geneid | 91801 |
---|---|
ensemblid | ENSG00000137760.15 |
hgncid | 25189 |
symbol | ALKBH8 |
name | alkB homolog 8, tRNA methyltransferase |
refseq_nuc | NM_138775.3 |
refseq_prot | NP_620130.2 |
ensembl_nuc | ENST00000428149.7 |
ensembl_prot | ENSP00000415885.2 |
mane_status | MANE Select |
chr | chr11 |
start | 107502727 |
end | 107565735 |
strand | - |
ver | v1.2 |
region | chr11:107502727-107565735 |
region5000 | chr11:107497727-107570735 |
regionname0 | ALKBH8_chr11_107502727_107565735 |
regionname5000 | ALKBH8_chr11_107497727_107570735 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 664 | 359 | 65 | 66 | 184 | 12 | 30 | 154 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0002 | 0/0 | 664 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0003 | 0/0 | 664 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0004 | 0/0 | 664 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0005 | 0/0 | 664 | 4 | 0 | 1 | 0 | 1 | 2 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0006 | 0/0 | 664 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0007 | 0/0 | 664 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0008 | 0/0 | 664 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0009 | 0/0 | 664 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0010 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0011 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0012 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0013 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0014 | 0/0 | 664 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0015 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0016 | 0/0 | 664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1995 | 238 | 29 | 43 | 127 | 11 | 27 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0002 | 1/0 | 1995 | 96 | 13 | 22 | 56 | 1 | 3 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0003 | 0/0 | 1995 | 20 | 19 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0004 | 0/0 | 1995 | 10 | 8 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0005 | 0/0 | 1995 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0006 | 0/0 | 1995 | 5 | 0 | 0 | 5 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0007 | 0/0 | 1995 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0008 | 0/0 | 1995 | 4 | 0 | 1 | 0 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0009 | 0/0 | 1995 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0010 | 0/0 | 1995 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0011 | 0/0 | 1995 | 2 | 0 | 0 | 0 | 1 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0012 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0013 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0014 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0015 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0016 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0017 | 0/0 | 1995 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0018 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0019 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0020 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0021 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
c0022 | 0/0 | 1995 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2073 | 276 | 56 | 53 | 143 | 7 | 16 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0002 | 0/1 | 2073 | 76 | 0 | 16 | 39 | 6 | 14 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0003 | 0/0 | 2073 | 9 | 9 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0004 | 0/0 | 2073 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0005 | 0/0 | 2073 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0006 | 0/0 | 2073 | 4 | 0 | 1 | 0 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0007 | 0/0 | 2073 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0008 | 0/0 | 2077 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0009 | 0/0 | 2073 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0010 | 0/0 | 2077 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0011 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0012 | 0/0 | 2073 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0013 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0014 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0015 | 0/0 | 2073 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0016 | 0/0 | 2073 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0017 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0018 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0019 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
t0020 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
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 | 2 | 6 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0003 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0011 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0012 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
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 | 0/1 | 1995 | 238 | 29 | 43 | 127 | 11 | 27 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002 | 1/0 | 1995 | 96 | 13 | 22 | 56 | 1 | 3 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003 | 0/0 | 1995 | 20 | 19 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0007 | 0/0 | 1995 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0019 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0002c0004 | 0/0 | 1995 | 10 | 8 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0003c0005 | 0/0 | 1995 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0004c0006 | 0/0 | 1995 | 5 | 0 | 0 | 5 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0005c0008 | 0/0 | 1995 | 4 | 0 | 1 | 0 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0006c0011 | 0/0 | 1995 | 2 | 0 | 0 | 0 | 1 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0006c0017 | 0/0 | 1995 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0007c0009 | 0/0 | 1995 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0008c0010 | 0/0 | 1995 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0009c0012 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0009c0016 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0010c0021 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0011c0020 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0012c0015 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0013c0014 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0014c0018 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0015c0013 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0016c0022 | 0/0 | 1995 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4067 | 154 | 28 | 26 | 83 | 5 | 12 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0002 | 0/1 | 4067 | 76 | 0 | 16 | 39 | 6 | 14 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0005 | 0/0 | 4067 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0012 | 0/0 | 4067 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0014 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0015 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0019 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0001t0020 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0001 | 1/0 | 4067 | 89 | 10 | 21 | 54 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0003 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0005 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0010 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0016 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0017 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0002t0018 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003t0001 | 0/0 | 4067 | 3 | 2 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003t0003 | 0/0 | 4067 | 6 | 6 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003t0007 | 0/0 | 4067 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003t0008 | 0/0 | 4071 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003t0010 | 0/0 | 4071 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0003t0013 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0007t0001 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0007t0011 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0001c0019t0005 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0002c0004t0001 | 0/0 | 4067 | 10 | 8 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0003c0005t0004 | 0/0 | 4067 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0004c0006t0001 | 0/0 | 4067 | 5 | 0 | 0 | 5 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0005c0008t0006 | 0/0 | 4067 | 4 | 0 | 1 | 0 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0006c0011t0001 | 0/0 | 4067 | 2 | 0 | 0 | 0 | 1 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0006c0017t0001 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0007c0009t0001 | 0/0 | 4067 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0008c0010t0001 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0009c0012t0009 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0009c0016t0009 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0010c0021t0001 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0011c0020t0009 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0012c0015t0003 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0013c0014t0001 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0014c0018t0001 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0015c0013t0001 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
a0016c0022t0001 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | copy fasta | chr11 | 107497727 | 107570735 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0015g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0001t0020g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0016g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0017g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0002t0018g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0008g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0003t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0007t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0007t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0007t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0001c0019t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0002c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0003c0005t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0003c0005t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0003c0005t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0003c0005t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0003c0005t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0004c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0004c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0004c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0004c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0004c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0005c0008t0006g0012 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0005c0008t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0006c0011t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0006c0011t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0006c0017t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0007c0009t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0007c0009t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0007c0009t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0008c0010t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0008c0010t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0009c0012t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0009c0016t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0010c0021t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0011c0020t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0012c0015t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0013c0014t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0014c0018t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0015c0013t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
a0016c0022t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00140 | hp1 | a0006 | c0011 | t0001 | g0247 | EUR | GBR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | GBR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00280 | hp1 | a0005 | c0008 | t0006 | g0012 | EUR | FIN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0100 | EUR | FIN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00408 | hp2 | a0014 | c0018 | t0001 | g0142 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00673 | hp1 | a0004 | c0006 | t0001 | g0239 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01081 | hp2 | a0002 | c0004 | t0001 | g0272 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01106 | hp2 | a0008 | c0010 | t0001 | g0094 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01167 | hp1 | a0001 | c0001 | t0015 | g0285 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01192 | hp2 | a0016 | c0022 | t0001 | g0181 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01243 | hp1 | a0002 | c0004 | t0001 | g0210 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01358 | hp2 | a0001 | c0002 | t0016 | g0121 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01361 | hp1 | a0008 | c0010 | t0001 | g0095 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01433 | hp1 | a0005 | c0008 | t0006 | g0253 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0261 | EUR | IBS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01891 | hp1 | a0001 | c0007 | t0011 | g0049 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01891 | hp2 | a0001 | c0003 | t0003 | g0282 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02055 | hp2 | a0001 | c0007 | t0001 | g0216 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0126 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02165 | hp1 | a0001 | c0001 | t0012 | g0150 | EAS | CDX | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CDX | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02257 | hp2 | a0003 | c0005 | t0004 | g0212 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02258 | hp1 | a0001 | c0003 | t0007 | g0230 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02280 | hp1 | a0001 | c0007 | t0001 | g0204 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0283 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02572 | hp1 | a0001 | c0003 | t0003 | g0284 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02572 | hp2 | a0001 | c0003 | t0008 | g0326 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02615 | hp1 | a0001 | c0003 | t0008 | g0015 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02615 | hp2 | a0002 | c0004 | t0001 | g0274 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02622 | hp2 | a0002 | c0004 | t0001 | g0275 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02630 | hp2 | a0002 | c0004 | t0001 | g0271 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02647 | hp1 | a0009 | c0016 | t0009 | g0207 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02683 | hp2 | a0006 | c0011 | t0001 | g0248 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02717 | hp1 | a0009 | c0012 | t0009 | g0227 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02717 | hp2 | a0002 | c0004 | t0001 | g0273 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02723 | hp2 | a0001 | c0003 | t0010 | g0280 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02809 | hp2 | a0007 | c0009 | t0001 | g0226 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02818 | hp1 | a0010 | c0021 | t0001 | g0205 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02818 | hp2 | a0002 | c0004 | t0001 | g0276 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02886 | hp1 | a0011 | c0020 | t0009 | g0318 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02895 | hp1 | a0001 | c0003 | t0013 | g0301 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02895 | hp2 | a0003 | c0005 | t0004 | g0215 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02896 | hp1 | a0001 | c0003 | t0007 | g0229 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02896 | hp2 | a0002 | c0004 | t0001 | g0040 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02897 | hp1 | a0003 | c0005 | t0004 | g0214 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02897 | hp2 | a0002 | c0004 | t0001 | g0040 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02922 | hp1 | a0013 | c0014 | t0001 | g0198 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02965 | hp1 | a0001 | c0003 | t0003 | g0220 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03041 | hp1 | a0007 | c0009 | t0001 | g0225 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03130 | hp1 | a0002 | c0004 | t0001 | g0277 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03139 | hp1 | a0001 | c0001 | t0020 | g0327 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0200 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03225 | hp2 | a0001 | c0003 | t0007 | g0233 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03491 | hp2 | a0005 | c0008 | t0006 | g0012 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03492 | hp2 | a0005 | c0008 | t0006 | g0012 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03540 | hp1 | a0001 | c0007 | t0011 | g0050 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03710 | hp1 | a0006 | c0017 | t0001 | g0222 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03834 | hp1 | a0001 | c0002 | t0017 | g0098 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03942 | hp1 | a0001 | c0001 | t0019 | g0240 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | STU | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | STU | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | STU | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18953 | hp2 | a0001 | c0002 | t0005 | g0132 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18971 | hp1 | a0004 | c0006 | t0001 | g0059 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18974 | hp1 | a0001 | c0001 | t0012 | g0151 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18979 | hp1 | a0004 | c0006 | t0001 | g0065 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18997 | hp1 | a0004 | c0006 | t0001 | g0061 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18998 | hp1 | a0001 | c0001 | t0014 | g0084 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19005 | hp1 | a0001 | c0019 | t0005 | g0161 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19005 | hp2 | a0001 | c0002 | t0018 | g0237 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | LWK | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19043 | hp1 | a0015 | c0013 | t0001 | g0206 | AFR | LWK | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | LWK | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19060 | hp1 | a0004 | c0006 | t0001 | g0090 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19240 | hp1 | a0012 | c0015 | t0003 | g0199 | AFR | YRI | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0286 | EUR | TSI | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02109 | hp1 | a0001 | c0003 | t0008 | g0015 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0232 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02486 | hp1 | a0007 | c0009 | t0001 | g0218 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02486 | hp2 | a0003 | c0005 | t0004 | g0324 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0219 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0224 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG03471 | hp2 | a0001 | c0003 | t0008 | g0015 | AFR | MSL | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | USA | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
HG06807 | hp2 | a0001 | c0003 | t0010 | g0231 | AFR | USA | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA20300 | hp1 | a0001 | c0002 | t0010 | g0128 | AFR | USA | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA20300 | hp2 | a0001 | c0003 | t0007 | g0228 | AFR | USA | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA21309 | hp1 | a0003 | c0005 | t0004 | g0213 | AFR | LWK | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0258 | REF | REF | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0066 | REF | REF | ALKBH8_chr11_107497727_107570735 | ALKBH8 | chr11 | 107497727 | 107570735 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:107504696
|
C | A | 1 | a0006 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.1957G>T | p.Asp653Tyr | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 2098/4067 | 1957/1995 | 653/664 | chr11 | 107504696 | ||
chr11:107504761
|
C | T | 1 | a0003 | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.1892G>A | p.Arg631His | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 2033/4067 | 1892/1995 | 631/664 | chr11 | 107504761 | ||
chr11:107504819
|
C | A | 1 | a0002 | 10 | HG01081.hp2 HG01243.hp1 HG02615.hp2 others(7): Show |
missense_variant | MODERATE | c.1834G>T | p.Gly612Cys | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1975/4067 | 1834/1995 | 612/664 | chr11 | 107504819 | ||
chr11:107504833
|
G | C | 1 | a0004 | 5 | HG00673.hp1 NA18971.hp1 NA18979.hp1 others(2): Show |
missense_variant | MODERATE | c.1820C>G | p.Pro607Arg | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1961/4067 | 1820/1995 | 607/664 | chr11 | 107504833 | ||
chr11:107504941
|
C | T | 1 | a0012 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1712G>A | p.Arg571Lys | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1853/4067 | 1712/1995 | 571/664 | chr11 | 107504941 | ||
chr11:107504953
|
C | T | 1 | a0005 | 4 | HG00280.hp1 HG01433.hp1 HG03491.hp2 others(1): Show |
missense_variant | MODERATE | c.1700G>A | p.Gly567Glu | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1841/4067 | 1700/1995 | 567/664 | chr11 | 107504953 | ||
chr11:107510892
|
T | C | 1 | a0014 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1432A>G | p.Thr478Ala | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/12 | 1573/4067 | 1432/1995 | 478/664 | chr11 | 107510892 | ||
chr11:107510904
|
G | T | 1 | a0008 | 2 | HG01106.hp2 HG01361.hp1 |
missense_variant | MODERATE | c.1420C>A | p.His474Asn | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/12 | 1561/4067 | 1420/1995 | 474/664 | chr11 | 107510904 | ||
chr11:107525446
|
T | C | 1 | a0015 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1025A>G | p.Asn342Ser | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/12 | 1166/4067 | 1025/1995 | 342/664 | chr11 | 107525446 | ||
chr11:107525585
|
A | C | 2 | a0009a0011 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
missense_variant | MODERATE | c.886T>G | p.Cys296Gly | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/12 | 1027/4067 | 886/1995 | 296/664 | chr11 | 107525585 | ||
chr11:107551809
|
T | G | 4 | a0010a0011a0012others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.699A>C | p.Gln233His | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/12 | 840/4067 | 699/1995 | 233/664 | chr11 | 107551809 | ||
chr11:107556896
|
G | C | 2 | a0010a0011 | 2 | HG02818.hp1 HG02886.hp1 |
missense_variant | MODERATE | c.237C>G | p.Asn79Lys | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/12 | 378/4067 | 237/1995 | 79/664 | chr11 | 107556896 | ||
chr11:107556961
|
G | A | 1 | a0016 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.172C>T | p.Arg58Trp | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/12 | 313/4067 | 172/1995 | 58/664 | chr11 | 107556961 | ||
chr11:107556987
|
T | C | 1 | a0007 | 3 | HG02486.hp1 HG02809.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.146A>G | p.Asn49Ser | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/12 | 287/4067 | 146/1995 | 49/664 | chr11 | 107556987 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:107510956
|
T | G | 1 | a0001c0019 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1368A>C | p.Ala456Ala | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/12 | 1509/4067 | 1368/1995 | 456/664 | chr11 | 107510956 | ||
chr11:107549804
|
A | G | 13 | a0001c0001a0001c0007a0001c0019others(10): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
synonymous_variant | LOW | c.720T>C | p.Asp240Asp | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/12 | 861/4067 | 720/1995 | 240/664 | chr11 | 107549804 | ||
chr11:107553959
|
C | T | 2 | a0010c0021a0011c0020 | 2 | HG02818.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.387G>A | p.Arg129Arg | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/12 | 528/4067 | 387/1995 | 129/664 | chr11 | 107553959 | ||
chr11:107556890
|
C | G | 9 | a0001c0003a0001c0007a0002c0004others(6): Show | 40 | HG01081.hp2 HG01109.hp2 HG01243.hp1 others(37): Show |
synonymous_variant | LOW | c.243G>C | p.Pro81Pro | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/12 | 384/4067 | 243/1995 | 81/664 | chr11 | 107556890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:107502752
|
T | C | 1 | a0001c0001t0014 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1906A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1906 | chr11 | 107502752 | |||||
chr11:107502782
|
T | C | 7 | a0001c0002t0003a0001c0003t0003a0001c0003t0013others(4): Show | 13 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1876A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1876 | chr11 | 107502782 | |||||
chr11:107502852
|
T | A | 1 | a0001c0002t0018 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1806A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1806 | chr11 | 107502852 | |||||
chr11:107502942
|
G | A | 1 | a0001c0007t0011 | 2 | HG01891.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1716C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1716 | chr11 | 107502942 | |||||
chr11:107503015
|
G | A | 3 | a0001c0001t0005a0001c0002t0005a0001c0019t0005 | 4 | NA18946.hp2 NA18953.hp2 NA18995.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1643C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1643 | chr11 | 107503015 | |||||
chr11:107503087
|
T | A | 1 | a0001c0001t0015 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1571A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1571 | chr11 | 107503087 | |||||
chr11:107503212
|
T | C | 2 | a0001c0001t0019a0001c0002t0017 | 2 | HG03834.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1446A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1446 | chr11 | 107503212 | |||||
chr11:107503260
|
C | T | 1 | a0003c0005t0004 | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1398G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1398 | chr11 | 107503260 | |||||
chr11:107503381
|
C | T | 3 | a0009c0012t0009a0009c0016t0009a0011c0020t0009 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1277G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1277 | chr11 | 107503381 | |||||
chr11:107503483
|
C | T | 1 | a0001c0002t0017 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1175 | chr11 | 107503483 | |||||
chr11:107503501
|
A | C | 1 | a0001c0002t0016 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1157T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1157 | chr11 | 107503501 | |||||
chr11:107503594
|
CTG | C | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1062_*1063delCA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1062 | chr11 | 107503594 | |||||
chr11:107503597
|
G | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1061C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1061 | chr11 | 107503597 | |||||
chr11:107503598
|
G | C | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1060C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1060 | chr11 | 107503598 | |||||
chr11:107503598
|
G | T | 4 | a0001c0002t0003a0001c0003t0003a0001c0003t0013others(1): Show | 10 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1060C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1060 | chr11 | 107503598 | |||||
chr11:107503601
|
A | AC | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1056dupG | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1056 | chr11 | 107503601 | |||||
chr11:107503604
|
A | AAG | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054insCT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1053 | chr11 | 107503604 | |||||
chr11:107503607
|
AT | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1050delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1050 | chr11 | 107503607 | |||||
chr11:107503609
|
G | C | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1049 | chr11 | 107503609 | |||||
chr11:107503612
|
A | C | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1046T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1046 | chr11 | 107503612 | |||||
chr11:107503614
|
A | T | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1044T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1044 | chr11 | 107503614 | |||||
chr11:107503615
|
T | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1043A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1043 | chr11 | 107503615 | |||||
chr11:107503616
|
T | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1042A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1042 | chr11 | 107503616 | |||||
chr11:107503620
|
C | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1038G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1038 | chr11 | 107503620 | |||||
chr11:107503621
|
A | C | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1037T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1037 | chr11 | 107503621 | |||||
chr11:107503622
|
G | T | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1036C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1036 | chr11 | 107503622 | |||||
chr11:107503624
|
T | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1034A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1034 | chr11 | 107503624 | |||||
chr11:107503625
|
C | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1033G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1033 | chr11 | 107503625 | |||||
chr11:107503627
|
T | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1031A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1031 | chr11 | 107503627 | |||||
chr11:107503628
|
A | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1030T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1030 | chr11 | 107503628 | |||||
chr11:107503629
|
A | T | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1029T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1029 | chr11 | 107503629 | |||||
chr11:107503632
|
A | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1026T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1026 | chr11 | 107503632 | |||||
chr11:107503634
|
A | T | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1024T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1024 | chr11 | 107503634 | |||||
chr11:107503638
|
C | T | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1020G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1020 | chr11 | 107503638 | |||||
chr11:107503639
|
G | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1019C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1019 | chr11 | 107503639 | |||||
chr11:107503641
|
T | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1017A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1017 | chr11 | 107503641 | |||||
chr11:107503643
|
G | GGT | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1014_*1015insAC | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1014 | chr11 | 107503643 | |||||
chr11:107503648
|
TG | T | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1009delC | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1009 | chr11 | 107503648 | |||||
chr11:107503650
|
G | A | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1008C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1008 | chr11 | 107503650 | |||||
chr11:107503652
|
T | G | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1006A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1006 | chr11 | 107503652 | |||||
chr11:107503655
|
G | GTAA | 3 | a0001c0002t0010a0001c0003t0008a0001c0003t0010 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1002_*1003insTTA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 1002 | chr11 | 107503655 | |||||
chr11:107503805
|
C | T | 4 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(1): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*853G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 853 | chr11 | 107503805 | |||||
chr11:107503905
|
C | T | 1 | a0001c0003t0013 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 753 | chr11 | 107503905 | |||||
chr11:107504163
|
C | T | 7 | a0001c0002t0003a0001c0003t0003a0001c0003t0013others(4): Show | 13 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*495G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 495 | chr11 | 107504163 | |||||
chr11:107504433
|
C | A | 1 | a0001c0001t0012 | 2 | HG02165.hp1 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*225G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 225 | chr11 | 107504433 | |||||
chr11:107504457
|
G | A | 1 | a0005c0008t0006 | 4 | HG00280.hp1 HG01433.hp1 HG03491.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 201 | chr11 | 107504457 | |||||
chr11:107504467
|
C | A | 1 | a0001c0003t0007 | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*191G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 12/12 | 191 | chr11 | 107504467 | |||||
chr11:107565729
|
G | C | 2 | a0001c0001t0020a0001c0003t0008 | 5 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-135C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/12 | chr11 | 107565729 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:107505318
|
T | A | 18 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(15): Show | 20 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1438-103A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505318 | ||||||
chr11:107505367
|
A | G | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1438-152T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505367 | ||||||
chr11:107505520
|
G | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1438-305C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505520 | ||||||
chr11:107505527
|
T | C | 5 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0260others(2): Show | 5 | HG00140.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1438-312A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505527 | ||||||
chr11:107505610
|
C | T | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1438-395G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505610 | ||||||
chr11:107505629
|
A | G | 58 | a0001c0001t0001g0281a0001c0001t0002g0002a0001c0001t0002g0003others(55): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1438-414T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505629 | ||||||
chr11:107505681
|
A | C | 3 | a0001c0001t0002g0256a0001c0001t0002g0286a0001c0001t0015g0285 | 3 | HG01167.hp1 HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1438-466T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505681 | ||||||
chr11:107505872
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1438-657C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505872 | ||||||
chr11:107505878
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1438-663T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107505878 | ||||||
chr11:107506123
|
A | G | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(220): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1438-908T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506123 | ||||||
chr11:107506284
|
C | G | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(191): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1438-1069G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506284 | ||||||
chr11:107506384
|
G | T | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1438-1169C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506384 | ||||||
chr11:107506398
|
T | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(220): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1438-1183A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506398 | ||||||
chr11:107506425
|
T | C | 20 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(17): Show | 22 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1438-1210A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506425 | ||||||
chr11:107506663
|
A | G | 1 | a0007c0009t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1438-1448T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506663 | ||||||
chr11:107506895
|
T | C | 48 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(45): Show | 58 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1438-1680A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107506895 | ||||||
chr11:107507008
|
A | AT | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(188): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1438-1794dupA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507008 | ||||||
chr11:107507173
|
A | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0133a0001c0001t0001g0139 | 4 | NA18955.hp1 NA18956.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1438-1958T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507173 | ||||||
chr11:107507409
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1438-2194C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507409 | ||||||
chr11:107507481
|
C | T | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438-2266G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507481 | ||||||
chr11:107507522
|
T | C | 1 | a0001c0002t0001g0053 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1438-2307A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507522 | ||||||
chr11:107507538
|
C | A | 1 | a0001c0003t0007g0229 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1438-2323G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507538 | ||||||
chr11:107507702
|
C | T | 17 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(14): Show | 19 | HG00140.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1438-2487G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507702 | ||||||
chr11:107507703
|
G | A | 1 | a0001c0002t0001g0022 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1438-2488C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507703 | ||||||
chr11:107507731
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1438-2516A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507731 | ||||||
chr11:107507847
|
A | C | 160 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(157): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1438-2632T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507847 | ||||||
chr11:107507899
|
C | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0133others(6): Show | 10 | HG02602.hp1 HG03239.hp2 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.1438-2684G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507899 | ||||||
chr11:107507904
|
T | G | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1438-2689A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107507904 | ||||||
chr11:107508026
|
A | T | 3 | a0007c0009t0001g0218a0007c0009t0001g0225a0007c0009t0001g0226 | 3 | HG02486.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1438-2811T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508026 | ||||||
chr11:107508079
|
A | T | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1437+2808T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508079 | ||||||
chr11:107508109
|
T | C | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1437+2778A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508109 | ||||||
chr11:107508173
|
C | CT | 18 | a0001c0001t0001g0047a0001c0001t0001g0093a0001c0001t0001g0123others(15): Show | 18 | HG00140.hp1 HG01109.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.1437+2713dupA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508173 | ||||||
chr11:107508173
|
CT | C | 28 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0306others(25): Show | 31 | HG00735.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.1437+2713delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508173 | ||||||
chr11:107508194
|
G | C | 2 | a0008c0010t0001g0094a0008c0010t0001g0095 | 2 | HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1437+2693C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508194 | ||||||
chr11:107508239
|
C | T | 5 | a0001c0002t0010g0128a0001c0003t0008g0015a0001c0003t0008g0326others(2): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1437+2648G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508239 | ||||||
chr11:107508275
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1437+2612A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508275 | ||||||
chr11:107508365
|
G | T | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1437+2522C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508365 | ||||||
chr11:107508412
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1437+2475T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508412 | ||||||
chr11:107508414
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0279a0001c0007t0001g0204 | 3 | HG02280.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1437+2473G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508414 | ||||||
chr11:107508619
|
C | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0250 | 3 | HG01256.hp1 HG01257.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1437+2268G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508619 | ||||||
chr11:107508675
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1437+2212G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508675 | ||||||
chr11:107508690
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1437+2197C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508690 | ||||||
chr11:107508752
|
G | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1437+2135C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508752 | ||||||
chr11:107508888
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(273): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1437+1999C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508888 | ||||||
chr11:107508906
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1437+1981A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508906 | ||||||
chr11:107508969
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG02451.hp1 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1437+1918C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107508969 | ||||||
chr11:107509032
|
A | G | 1 | a0001c0002t0001g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1437+1855T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509032 | ||||||
chr11:107509221
|
T | C | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1437+1666A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509221 | ||||||
chr11:107509319
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1437+1568A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509319 | ||||||
chr11:107509322
|
C | A | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1437+1565G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509322 | ||||||
chr11:107509390
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1437+1497A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509390 | ||||||
chr11:107509410
|
C | G | 1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1437+1477G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509410 | ||||||
chr11:107509454
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1437+1433G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509454 | ||||||
chr11:107509472
|
G | C | 1 | a0001c0001t0001g0291 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1437+1415C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509472 | ||||||
chr11:107509496
|
A | G | 9 | a0002c0004t0001g0040a0002c0004t0001g0210a0002c0004t0001g0271others(6): Show | 10 | HG01081.hp2 HG01243.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1437+1391T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509496 | ||||||
chr11:107509575
|
TACA | T | 10 | a0002c0004t0001g0040a0002c0004t0001g0210a0002c0004t0001g0271others(7): Show | 11 | HG01081.hp2 HG01243.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1437+1309_1437+131 others(7): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509575 | ||||||
chr11:107509754
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1437+1133A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509754 | ||||||
chr11:107509788
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(51): Show | 69 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1437+1099G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509788 | ||||||
chr11:107509837
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1437+1050T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509837 | ||||||
chr11:107509888
|
C | G | 1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1437+999G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509888 | ||||||
chr11:107509938
|
T | C | 1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1437+949A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509938 | ||||||
chr11:107509968
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1437+919C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107509968 | ||||||
chr11:107510045
|
G | C | 5 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(2): Show | 5 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1437+842C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510045 | ||||||
chr11:107510083
|
T | G | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1437+804A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510083 | ||||||
chr11:107510168
|
T | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1437+719A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510168 | ||||||
chr11:107510322
|
T | C | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1437+565A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510322 | ||||||
chr11:107510454
|
C | A | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1437+433G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510454 | ||||||
chr11:107510807
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1437+80C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510807 | ||||||
chr11:107510848
|
T | C | 3 | a0001c0003t0001g0232a0010c0021t0001g0205a0012c0015t0003g0199 | 3 | HG02109.hp2 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1437+39A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 11/11 | chr11 | 107510848 | ||||||
chr11:107511039
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
splice_region_variant&intron_variant | LOW | c.1288-3C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511039 | ||||||
chr11:107511172
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1288-136A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511172 | ||||||
chr11:107511206
|
T | C | 18 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0003t0003g0219others(15): Show | 19 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1288-170A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511206 | ||||||
chr11:107511242
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0139 | 2 | NA19012.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1288-206T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511242 | ||||||
chr11:107511327
|
T | C | 2 | a0001c0003t0001g0232a0010c0021t0001g0205 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1288-291A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511327 | ||||||
chr11:107511338
|
T | C | 1 | a0001c0001t0002g0035 | 2 | NA18939.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1288-302A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511338 | ||||||
chr11:107511389
|
A | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1288-353T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511389 | ||||||
chr11:107511440
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0238 | 2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1288-404T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511440 | ||||||
chr11:107511455
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0279a0001c0007t0001g0204 | 3 | HG02280.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1288-419C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511455 | ||||||
chr11:107511504
|
T | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1288-468A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511504 | ||||||
chr11:107511568
|
A | C | 5 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(2): Show | 5 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-532T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511568 | ||||||
chr11:107511637
|
C | T | 57 | a0001c0001t0001g0130a0001c0001t0001g0176a0001c0001t0001g0177others(54): Show | 67 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1288-601G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511637 | ||||||
chr11:107511702
|
AAGTAGCT | A | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1288-673_1288-667d others(9): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511702 | ||||||
chr11:107511822
|
C | T | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-786G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511822 | ||||||
chr11:107511823
|
G | A | 1 | a0001c0001t0001g0025 | 2 | NA18955.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1288-787C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511823 | ||||||
chr11:107511852
|
G | A | 48 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(45): Show | 58 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1288-816C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107511852 | ||||||
chr11:107512195
|
T | C | 2 | a0001c0007t0001g0216a0015c0013t0001g0206 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1288-1159A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512195 | ||||||
chr11:107512217
|
GAC | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(158): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1288-1183_1288-118 others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512217 | ||||||
chr11:107512303
|
G | GGTTT | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(85): Show | 107 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1288-1268_1288-126 others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512303 | ||||||
chr11:107512309
|
T | G | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(86): Show | 108 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.1288-1273A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512309 | ||||||
chr11:107512309
|
T | TTTTG | 88 | a0001c0001t0001g0130a0001c0001t0001g0153a0001c0001t0001g0208others(85): Show | 99 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.1288-1277_1288-127 others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512309 | ||||||
chr11:107512315
|
T | C | 1 | a0001c0001t0002g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1288-1279A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512315 | ||||||
chr11:107512315
|
T | TTGTC | 106 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1288-1280_1288-127 others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512315 | ||||||
chr11:107512727
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18939.hp1 NA18992.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1288-1691T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512727 | ||||||
chr11:107512730
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0133a0001c0001t0001g0139 | 4 | NA18955.hp1 NA18956.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288-1694A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512730 | ||||||
chr11:107512781
|
TGATCCTC others(4592): Show |
T | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1287+4919_1288-174 others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512781 | ||||||
chr11:107512805
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1288-1769T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107512805 | ||||||
chr11:107513080
|
C | T | 1 | a0001c0002t0001g0104 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1288-2044G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513080 | ||||||
chr11:107513172
|
A | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0211 | 2 | HG01070.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1288-2136T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513172 | ||||||
chr11:107513350
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1288-2314G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513350 | ||||||
chr11:107513388
|
C | CA | 5 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(2): Show | 5 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-2353dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513388 | ||||||
chr11:107513413
|
T | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1288-2377A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513413 | ||||||
chr11:107513629
|
T | C | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-2593A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513629 | ||||||
chr11:107513643
|
G | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1288-2607C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513643 | ||||||
chr11:107513818
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1288-2782C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513818 | ||||||
chr11:107513858
|
A | C | 1 | a0001c0001t0001g0320 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1288-2822T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513858 | ||||||
chr11:107513911
|
T | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(273): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1288-2875A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107513911 | ||||||
chr11:107514029
|
C | T | 53 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(50): Show | 63 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1288-2993G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514029 | ||||||
chr11:107514117
|
T | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(273): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1288-3081A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514117 | ||||||
chr11:107514118
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(273): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1288-3082C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514118 | ||||||
chr11:107514144
|
A | C | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-3108T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514144 | ||||||
chr11:107514210
|
A | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0322 | 3 | HG02129.hp2 NA18945.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1288-3174T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514210 | ||||||
chr11:107514324
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1288-3288T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514324 | ||||||
chr11:107514427
|
G | C | 55 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(52): Show | 65 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.1288-3391C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514427 | ||||||
chr11:107514458
|
A | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1288-3422T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514458 | ||||||
chr11:107514852
|
G | A | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-3816C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107514852 | ||||||
chr11:107515307
|
T | C | 1 | a0013c0014t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1288-4271A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107515307 | ||||||
chr11:107515327
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0279 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1288-4291T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107515327 | ||||||
chr11:107515732
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1288-4696T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107515732 | ||||||
chr11:107515859
|
T | C | 2 | a0001c0007t0001g0216a0015c0013t0001g0206 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1288-4823A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107515859 | ||||||
chr11:107516061
|
C | A | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1288-5025G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516061 | ||||||
chr11:107516316
|
C | G | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-5280G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516316 | ||||||
chr11:107516362
|
G | A | 1 | a0001c0003t0007g0229 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1288-5326C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516362 | ||||||
chr11:107516478
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1288-5442C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516478 | ||||||
chr11:107516800
|
C | G | 2 | a0001c0007t0011g0049a0001c0007t0011g0050 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1287+5499G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516800 | ||||||
chr11:107516847
|
A | G | 2 | a0001c0003t0001g0232a0010c0021t0001g0205 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1287+5452T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516847 | ||||||
chr11:107516930
|
G | A | 107 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(104): Show | 126 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.1287+5369C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107516930 | ||||||
chr11:107517000
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(79): Show | 98 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1287+5299C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107517000 | ||||||
chr11:107517247
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1287+5052G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107517247 | ||||||
chr11:107517322
|
T | C | 1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1287+4977A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107517322 | ||||||
chr11:107517439
|
C | T | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1287+4860G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107517439 | ||||||
chr11:107517546
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1287+4753G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107517546 | ||||||
chr11:107517691
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1287+4608A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107517691 | ||||||
chr11:107518079
|
AAT | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(53): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1287+4218_1287+421 others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518079 | ||||||
chr11:107518083
|
C | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(282): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1287+4216G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518083 | ||||||
chr11:107518124
|
A | C | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1287+4175T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518124 | ||||||
chr11:107518125
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1287+4174A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518125 | ||||||
chr11:107518227
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1287+4072G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518227 | ||||||
chr11:107518282
|
T | A | 1 | a0001c0001t0002g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1287+4017A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518282 | ||||||
chr11:107518300
|
T | G | 1 | a0008c0010t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1287+3999A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518300 | ||||||
chr11:107518326
|
C | T | 1 | a0001c0003t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1287+3973G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518326 | ||||||
chr11:107518419
|
G | GC | 6 | a0001c0001t0001g0006a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 9 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1287+3879dupG | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518419 | ||||||
chr11:107518443
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1287+3856A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518443 | ||||||
chr11:107518444
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1287+3855C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518444 | ||||||
chr11:107518461
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | NA18939.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1287+3838A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518461 | ||||||
chr11:107518498
|
T | A | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1287+3801A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518498 | ||||||
chr11:107518529
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1287+3770C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518529 | ||||||
chr11:107518610
|
A | C | 1 | a0001c0002t0001g0119 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1287+3689T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518610 | ||||||
chr11:107518635
|
G | A | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287+3664C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518635 | ||||||
chr11:107518680
|
G | A | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1287+3619C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518680 | ||||||
chr11:107518723
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1287+3576G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518723 | ||||||
chr11:107518724
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1287+3575G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518724 | ||||||
chr11:107518725
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1287+3574T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518725 | ||||||
chr11:107518765
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1287+3534T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518765 | ||||||
chr11:107518816
|
C | CTGTT | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1287+3482_1287+348 others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107518816 | ||||||
chr11:107519122
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1287+3177A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519122 | ||||||
chr11:107519255
|
G | A | 5 | a0001c0002t0010g0128a0001c0003t0008g0015a0001c0003t0008g0326others(2): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1287+3044C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519255 | ||||||
chr11:107519298
|
T | G | 5 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(2): Show | 5 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+3001A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519298 | ||||||
chr11:107519312
|
T | G | 1 | a0001c0001t0001g0031 | 2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1287+2987A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519312 | ||||||
chr11:107519349
|
T | C | 1 | a0001c0001t0002g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1287+2950A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519349 | ||||||
chr11:107519474
|
T | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1287+2825A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519474 | ||||||
chr11:107519520
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0140others(5): Show | 9 | HG02602.hp1 HG03239.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287+2779G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519520 | ||||||
chr11:107519585
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1287+2714G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107519585 | ||||||
chr11:107520025
|
T | C | 2 | a0001c0007t0011g0049a0001c0007t0011g0050 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1287+2274A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520025 | ||||||
chr11:107520065
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1287+2234G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520065 | ||||||
chr11:107520096
|
A | G | 1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1287+2203T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520096 | ||||||
chr11:107520224
|
C | G | 4 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0052others(1): Show | 6 | HG02027.hp2 HG02165.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287+2075G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520224 | ||||||
chr11:107520297
|
G | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(282): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1287+2002C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520297 | ||||||
chr11:107520386
|
C | T | 1 | a0010c0021t0001g0205 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1287+1913G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520386 | ||||||
chr11:107520478
|
T | A | 2 | a0001c0002t0001g0107a0001c0002t0001g0211 | 2 | HG01070.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1287+1821A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520478 | ||||||
chr11:107520532
|
A | G | 1 | a0011c0020t0009g0318 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1287+1767T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520532 | ||||||
chr11:107520552
|
T | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1287+1747A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520552 | ||||||
chr11:107520573
|
T | C | 1 | a0001c0002t0001g0070 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1287+1726A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520573 | ||||||
chr11:107520739
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0149others(2): Show | 6 | NA18942.hp2 NA18997.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287+1560A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520739 | ||||||
chr11:107520766
|
A | G | 9 | a0002c0004t0001g0040a0002c0004t0001g0210a0002c0004t0001g0271others(6): Show | 10 | HG01081.hp2 HG01243.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1287+1533T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520766 | ||||||
chr11:107520784
|
C | T | 1 | a0001c0002t0003g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1287+1515G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520784 | ||||||
chr11:107520800
|
A | G | 5 | a0001c0001t0001g0033a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG01109.hp2 HG01123.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287+1499T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520800 | ||||||
chr11:107520890
|
T | A | 4 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287+1409A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107520890 | ||||||
chr11:107521100
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1287+1199T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521100 | ||||||
chr11:107521248
|
G | C | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1287+1051C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521248 | ||||||
chr11:107521263
|
C | T | 4 | a0001c0002t0001g0019a0001c0002t0001g0057a0001c0002t0001g0062others(1): Show | 5 | NA18941.hp1 NA18995.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+1036G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521263 | ||||||
chr11:107521284
|
T | C | 1 | a0001c0007t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1287+1015A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521284 | ||||||
chr11:107521353
|
G | A | 48 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(45): Show | 58 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1287+946C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521353 | ||||||
chr11:107521376
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1287+923T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521376 | ||||||
chr11:107521743
|
T | G | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1287+556A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521743 | ||||||
chr11:107521920
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1287+379G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107521920 | ||||||
chr11:107522089
|
A | G | 1 | a0001c0002t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1287+210T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 10/11 | chr11 | 107522089 | ||||||
chr11:107522627
|
G | GA | 8 | a0001c0002t0001g0064a0001c0002t0001g0069a0001c0002t0001g0117others(5): Show | 8 | HG01978.hp1 HG02040.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1031-73dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522627 | ||||||
chr11:107522637
|
A | T | 3 | a0001c0002t0001g0056a0001c0002t0001g0060a0001c0002t0001g0068 | 3 | NA18957.hp2 NA18966.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1031-82T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522637 | ||||||
chr11:107522679
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1031-124C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522679 | ||||||
chr11:107522754
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1031-199A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522754 | ||||||
chr11:107522759
|
T | TC | 5 | a0004c0006t0001g0059a0004c0006t0001g0061a0004c0006t0001g0065others(2): Show | 5 | HG00673.hp1 NA18971.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1031-205dupG | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522759 | ||||||
chr11:107522795
|
G | C | 9 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(6): Show | 9 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1031-240C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522795 | ||||||
chr11:107522813
|
AC | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1031-259delG | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522813 | ||||||
chr11:107522844
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1031-289C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522844 | ||||||
chr11:107522866
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1031-311T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522866 | ||||||
chr11:107522871
|
T | C | 51 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(48): Show | 61 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1031-316A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522871 | ||||||
chr11:107522881
|
G | A | 8 | a0002c0004t0001g0040a0002c0004t0001g0271a0002c0004t0001g0272others(5): Show | 9 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1031-326C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107522881 | ||||||
chr11:107523011
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1031-456C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523011 | ||||||
chr11:107523050
|
CA | C | 53 | a0001c0001t0001g0130a0001c0001t0002g0265a0001c0001t0019g0240others(50): Show | 63 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1031-496delT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523050 | ||||||
chr11:107523050
|
CAA | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1031-497_1031-496d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523050 | ||||||
chr11:107523140
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0299a0001c0001t0001g0300others(1): Show | 5 | NA18959.hp1 NA18968.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1031-585G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523140 | ||||||
chr11:107523141
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1031-586C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523141 | ||||||
chr11:107523164
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1031-609T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523164 | ||||||
chr11:107523253
|
T | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(108): Show | 131 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.1031-698A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523253 | ||||||
chr11:107523390
|
G | C | 2 | a0001c0003t0008g0015a0001c0003t0008g0326 | 4 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031-835C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523390 | ||||||
chr11:107523401
|
A | G | 1 | a0001c0002t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1031-846T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523401 | ||||||
chr11:107523423
|
G | C | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1031-868C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523423 | ||||||
chr11:107523481
|
G | A | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-926C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523481 | ||||||
chr11:107523602
|
CT | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(258): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1031-1048delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523602 | ||||||
chr11:107523602
|
CTT | C | 8 | a0001c0001t0001g0173a0001c0001t0002g0087a0001c0003t0001g0232others(5): Show | 8 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1031-1049_1031-104 others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523602 | ||||||
chr11:107523796
|
T | G | 18 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(15): Show | 18 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1031-1241A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523796 | ||||||
chr11:107523821
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1031-1266G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523821 | ||||||
chr11:107523856
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 64 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1031-1301G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523856 | ||||||
chr11:107523879
|
G | T | 10 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0210others(7): Show | 10 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1031-1324C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107523879 | ||||||
chr11:107524120
|
G | A | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1030+1321C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524120 | ||||||
chr11:107524171
|
G | A | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1030+1270C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524171 | ||||||
chr11:107524802
|
C | T | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1030+639G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524802 | ||||||
chr11:107524813
|
T | C | 3 | a0001c0002t0001g0053a0001c0002t0001g0184a0001c0002t0001g0187 | 3 | NA18978.hp1 NA18987.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1030+628A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524813 | ||||||
chr11:107524839
|
T | A | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1030+602A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524839 | ||||||
chr11:107524906
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1030+535A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524906 | ||||||
chr11:107524945
|
A | T | 2 | a0005c0008t0006g0012a0005c0008t0006g0253 | 4 | HG00280.hp1 HG01433.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030+496T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107524945 | ||||||
chr11:107525007
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1030+434G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107525007 | ||||||
chr11:107525116
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1030+325C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107525116 | ||||||
chr11:107525293
|
A | G | 3 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128 | 3 | HG02145.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1030+148T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107525293 | ||||||
chr11:107525432
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1030+9A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 9/11 | chr11 | 107525432 | ||||||
chr11:107525629
|
T | A | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.879-37A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107525629 | ||||||
chr11:107525660
|
T | C | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.879-68A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107525660 | ||||||
chr11:107525747
|
A | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.879-155T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107525747 | ||||||
chr11:107526044
|
C | A | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.879-452G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526044 | ||||||
chr11:107526084
|
T | G | 1 | a0001c0002t0001g0104 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.879-492A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526084 | ||||||
chr11:107526110
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.879-518C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526110 | ||||||
chr11:107526242
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.879-650T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526242 | ||||||
chr11:107526288
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.879-696C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526288 | ||||||
chr11:107526341
|
TTTAAG | T | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.879-754_879-750del others(5): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526341 | ||||||
chr11:107526420
|
T | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.879-828A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526420 | ||||||
chr11:107526520
|
C | T | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.879-928G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526520 | ||||||
chr11:107526731
|
T | C | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.879-1139A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526731 | ||||||
chr11:107526738
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.879-1146G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526738 | ||||||
chr11:107526861
|
T | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(85): Show | 107 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.879-1269A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107526861 | ||||||
chr11:107527337
|
C | T | 3 | a0006c0011t0001g0247a0006c0011t0001g0248a0006c0017t0001g0222 | 3 | HG00140.hp1 HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.879-1745G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527337 | ||||||
chr11:107527383
|
C | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(92): Show | 114 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.879-1791G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527383 | ||||||
chr11:107527482
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.879-1890T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527482 | ||||||
chr11:107527683
|
C | T | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879-2091G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527683 | ||||||
chr11:107527713
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.879-2121T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527713 | ||||||
chr11:107527849
|
G | C | 4 | a0001c0002t0001g0029a0001c0002t0001g0036a0001c0002t0001g0125others(1): Show | 6 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.879-2257C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527849 | ||||||
chr11:107527869
|
G | A | 1 | a0001c0003t0013g0301 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879-2277C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527869 | ||||||
chr11:107527972
|
C | T | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.879-2380G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107527972 | ||||||
chr11:107528008
|
G | A | 1 | a0001c0019t0005g0161 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.879-2416C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528008 | ||||||
chr11:107528015
|
A | T | 3 | a0001c0003t0003g0282a0001c0003t0003g0283a0001c0003t0003g0284 | 3 | HG01891.hp2 HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.879-2423T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528015 | ||||||
chr11:107528060
|
A | G | 2 | a0001c0002t0001g0196a0001c0002t0001g0197 | 2 | NA18962.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.879-2468T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528060 | ||||||
chr11:107528242
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.879-2650T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528242 | ||||||
chr11:107528367
|
C | CT | 43 | a0001c0001t0001g0130a0001c0001t0019g0240a0001c0002t0001g0004others(40): Show | 51 | HG00280.hp2 HG00741.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.879-2776dupA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528367 | ||||||
chr11:107528419
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.879-2827C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528419 | ||||||
chr11:107528435
|
A | G | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.879-2843T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528435 | ||||||
chr11:107528456
|
G | T | 5 | a0002c0004t0001g0040a0002c0004t0001g0273a0002c0004t0001g0274others(2): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-2864C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528456 | ||||||
chr11:107528493
|
G | A | 1 | a0001c0003t0001g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879-2901C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528493 | ||||||
chr11:107528600
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.879-3008T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528600 | ||||||
chr11:107528650
|
T | C | 3 | a0003c0005t0004g0214a0003c0005t0004g0215a0003c0005t0004g0324 | 3 | HG02486.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.879-3058A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528650 | ||||||
chr11:107528770
|
T | C | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879-3178A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528770 | ||||||
chr11:107528780
|
C | T | 2 | a0001c0001t0001g0321a0013c0014t0001g0198 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.879-3188G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528780 | ||||||
chr11:107528857
|
A | G | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.879-3265T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107528857 | ||||||
chr11:107529035
|
G | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.878+3265C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529035 | ||||||
chr11:107529376
|
A | T | 1 | a0001c0001t0001g0311 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.878+2924T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529376 | ||||||
chr11:107529410
|
G | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.878+2890C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529410 | ||||||
chr11:107529456
|
T | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0302 | 4 | NA18955.hp2 NA18966.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.878+2844A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529456 | ||||||
chr11:107529508
|
A | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.878+2792T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529508 | ||||||
chr11:107529510
|
TTC | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.878+2788_878+2789d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529510 | ||||||
chr11:107529511
|
TC | T | 82 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(79): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.878+2788delG | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529511 | ||||||
chr11:107529565
|
C | T | 1 | a0001c0001t0012g0151 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.878+2735G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529565 | ||||||
chr11:107529649
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.878+2651G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529649 | ||||||
chr11:107529672
|
T | TTTTTGTA others(311): Show |
3 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0210 | 3 | HG01243.hp1 HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.878+2627_878+2628i others(320): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529672 | ||||||
chr11:107529672
|
T | TTTTTGTA others(312): Show |
6 | a0002c0004t0001g0040a0002c0004t0001g0271a0002c0004t0001g0272others(3): Show | 7 | HG01081.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.878+2627_878+2628i others(321): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529672 | ||||||
chr11:107529672
|
T | TTTTTGTA others(313): Show |
1 | a0002c0004t0001g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.878+2627_878+2628i others(322): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529672 | ||||||
chr11:107529672
|
T | TTTTTGTA others(314): Show |
1 | a0002c0004t0001g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.878+2627_878+2628i others(323): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529672 | ||||||
chr11:107529735
|
C | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878+2565G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529735 | ||||||
chr11:107529742
|
T | C | 6 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.878+2558A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529742 | ||||||
chr11:107529762
|
A | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0306 | 3 | NA18975.hp2 NA19072.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.878+2538T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529762 | ||||||
chr11:107529798
|
G | A | 2 | a0001c0001t0001g0321a0013c0014t0001g0198 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.878+2502C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529798 | ||||||
chr11:107529916
|
T | C | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.878+2384A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529916 | ||||||
chr11:107529988
|
T | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.878+2312A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529988 | ||||||
chr11:107529992
|
G | GACACACA others(20): Show |
1 | a0001c0002t0001g0099 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.878+2281_878+2307d others(29): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107529992 | ||||||
chr11:107530155
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.878+2145A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530155 | ||||||
chr11:107530247
|
G | C | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.878+2053C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530247 | ||||||
chr11:107530419
|
A | T | 1 | a0001c0001t0001g0321 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.878+1881T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530419 | ||||||
chr11:107530439
|
A | G | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878+1861T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530439 | ||||||
chr11:107530481
|
TA | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0279a0001c0007t0001g0204 | 3 | HG02280.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.878+1818delT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530481 | ||||||
chr11:107530564
|
CCT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.878+1734_878+1735d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530564 | ||||||
chr11:107530600
|
A | AAC | 11 | a0001c0001t0019g0240a0001c0002t0001g0029a0001c0002t0001g0036others(8): Show | 13 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.878+1698_878+1699d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
A | AACAC | 27 | a0001c0001t0001g0093a0001c0001t0001g0130a0001c0002t0001g0004others(24): Show | 31 | HG00280.hp2 HG00558.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.878+1696_878+1699d others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
A | AACACAC | 27 | a0001c0002t0001g0019a0001c0002t0001g0053a0001c0002t0001g0054others(24): Show | 28 | HG00140.hp1 HG00673.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.878+1694_878+1699d others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
A | AACACACA others(1): Show |
13 | a0001c0002t0001g0017a0001c0002t0001g0056a0001c0002t0001g0060others(10): Show | 14 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.878+1692_878+1699d others(10): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
A | AACACACA others(3): Show |
2 | a0001c0002t0001g0107a0004c0006t0001g0059 | 2 | HG01070.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.878+1690_878+1699d others(12): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
A | AACACACA others(5): Show |
1 | a0001c0002t0001g0058 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.878+1688_878+1699d others(14): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AAC | A | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0002t0001g0118others(6): Show | 9 | HG00738.hp1 HG01099.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.878+1698_878+1699d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACAC | A | 13 | a0001c0001t0001g0217a0001c0002t0001g0156a0001c0002t0003g0126others(10): Show | 14 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.878+1696_878+1699d others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACAC | A | 5 | a0001c0001t0001g0281a0001c0003t0003g0282a0001c0003t0003g0284others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.878+1694_878+1699d others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(1): Show |
A | 18 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0133others(15): Show | 19 | HG01123.hp2 HG01934.hp1 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.878+1692_878+1699d others(10): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(3): Show |
A | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(67): Show | 90 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.878+1690_878+1699d others(12): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(5): Show |
A | 3 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230 | 3 | HG02258.hp1 HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.878+1688_878+1699d others(14): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(7): Show |
A | 3 | a0001c0001t0001g0223a0001c0001t0001g0305a0001c0001t0001g0317 | 3 | HG03579.hp1 NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.878+1686_878+1699d others(16): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(9): Show |
A | 4 | a0001c0001t0001g0042a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 5 | NA18969.hp2 NA18975.hp2 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.878+1684_878+1699d others(18): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(11): Show |
A | 2 | a0001c0001t0002g0038a0001c0001t0002g0263 | 3 | HG01256.hp1 HG01257.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.878+1682_878+1699d others(20): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530600
|
AACACACA others(13): Show |
A | 98 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.878+1680_878+1699d others(22): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530600 | ||||||
chr11:107530618
|
C | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0078others(10): Show | 15 | HG01255.hp2 HG02040.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.878+1682G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530618 | ||||||
chr11:107530622
|
C | A | 1 | a0001c0002t0001g0070 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.878+1678G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530622 | ||||||
chr11:107530661
|
C | T | 1 | a0001c0001t0002g0039 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.878+1639G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107530661 | ||||||
chr11:107531086
|
T | G | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.878+1214A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531086 | ||||||
chr11:107531113
|
G | GA | 16 | a0001c0001t0001g0223a0001c0001t0001g0279a0001c0001t0001g0281others(13): Show | 17 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.878+1186dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531113 | ||||||
chr11:107531174
|
G | C | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.878+1126C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531174 | ||||||
chr11:107531210
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.878+1090C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531210 | ||||||
chr11:107531260
|
A | T | 1 | a0001c0001t0002g0167 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.878+1040T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531260 | ||||||
chr11:107531433
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 4 | NA18940.hp2 NA18952.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.878+867T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531433 | ||||||
chr11:107531493
|
A | T | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.878+807T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531493 | ||||||
chr11:107531502
|
A | T | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.878+798T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531502 | ||||||
chr11:107531537
|
A | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0250 | 3 | HG01256.hp1 HG01257.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.878+763T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531537 | ||||||
chr11:107531604
|
G | A | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.878+696C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107531604 | ||||||
chr11:107532161
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(85): Show | 105 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.878+139C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107532161 | ||||||
chr11:107532269
|
A | T | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(109): Show | 130 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.878+31T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 8/11 | chr11 | 107532269 | ||||||
chr11:107532435
|
C | A | 1 | a0001c0003t0010g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.772-29G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532435 | ||||||
chr11:107532476
|
TAG | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(85): Show | 105 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.772-72_772-71delCT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532476 | ||||||
chr11:107532537
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.772-131G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532537 | ||||||
chr11:107532603
|
T | G | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.772-197A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532603 | ||||||
chr11:107532784
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.772-378T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532784 | ||||||
chr11:107532792
|
C | T | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.772-386G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532792 | ||||||
chr11:107532895
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.772-489A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532895 | ||||||
chr11:107532929
|
T | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-523A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532929 | ||||||
chr11:107532950
|
T | C | 8 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(5): Show | 10 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-544A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107532950 | ||||||
chr11:107533064
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | NA18939.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.772-658G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533064 | ||||||
chr11:107533205
|
T | C | 2 | a0001c0003t0003g0283a0001c0003t0003g0284 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.772-799A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533205 | ||||||
chr11:107533447
|
A | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-1041T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533447 | ||||||
chr11:107533463
|
T | A | 1 | a0001c0002t0001g0055 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.772-1057A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533463 | ||||||
chr11:107533463
|
T | C | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.772-1057A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533463 | ||||||
chr11:107533634
|
G | C | 1 | a0001c0002t0017g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.772-1228C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533634 | ||||||
chr11:107533642
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.772-1236A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533642 | ||||||
chr11:107533740
|
T | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(53): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.772-1334A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533740 | ||||||
chr11:107533775
|
A | C | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.772-1369T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533775 | ||||||
chr11:107533780
|
A | C | 1 | a0002c0004t0001g0274 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.772-1374T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533780 | ||||||
chr11:107533782
|
C | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.772-1376G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533782 | ||||||
chr11:107533854
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.772-1448G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533854 | ||||||
chr11:107533872
|
T | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(85): Show | 105 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.772-1466A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107533872 | ||||||
chr11:107534046
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.772-1640G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534046 | ||||||
chr11:107534263
|
C | T | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.772-1857G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534263 | ||||||
chr11:107534264
|
G | A | 5 | a0001c0001t0002g0249a0001c0002t0001g0029a0001c0002t0001g0036others(2): Show | 7 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-1858C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534264 | ||||||
chr11:107534352
|
T | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-1946A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534352 | ||||||
chr11:107534410
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.772-2004C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534410 | ||||||
chr11:107534559
|
C | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0002t0001g0292others(1): Show | 4 | HG00408.hp1 HG00438.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.772-2153G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534559 | ||||||
chr11:107534579
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.772-2173T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534579 | ||||||
chr11:107534742
|
T | C | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.772-2336A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534742 | ||||||
chr11:107534757
|
C | CT | 125 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(122): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.772-2352dupA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534757 | ||||||
chr11:107534757
|
C | CTT | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0016others(77): Show | 95 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.772-2353_772-2352d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534757 | ||||||
chr11:107534779
|
T | A | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-2373A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534779 | ||||||
chr11:107534876
|
T | C | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.772-2470A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534876 | ||||||
chr11:107534909
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.772-2503C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534909 | ||||||
chr11:107534911
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.772-2505T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534911 | ||||||
chr11:107534913
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.772-2507G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534913 | ||||||
chr11:107534922
|
A | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(109): Show | 130 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.772-2516T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107534922 | ||||||
chr11:107535072
|
G | A | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.772-2666C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535072 | ||||||
chr11:107535115
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0143a0001c0001t0001g0155others(1): Show | 7 | HG02451.hp2 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-2709T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535115 | ||||||
chr11:107535207
|
C | T | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.772-2801G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535207 | ||||||
chr11:107535318
|
A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0043others(10): Show | 23 | HG00673.hp2 HG01123.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.772-2912T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535318 | ||||||
chr11:107535331
|
T | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.772-2925A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535331 | ||||||
chr11:107535339
|
C | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-2933G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535339 | ||||||
chr11:107535344
|
T | C | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.772-2938A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535344 | ||||||
chr11:107535368
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.772-2962G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535368 | ||||||
chr11:107535552
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.772-3146A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535552 | ||||||
chr11:107535599
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.772-3193A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535599 | ||||||
chr11:107535602
|
T | C | 2 | a0001c0003t0008g0015a0001c0003t0008g0326 | 4 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-3196A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535602 | ||||||
chr11:107535826
|
G | A | 8 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(5): Show | 10 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-3420C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535826 | ||||||
chr11:107535855
|
G | A | 2 | a0001c0001t0012g0150a0001c0001t0012g0151 | 2 | HG02165.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.772-3449C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535855 | ||||||
chr11:107535871
|
C | T | 1 | a0006c0011t0001g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.772-3465G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535871 | ||||||
chr11:107535955
|
A | G | 2 | a0001c0001t0002g0269a0006c0011t0001g0247 | 2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.772-3549T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107535955 | ||||||
chr11:107536120
|
G | A | 1 | a0001c0003t0003g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.772-3714C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536120 | ||||||
chr11:107536284
|
A | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(54): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.772-3878T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536284 | ||||||
chr11:107536398
|
T | C | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.772-3992A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536398 | ||||||
chr11:107536405
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0112 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.772-3999C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536405 | ||||||
chr11:107536406
|
TA | T | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(20): Show | 24 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.772-4001delT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536406 | ||||||
chr11:107536600
|
T | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.772-4194A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536600 | ||||||
chr11:107536656
|
G | A | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.772-4250C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536656 | ||||||
chr11:107536686
|
G | A | 1 | a0002c0004t0001g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.772-4280C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536686 | ||||||
chr11:107536798
|
C | T | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.772-4392G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536798 | ||||||
chr11:107536911
|
C | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(124): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.772-4505G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107536911 | ||||||
chr11:107537301
|
A | G | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.772-4895T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537301 | ||||||
chr11:107537357
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.772-4951A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537357 | ||||||
chr11:107537421
|
G | A | 1 | a0007c0009t0001g0226 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.772-5015C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537421 | ||||||
chr11:107537497
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-5091A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537497 | ||||||
chr11:107537513
|
A | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-5107T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537513 | ||||||
chr11:107537570
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.772-5164C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537570 | ||||||
chr11:107537630
|
A | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(86): Show | 106 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.772-5224T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537630 | ||||||
chr11:107537719
|
C | CGGCCGGG others(340): Show |
1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.772-5314_772-5313i others(349): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537719 | ||||||
chr11:107537719
|
CA | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.772-5314delT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537719 | ||||||
chr11:107537720
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.772-5314T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537720 | ||||||
chr11:107537866
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-5460A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537866 | ||||||
chr11:107537972
|
A | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(53): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.772-5566T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107537972 | ||||||
chr11:107538014
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.772-5608G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538014 | ||||||
chr11:107538063
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(89): Show | 110 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.772-5657A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538063 | ||||||
chr11:107538156
|
T | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0043others(11): Show | 24 | HG00673.hp2 HG01123.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.772-5750A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538156 | ||||||
chr11:107538221
|
A | AG | 126 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(123): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.772-5816_772-5815i others(3): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538221 | ||||||
chr11:107538325
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-5919G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538325 | ||||||
chr11:107538598
|
C | T | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.772-6192G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538598 | ||||||
chr11:107538683
|
C | T | 2 | a0001c0001t0001g0321a0013c0014t0001g0198 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.772-6277G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538683 | ||||||
chr11:107538783
|
A | G | 1 | a0001c0002t0001g0057 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.772-6377T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538783 | ||||||
chr11:107538784
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-6378G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538784 | ||||||
chr11:107538906
|
C | T | 1 | a0001c0002t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.772-6500G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107538906 | ||||||
chr11:107539010
|
C | T | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.772-6604G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539010 | ||||||
chr11:107539370
|
T | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-6964A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539370 | ||||||
chr11:107539397
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.772-6991A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539397 | ||||||
chr11:107539476
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-7070T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539476 | ||||||
chr11:107539502
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.772-7096C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539502 | ||||||
chr11:107539590
|
A | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-7184T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539590 | ||||||
chr11:107539596
|
C | CA | 86 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(83): Show | 103 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.772-7191dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539596 | ||||||
chr11:107539658
|
TC | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-7253delG | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539658 | ||||||
chr11:107539749
|
G | A | 5 | a0001c0002t0001g0022a0001c0002t0001g0024a0001c0002t0001g0119others(2): Show | 7 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-7343C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539749 | ||||||
chr11:107539791
|
T | TA | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.772-7386dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539791 | ||||||
chr11:107539801
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.772-7395C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539801 | ||||||
chr11:107539910
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.772-7504C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539910 | ||||||
chr11:107539947
|
A | T | 2 | a0001c0002t0001g0101a0001c0002t0001g0245 | 2 | NA18963.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.772-7541T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107539947 | ||||||
chr11:107540087
|
G | A | 1 | a0001c0001t0005g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.772-7681C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540087 | ||||||
chr11:107540114
|
G | A | 1 | a0001c0002t0016g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.772-7708C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540114 | ||||||
chr11:107540233
|
A | G | 1 | a0010c0021t0001g0205 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.772-7827T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540233 | ||||||
chr11:107540481
|
T | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-8075A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540481 | ||||||
chr11:107540483
|
C | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.772-8077G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540483 | ||||||
chr11:107540571
|
A | C | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.772-8165T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540571 | ||||||
chr11:107540660
|
A | G | 8 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(5): Show | 10 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-8254T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540660 | ||||||
chr11:107540777
|
T | G | 3 | a0009c0012t0009g0227a0009c0016t0009g0207a0011c0020t0009g0318 | 3 | HG02647.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.772-8371A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540777 | ||||||
chr11:107540803
|
A | G | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-8397T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540803 | ||||||
chr11:107540925
|
T | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.772-8519A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540925 | ||||||
chr11:107540935
|
G | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.772-8529C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540935 | ||||||
chr11:107540959
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.772-8553G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540959 | ||||||
chr11:107540967
|
T | C | 44 | a0001c0001t0001g0130a0001c0001t0002g0129a0001c0001t0019g0240others(41): Show | 52 | HG00280.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.772-8561A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107540967 | ||||||
chr11:107541152
|
C | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+8601G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541152 | ||||||
chr11:107541179
|
C | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+8574G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541179 | ||||||
chr11:107541194
|
C | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+8559G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541194 | ||||||
chr11:107541328
|
G | A | 8 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0082others(5): Show | 10 | HG00423.hp2 NA18953.hp1 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.771+8425C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541328 | ||||||
chr11:107541333
|
T | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+8420A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541333 | ||||||
chr11:107541402
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.771+8351T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541402 | ||||||
chr11:107541488
|
G | A | 6 | a0001c0003t0003g0219a0001c0003t0003g0220a0001c0003t0003g0224others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+8265C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541488 | ||||||
chr11:107541543
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.771+8210T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541543 | ||||||
chr11:107541667
|
C | T | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+8086G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541667 | ||||||
chr11:107541705
|
T | C | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.771+8048A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541705 | ||||||
chr11:107541756
|
T | C | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+7997A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541756 | ||||||
chr11:107541766
|
G | T | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.771+7987C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541766 | ||||||
chr11:107541816
|
C | T | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+7937G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541816 | ||||||
chr11:107541968
|
G | A | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.771+7785C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541968 | ||||||
chr11:107541983
|
A | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0123others(5): Show | 10 | HG01106.hp1 HG01169.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+7770T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107541983 | ||||||
chr11:107542131
|
T | A | 11 | a0001c0007t0011g0049a0001c0007t0011g0050a0002c0004t0001g0040others(8): Show | 12 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.771+7622A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542131 | ||||||
chr11:107542159
|
A | G | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+7594T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542159 | ||||||
chr11:107542213
|
A | C | 1 | a0001c0001t0002g0114 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.771+7540T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542213 | ||||||
chr11:107542216
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.771+7537G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542216 | ||||||
chr11:107542260
|
G | C | 1 | a0001c0001t0002g0251 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.771+7493C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542260 | ||||||
chr11:107542299
|
C | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(282): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.771+7454G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542299 | ||||||
chr11:107542302
|
A | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+7451T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542302 | ||||||
chr11:107542554
|
T | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.771+7199A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542554 | ||||||
chr11:107542570
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.771+7183C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542570 | ||||||
chr11:107542581
|
G | C | 8 | a0002c0004t0001g0040a0002c0004t0001g0271a0002c0004t0001g0272others(5): Show | 9 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.771+7172C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542581 | ||||||
chr11:107542712
|
C | A | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+7041G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542712 | ||||||
chr11:107542729
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(53): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.771+7024C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542729 | ||||||
chr11:107542772
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+6981A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542772 | ||||||
chr11:107542802
|
A | T | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(4): Show | 7 | HG00738.hp1 HG01099.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+6951T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542802 | ||||||
chr11:107542848
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+6905G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542848 | ||||||
chr11:107542985
|
A | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.771+6768T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107542985 | ||||||
chr11:107543023
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.771+6730C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543023 | ||||||
chr11:107543026
|
C | T | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(53): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.771+6727G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543026 | ||||||
chr11:107543029
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+6724A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543029 | ||||||
chr11:107543034
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+6719G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543034 | ||||||
chr11:107543110
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+6643C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543110 | ||||||
chr11:107543229
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+6524A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543229 | ||||||
chr11:107543655
|
A | C | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.771+6098T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107543655 | ||||||
chr11:107544016
|
T | C | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.771+5737A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544016 | ||||||
chr11:107544050
|
C | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.771+5703G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544050 | ||||||
chr11:107544070
|
A | C | 6 | a0001c0002t0001g0100a0001c0002t0001g0105a0001c0002t0001g0106others(3): Show | 6 | HG00280.hp2 HG01106.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.771+5683T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544070 | ||||||
chr11:107544197
|
A | T | 1 | a0002c0004t0001g0273 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.771+5556T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544197 | ||||||
chr11:107544230
|
G | C | 1 | a0001c0002t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.771+5523C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544230 | ||||||
chr11:107544263
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.771+5490A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544263 | ||||||
chr11:107544449
|
G | A | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.771+5304C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544449 | ||||||
chr11:107544662
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.771+5091G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544662 | ||||||
chr11:107544815
|
C | CCA | 17 | a0001c0001t0001g0223a0001c0002t0001g0068a0001c0002t0001g0069others(14): Show | 18 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.771+4936_771+4937d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
C | CCACA | 6 | a0001c0001t0001g0279a0001c0002t0001g0029a0001c0002t0001g0036others(3): Show | 8 | HG00140.hp1 HG00733.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.771+4934_771+4937d others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCA | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0093others(27): Show | 34 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.771+4936_771+4937d others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCACA | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0026others(127): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.771+4934_771+4937d others(6): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCACACA | C | 22 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0138others(19): Show | 23 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.771+4932_771+4937d others(8): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCACACAC others(1): Show |
C | 25 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0033others(22): Show | 32 | HG01106.hp2 HG01109.hp2 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.771+4930_771+4937d others(10): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCACACAC others(3): Show |
C | 10 | a0001c0001t0001g0307a0001c0001t0001g0314a0001c0001t0001g0321others(7): Show | 12 | HG00099.hp2 HG01981.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.771+4928_771+4937d others(12): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCACACAC others(5): Show |
C | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 57 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.771+4926_771+4937d others(14): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544815
|
CCACACAC others(7): Show |
C | 1 | a0001c0001t0001g0300 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.771+4924_771+4937d others(16): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544815 | ||||||
chr11:107544850
|
CACACACA others(4): Show |
C | 1 | a0001c0002t0001g0293 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.771+4892_771+4902d others(13): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544850 | ||||||
chr11:107544858
|
CACA | C | 3 | a0001c0001t0001g0170a0001c0001t0002g0250a0001c0002t0001g0107 | 3 | HG01070.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.771+4892_771+4894d others(5): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544858 | ||||||
chr11:107544862
|
A | C | 1 | a0001c0002t0001g0056 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.771+4891T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544862 | ||||||
chr11:107544887
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.771+4866C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544887 | ||||||
chr11:107544893
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+4860A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544893 | ||||||
chr11:107544948
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+4805A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107544948 | ||||||
chr11:107545040
|
A | G | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+4713T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545040 | ||||||
chr11:107545183
|
A | G | 1 | a0001c0001t0002g0183 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.771+4570T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545183 | ||||||
chr11:107545221
|
A | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+4532T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545221 | ||||||
chr11:107545231
|
T | C | 1 | a0001c0001t0002g0039 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.771+4522A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545231 | ||||||
chr11:107545490
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+4263C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545490 | ||||||
chr11:107545643
|
C | G | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(4): Show | 7 | HG00738.hp1 HG01099.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+4110G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545643 | ||||||
chr11:107545699
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.771+4054A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545699 | ||||||
chr11:107545886
|
C | T | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(103): Show | 124 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.771+3867G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545886 | ||||||
chr11:107545918
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+3835G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545918 | ||||||
chr11:107545947
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+3806G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545947 | ||||||
chr11:107545948
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+3805T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545948 | ||||||
chr11:107545950
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.771+3803G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107545950 | ||||||
chr11:107546058
|
T | C | 37 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 45 | HG00408.hp2 HG00639.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.771+3695A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546058 | ||||||
chr11:107546137
|
T | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(4): Show | 7 | HG00738.hp1 HG01099.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+3616A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546137 | ||||||
chr11:107546167
|
C | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(103): Show | 124 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.771+3586G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546167 | ||||||
chr11:107546268
|
T | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0079others(30): Show | 38 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.771+3485A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546268 | ||||||
chr11:107546271
|
G | A | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+3482C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546271 | ||||||
chr11:107546342
|
CATCTCTC others(4): Show |
C | 1 | a0001c0002t0001g0187 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.771+3400_771+3410d others(13): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546342 | ||||||
chr11:107546469
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.771+3284G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546469 | ||||||
chr11:107546512
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 178 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.771+3241G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546512 | ||||||
chr11:107546560
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0300 | 3 | NA18959.hp1 NA18968.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.771+3193G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546560 | ||||||
chr11:107546575
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.771+3178G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546575 | ||||||
chr11:107546576
|
G | T | 1 | a0001c0002t0001g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.771+3177C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546576 | ||||||
chr11:107546591
|
G | A | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(4): Show | 7 | HG00738.hp1 HG01099.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+3162C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546591 | ||||||
chr11:107546736
|
C | T | 5 | a0001c0003t0001g0232a0009c0012t0009g0227a0009c0016t0009g0207others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.771+3017G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546736 | ||||||
chr11:107546890
|
T | C | 18 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(15): Show | 19 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.771+2863A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546890 | ||||||
chr11:107546943
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.771+2810C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107546943 | ||||||
chr11:107547075
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.771+2678T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547075 | ||||||
chr11:107547092
|
C | T | 1 | a0005c0008t0006g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.771+2661G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547092 | ||||||
chr11:107547093
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.771+2660C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547093 | ||||||
chr11:107547226
|
A | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(103): Show | 124 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.771+2527T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547226 | ||||||
chr11:107547258
|
G | A | 2 | a0001c0002t0001g0292a0001c0002t0001g0293 | 2 | HG00438.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.771+2495C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547258 | ||||||
chr11:107547265
|
AAGGTGCT others(88): Show |
A | 1 | a0001c0001t0002g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.771+2393_771+2487d others(97): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547265 | ||||||
chr11:107547378
|
T | C | 2 | a0001c0001t0001g0321a0013c0014t0001g0198 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.771+2375A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547378 | ||||||
chr11:107547439
|
C | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+2314G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547439 | ||||||
chr11:107547474
|
G | A | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(94): Show | 115 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.771+2279C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547474 | ||||||
chr11:107547599
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.771+2154A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547599 | ||||||
chr11:107547629
|
G | A | 1 | a0001c0002t0001g0070 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.771+2124C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547629 | ||||||
chr11:107547668
|
T | TAAG | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771+2082_771+2084d others(5): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547668 | ||||||
chr11:107547683
|
G | A | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+2070C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547683 | ||||||
chr11:107547820
|
C | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.771+1933G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547820 | ||||||
chr11:107547860
|
G | C | 1 | a0001c0003t0003g0219 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.771+1893C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547860 | ||||||
chr11:107547967
|
C | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01496.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.771+1786G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547967 | ||||||
chr11:107547975
|
G | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.771+1778C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107547975 | ||||||
chr11:107548087
|
T | C | 4 | a0001c0001t0001g0130a0001c0002t0001g0004a0001c0002t0001g0110others(1): Show | 7 | HG01243.hp2 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+1666A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548087 | ||||||
chr11:107548406
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.771+1347C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548406 | ||||||
chr11:107548549
|
C | T | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.771+1204G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548549 | ||||||
chr11:107548594
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.771+1159A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548594 | ||||||
chr11:107548615
|
G | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 178 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.771+1138C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548615 | ||||||
chr11:107548620
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.771+1133T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548620 | ||||||
chr11:107548855
|
C | CT | 14 | a0001c0002t0001g0187a0001c0002t0003g0126a0001c0002t0003g0127others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.771+897dupA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548855 | ||||||
chr11:107548855
|
CT | C | 12 | a0001c0001t0001g0113a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG00738.hp2 HG01081.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.771+897delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548855 | ||||||
chr11:107548855
|
CTT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.771+896_771+897del others(2): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548855 | ||||||
chr11:107548857
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.771+896A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548857 | ||||||
chr11:107548932
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.771+821G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548932 | ||||||
chr11:107548999
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.771+754A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107548999 | ||||||
chr11:107549011
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 97 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.771+742G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549011 | ||||||
chr11:107549059
|
G | A | 1 | a0002c0004t0001g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.771+694C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549059 | ||||||
chr11:107549092
|
C | T | 1 | a0009c0016t0009g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771+661G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549092 | ||||||
chr11:107549093
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.771+660A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549093 | ||||||
chr11:107549099
|
C | T | 8 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(5): Show | 10 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.771+654G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549099 | ||||||
chr11:107549115
|
T | C | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.771+638A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549115 | ||||||
chr11:107549141
|
G | A | 12 | a0001c0002t0001g0071a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.771+612C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549141 | ||||||
chr11:107549344
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.771+409A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549344 | ||||||
chr11:107549466
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.771+287C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 7/11 | chr11 | 107549466 | ||||||
chr11:107549883
|
G | GCTTATGC others(88): Show |
1 | a0001c0001t0002g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.701-61_701-60insGG others(93): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107549883 | ||||||
chr11:107550087
|
C | G | 1 | a0001c0001t0002g0052 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.701-264G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550087 | ||||||
chr11:107550185
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0279a0001c0007t0001g0204 | 3 | HG02280.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.701-362C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550185 | ||||||
chr11:107550349
|
C | T | 1 | a0001c0003t0003g0224 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.701-526G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550349 | ||||||
chr11:107550543
|
C | T | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.701-720G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550543 | ||||||
chr11:107550778
|
C | G | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(84): Show | 104 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.701-955G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550778 | ||||||
chr11:107550788
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.701-965G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550788 | ||||||
chr11:107550789
|
G | A | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(84): Show | 105 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.701-966C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550789 | ||||||
chr11:107550893
|
A | G | 1 | a0012c0015t0003g0199 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.700+915T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550893 | ||||||
chr11:107550944
|
T | C | 12 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(9): Show | 14 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.700+864A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107550944 | ||||||
chr11:107551155
|
T | C | 1 | a0001c0002t0001g0197 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.700+653A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551155 | ||||||
chr11:107551189
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.700+619T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551189 | ||||||
chr11:107551314
|
T | C | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+494A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551314 | ||||||
chr11:107551396
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 59 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.700+412T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551396 | ||||||
chr11:107551465
|
G | A | 2 | a0012c0015t0003g0199a0013c0014t0001g0198 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.700+343C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551465 | ||||||
chr11:107551480
|
G | A | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+328C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551480 | ||||||
chr11:107551640
|
A | G | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+168T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551640 | ||||||
chr11:107551642
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.700+166G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551642 | ||||||
chr11:107551650
|
C | T | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+158G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551650 | ||||||
chr11:107551651
|
G | A | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.700+157C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551651 | ||||||
chr11:107551653
|
C | T | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+155G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551653 | ||||||
chr11:107551667
|
A | C | 1 | a0001c0001t0002g0250 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.700+141T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551667 | ||||||
chr11:107551667
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.700+141T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551667 | ||||||
chr11:107551675
|
C | A | 6 | a0001c0002t0001g0029a0001c0002t0001g0036a0001c0002t0001g0125others(3): Show | 8 | HG00140.hp1 HG00733.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.700+133G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551675 | ||||||
chr11:107551694
|
C | CA | 67 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 81 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.700+113dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551694 | ||||||
chr11:107551705
|
A | AT | 3 | a0001c0003t0003g0219a0001c0003t0003g0282a0003c0005t0004g0212 | 3 | HG01891.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.700+102_700+103ins others(1): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551705 | ||||||
chr11:107551705
|
A | T | 47 | a0001c0001t0002g0003a0001c0001t0002g0011a0001c0001t0002g0020others(44): Show | 62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.700+103T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551705 | ||||||
chr11:107551706
|
AATAAT | A | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+97_700+101delA others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551706 | ||||||
chr11:107551707
|
AT | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0137a0001c0001t0001g0164others(1): Show | 4 | HG03239.hp1 NA18951.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+100delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551707 | ||||||
chr11:107551708
|
T | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 180 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.700+100A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551708 | ||||||
chr11:107551711
|
T | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 131 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.700+97A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551711 | ||||||
chr11:107551714
|
T | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 96 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.700+94A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551714 | ||||||
chr11:107551738
|
C | T | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+70G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 6/11 | chr11 | 107551738 | ||||||
chr11:107552018
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.596-106T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552018 | ||||||
chr11:107552032
|
T | TTAATA | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-125_596-121dup others(5): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552032 | ||||||
chr11:107552103
|
AT | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(80): Show | 100 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.596-192delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552103 | ||||||
chr11:107552215
|
T | C | 9 | a0001c0003t0001g0221a0001c0003t0001g0232a0001c0003t0003g0219others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.596-303A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552215 | ||||||
chr11:107552357
|
C | G | 3 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128 | 3 | HG02145.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.596-445G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552357 | ||||||
chr11:107552358
|
TTAAG | T | 40 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0022others(37): Show | 48 | HG00280.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.596-450_596-447del others(4): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552358 | ||||||
chr11:107552386
|
T | C | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.596-474A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552386 | ||||||
chr11:107552395
|
T | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0008others(55): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.596-483A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552395 | ||||||
chr11:107552519
|
C | A | 6 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+589G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552519 | ||||||
chr11:107552705
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.595+403T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552705 | ||||||
chr11:107552893
|
G | A | 2 | a0001c0007t0001g0204a0015c0013t0001g0206 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.595+215C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 5/11 | chr11 | 107552893 | ||||||
chr11:107553246
|
T | C | 9 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(6): Show | 11 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.500-43A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553246 | ||||||
chr11:107553307
|
T | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 61 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.500-104A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553307 | ||||||
chr11:107553422
|
T | C | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.500-219A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553422 | ||||||
chr11:107553514
|
C | G | 4 | a0001c0002t0001g0029a0001c0002t0001g0036a0001c0002t0001g0246others(1): Show | 6 | HG00733.hp1 HG00741.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-311G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553514 | ||||||
chr11:107553580
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.499+267C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553580 | ||||||
chr11:107553608
|
C | T | 2 | a0001c0003t0010g0280a0009c0012t0009g0227 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.499+239G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553608 | ||||||
chr11:107553674
|
A | C | 20 | a0001c0002t0001g0007a0001c0002t0001g0096a0001c0002t0001g0097others(17): Show | 22 | HG00280.hp2 HG01106.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.499+173T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553674 | ||||||
chr11:107553674
|
A | T | 8 | a0002c0004t0001g0040a0002c0004t0001g0271a0002c0004t0001g0272others(5): Show | 9 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.499+173T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 4/11 | chr11 | 107553674 | ||||||
chr11:107553983
|
G | A | 3 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128 | 3 | HG02145.hp1 HG03098.hp2 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.368-5C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107553983 | ||||||
chr11:107554329
|
T | C | 18 | a0001c0003t0001g0221a0001c0003t0001g0232a0001c0003t0003g0219others(15): Show | 20 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.368-351A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554329 | ||||||
chr11:107554556
|
AAG | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(81): Show | 101 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.368-580_368-579del others(2): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554556 | ||||||
chr11:107554563
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.368-585A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554563 | ||||||
chr11:107554635
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.368-657C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554635 | ||||||
chr11:107554819
|
T | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(79): Show | 99 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.368-841A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554819 | ||||||
chr11:107554907
|
AT | A | 3 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128 | 3 | HG02145.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.368-930delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554907 | ||||||
chr11:107554960
|
C | T | 2 | a0010c0021t0001g0205a0011c0020t0009g0318 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.368-982G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554960 | ||||||
chr11:107554988
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(83): Show | 103 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.368-1010C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554988 | ||||||
chr11:107554998
|
A | G | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1020T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107554998 | ||||||
chr11:107555023
|
T | G | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1045A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555023 | ||||||
chr11:107555025
|
C | T | 21 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.368-1047G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555025 | ||||||
chr11:107555056
|
A | G | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1078T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555056 | ||||||
chr11:107555089
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368-1111G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555089 | ||||||
chr11:107555110
|
A | T | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1132T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555110 | ||||||
chr11:107555116
|
C | T | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-1138G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555116 | ||||||
chr11:107555187
|
G | C | 18 | a0001c0003t0001g0221a0001c0003t0001g0232a0001c0003t0003g0219others(15): Show | 20 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.368-1209C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555187 | ||||||
chr11:107555250
|
A | G | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-1272T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555250 | ||||||
chr11:107555252
|
T | G | 2 | a0001c0001t0002g0052a0001c0002t0001g0187 | 2 | NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.368-1274A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555252 | ||||||
chr11:107555270
|
A | T | 9 | a0001c0003t0001g0221a0001c0003t0001g0232a0001c0003t0003g0219others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.368-1292T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555270 | ||||||
chr11:107555360
|
T | C | 2 | a0012c0015t0003g0199a0013c0014t0001g0198 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.368-1382A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555360 | ||||||
chr11:107555395
|
CA | C | 9 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(6): Show | 11 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+1370delT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555395 | ||||||
chr11:107555403
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 61 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.367+1363T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555403 | ||||||
chr11:107555425
|
A | G | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1341T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555425 | ||||||
chr11:107555433
|
C | A | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.367+1333G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555433 | ||||||
chr11:107555442
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.367+1324G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555442 | ||||||
chr11:107555531
|
A | C | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1235T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555531 | ||||||
chr11:107555549
|
A | G | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.367+1217T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555549 | ||||||
chr11:107555555
|
G | A | 2 | a0012c0015t0003g0199a0013c0014t0001g0198 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.367+1211C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555555 | ||||||
chr11:107555653
|
G | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.367+1113C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555653 | ||||||
chr11:107555694
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.367+1072A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555694 | ||||||
chr11:107555902
|
T | C | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+864A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107555902 | ||||||
chr11:107556051
|
A | G | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+715T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556051 | ||||||
chr11:107556095
|
C | A | 1 | a0001c0003t0013g0301 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.367+671G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556095 | ||||||
chr11:107556095
|
C | T | 6 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0010g0128others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.367+671G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556095 | ||||||
chr11:107556121
|
T | C | 1 | a0001c0007t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+645A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556121 | ||||||
chr11:107556278
|
C | CA | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+487dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556278 | ||||||
chr11:107556284
|
G | A | 16 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(13): Show | 17 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.367+482C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556284 | ||||||
chr11:107556285
|
C | A | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.367+481G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556285 | ||||||
chr11:107556289
|
A | C | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+477T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556289 | ||||||
chr11:107556289
|
A | T | 12 | a0001c0003t0001g0200a0001c0007t0011g0049a0001c0007t0011g0050others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.367+477T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556289 | ||||||
chr11:107556293
|
T | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.367+473A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556293 | ||||||
chr11:107556387
|
C | T | 9 | a0001c0003t0007g0228a0001c0003t0007g0229a0001c0003t0007g0230others(6): Show | 11 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+379G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556387 | ||||||
chr11:107556433
|
G | A | 5 | a0003c0005t0004g0212a0003c0005t0004g0213a0003c0005t0004g0214others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+333C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556433 | ||||||
chr11:107556519
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 9 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.367+247T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556519 | ||||||
chr11:107556523
|
A | T | 1 | a0001c0001t0001g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.367+243T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556523 | ||||||
chr11:107556665
|
T | A | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+101A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 3/11 | chr11 | 107556665 | ||||||
chr11:107557011
|
A | G | 2 | a0010c0021t0001g0205a0011c0020t0009g0318 | 2 | HG02818.hp1 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.130-8T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557011 | ||||||
chr11:107557017
|
C | A | 2 | a0010c0021t0001g0205a0011c0020t0009g0318 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130-14G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557017 | ||||||
chr11:107557086
|
T | A | 2 | a0012c0015t0003g0199a0013c0014t0001g0198 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.130-83A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557086 | ||||||
chr11:107557087
|
A | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.130-84T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557087 | ||||||
chr11:107557241
|
C | T | 2 | a0010c0021t0001g0205a0011c0020t0009g0318 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130-238G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557241 | ||||||
chr11:107557339
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0279 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.130-336C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557339 | ||||||
chr11:107557340
|
G | C | 4 | a0010c0021t0001g0205a0011c0020t0009g0318a0012c0015t0003g0199others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-337C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557340 | ||||||
chr11:107557484
|
G | C | 2 | a0012c0015t0003g0199a0013c0014t0001g0198 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.130-481C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557484 | ||||||
chr11:107557545
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-542A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557545 | ||||||
chr11:107557629
|
T | C | 1 | a0009c0016t0009g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.130-626A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557629 | ||||||
chr11:107557724
|
G | A | 3 | a0001c0007t0001g0204a0001c0007t0001g0216a0015c0013t0001g0206 | 3 | HG02055.hp2 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.130-721C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557724 | ||||||
chr11:107557835
|
A | G | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.130-832T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557835 | ||||||
chr11:107557957
|
T | G | 1 | a0006c0017t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.130-954A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557957 | ||||||
chr11:107557968
|
C | T | 40 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0022others(37): Show | 48 | HG00280.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.130-965G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107557968 | ||||||
chr11:107558006
|
T | C | 1 | a0001c0007t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.130-1003A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558006 | ||||||
chr11:107558294
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.130-1291C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558294 | ||||||
chr11:107558351
|
A | G | 2 | a0010c0021t0001g0205a0011c0020t0009g0318 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130-1348T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558351 | ||||||
chr11:107558624
|
T | C | 2 | a0001c0002t0001g0019a0001c0002t0001g0081 | 3 | NA18941.hp1 NA19004.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.130-1621A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558624 | ||||||
chr11:107558691
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | NA18971.hp2 NA18975.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.130-1688A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558691 | ||||||
chr11:107558697
|
T | G | 78 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0147others(75): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.130-1694A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558697 | ||||||
chr11:107558721
|
T | C | 1 | a0001c0001t0001g0319 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.130-1718A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558721 | ||||||
chr11:107558923
|
C | T | 1 | a0015c0013t0001g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+1842G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558923 | ||||||
chr11:107558940
|
T | C | 1 | a0009c0016t0009g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129+1825A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107558940 | ||||||
chr11:107559033
|
T | C | 1 | a0001c0002t0001g0089 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.129+1732A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559033 | ||||||
chr11:107559111
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0223a0001c0001t0001g0279 | 3 | HG02451.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.129+1654A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559111 | ||||||
chr11:107559139
|
A | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0041others(60): Show | 73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.129+1626T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559139 | ||||||
chr11:107559171
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0155others(9): Show | 15 | HG00738.hp1 HG01099.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.129+1594A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559171 | ||||||
chr11:107559185
|
C | T | 1 | a0001c0002t0001g0053 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.129+1580G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559185 | ||||||
chr11:107559328
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 63 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.129+1437T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559328 | ||||||
chr11:107559331
|
A | C | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.129+1434T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559331 | ||||||
chr11:107559350
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 61 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.129+1415A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559350 | ||||||
chr11:107559505
|
A | AT | 51 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(48): Show | 67 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.129+1259dupA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559505 | ||||||
chr11:107559505
|
AT | A | 6 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0188others(3): Show | 6 | NA18971.hp2 NA18972.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+1259delA | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559505 | ||||||
chr11:107559542
|
T | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0279a0001c0001t0001g0281 | 3 | HG02723.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.129+1223A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559542 | ||||||
chr11:107559574
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 60 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.129+1191A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559574 | ||||||
chr11:107559574
|
T | C | 113 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0045others(110): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.129+1191A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559574 | ||||||
chr11:107559614
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 59 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+1151A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559614 | ||||||
chr11:107559620
|
C | A | 1 | a0009c0016t0009g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129+1145G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559620 | ||||||
chr11:107559771
|
C | G | 1 | a0010c0021t0001g0205 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.129+994G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559771 | ||||||
chr11:107559888
|
T | A | 1 | a0001c0003t0007g0233 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129+877A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107559888 | ||||||
chr11:107560020
|
A | G | 1 | a0001c0002t0001g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.129+745T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107560020 | ||||||
chr11:107560247
|
C | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 59 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+518G>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107560247 | ||||||
chr11:107560387
|
A | T | 2 | a0001c0001t0001g0159a0001c0002t0001g0158 | 2 | NA18993.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.129+378T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107560387 | ||||||
chr11:107560454
|
A | G | 9 | a0001c0001t0001g0270a0002c0004t0001g0040a0002c0004t0001g0271others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+311T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107560454 | ||||||
chr11:107560514
|
A | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217 | 3 | HG00738.hp1 HG01099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.129+251T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 2/11 | chr11 | 107560514 | ||||||
chr11:107560911
|
C | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(145): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-6-12G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107560911 | ||||||
chr11:107560935
|
A | C | 3 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0234 | 5 | HG02027.hp2 HG02165.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-36T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107560935 | ||||||
chr11:107560963
|
T | C | 2 | a0001c0003t0003g0283a0001c0003t0003g0284 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-6-64A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107560963 | ||||||
chr11:107561233
|
G | A | 1 | a0001c0003t0008g0015 | 3 | HG02109.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-6-334C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561233 | ||||||
chr11:107561263
|
C | T | 79 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0217others(76): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-6-364G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561263 | ||||||
chr11:107561275
|
A | G | 2 | a0008c0010t0001g0094a0008c0010t0001g0095 | 2 | HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-6-376T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561275 | ||||||
chr11:107561428
|
G | A | 20 | a0001c0001t0001g0270a0001c0003t0001g0232a0001c0003t0003g0224others(17): Show | 21 | HG01081.hp2 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-529C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561428 | ||||||
chr11:107561557
|
T | C | 1 | a0001c0003t0010g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-6-658A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561557 | ||||||
chr11:107561572
|
C | A | 1 | a0001c0007t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-6-673G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561572 | ||||||
chr11:107561776
|
T | C | 54 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0242others(51): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.-6-877A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561776 | ||||||
chr11:107561850
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 59 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-6-951A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107561850 | ||||||
chr11:107562013
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-6-1114C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562013 | ||||||
chr11:107562207
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-6-1308C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562207 | ||||||
chr11:107562214
|
G | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0092 | 2 | HG02080.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-6-1315C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562214 | ||||||
chr11:107562297
|
C | CA | 103 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0046others(100): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-6-1399dupT | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562297 | ||||||
chr11:107562297
|
C | CAA | 12 | a0001c0001t0001g0270a0001c0001t0002g0278a0001c0007t0011g0049others(9): Show | 13 | HG01081.hp2 HG01891.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-1400_-6-1399dup others(2): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562297 | ||||||
chr11:107562688
|
G | T | 1 | a0001c0001t0002g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-6-1789C>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562688 | ||||||
chr11:107562726
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-6-1827C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562726 | ||||||
chr11:107562768
|
T | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(34): Show | 46 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.-6-1869A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562768 | ||||||
chr11:107562845
|
G | C | 1 | a0001c0001t0001g0322 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-6-1946C>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562845 | ||||||
chr11:107562886
|
G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-6-1987C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562886 | ||||||
chr11:107562896
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-6-1997C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562896 | ||||||
chr11:107562983
|
G | A | 1 | a0009c0016t0009g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-6-2084C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107562983 | ||||||
chr11:107563109
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0031others(44): Show | 59 | HG00099.hp1 HG00609.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-6-2210C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563109 | ||||||
chr11:107563175
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-6-2276T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563175 | ||||||
chr11:107563303
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(149): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-7+2298G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563303 | ||||||
chr11:107563468
|
A | C | 2 | a0001c0001t0001g0217a0001c0007t0001g0216 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-7+2133T>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563468 | ||||||
chr11:107563519
|
AATTTATT others(7): Show |
A | 105 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(102): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.-7+2068_-7+2081del others(14): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563519 | ||||||
chr11:107563659
|
A | G | 9 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0002t0001g0211others(6): Show | 9 | HG00738.hp1 HG01099.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+1942T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563659 | ||||||
chr11:107563820
|
G | A | 2 | a0001c0002t0001g0196a0001c0002t0001g0197 | 2 | NA18962.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-7+1781C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563820 | ||||||
chr11:107563876
|
A | G | 2 | a0009c0016t0009g0207a0015c0013t0001g0206 | 2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-7+1725T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563876 | ||||||
chr11:107563951
|
T | C | 1 | a0001c0003t0010g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-7+1650A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563951 | ||||||
chr11:107563980
|
C | T | 5 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 5 | HG01255.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1621G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107563980 | ||||||
chr11:107564141
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-7+1460C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564141 | ||||||
chr11:107564334
|
A | G | 1 | a0001c0003t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-7+1267T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564334 | ||||||
chr11:107564360
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+1241A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564360 | ||||||
chr11:107564388
|
T | A | 3 | a0001c0003t0003g0282a0001c0003t0003g0283a0001c0003t0003g0284 | 3 | HG01891.hp2 HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-7+1213A>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564388 | ||||||
chr11:107564403
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-7+1198G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564403 | ||||||
chr11:107564414
|
T | G | 2 | a0001c0001t0002g0286a0001c0001t0015g0285 | 2 | HG01167.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-7+1187A>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564414 | ||||||
chr11:107564459
|
A | G | 2 | a0012c0015t0003g0199a0013c0014t0001g0198 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7+1142T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564459 | ||||||
chr11:107564466
|
C | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(146): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-7+1135G>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564466 | ||||||
chr11:107564585
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 57 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7+1016A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564585 | ||||||
chr11:107564667
|
A | G | 2 | a0001c0007t0011g0049a0001c0007t0011g0050 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-7+934T>C | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564667 | ||||||
chr11:107564744
|
C | CACTCTCA others(13): Show |
1 | a0001c0001t0001g0048 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-7+837_-7+856dupAT others(18): Show |
ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564744 | ||||||
chr11:107564792
|
A | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 57 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7+809T>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564792 | ||||||
chr11:107564794
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG03130.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-7+807G>A | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107564794 | ||||||
chr11:107565186
|
T | C | 1 | a0001c0001t0002g0287 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-7+415A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107565186 | ||||||
chr11:107565270
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 57 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7+331A>G | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107565270 | ||||||
chr11:107565376
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-7+225C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107565376 | ||||||
chr11:107565529
|
G | A | 1 | a0003c0005t0004g0324 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7+72C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107565529 | ||||||
chr11:107565579
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-7+22C>T | ALKBH8 | ENSG00000137760.15 | transcript | ENST00000428149.7 | protein_coding | 1/11 | chr11 | 107565579 |