ||||||
chr12:52303823
|
G | A | 3 | a0001c0001t0005g0134a0001c0001t0005g0141a0001c0001t0005g0147 | 3 | HG01069.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.579-288G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303823 | ||||||
chr12:52303960
|
T | C | 261 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(258): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.579-151T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303960 | ||||||
chr12:52303964
|
A | C | 261 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(258): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.579-147A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303964 | ||||||
chr12:52303967
|
C | G | 261 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(258): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.579-144C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303967 | ||||||
chr12:52303988
|
C | T | 1 | a0001c0001t0005g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.579-123C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303988 | ||||||
chr12:52304018
|
T | C | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579-93T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304018 | ||||||
chr12:52304022
|
C | T | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579-89C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304022 | ||||||
chr12:52304025
|
G | C | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579-86G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304025 | ||||||
chr12:52304053
|
G | A | 3 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0016t0005g0333 | 3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.579-58G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304053 | ||||||
chr12:52304083
|
C | T | 1 | a0001c0001t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.579-28C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304083 | ||||||
chr12:52304223
|
G | A | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+52G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304223 | ||||||
chr12:52304224
|
A | G | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+53A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304224 | ||||||
chr12:52304225
|
T | C | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+54T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304225 | ||||||
chr12:52304230
|
C | T | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+59C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304230 | ||||||
chr12:52304261
|
C | T | 170 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(167): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.639+90C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304261 | ||||||
chr12:52304268
|
C | T | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+97C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304268 | ||||||
chr12:52304269
|
A | G | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+98A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304269 | ||||||
chr12:52304340
|
C | A | 1 | a0001c0001t0002g0082 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.639+169C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304340 | ||||||
chr12:52304354
|
T | C | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+183T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304354 | ||||||
chr12:52304365
|
T | C | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+194T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304365 | ||||||
chr12:52304370
|
G | A | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+199G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304370 | ||||||
chr12:52304376
|
A | C | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.639+205A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304376 | ||||||
chr12:52304376
|
A | G | 263 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(260): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+205A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304376 | ||||||
chr12:52304379
|
T | C | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+208T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304379 | ||||||
chr12:52304384
|
C | T | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+213C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304384 | ||||||
chr12:52304385
|
A | G | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+214A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304385 | ||||||
chr12:52304389
|
G | A | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+218G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304389 | ||||||
chr12:52304440
|
C | T | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+269C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304440 | ||||||
chr12:52304442
|
A | G | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+271A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304442 | ||||||
chr12:52304444
|
T | G | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+273T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304444 | ||||||
chr12:52304446
|
C | T | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+275C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304446 | ||||||
chr12:52304448
|
G | T | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.639+277G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304448 | ||||||
chr12:52304451
|
G | T | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+280G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304451 | ||||||
chr12:52304452
|
C | T | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+281C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304452 | ||||||
chr12:52304461
|
C | A | 264 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(261): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+290C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304461 | ||||||
chr12:52304469
|
G | GATTCT | 3 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0016t0005g0333 | 3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+300_639+301ins others(5): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 52304469 | |||||
chr12:52304472
|
A | G | 3 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0016t0005g0333 | 3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+301A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304472 | ||||||
chr12:52304472
|
A | T | 261 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(258): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.639+301A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304472 | ||||||
chr12:52304474
|
A | T | 3 | a0001c0002t0011g0346a0001c0002t0020g0345a0001c0016t0005g0333 | 3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+303A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304474 | ||||||
chr12:52304490
|
G | C | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.639+319G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304490 | ||||||
chr12:52304552
|
T | G | 5 | a0001c0001t0002g0049a0001c0001t0005g0128a0001c0007t0003g0067others(2): Show | 5 | HG00438.hp1 NA18944.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-380T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304552 | ||||||
chr12:52304582
|
T | C | 5 | a0001c0001t0002g0052a0001c0001t0002g0090a0001c0007t0003g0067others(2): Show | 5 | HG01168.hp2 HG01169.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-350T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304582 | ||||||
chr12:52304587
|
C | A | 5 | a0001c0001t0002g0052a0001c0001t0002g0090a0001c0007t0003g0067others(2): Show | 5 | HG01168.hp2 HG01169.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-345C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304587 | ||||||
chr12:52304588
|
T | C | 5 | a0001c0001t0002g0052a0001c0001t0002g0090a0001c0007t0003g0067others(2): Show | 5 | HG01168.hp2 HG01169.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-344T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304588 | ||||||
chr12:52304595
|
T | C | 6 | a0001c0001t0002g0052a0001c0001t0002g0083a0001c0001t0002g0090others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-337T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304595 | ||||||
chr12:52304606
|
G | T | 10 | a0001c0001t0002g0052a0001c0001t0002g0059a0001c0001t0002g0083others(7): Show | 10 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-326G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304606 | ||||||
chr12:52304607
|
C | G | 10 | a0001c0001t0002g0052a0001c0001t0002g0059a0001c0001t0002g0083others(7): Show | 10 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-325C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304607 | ||||||
chr12:52304678
|
G | T | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-254G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304678 | ||||||
chr12:52304680
|
G | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-252G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304680 | ||||||
chr12:52304686
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-246A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304686 | ||||||
chr12:52304694
|
T | C | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-238T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304694 | ||||||
chr12:52304696
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-236A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304696 | ||||||
chr12:52304702
|
T | C | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-230T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304702 | ||||||
chr12:52304709
|
C | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-223C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304709 | ||||||
chr12:52304710
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-222A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304710 | ||||||
chr12:52304727
|
C | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-205C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304727 | ||||||
chr12:52304729
|
G | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-203G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304729 | ||||||
chr12:52304732
|
C | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-200C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304732 | ||||||
chr12:52304733
|
C | T | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-199C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304733 | ||||||
chr12:52304738
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-194A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304738 | ||||||
chr12:52304754
|
C | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-178C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304754 | ||||||
chr12:52304760
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-172A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304760 | ||||||
chr12:52304761
|
T | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-171T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304761 | ||||||
chr12:52304763
|
G | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-169G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304763 | ||||||
chr12:52304777
|
G | C | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-155G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304777 | ||||||
chr12:52304781
|
C | T | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-151C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304781 | ||||||
chr12:52304784
|
C | T | 1 | a0001c0002t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.640-148C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304784 | ||||||
chr12:52304785
|
G | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-147G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304785 | ||||||
chr12:52304787
|
G | C | 2 | a0001c0005t0006g0139a0001c0005t0006g0166 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.640-145G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304787 | ||||||
chr12:52304792
|
GC | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-138delC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 52304792 | |||||
chr12:52304802
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-130A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304802 | ||||||
chr12:52304806
|
AG | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-125delG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304806 | ||||||
chr12:52304809
|
G | A | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-123G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304809 | ||||||
chr12:52304822
|
A | G | 3 | a0001c0007t0003g0067a0001c0007t0003g0289a0001c0007t0003g0292 | 3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-110A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304822 | ||||||
chr12:52305032
|
G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.735+5G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305032 | ||||||
chr12:52305051
|
A | C | 4 | a0001c0001t0002g0058a0001c0001t0002g0085a0001c0001t0002g0089others(1): Show | 4 | HG00741.hp1 HG01243.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+24A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305051 | ||||||
chr12:52305056
|
T | C | 3 | a0001c0002t0001g0178a0001c0002t0001g0181a0001c0002t0001g0221 | 3 | NA18972.hp2 NA19001.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.735+29T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305056 | ||||||
chr12:52305066
|
CAG | C | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+44_735+45delAG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 52305066 | |||||
chr12:52305147
|
G | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0301 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.736-93G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305147 | ||||||
chr12:52305180
|
T | C | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.736-60T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305180 | ||||||
chr12:52305192
|
G | A | 1 | a0001c0002t0011g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.736-48G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305192 | ||||||
chr12:52305429
|
G | T | 100 | a0001c0001t0004g0253a0001c0001t0005g0008a0001c0001t0005g0025others(97): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.900+25G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305429 | ||||||
chr12:52305507
|
A | G | 1 | a0001c0007t0005g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.900+103A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305507 | ||||||
chr12:52305518
|
C | T | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.900+114C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305518 | ||||||
chr12:52305573
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.901-90A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305573 | ||||||
chr12:52305635
|
A | G | 10 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(7): Show | 11 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-28A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305635 | ||||||
chr12:52305837
|
G | T | 3 | a0001c0001t0005g0038a0001c0001t0005g0330a0001c0001t0005g0340 | 4 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+49G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305837 | ||||||
chr12:52305899
|
A | G | 1 | a0001c0001t0002g0018 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1026+111A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305899 | ||||||
chr12:52305913
|
G | A | 2 | a0001c0003t0004g0280a0001c0003t0004g0300 | 2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1026+125G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305913 | ||||||
chr12:52305930
|
T | A | 1 | a0001c0003t0004g0323 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1027-130T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305930 | ||||||
chr12:52305944
|
G | A | 166 | a0001c0001t0004g0045a0001c0001t0004g0253a0001c0001t0005g0008others(163): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1027-116G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305944 | ||||||
chr12:52305987
|
C | T | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-73C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305987 | ||||||
chr12:52305988
|
A | G | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-72A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305988 | ||||||
chr12:52306045
|
C | T | 2 | a0001c0002t0001g0165a0001c0002t0001g0188 | 2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1027-15C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52306045 | ||||||
chr12:52306316
|
C | A | 160 | a0001c0001t0004g0045a0001c0001t0004g0253a0001c0001t0005g0008others(157): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1247+36C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306316 | ||||||
chr12:52306416
|
C | T | 1 | a0001c0001t0002g0046 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1247+136C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306416 | ||||||
chr12:52306573
|
G | T | 1 | a0005c0013t0001g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1247+293G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306573 | ||||||
chr12:52306609
|
G | A | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1247+329G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306609 | ||||||
chr12:52306925
|
A | G | 1 | a0011c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1247+645A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306925 | ||||||
chr12:52307047
|
C | CT | 47 | a0001c0001t0004g0045a0001c0003t0004g0007a0001c0003t0004g0040others(44): Show | 51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1247+776dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 52307047 | |||||
chr12:52307061
|
A | T | 1 | a0001c0003t0004g0321 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1247+781A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307061 | ||||||
chr12:52307084
|
G | A | 1 | a0011c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1247+804G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307084 | ||||||
chr12:52307183
|
C | T | 176 | a0001c0001t0004g0045a0001c0001t0004g0253a0001c0001t0005g0008others(173): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1247+903C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307183 | ||||||
chr12:52307420
|
T | A | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248-813T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307420 | ||||||
chr12:52307461
|
C | T | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1248-772C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307461 | ||||||
chr12:52307537
|
G | A | 1 | a0001c0002t0003g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1248-696G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307537 | ||||||
chr12:52307609
|
C | T | 7 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0005g0027others(4): Show | 9 | HG00733.hp1 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1248-624C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307609 | ||||||
chr12:52307625
|
C | T | 55 | a0001c0002t0003g0015a0001c0002t0003g0041a0001c0002t0003g0043others(52): Show | 62 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1248-608C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307625 | ||||||
chr12:52307739
|
A | G | 5 | a0001c0003t0004g0258a0001c0003t0004g0276a0001c0003t0004g0286others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248-494A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307739 | ||||||
chr12:52307740
|
G | A | 1 | a0001c0002t0003g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248-493G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307740 | ||||||
chr12:52307776
|
C | T | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248-457C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307776 | ||||||
chr12:52307820
|
T | G | 1 | a0001c0002t0001g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1248-413T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307820 | ||||||
chr12:52307874
|
G | A | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1248-359G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307874 | ||||||
chr12:52307919
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1248-314G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307919 | ||||||
chr12:52307924
|
T | C | 16 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(13): Show | 17 | HG00099.hp2 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1248-309T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307924 | ||||||
chr12:52307926
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1248-307C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307926 | ||||||
chr12:52307962
|
T | C | 7 | a0001c0005t0004g0028a0001c0005t0004g0151a0001c0005t0004g0153others(4): Show | 8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248-271T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307962 | ||||||
chr12:52308049
|
A | C | 1 | a0001c0002t0003g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1248-184A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52308049 | ||||||
chr12:52308050
|
G | T | 1 | a0001c0002t0003g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1248-183G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52308050 | ||||||
chr12:52308081
|
C | T | 3 | a0001c0010t0010g0030a0001c0010t0010g0161a0001c0010t0022g0030 | 3 | HG00099.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1248-152C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52308081 | ||||||
chr12:52308347
|
C | T | 6 | a0001c0006t0006g0159a0001c0006t0006g0273a0001c0006t0006g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-57C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 10/10 | chr12 | 52308347 |