geneid | 221120 |
---|---|
ensemblid | ENSG00000166199.13 |
hgncid | 30141 |
symbol | ALKBH3 |
name | alkB homolog 3, alpha-ketoglutarate dependent dioxygenase |
refseq_nuc | NM_139178.4 |
refseq_prot | NP_631917.1 |
ensembl_nuc | ENST00000302708.9 |
ensembl_prot | ENSP00000302232.4 |
mane_status | MANE Select |
chr | chr11 |
start | 43880831 |
end | 43920274 |
strand | + |
ver | v1.2 |
region | chr11:43880831-43920274 |
region5000 | chr11:43875831-43925274 |
regionname0 | ALKBH3_chr11_43880831_43920274 |
regionname5000 | ALKBH3_chr11_43875831_43925274 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 286 | 319 | 85 | 67 | 126 | 12 | 28 | 98 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0002 | 0/0 | 286 | 51 | 11 | 11 | 17 | 2 | 10 | 13 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0003 | 0/1 | 69 | 2 | 0 | 0 | 1 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0004 | 0/0 | 286 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0005 | 0/0 | 286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0006 | 0/0 | 286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
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 | 0/0 | 861 | 196 | 22 | 34 | 107 | 9 | 24 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0002 | 0/0 | 861 | 93 | 57 | 17 | 14 | 3 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0003 | 0/0 | 861 | 51 | 11 | 11 | 17 | 2 | 10 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0004 | 0/0 | 861 | 27 | 5 | 15 | 5 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0005 | 0/0 | 861 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0006 | 1/0 | 861 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0007 | 0/0 | 861 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0008 | 0/0 | 861 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0009 | 0/1 | 861 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0010 | 0/0 | 861 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
c0011 | 0/0 | 861 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
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 | 1/1 | 684 | 225 | 29 | 38 | 122 | 9 | 25 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0002 | 0/0 | 684 | 68 | 25 | 13 | 18 | 2 | 10 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0003 | 0/0 | 684 | 27 | 5 | 15 | 5 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0004 | 0/0 | 684 | 25 | 18 | 6 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0005 | 0/0 | 684 | 15 | 10 | 4 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0006 | 0/0 | 684 | 8 | 6 | 0 | 0 | 2 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0007 | 0/0 | 684 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0008 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0009 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
t0010 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
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 | 26 | 0 | 1 | 23 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0003 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0004 | 0/0 | 9 | 0 | 6 | 1 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0005 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0007 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0017 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0025 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0049 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0050 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
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 | 0/0 | 861 | 196 | 22 | 34 | 107 | 9 | 24 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0002 | 0/0 | 861 | 93 | 57 | 17 | 14 | 3 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0004 | 0/0 | 861 | 27 | 5 | 15 | 5 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0006 | 1/0 | 861 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0007 | 0/0 | 861 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0002c0003 | 0/0 | 861 | 51 | 11 | 11 | 17 | 2 | 10 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0003c0009 | 0/1 | 861 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0003c0010 | 0/0 | 861 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0004c0005 | 0/0 | 861 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0005c0011 | 0/0 | 861 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0006c0008 | 0/0 | 861 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1544 | 179 | 12 | 29 | 106 | 9 | 23 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0001t0005 | 0/0 | 1544 | 14 | 10 | 3 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0001t0008 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0001t0009 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0001t0010 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0002t0001 | 0/0 | 1544 | 40 | 15 | 9 | 14 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0002t0002 | 0/0 | 1544 | 15 | 13 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0002t0004 | 0/0 | 1544 | 25 | 18 | 6 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0002t0006 | 0/0 | 1544 | 8 | 6 | 0 | 0 | 2 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0002t0007 | 0/0 | 1544 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0004t0003 | 0/0 | 1544 | 27 | 5 | 15 | 5 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0006t0001 | 1/0 | 1544 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0001c0007t0005 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0002c0003t0002 | 0/0 | 1544 | 51 | 11 | 11 | 17 | 2 | 10 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0003c0009t0001 | 0/1 | 1544 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0003c0010t0002 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0004c0005t0001 | 0/0 | 1544 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0005c0011t0002 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
a0006c0008t0001 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | copy fasta | chr11 | 43875831 | 43925274 |
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 | 26 | 0 | 1 | 23 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0009g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0001t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0002g0003 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0002g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0006g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0006g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0007g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0002t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0004 | 0/0 | 9 | 0 | 6 | 1 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0004t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0006t0001g0025 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0001c0007t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0007 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0017 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0049 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0050 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0002c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0003c0009t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0003c0010t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0004c0005t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0005c0011t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
a0006c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00140 | hp2 | a0001 | c0002 | t0006 | g0051 | EUR | GBR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00423 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00438 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0012 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00609 | hp2 | a0001 | c0004 | t0003 | g0027 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00621 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00639 | hp1 | a0001 | c0004 | t0003 | g0028 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0014 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00642 | hp1 | a0001 | c0004 | t0003 | g0060 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00735 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG00741 | hp2 | a0002 | c0003 | t0002 | g0173 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0108 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01069 | hp2 | a0001 | c0004 | t0003 | g0063 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01070 | hp2 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01071 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01074 | hp1 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0179 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01081 | hp1 | a0001 | c0004 | t0003 | g0066 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01081 | hp2 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01168 | hp1 | a0001 | c0007 | t0005 | g0191 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0185 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0058 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01258 | hp1 | a0001 | c0002 | t0004 | g0058 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0150 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0186 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01358 | hp2 | a0001 | c0002 | t0004 | g0223 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01361 | hp1 | a0001 | c0004 | t0003 | g0065 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0103 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01433 | hp1 | a0001 | c0002 | t0004 | g0224 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01433 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01515 | hp2 | a0002 | c0003 | t0002 | g0167 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01884 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01928 | hp2 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01934 | hp2 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01943 | hp1 | a0002 | c0003 | t0002 | g0166 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01952 | hp1 | a0001 | c0004 | t0003 | g0062 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01978 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01993 | hp1 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02004 | hp2 | a0002 | c0003 | t0002 | g0184 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02055 | hp2 | a0002 | c0003 | t0002 | g0049 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02132 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02135 | hp2 | a0002 | c0003 | t0002 | g0018 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02145 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0187 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02258 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02258 | hp2 | a0001 | c0004 | t0003 | g0028 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02273 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02451 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02451 | hp2 | a0002 | c0003 | t0002 | g0047 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02572 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0064 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0211 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02630 | hp2 | a0002 | c0003 | t0002 | g0169 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0176 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02683 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02698 | hp2 | a0002 | c0003 | t0002 | g0174 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02717 | hp2 | a0001 | c0002 | t0007 | g0215 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02723 | hp1 | a0006 | c0008 | t0001 | g0171 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02723 | hp2 | a0001 | c0002 | t0004 | g0217 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02735 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0192 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02818 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02886 | hp1 | a0002 | c0003 | t0002 | g0165 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02886 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02922 | hp2 | a0002 | c0003 | t0002 | g0050 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02970 | hp2 | a0001 | c0002 | t0006 | g0190 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03017 | hp1 | a0002 | c0003 | t0002 | g0151 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03041 | hp1 | a0005 | c0011 | t0002 | g0149 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0212 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0052 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03139 | hp1 | a0001 | c0002 | t0007 | g0026 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03195 | hp2 | a0002 | c0003 | t0002 | g0007 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03225 | hp2 | a0001 | c0002 | t0007 | g0026 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03453 | hp1 | a0002 | c0003 | t0002 | g0168 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03491 | hp2 | a0001 | c0004 | t0003 | g0004 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03492 | hp1 | a0001 | c0004 | t0003 | g0004 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03516 | hp1 | a0002 | c0003 | t0002 | g0172 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03516 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0052 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0049 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03669 | hp1 | a0002 | c0003 | t0002 | g0106 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0177 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03942 | hp2 | a0002 | c0003 | t0002 | g0017 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04115 | hp2 | a0002 | c0003 | t0002 | g0183 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG04228 | hp2 | a0002 | c0003 | t0002 | g0181 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18522 | hp1 | a0001 | c0006 | t0001 | g0025 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18939 | hp1 | a0002 | c0003 | t0002 | g0105 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18940 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18942 | hp2 | a0002 | c0003 | t0002 | g0101 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18946 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18947 | hp2 | a0004 | c0005 | t0001 | g0030 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18951 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0102 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18964 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18972 | hp1 | a0002 | c0003 | t0002 | g0180 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18978 | hp2 | a0002 | c0003 | t0002 | g0178 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18983 | hp1 | a0001 | c0004 | t0003 | g0027 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18994 | hp2 | a0004 | c0005 | t0001 | g0030 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA18995 | hp2 | a0003 | c0010 | t0002 | g0033 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19030 | hp1 | a0001 | c0004 | t0003 | g0067 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19030 | hp2 | a0001 | c0002 | t0007 | g0026 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19043 | hp1 | a0001 | c0002 | t0004 | g0221 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19043 | hp2 | a0002 | c0003 | t0002 | g0175 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19056 | hp2 | a0001 | c0004 | t0003 | g0061 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19060 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19063 | hp1 | a0001 | c0004 | t0003 | g0009 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19070 | hp1 | a0002 | c0003 | t0002 | g0050 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19089 | hp2 | a0002 | c0003 | t0002 | g0033 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19090 | hp2 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19240 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ASW | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ASW | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20752 | hp1 | a0002 | c0003 | t0002 | g0182 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0222 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20805 | hp2 | a0001 | c0002 | t0006 | g0051 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01123 | hp1 | a0001 | c0004 | t0003 | g0004 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02109 | hp1 | a0001 | c0002 | t0004 | g0195 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02109 | hp2 | a0001 | c0002 | t0006 | g0188 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0201 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG02559 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG03471 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG06807 | hp1 | a0001 | c0002 | t0007 | g0216 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0208 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA21309 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
homoSapiens_chm13v2 | hp1 | a0003 | c0009 | t0001 | g0093 | REF | REF | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
homoSapiens_grch38 | hp1 | a0001 | c0006 | t0001 | g0025 | REF | REF | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:43883120
|
G | T | 1 | a0005 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.115G>T | p.Gly39Cys | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/10 | 534/1544 | 115/861 | 39/286 | chr11 | 43883120 | ||
chr11:43884007
|
C | T | 1 | a0003 | 2 | NA18995.hp2 homoSapiens_chm13v2.hp1 |
stop_gained | HIGH | c.208C>T | p.Arg70* | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/10 | 627/1544 | 208/861 | 70/286 | chr11 | 43884007 | ||
chr11:43892127
|
C | G | 1 | a0006 | 1 | HG02723.hp1 | missense_variant&splice_region_variant | MODERATE | c.457C>G | p.His153Asp | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/10 | 876/1544 | 457/861 | 153/286 | chr11 | 43892127 | ||
chr11:43901546
|
C | T | 1 | a0004 | 2 | NA18947.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.490C>T | p.Arg164Cys | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/10 | 909/1544 | 490/861 | 164/286 | chr11 | 43901546 | ||
chr11:43919052
|
C | G | 2 | a0002a0003 | 52 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
missense_variant | MODERATE | c.684C>G | p.Asp228Glu | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/10 | 1103/1544 | 684/861 | 228/286 | chr11 | 43919052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:43883086
|
T | G | 1 | a0001c0007 | 1 | HG01168.hp1 | splice_region_variant&synonymous_variant | LOW | c.81T>G | p.Ala27Ala | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/10 | 500/1544 | 81/861 | 27/286 | chr11 | 43883086 | ||
chr11:43889815
|
T | C | 10 | a0001c0001a0001c0002a0001c0004others(7): Show | 374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
synonymous_variant | LOW | c.357T>C | p.Thr119Thr | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/10 | 776/1544 | 357/861 | 119/286 | chr11 | 43889815 | ||
chr11:43892054
|
G | A | 1 | a0001c0004 | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
synonymous_variant | LOW | c.384G>A | p.Gln128Gln | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/10 | 803/1544 | 384/861 | 128/286 | chr11 | 43892054 | ||
chr11:43919094
|
G | T | 6 | a0001c0001a0001c0004a0001c0007others(3): Show | 228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
synonymous_variant | LOW | c.726G>T | p.Gly242Gly | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/10 | 1145/1544 | 726/861 | 242/286 | chr11 | 43919094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:43880873
|
C | T | 2 | a0001c0001t0005a0001c0007t0005 | 15 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-377C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | chr11 | 43880873 | ||||||
chr11:43880975
|
T | C | 1 | a0001c0002t0006 | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-275T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1678 | chr11 | 43880975 | |||||
chr11:43881070
|
G | A | 2 | a0001c0002t0007a0001c0004t0003 | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1583 | chr11 | 43881070 | |||||
chr11:43881100
|
G | A | 1 | a0001c0001t0008 | 1 | HG01069.hp1 | 5_prime_UTR_variant | MODIFIER | c.-150G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1553 | chr11 | 43881100 | |||||
chr11:43881131
|
G | T | 1 | a0001c0002t0004 | 25 | HG00735.hp1 HG01167.hp1 HG01256.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-119G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1522 | chr11 | 43881131 | |||||
chr11:43882598
|
T | A | 1 | a0001c0001t0009 | 1 | HG00639.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/10 | chr11 | 43882598 | ||||||
chr11:43920012
|
G | A | 1 | a0001c0001t0010 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 10/10 | 2 | chr11 | 43920012 | |||||
chr11:43920087
|
C | G | 1 | a0001c0002t0007 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 10/10 | 77 | chr11 | 43920087 | |||||
chr11:43920227
|
C | G | 4 | a0001c0002t0002a0002c0003t0002a0003c0010t0002others(1): Show | 68 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 10/10 | 217 | chr11 | 43920227 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:43881231
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-71+52C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881231 | ||||||
chr11:43881286
|
A | G | 6 | a0001c0002t0004g0058a0001c0002t0004g0059a0001c0002t0004g0221others(3): Show | 8 | HG00735.hp1 HG01167.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+107A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881286 | ||||||
chr11:43881344
|
G | A | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-71+165G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881344 | ||||||
chr11:43881427
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG03927.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-71+248C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881427 | ||||||
chr11:43881637
|
C | T | 1 | a0001c0002t0004g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-71+458C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881637 | ||||||
chr11:43881640
|
C | T | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+461C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881640 | ||||||
chr11:43881707
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-71+528G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881707 | ||||||
chr11:43881778
|
G | C | 8 | a0002c0003t0002g0033a0002c0003t0002g0101a0002c0003t0002g0102others(5): Show | 8 | HG01361.hp2 HG03669.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+599G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881778 | ||||||
chr11:43881828
|
T | C | 16 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216others(13): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-71+649T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881828 | ||||||
chr11:43881841
|
T | G | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-71+662T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881841 | ||||||
chr11:43882050
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-70-533G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882050 | ||||||
chr11:43882070
|
T | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-70-513T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882070 | ||||||
chr11:43882167
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-70-416T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882167 | ||||||
chr11:43882223
|
A | T | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-70-360A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882223 | ||||||
chr11:43882248
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-70-335G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882248 | ||||||
chr11:43882292
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-70-291G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882292 | ||||||
chr11:43882306
|
A | G | 4 | a0001c0001t0005g0053a0001c0001t0005g0192a0001c0001t0005g0193others(1): Show | 5 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-277A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882306 | ||||||
chr11:43882520
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-70-63C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882520 | ||||||
chr11:43882741
|
T | C | 1 | a0001c0001t0008g0108 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79+10T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/9 | chr11 | 43882741 | ||||||
chr11:43882833
|
C | T | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+102C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/9 | chr11 | 43882833 | ||||||
chr11:43882903
|
T | C | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+172T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/9 | chr11 | 43882903 | ||||||
chr11:43883196
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.183+8C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883196 | ||||||
chr11:43883326
|
GA | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(89): Show | 150 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.183+139delA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883326 | ||||||
chr11:43883327
|
A | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.183+139A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883327 | ||||||
chr11:43883389
|
C | A | 2 | a0001c0002t0004g0058a0001c0002t0004g0221 | 3 | HG01256.hp2 HG01258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+201C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883389 | ||||||
chr11:43883510
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.183+322A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883510 | ||||||
chr11:43883525
|
T | C | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+337T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883525 | ||||||
chr11:43883546
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.183+358T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883546 | ||||||
chr11:43883690
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.184-293A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883690 | ||||||
chr11:43883890
|
C | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.184-93C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883890 | ||||||
chr11:43883934
|
T | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.184-49T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883934 | ||||||
chr11:43883967
|
G | T | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.184-16G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883967 | ||||||
chr11:43884057
|
T | TG | 1 | a0001c0002t0007g0026 | 3 | HG03139.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.218+41dupG | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884057 | |||||
chr11:43884305
|
C | T | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.218+288C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884305 | ||||||
chr11:43884374
|
T | C | 1 | a0002c0003t0002g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.218+357T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884374 | ||||||
chr11:43884375
|
CT | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 168 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.218+378delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | |||||
chr11:43884375
|
CTT | C | 19 | a0001c0001t0001g0034a0001c0001t0001g0110a0001c0001t0001g0148others(16): Show | 34 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.218+377_218+378del others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | |||||
chr11:43884375
|
CTTT | C | 5 | a0001c0001t0001g0098a0001c0001t0001g0225a0001c0002t0007g0026others(2): Show | 7 | HG00323.hp2 HG01261.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+376_218+378del others(3): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | |||||
chr11:43884375
|
CTTTT | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 84 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.218+375_218+378del others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | |||||
chr11:43884437
|
T | A | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.218+420T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884437 | ||||||
chr11:43884892
|
C | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.218+875C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884892 | ||||||
chr11:43884975
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.218+958C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884975 | ||||||
chr11:43884985
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(89): Show | 150 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.218+968G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884985 | ||||||
chr11:43885146
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.218+1129T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885146 | ||||||
chr11:43885150
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.218+1133A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885150 | ||||||
chr11:43885272
|
C | T | 16 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216others(13): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.218+1255C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885272 | ||||||
chr11:43885398
|
T | C | 2 | a0002c0003t0002g0168a0002c0003t0002g0169 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.219-1208T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885398 | ||||||
chr11:43885524
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.219-1082G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885524 | ||||||
chr11:43885538
|
G | C | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1068G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885538 | ||||||
chr11:43885637
|
C | G | 1 | a0001c0002t0001g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-969C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885637 | ||||||
chr11:43885778
|
A | G | 5 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0188others(2): Show | 7 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-828A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885778 | ||||||
chr11:43885936
|
A | G | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.219-670A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885936 | ||||||
chr11:43885949
|
A | G | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-657A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885949 | ||||||
chr11:43886011
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.219-595A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886011 | ||||||
chr11:43886035
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.219-571G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886035 | ||||||
chr11:43886062
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.219-544C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886062 | ||||||
chr11:43886129
|
A | G | 3 | a0001c0002t0004g0056a0001c0002t0004g0211a0001c0002t0004g0212 | 4 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-477A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886129 | ||||||
chr11:43886243
|
C | T | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-363C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886243 | ||||||
chr11:43886365
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.219-241A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886365 | ||||||
chr11:43886406
|
C | A | 2 | a0001c0001t0001g0170a0006c0008t0001g0171 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.219-200C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886406 | ||||||
chr11:43886554
|
T | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.219-52T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886554 | ||||||
chr11:43886680
|
C | T | 23 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0053others(20): Show | 40 | HG00140.hp2 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.266+27C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43886680 | ||||||
chr11:43886916
|
A | G | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.266+263A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43886916 | ||||||
chr11:43886965
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.266+312T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43886965 | ||||||
chr11:43887082
|
GCATATGT others(4): Show |
G | 1 | a0002c0003t0002g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.266+432_266+442del others(11): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887082 | |||||
chr11:43887087
|
T | C | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.266+434T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887087 | ||||||
chr11:43887122
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.266+469C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887122 | ||||||
chr11:43887164
|
G | A | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+511G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887164 | ||||||
chr11:43887212
|
A | G | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.266+559A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887212 | ||||||
chr11:43887286
|
G | C | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+633G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887286 | ||||||
chr11:43887535
|
C | T | 1 | a0002c0003t0002g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.266+882C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887535 | ||||||
chr11:43887544
|
A | G | 1 | a0001c0002t0004g0224 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.266+891A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887544 | ||||||
chr11:43887698
|
A | G | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.266+1045A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887698 | ||||||
chr11:43887703
|
A | G | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.266+1050A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887703 | ||||||
chr11:43887785
|
G | GT | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 87 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.266+1141dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887785 | |||||
chr11:43887813
|
G | C | 2 | a0002c0003t0002g0047a0002c0003t0002g0172 | 3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.266+1160G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887813 | ||||||
chr11:43887914
|
G | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0145 | 2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.266+1261G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887914 | ||||||
chr11:43887936
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0111a0001c0001t0001g0112 | 4 | HG01255.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+1283G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887936 | ||||||
chr11:43887955
|
A | AT | 27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(24): Show | 48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.266+1317dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887955 | |||||
chr11:43887955
|
AT | A | 3 | a0001c0001t0001g0036a0001c0002t0002g0003a0001c0002t0002g0016 | 16 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.266+1317delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887955 | |||||
chr11:43887964
|
T | A | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.266+1311T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887964 | ||||||
chr11:43887971
|
G | T | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.266+1318G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887971 | ||||||
chr11:43887999
|
G | A | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.266+1346G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887999 | ||||||
chr11:43888043
|
TGCCTTGG others(299): Show |
T | 123 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.266+1424_267-1343d others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43888043 | |||||
chr11:43888382
|
C | T | 35 | a0002c0003t0002g0007a0002c0003t0002g0017a0002c0003t0002g0018others(32): Show | 50 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.267-1343C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888382 | ||||||
chr11:43888537
|
A | G | 3 | a0001c0002t0001g0055a0001c0002t0001g0209a0001c0002t0001g0210 | 4 | HG01243.hp1 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-1188A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888537 | ||||||
chr11:43888693
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.267-1032C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888693 | ||||||
chr11:43888807
|
G | A | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.267-918G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888807 | ||||||
chr11:43888875
|
A | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.267-850A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888875 | ||||||
chr11:43889085
|
A | G | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.267-640A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889085 | ||||||
chr11:43889092
|
C | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.267-633C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889092 | ||||||
chr11:43889111
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0130 | 3 | HG00597.hp1 NA19005.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.267-614C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889111 | ||||||
chr11:43889115
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.267-610A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889115 | ||||||
chr11:43889188
|
C | G | 1 | a0002c0003t0002g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.267-537C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889188 | ||||||
chr11:43889211
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.267-514G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889211 | ||||||
chr11:43889213
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0001g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.267-512C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889213 | ||||||
chr11:43889223
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.267-502C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889223 | ||||||
chr11:43889261
|
G | A | 2 | a0001c0002t0006g0188a0001c0002t0006g0189 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.267-464G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889261 | ||||||
chr11:43889581
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.267-144G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889581 | ||||||
chr11:43889661
|
A | G | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.267-64A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889661 | ||||||
chr11:43889706
|
A | G | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.267-19A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889706 | ||||||
chr11:43889918
|
A | T | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.370+90A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43889918 | ||||||
chr11:43890137
|
C | CTA | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.370+310_370+311ins others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 43890137 | |||||
chr11:43890218
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.370+390C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890218 | ||||||
chr11:43890365
|
C | T | 1 | a0001c0002t0004g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.370+537C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890365 | ||||||
chr11:43890366
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.370+538G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890366 | ||||||
chr11:43890418
|
C | T | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.370+590C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890418 | ||||||
chr11:43890587
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.370+759T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890587 | ||||||
chr11:43890632
|
G | A | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.370+804G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890632 | ||||||
chr11:43890812
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.370+984C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890812 | ||||||
chr11:43890819
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370+991G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890819 | ||||||
chr11:43890820
|
C | T | 3 | a0002c0003t0002g0167a0002c0003t0002g0181a0002c0003t0002g0182 | 3 | HG01515.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.370+992C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890820 | ||||||
chr11:43890982
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.371-1059A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890982 | ||||||
chr11:43891117
|
C | T | 11 | a0001c0001t0005g0043a0001c0001t0005g0044a0001c0001t0005g0053others(8): Show | 14 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.371-924C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891117 | ||||||
chr11:43891241
|
T | C | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.371-800T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891241 | ||||||
chr11:43891326
|
AAAATT | A | 4 | a0001c0001t0005g0053a0001c0001t0005g0192a0001c0001t0005g0193others(1): Show | 5 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-707_371-703del others(5): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 43891326 | |||||
chr11:43891375
|
C | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.371-666C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891375 | ||||||
chr11:43891504
|
T | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.371-537T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891504 | ||||||
chr11:43891581
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.371-460C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891581 | ||||||
chr11:43891687
|
CAG | C | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.371-353_371-352del others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891687 | ||||||
chr11:43891836
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.371-205T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891836 | ||||||
chr11:43891912
|
T | C | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.371-129T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891912 | ||||||
chr11:43891930
|
T | C | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.371-111T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891930 | ||||||
chr11:43891970
|
A | G | 1 | a0001c0004t0003g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.371-71A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891970 | ||||||
chr11:43892157
|
G | A | 16 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216others(13): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.459+28G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892157 | ||||||
chr11:43892406
|
G | T | 5 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0188others(2): Show | 7 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+277G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892406 | ||||||
chr11:43892478
|
A | G | 8 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG00673.hp1 HG02129.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+349A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892478 | ||||||
chr11:43892483
|
C | A | 6 | a0002c0003t0002g0017a0002c0003t0002g0048a0002c0003t0002g0166others(3): Show | 10 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.459+354C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892483 | ||||||
chr11:43892651
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+522T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892651 | ||||||
chr11:43892663
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.459+534A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892663 | ||||||
chr11:43892863
|
GC | G | 35 | a0002c0003t0002g0007a0002c0003t0002g0017a0002c0003t0002g0018others(32): Show | 50 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.459+735delC | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892863 | ||||||
chr11:43892940
|
A | G | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+811A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892940 | ||||||
chr11:43892966
|
A | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0069a0001c0001t0001g0097 | 6 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+837A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892966 | ||||||
chr11:43892988
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.459+859C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892988 | ||||||
chr11:43893002
|
T | G | 1 | a0002c0003t0002g0048 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.459+873T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893002 | ||||||
chr11:43893008
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.459+879G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893008 | ||||||
chr11:43893022
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.459+893G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893022 | ||||||
chr11:43893262
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.459+1133T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893262 | ||||||
chr11:43893327
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.459+1198A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893327 | ||||||
chr11:43893402
|
C | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+1273C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893402 | ||||||
chr11:43893463
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.459+1334C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893463 | ||||||
chr11:43893786
|
G | A | 3 | a0002c0003t0002g0033a0002c0003t0002g0102a0003c0010t0002g0033 | 3 | NA18961.hp1 NA18995.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.459+1657G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893786 | ||||||
chr11:43894017
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+1888T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894017 | ||||||
chr11:43894320
|
T | C | 1 | a0001c0002t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.459+2191T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894320 | ||||||
chr11:43894703
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.459+2574G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894703 | ||||||
chr11:43894715
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.459+2586C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894715 | ||||||
chr11:43894800
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.459+2671C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894800 | ||||||
chr11:43894832
|
T | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.459+2703T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894832 | ||||||
chr11:43895006
|
C | G | 1 | a0001c0001t0001g0041 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459+2877C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895006 | ||||||
chr11:43895267
|
G | A | 8 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG00673.hp1 HG02129.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+3138G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895267 | ||||||
chr11:43895308
|
G | A | 1 | a0001c0004t0003g0027 | 2 | HG00609.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.459+3179G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895308 | ||||||
chr11:43895360
|
C | A | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.459+3231C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895360 | ||||||
chr11:43895491
|
A | G | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+3362A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895491 | ||||||
chr11:43895692
|
C | T | 2 | a0001c0001t0005g0053a0001c0001t0005g0193 | 3 | HG00741.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.459+3563C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895692 | ||||||
chr11:43896021
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.459+3892C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896021 | ||||||
chr11:43896037
|
T | C | 1 | a0002c0003t0002g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.459+3908T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896037 | ||||||
chr11:43896068
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.459+3939G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896068 | ||||||
chr11:43896102
|
C | T | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+3973C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896102 | ||||||
chr11:43896159
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.459+4030T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896159 | ||||||
chr11:43896217
|
G | A | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+4088G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896217 | ||||||
chr11:43896268
|
T | TAC | 28 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0001g0111others(25): Show | 45 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.459+4170_459+4171d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896268
|
T | TACAC | 10 | a0001c0002t0001g0055a0001c0002t0006g0052a0001c0002t0006g0187others(7): Show | 14 | HG02145.hp2 HG02572.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.459+4168_459+4171d others(6): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896268
|
T | TACACAC | 3 | a0001c0001t0001g0110a0001c0002t0006g0051a0001c0002t0006g0188 | 4 | HG00140.hp2 HG02109.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+4166_459+4171d others(8): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896268
|
TAC | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG00673.hp1 HG00741.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.459+4170_459+4171d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896268
|
TACAC | T | 35 | a0001c0001t0001g0021a0001c0001t0001g0125a0001c0001t0001g0126others(32): Show | 52 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.459+4168_459+4171d others(6): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896268
|
TACACACA others(3): Show |
T | 3 | a0001c0001t0001g0088a0001c0001t0001g0148a0001c0001t0005g0158 | 3 | HG02280.hp2 HG03486.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.459+4162_459+4171d others(12): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896268
|
TACACACA others(5): Show |
T | 47 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(44): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.459+4160_459+4171d others(14): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | |||||
chr11:43896426
|
C | T | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+4297C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896426 | ||||||
chr11:43896603
|
C | A | 1 | a0001c0001t0005g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+4474C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896603 | ||||||
chr11:43896726
|
A | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4597A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896726 | ||||||
chr11:43896735
|
T | C | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4606T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896735 | ||||||
chr11:43896736
|
G | A | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4607G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896736 | ||||||
chr11:43896737
|
C | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4608C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896737 | ||||||
chr11:43896737
|
CT | C | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+4609delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896737 | ||||||
chr11:43896828
|
G | A | 1 | a0002c0003t0002g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.460-4688G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896828 | ||||||
chr11:43896856
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.460-4660T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896856 | ||||||
chr11:43896990
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.460-4526T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896990 | ||||||
chr11:43897256
|
G | A | 2 | a0001c0002t0004g0058a0001c0002t0004g0222 | 3 | HG01256.hp2 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.460-4260G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897256 | ||||||
chr11:43897279
|
C | T | 1 | a0001c0002t0006g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.460-4237C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897279 | ||||||
chr11:43897542
|
G | C | 4 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(1): Show | 4 | HG01243.hp2 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3974G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897542 | ||||||
chr11:43897594
|
A | G | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-3922A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897594 | ||||||
chr11:43897686
|
C | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02132.hp1 HG02135.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.460-3830C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897686 | ||||||
chr11:43897703
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.460-3813A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897703 | ||||||
chr11:43897707
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 6 | NA18944.hp1 NA18947.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-3809C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897707 | ||||||
chr11:43897836
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.460-3680A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897836 | ||||||
chr11:43897861
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.460-3655A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897861 | ||||||
chr11:43898068
|
CAAG | C | 16 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216others(13): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.460-3447_460-3445d others(5): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898068 | ||||||
chr11:43898112
|
C | G | 2 | a0002c0003t0002g0047a0002c0003t0002g0172 | 3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.460-3404C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898112 | ||||||
chr11:43898144
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(113): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.460-3372C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898144 | ||||||
chr11:43898228
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(113): Show | 191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.460-3288C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898228 | ||||||
chr11:43898236
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(121): Show | 201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.460-3280C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898236 | ||||||
chr11:43898365
|
C | T | 2 | a0002c0003t0002g0047a0002c0003t0002g0172 | 3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.460-3151C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898365 | ||||||
chr11:43898431
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.460-3085C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898431 | ||||||
chr11:43898456
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.460-3060A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898456 | ||||||
chr11:43898488
|
C | T | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.460-3028C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898488 | ||||||
chr11:43898503
|
C | T | 3 | a0001c0004t0003g0028a0001c0004t0003g0029a0001c0004t0003g0066 | 5 | HG00639.hp1 HG01081.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-3013C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898503 | ||||||
chr11:43898559
|
G | A | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-2957G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898559 | ||||||
chr11:43898766
|
C | T | 1 | a0001c0001t0005g0053 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.460-2750C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898766 | ||||||
chr11:43899119
|
A | G | 1 | a0001c0002t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.460-2397A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899119 | ||||||
chr11:43899173
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.460-2343C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899173 | ||||||
chr11:43899295
|
C | T | 1 | a0002c0003t0002g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.460-2221C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899295 | ||||||
chr11:43899403
|
C | T | 1 | a0001c0002t0001g0204 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.460-2113C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899403 | ||||||
chr11:43899429
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(224): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.460-2087G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899429 | ||||||
chr11:43899447
|
G | A | 16 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216others(13): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.460-2069G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899447 | ||||||
chr11:43899504
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.460-2012T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899504 | ||||||
chr11:43899605
|
C | T | 3 | a0001c0002t0006g0051a0001c0002t0006g0188a0001c0002t0006g0189 | 4 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1911C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899605 | ||||||
chr11:43899647
|
A | T | 2 | a0001c0001t0005g0156a0001c0001t0005g0157 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.460-1869A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899647 | ||||||
chr11:43899816
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-1700G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899816 | ||||||
chr11:43899861
|
C | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0002t0001g0203others(8): Show | 11 | HG00140.hp1 HG01361.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-1655C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899861 | ||||||
chr11:43899872
|
G | GA | 72 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.460-1627dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43899872 | |||||
chr11:43899872
|
G | GAA | 22 | a0001c0001t0001g0114a0001c0001t0001g0205a0001c0001t0005g0043others(19): Show | 38 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.460-1628_460-1627d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43899872 | |||||
chr11:43900083
|
A | AAG | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(189): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.460-1432_460-1431i others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900083 | |||||
chr11:43900087
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.460-1429T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900087 | ||||||
chr11:43900215
|
A | AATT | 19 | a0001c0001t0001g0032a0001c0001t0001g0071a0001c0001t0001g0074others(16): Show | 33 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.460-1301_460-1300i others(5): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900215 | ||||||
chr11:43900215
|
A | AATTT | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(34): Show | 67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.460-1301_460-1300i others(6): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900215 | ||||||
chr11:43900215
|
A | AATTTT | 11 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0031others(8): Show | 19 | HG00735.hp2 HG01175.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-1301_460-1300i others(7): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900215 | ||||||
chr11:43900215
|
A | AT | 11 | a0001c0002t0001g0046a0001c0002t0001g0055a0001c0002t0001g0199others(8): Show | 18 | HG01109.hp1 HG01109.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.460-1275dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900215 | |||||
chr11:43900215
|
AT | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(75): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.460-1275delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900215 | |||||
chr11:43900215
|
ATT | A | 5 | a0002c0003t0002g0048a0002c0003t0002g0167a0002c0003t0002g0174others(2): Show | 6 | HG01070.hp2 HG01081.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-1276_460-1275d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900215 | |||||
chr11:43900219
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.460-1297T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900219 | ||||||
chr11:43900244
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(91): Show | 152 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.460-1272G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900244 | ||||||
chr11:43900249
|
A | G | 16 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216others(13): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.460-1267A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900249 | ||||||
chr11:43900368
|
C | T | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-1148C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900368 | ||||||
chr11:43900415
|
G | A | 1 | a0001c0002t0004g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-1101G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900415 | ||||||
chr11:43900455
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.460-1061C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900455 | ||||||
chr11:43900469
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.460-1047G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900469 | ||||||
chr11:43900474
|
G | T | 1 | a0006c0008t0001g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-1042G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900474 | ||||||
chr11:43900517
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.460-999T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900517 | ||||||
chr11:43901186
|
G | A | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.460-330G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43901186 | ||||||
chr11:43901226
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.460-290G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43901226 | ||||||
chr11:43901378
|
G | A | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.460-138G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43901378 | ||||||
chr11:43901761
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.669+36C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43901761 | ||||||
chr11:43901913
|
A | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(189): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.669+188A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43901913 | ||||||
chr11:43901994
|
A | G | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+269A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43901994 | ||||||
chr11:43902024
|
T | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(189): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.669+299T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902024 | ||||||
chr11:43902055
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.669+330G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902055 | ||||||
chr11:43902565
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.669+840G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902565 | ||||||
chr11:43902627
|
A | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+902A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902627 | ||||||
chr11:43902710
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.669+985C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902710 | ||||||
chr11:43902721
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.669+996C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902721 | ||||||
chr11:43902779
|
G | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(190): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.669+1054G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902779 | ||||||
chr11:43902899
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.669+1174G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902899 | ||||||
chr11:43902927
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+1202A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902927 | ||||||
chr11:43902960
|
C | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+1235C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902960 | ||||||
chr11:43903011
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 43 | HG00423.hp1 HG00735.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.669+1286G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903011 | ||||||
chr11:43903080
|
T | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 75 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.669+1355T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903080 | ||||||
chr11:43903156
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.669+1431G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903156 | ||||||
chr11:43903172
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.669+1447G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903172 | ||||||
chr11:43903196
|
C | T | 1 | a0001c0002t0006g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+1471C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903196 | ||||||
chr11:43903197
|
T | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(49): Show | 85 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.669+1472T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903197 | ||||||
chr11:43903245
|
G | A | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+1520G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903245 | ||||||
chr11:43903259
|
T | C | 1 | a0001c0002t0007g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+1534T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903259 | ||||||
chr11:43903338
|
A | G | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.669+1613A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903338 | ||||||
chr11:43903378
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(47): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.669+1653C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903378 | ||||||
chr11:43903466
|
A | T | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.669+1741A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903466 | ||||||
chr11:43903516
|
G | A | 17 | a0001c0001t0001g0032a0001c0002t0007g0026a0001c0002t0007g0215others(14): Show | 34 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.669+1791G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903516 | ||||||
chr11:43903519
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.669+1794A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903519 | ||||||
chr11:43903528
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(224): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.669+1803T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903528 | ||||||
chr11:43903529
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(41): Show | 67 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.669+1804G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903529 | ||||||
chr11:43903602
|
C | T | 3 | a0002c0003t0002g0167a0002c0003t0002g0181a0002c0003t0002g0182 | 3 | HG01515.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.669+1877C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903602 | ||||||
chr11:43903612
|
A | G | 1 | a0001c0002t0001g0161 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.669+1887A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903612 | ||||||
chr11:43903703
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.669+1978G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903703 | ||||||
chr11:43903884
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0001g0207 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.669+2159G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903884 | ||||||
chr11:43903890
|
T | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+2165T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903890 | ||||||
chr11:43903988
|
A | T | 3 | a0001c0002t0001g0055a0001c0002t0001g0209a0001c0002t0001g0210 | 4 | HG01243.hp1 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+2263A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903988 | ||||||
chr11:43904379
|
C | T | 1 | a0001c0004t0003g0065 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.669+2654C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904379 | ||||||
chr11:43904674
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+2949A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904674 | ||||||
chr11:43904772
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.669+3047G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904772 | ||||||
chr11:43904800
|
C | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+3075C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904800 | ||||||
chr11:43905099
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.669+3374A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905099 | ||||||
chr11:43905118
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.669+3393G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905118 | ||||||
chr11:43905127
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+3402C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905127 | ||||||
chr11:43905192
|
T | TG | 3 | a0001c0001t0001g0040a0001c0001t0001g0132a0001c0001t0001g0145 | 4 | HG00408.hp2 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+3468dupG | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43905192 | |||||
chr11:43905396
|
C | T | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.669+3671C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905396 | ||||||
chr11:43905442
|
G | GT | 16 | a0001c0001t0001g0068a0001c0002t0004g0058a0001c0004t0003g0004others(13): Show | 31 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.669+3728dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43905442 | |||||
chr11:43905465
|
G | T | 6 | a0001c0002t0001g0008a0001c0002t0001g0057a0001c0002t0001g0194others(3): Show | 12 | HG00544.hp1 HG00673.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+3740G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905465 | ||||||
chr11:43905527
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0001t0001g0132others(1): Show | 5 | HG00408.hp2 HG02165.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+3802A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905527 | ||||||
chr11:43905658
|
T | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+3933T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905658 | ||||||
chr11:43905714
|
G | A | 2 | a0002c0003t0002g0047a0002c0003t0002g0172 | 3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.669+3989G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905714 | ||||||
chr11:43905740
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(190): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.669+4015A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905740 | ||||||
chr11:43905846
|
T | C | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+4121T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905846 | ||||||
chr11:43906046
|
C | A | 1 | a0001c0002t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.669+4321C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906046 | ||||||
chr11:43906123
|
T | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.669+4398T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906123 | ||||||
chr11:43906138
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.669+4413T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906138 | ||||||
chr11:43906229
|
C | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.669+4504C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906229 | ||||||
chr11:43906237
|
T | C | 6 | a0001c0001t0005g0053a0001c0001t0005g0192a0001c0001t0005g0193others(3): Show | 7 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+4512T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906237 | ||||||
chr11:43906306
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.669+4581A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906306 | ||||||
chr11:43906745
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.669+5020A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906745 | ||||||
chr11:43906747
|
C | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.669+5022C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906747 | ||||||
chr11:43906973
|
T | G | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+5248T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906973 | ||||||
chr11:43907115
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.669+5390T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907115 | ||||||
chr11:43907212
|
A | AGT | 16 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(13): Show | 29 | HG00423.hp2 HG00609.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.669+5503_669+5504d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43907212 | |||||
chr11:43907228
|
T | C | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+5503T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907228 | ||||||
chr11:43907249
|
A | T | 1 | a0001c0001t0001g0083 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.669+5524A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907249 | ||||||
chr11:43907308
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(46): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.669+5583G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907308 | ||||||
chr11:43907317
|
C | G | 2 | a0001c0002t0004g0056a0001c0002t0004g0211 | 3 | HG02451.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.669+5592C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907317 | ||||||
chr11:43907400
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.669+5675C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907400 | ||||||
chr11:43907667
|
G | A | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+5942G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907667 | ||||||
chr11:43907899
|
T | C | 1 | a0001c0004t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.669+6174T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907899 | ||||||
chr11:43907942
|
G | A | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+6217G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907942 | ||||||
chr11:43907949
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.669+6224A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907949 | ||||||
chr11:43908342
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.669+6617G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908342 | ||||||
chr11:43908451
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0084 | 2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.669+6726G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908451 | ||||||
chr11:43908458
|
G | A | 1 | a0001c0002t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.669+6733G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908458 | ||||||
chr11:43908461
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.669+6736A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908461 | ||||||
chr11:43908692
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.669+6967C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908692 | ||||||
chr11:43908694
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.669+6969G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908694 | ||||||
chr11:43908709
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.669+6984C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908709 | ||||||
chr11:43908754
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0113others(8): Show | 13 | HG00280.hp1 HG00323.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+7029C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908754 | ||||||
chr11:43908764
|
A | G | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+7039A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908764 | ||||||
chr11:43908891
|
G | A | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.669+7166G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908891 | ||||||
chr11:43909133
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0085 | 5 | HG00423.hp1 HG01943.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+7408G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909133 | ||||||
chr11:43909498
|
G | A | 1 | a0002c0003t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.669+7773G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909498 | ||||||
chr11:43909511
|
A | C | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+7786A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909511 | ||||||
chr11:43909876
|
C | G | 3 | a0001c0002t0006g0051a0001c0002t0006g0188a0001c0002t0006g0189 | 4 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+8151C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909876 | ||||||
chr11:43910063
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(46): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.669+8338G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910063 | ||||||
chr11:43910287
|
CT | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(21): Show | 45 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.669+8563delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910287 | ||||||
chr11:43910336
|
T | A | 2 | a0001c0002t0006g0052a0001c0002t0006g0190 | 3 | HG02970.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.669+8611T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910336 | ||||||
chr11:43910451
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.670-8587G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910451 | ||||||
chr11:43910562
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670-8476A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910562 | ||||||
chr11:43910624
|
C | T | 1 | a0001c0004t0003g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.670-8414C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910624 | ||||||
chr11:43910786
|
C | CT | 33 | a0001c0001t0001g0170a0001c0001t0005g0043a0001c0001t0005g0044others(30): Show | 62 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.670-8243dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43910786 | |||||
chr11:43910795
|
T | C | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0199 | 3 | HG01243.hp2 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-8243T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910795 | ||||||
chr11:43910948
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0100 | 2 | HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.670-8090G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910948 | ||||||
chr11:43911135
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.670-7903A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911135 | ||||||
chr11:43911290
|
G | A | 13 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0027others(10): Show | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.670-7748G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911290 | ||||||
chr11:43911309
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0072a0001c0001t0001g0074others(6): Show | 11 | HG00735.hp2 HG01175.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-7729G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911309 | ||||||
chr11:43911443
|
A | C | 3 | a0001c0001t0001g0205a0001c0002t0001g0054a0001c0002t0001g0202 | 4 | HG01109.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-7595A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911443 | ||||||
chr11:43911757
|
C | T | 4 | a0001c0002t0001g0008a0001c0002t0001g0194a0001c0002t0001g0200others(1): Show | 9 | HG00544.hp1 HG00673.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-7281C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911757 | ||||||
chr11:43911849
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(131): Show | 242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.670-7189G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911849 | ||||||
chr11:43911888
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(195): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.670-7150T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911888 | ||||||
chr11:43911919
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.670-7119G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911919 | ||||||
chr11:43911950
|
G | A | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-7088G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911950 | ||||||
chr11:43911983
|
C | T | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-7055C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911983 | ||||||
chr11:43911994
|
G | A | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-7044G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911994 | ||||||
chr11:43912078
|
G | A | 1 | a0006c0008t0001g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-6960G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912078 | ||||||
chr11:43912089
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0082 | 2 | NA19001.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.670-6949C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912089 | ||||||
chr11:43912139
|
C | CA | 38 | a0002c0003t0002g0007a0002c0003t0002g0017a0002c0003t0002g0018others(35): Show | 53 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.670-6893dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43912139 | |||||
chr11:43912268
|
T | C | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-6770T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912268 | ||||||
chr11:43912324
|
C | T | 1 | a0002c0003t0002g0182 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.670-6714C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912324 | ||||||
chr11:43912412
|
C | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.670-6626C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912412 | ||||||
chr11:43912571
|
G | A | 53 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(50): Show | 74 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.670-6467G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912571 | ||||||
chr11:43912921
|
T | C | 53 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(50): Show | 74 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.670-6117T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912921 | ||||||
chr11:43912992
|
TAAGTCAA others(12): Show |
T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.670-6026_670-6008d others(21): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43912992 | |||||
chr11:43913042
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.670-5996C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913042 | ||||||
chr11:43913106
|
T | TA | 15 | a0001c0001t0001g0078a0001c0002t0001g0045a0001c0002t0001g0046others(12): Show | 31 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.670-5916dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43913106 | |||||
chr11:43913133
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-5905C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913133 | ||||||
chr11:43913151
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.670-5887T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913151 | ||||||
chr11:43913167
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(133): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.670-5871A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913167 | ||||||
chr11:43913194
|
T | G | 1 | a0001c0002t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-5844T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913194 | ||||||
chr11:43913244
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.670-5794A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913244 | ||||||
chr11:43913297
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.670-5741C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913297 | ||||||
chr11:43913554
|
G | T | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-5484G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913554 | ||||||
chr11:43913557
|
C | T | 8 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(5): Show | 10 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-5481C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913557 | ||||||
chr11:43913573
|
C | T | 3 | a0002c0003t0002g0033a0002c0003t0002g0102a0003c0010t0002g0033 | 3 | NA18961.hp1 NA18995.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.670-5465C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913573 | ||||||
chr11:43913615
|
T | C | 5 | a0002c0003t0002g0049a0002c0003t0002g0179a0002c0003t0002g0184others(2): Show | 6 | HG01074.hp2 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-5423T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913615 | ||||||
chr11:43913796
|
T | A | 1 | a0004c0005t0001g0030 | 2 | NA18947.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.670-5242T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913796 | ||||||
chr11:43914139
|
G | T | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-4899G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914139 | ||||||
chr11:43914412
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670-4626G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914412 | ||||||
chr11:43914434
|
G | A | 53 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(50): Show | 74 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.670-4604G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914434 | ||||||
chr11:43914447
|
G | C | 1 | a0001c0001t0001g0035 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.670-4591G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914447 | ||||||
chr11:43914529
|
G | A | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-4509G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914529 | ||||||
chr11:43914566
|
T | TA | 42 | a0001c0001t0001g0225a0001c0002t0002g0003a0001c0002t0002g0016others(39): Show | 69 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.670-4462dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43914566 | |||||
chr11:43914566
|
TA | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.670-4462delA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43914566 | |||||
chr11:43914589
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(193): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.670-4449A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914589 | ||||||
chr11:43914653
|
C | T | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-4385C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914653 | ||||||
chr11:43915123
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.670-3915G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915123 | ||||||
chr11:43915124
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0123a0001c0001t0009g0014 | 5 | HG00639.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-3914C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915124 | ||||||
chr11:43915215
|
G | GA | 7 | a0001c0001t0001g0072a0001c0001t0001g0121a0001c0001t0005g0158others(4): Show | 7 | HG01981.hp1 HG02738.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-3807dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43915215 | |||||
chr11:43915215
|
GA | G | 10 | a0001c0001t0001g0077a0001c0002t0001g0008a0001c0002t0001g0057others(7): Show | 16 | HG00544.hp1 HG00673.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.670-3807delA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43915215 | |||||
chr11:43915247
|
T | A | 1 | a0001c0001t0005g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.670-3791T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915247 | ||||||
chr11:43915275
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.670-3763T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915275 | ||||||
chr11:43915395
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 163 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.670-3643T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915395 | ||||||
chr11:43915430
|
C | G | 8 | a0001c0002t0001g0045a0001c0002t0001g0046a0001c0002t0001g0159others(5): Show | 10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-3608C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915430 | ||||||
chr11:43915493
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670-3545C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915493 | ||||||
chr11:43915539
|
A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(85): Show | 148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.670-3499A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915539 | ||||||
chr11:43915540
|
A | T | 1 | a0001c0002t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.670-3498A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915540 | ||||||
chr11:43915567
|
A | G | 1 | a0001c0002t0001g0160 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.670-3471A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915567 | ||||||
chr11:43915589
|
C | T | 1 | a0001c0002t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.670-3449C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915589 | ||||||
chr11:43915662
|
AG | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(134): Show | 233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.670-3374delG | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43915662 | |||||
chr11:43915866
|
C | T | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-3172C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915866 | ||||||
chr11:43916037
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.670-3001T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916037 | ||||||
chr11:43916169
|
G | A | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-2869G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916169 | ||||||
chr11:43916244
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670-2794G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916244 | ||||||
chr11:43916409
|
C | A | 8 | a0001c0002t0004g0022a0001c0002t0004g0024a0001c0002t0004g0056others(5): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-2629C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916409 | ||||||
chr11:43916480
|
G | A | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-2558G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916480 | ||||||
chr11:43916526
|
T | TTTATCCT others(23): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0078others(3): Show | 9 | NA18978.hp1 NA18979.hp2 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-2509_670-2480d others(32): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43916526 | |||||
chr11:43916764
|
A | G | 1 | a0001c0004t0003g0062 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.670-2274A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916764 | ||||||
chr11:43916809
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.670-2229G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916809 | ||||||
chr11:43916889
|
G | A | 6 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(3): Show | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-2149G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916889 | ||||||
chr11:43917048
|
G | C | 37 | a0002c0003t0002g0007a0002c0003t0002g0017a0002c0003t0002g0018others(34): Show | 52 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.670-1990G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917048 | ||||||
chr11:43917117
|
G | A | 3 | a0001c0002t0007g0026a0001c0002t0007g0215a0001c0002t0007g0216 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-1921G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917117 | ||||||
chr11:43917226
|
C | A | 1 | a0005c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-1812C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917226 | ||||||
chr11:43917563
|
C | A | 1 | a0001c0001t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.670-1475C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917563 | ||||||
chr11:43917645
|
A | AT | 18 | a0001c0001t0001g0133a0001c0002t0001g0045a0001c0002t0001g0046others(15): Show | 24 | HG00140.hp2 HG01928.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.670-1383dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43917645 | |||||
chr11:43917947
|
T | G | 15 | a0001c0002t0001g0054a0001c0002t0001g0196a0001c0002t0001g0197others(12): Show | 23 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.670-1091T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917947 | ||||||
chr11:43918030
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG02004.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.670-1008T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918030 | ||||||
chr11:43918076
|
C | T | 9 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(6): Show | 13 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-962C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918076 | ||||||
chr11:43918078
|
G | A | 38 | a0002c0003t0002g0007a0002c0003t0002g0017a0002c0003t0002g0018others(35): Show | 53 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.670-960G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918078 | ||||||
chr11:43918214
|
C | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.670-824C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918214 | ||||||
chr11:43918230
|
G | A | 10 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 14 | HG00280.hp1 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-808G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918230 | ||||||
chr11:43918372
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(133): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.670-666C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918372 | ||||||
chr11:43918434
|
T | G | 2 | a0001c0002t0001g0046a0001c0002t0001g0162 | 3 | NA18969.hp2 NA18985.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.670-604T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918434 | ||||||
chr11:43918704
|
T | C | 9 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(6): Show | 13 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-334T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918704 | ||||||
chr11:43918916
|
T | C | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-122T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918916 | ||||||
chr11:43918956
|
AT | A | 9 | a0001c0002t0006g0051a0001c0002t0006g0052a0001c0002t0006g0187others(6): Show | 13 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-73delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43918956 | |||||
chr11:43919016
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(190): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.670-22T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43919016 | ||||||
chr11:43919212
|
G | C | 1 | a0001c0002t0001g0200 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.768+76G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919212 | ||||||
chr11:43919215
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.768+79A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919215 | ||||||
chr11:43919247
|
A | G | 1 | a0003c0009t0001g0093 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.768+111A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919247 | ||||||
chr11:43919353
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.768+217G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919353 | ||||||
chr11:43919576
|
A | G | 3 | a0001c0002t0002g0003a0001c0002t0002g0016a0001c0002t0002g0152 | 15 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.769-342A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919576 | ||||||
chr11:43919820
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.769-98G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919820 | ||||||
chr11:43919825
|
A | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.769-93A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919825 | ||||||
chr11:43919873
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.769-45G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919873 |