geneid | 63905 |
---|---|
ensemblid | ENSG00000101363.13 |
hgncid | 15799 |
symbol | MANBAL |
name | mannosidase beta like |
refseq_nuc | NM_001003897.2 |
refseq_prot | NP_001003897.1 |
ensembl_nuc | ENST00000373606.8 |
ensembl_prot | ENSP00000362708.3 |
mane_status | MANE Select |
chr | chr20 |
start | 37289655 |
end | 37317260 |
strand | + |
ver | v1.2 |
region | chr20:37289655-37317260 |
region5000 | chr20:37284655-37322260 |
regionname0 | MANBAL_chr20_37289655_37317260 |
regionname5000 | MANBAL_chr20_37284655_37322260 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 85 | 272 | 78 | 48 | 96 | 16 | 32 | 72 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 258 | 270 | 78 | 48 | 94 | 16 | 32 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
c0002 | 0/0 | 258 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 934 | 89 | 5 | 20 | 48 | 7 | 9 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0002 | 0/0 | 934 | 83 | 24 | 5 | 44 | 0 | 10 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0003 | 0/1 | 934 | 23 | 6 | 6 | 1 | 4 | 5 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0004 | 0/0 | 934 | 12 | 8 | 3 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0005 | 0/0 | 934 | 12 | 3 | 6 | 0 | 2 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0006 | 0/0 | 934 | 12 | 12 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0007 | 0/0 | 934 | 5 | 4 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0008 | 0/0 | 934 | 4 | 0 | 3 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0009 | 0/0 | 934 | 3 | 0 | 1 | 1 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0010 | 0/0 | 934 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0011 | 0/0 | 934 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0012 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0013 | 0/0 | 934 | 2 | 0 | 0 | 0 | 0 | 2 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0014 | 0/0 | 934 | 2 | 1 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0015 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0016 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0017 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0018 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0019 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0020 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0021 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0022 | 0/0 | 934 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0023 | 1/0 | 934 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0024 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0025 | 0/0 | 934 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0026 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0027 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0028 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0029 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0030 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
t0031 | 0/0 | 934 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
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 | 58 | 14 | 9 | 25 | 2 | 8 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0002 | 0/0 | 27 | 0 | 0 | 27 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0003 | 0/0 | 20 | 9 | 2 | 0 | 5 | 4 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0005 | 0/0 | 7 | 0 | 2 | 0 | 4 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0006 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0007 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0029 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 258 | 270 | 78 | 48 | 94 | 16 | 32 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0002 | 0/0 | 258 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1191 | 87 | 5 | 20 | 46 | 7 | 9 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0002 | 0/0 | 1191 | 83 | 24 | 5 | 44 | 0 | 10 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0003 | 0/1 | 1191 | 23 | 6 | 6 | 1 | 4 | 5 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0004 | 0/0 | 1191 | 12 | 8 | 3 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0005 | 0/0 | 1191 | 12 | 3 | 6 | 0 | 2 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0006 | 0/0 | 1191 | 12 | 12 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0007 | 0/0 | 1191 | 5 | 4 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0008 | 0/0 | 1191 | 4 | 0 | 3 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0009 | 0/0 | 1191 | 3 | 0 | 1 | 1 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0010 | 0/0 | 1191 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0011 | 0/0 | 1191 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0012 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0013 | 0/0 | 1191 | 2 | 0 | 0 | 0 | 0 | 2 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0014 | 0/0 | 1191 | 2 | 1 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0015 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0016 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0017 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0018 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0019 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0020 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0021 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0022 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0023 | 1/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0024 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0025 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0026 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0027 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0028 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0029 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0030 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0001t0031 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
a0001c0002t0001 | 0/0 | 1191 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | copy fasta | chr20 | 37284655 | 37322260 |
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 | 40 | 2 | 7 | 25 | 0 | 6 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 0 | 4 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0002 | 0/0 | 27 | 0 | 0 | 27 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0003 | 0/0 | 9 | 6 | 0 | 0 | 0 | 3 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0003 | 0/0 | 4 | 1 | 0 | 0 | 3 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0029 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0004g0001 | 0/0 | 6 | 5 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0004g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0005g0003 | 0/0 | 6 | 2 | 2 | 0 | 2 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0006g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0009g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0010g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0011g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0012g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0012g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0013g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0014g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0016g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0019g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0020g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0022g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0023g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0025g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0026g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0027g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0029g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0030g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0001t0031g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0001 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00323 | hp2 | a0001 | c0001 | t0025 | g0030 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01109 | hp2 | a0001 | c0001 | t0014 | g0063 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0110 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01243 | hp2 | a0001 | c0001 | t0022 | g0113 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01257 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01261 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0065 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0111 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02074 | hp2 | a0001 | c0001 | t0016 | g0090 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02145 | hp2 | a0001 | c0001 | t0019 | g0039 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02155 | hp2 | a0001 | c0001 | t0030 | g0023 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02273 | hp2 | a0001 | c0001 | t0031 | g0070 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02602 | hp1 | a0001 | c0001 | t0020 | g0078 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0107 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02622 | hp2 | a0001 | c0001 | t0028 | g0018 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02818 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02970 | hp2 | a0001 | c0001 | t0021 | g0033 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03130 | hp1 | a0001 | c0001 | t0017 | g0099 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03195 | hp2 | a0001 | c0001 | t0027 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03492 | hp2 | a0001 | c0001 | t0029 | g0006 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0102 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03669 | hp2 | a0001 | c0001 | t0026 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0094 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03710 | hp2 | a0001 | c0001 | t0024 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19002 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0035 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ASW | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ASW | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0106 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA20905 | hp2 | a0001 | c0001 | t0013 | g0074 | SAS | GIH | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02109 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0115 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | USA | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | USA | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0100 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0029 | REF | REF | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0023 | g0082 | REF | REF | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37316376
|
G | C | 1 | a0001c0002 | 2 | HG02071.hp1 HG02165.hp1 |
synonymous_variant | LOW | c.219G>C | p.Val73Val | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 307/1191 | 219/258 | 73/85 | chr20 | 37316376 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37316435
|
T | C | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 20 | chr20 | 37316435 | |||||
chr20:37316483
|
A | C | 1 | a0001c0001t0014 | 2 | HG01109.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 68 | chr20 | 37316483 | |||||
chr20:37316530
|
G | A | 1 | a0001c0001t0013 | 2 | HG03688.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 115 | chr20 | 37316530 | |||||
chr20:37316537
|
G | T | 1 | a0001c0001t0031 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*122G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 122 | chr20 | 37316537 | |||||
chr20:37316540
|
C | T | 1 | a0001c0001t0030 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 125 | chr20 | 37316540 | |||||
chr20:37316568
|
C | T | 1 | a0001c0001t0029 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 153 | chr20 | 37316568 | |||||
chr20:37316701
|
G | A | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | 207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*286G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 286 | chr20 | 37316701 | |||||
chr20:37316714
|
G | A | 4 | a0001c0001t0010a0001c0001t0012a0001c0001t0021others(1): Show | 7 | HG01243.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*299G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 299 | chr20 | 37316714 | |||||
chr20:37316745
|
C | A | 1 | a0001c0001t0015 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 330 | chr20 | 37316745 | |||||
chr20:37316750
|
T | A | 1 | a0001c0001t0016 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 335 | chr20 | 37316750 | |||||
chr20:37316771
|
G | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*356G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 356 | chr20 | 37316771 | |||||
chr20:37316819
|
G | A | 1 | a0001c0001t0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 404 | chr20 | 37316819 | |||||
chr20:37316835
|
C | G | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(17): Show | 170 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*420C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 420 | chr20 | 37316835 | |||||
chr20:37316855
|
G | A | 1 | a0001c0001t0024 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 440 | chr20 | 37316855 | |||||
chr20:37316940
|
T | C | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(11): Show | 136 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*525T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 525 | chr20 | 37316940 | |||||
chr20:37316993
|
A | G | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(14): Show | 154 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*578A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 578 | chr20 | 37316993 | |||||
chr20:37317007
|
C | A | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*592C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 592 | chr20 | 37317007 | |||||
chr20:37317009
|
G | A | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*594G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 594 | chr20 | 37317009 | |||||
chr20:37317010
|
C | T | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*595C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 595 | chr20 | 37317010 | |||||
chr20:37317018
|
C | T | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*603C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 603 | chr20 | 37317018 | |||||
chr20:37317021
|
T | G | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*606T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 606 | chr20 | 37317021 | |||||
chr20:37317037
|
T | A | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*622T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 622 | chr20 | 37317037 | |||||
chr20:37317038
|
G | T | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*623G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 623 | chr20 | 37317038 | |||||
chr20:37317049
|
T | G | 1 | a0001c0001t0019 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 634 | chr20 | 37317049 | |||||
chr20:37317091
|
G | A | 1 | a0001c0001t0028 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*676G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 676 | chr20 | 37317091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:37289713
|
T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+27T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37289713 | ||||||
chr20:37289735
|
C | G | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+49C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37289735 | ||||||
chr20:37289885
|
C | G | 1 | a0001c0001t0003g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-57+199C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37289885 | ||||||
chr20:37290107
|
A | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+421A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290107 | ||||||
chr20:37290154
|
C | T | 1 | a0001c0001t0022g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57+468C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290154 | ||||||
chr20:37290414
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57+728C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290414 | ||||||
chr20:37290441
|
C | CT | 20 | a0001c0001t0001g0016a0001c0001t0002g0032a0001c0001t0002g0104others(17): Show | 24 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-57+768dupT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37290441 | |||||
chr20:37290583
|
C | T | 1 | a0001c0001t0022g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57+897C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290583 | ||||||
chr20:37290584
|
G | A | 1 | a0001c0001t0021g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+898G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290584 | ||||||
chr20:37290702
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-57+1016A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290702 | ||||||
chr20:37290725
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-57+1039T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290725 | ||||||
chr20:37290809
|
A | G | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+1123A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290809 | ||||||
chr20:37290920
|
A | G | 1 | a0001c0001t0017g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-57+1234A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290920 | ||||||
chr20:37291007
|
T | G | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+1321T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291007 | ||||||
chr20:37291013
|
A | G | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+1327A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291013 | ||||||
chr20:37291032
|
T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+1346T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291032 | ||||||
chr20:37291084
|
GAGA | G | 5 | a0001c0001t0002g0032a0001c0001t0003g0031a0001c0001t0003g0032others(2): Show | 6 | HG01071.hp1 HG01192.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+1402_-57+1404d others(5): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37291084 | |||||
chr20:37291219
|
A | T | 1 | a0001c0001t0002g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57+1533A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291219 | ||||||
chr20:37291286
|
A | ATGT | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+1601_-57+1603d others(5): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37291286 | |||||
chr20:37291616
|
C | T | 1 | a0001c0001t0017g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-57+1930C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291616 | ||||||
chr20:37291698
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0096a0001c0001t0002g0097 | 4 | HG01192.hp1 HG02280.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+2012A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291698 | ||||||
chr20:37291832
|
T | C | 6 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0036others(3): Show | 8 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+2146T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291832 | ||||||
chr20:37291886
|
C | T | 1 | a0001c0001t0014g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-57+2200C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291886 | ||||||
chr20:37292087
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-57+2401C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292087 | ||||||
chr20:37292098
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0019g0039 | 3 | HG02145.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-57+2412T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292098 | ||||||
chr20:37292300
|
T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+2614T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292300 | ||||||
chr20:37292313
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-57+2627T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292313 | ||||||
chr20:37292340
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-57+2654C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292340 | ||||||
chr20:37292482
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+2796A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292482 | ||||||
chr20:37292862
|
T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+3176T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292862 | ||||||
chr20:37292968
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-57+3282C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292968 | ||||||
chr20:37293058
|
T | C | 1 | a0001c0001t0022g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57+3372T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293058 | ||||||
chr20:37293274
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-57+3588G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293274 | ||||||
chr20:37293309
|
G | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0109 | 2 | HG01175.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-57+3623G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293309 | ||||||
chr20:37293466
|
G | A | 1 | a0001c0001t0021g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+3780G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293466 | ||||||
chr20:37293488
|
G | A | 1 | a0001c0001t0007g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-57+3802G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293488 | ||||||
chr20:37293512
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-57+3826G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293512 | ||||||
chr20:37293687
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-57+4001T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293687 | ||||||
chr20:37293742
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-57+4056G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293742 | ||||||
chr20:37293774
|
G | A | 1 | a0001c0001t0001g0019 | 2 | NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-57+4088G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293774 | ||||||
chr20:37293823
|
C | T | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+4137C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293823 | ||||||
chr20:37294015
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-57+4329G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294015 | ||||||
chr20:37294182
|
C | G | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+4496C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294182 | ||||||
chr20:37294406
|
T | C | 3 | a0001c0001t0002g0006a0001c0001t0002g0098a0001c0001t0029g0006 | 5 | HG02683.hp2 HG03239.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+4720T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294406 | ||||||
chr20:37294430
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+4744C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294430 | ||||||
chr20:37294555
|
C | T | 1 | a0001c0001t0013g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-57+4869C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294555 | ||||||
chr20:37294697
|
G | C | 1 | a0001c0001t0003g0031 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-57+5011G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294697 | ||||||
chr20:37294752
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57+5066T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294752 | ||||||
chr20:37294923
|
C | T | 1 | a0001c0001t0006g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-57+5237C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294923 | ||||||
chr20:37295004
|
G | C | 1 | a0001c0001t0006g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-57+5318G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295004 | ||||||
chr20:37295273
|
A | G | 1 | a0001c0001t0003g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-57+5587A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295273 | ||||||
chr20:37295299
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+5613A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295299 | ||||||
chr20:37295545
|
T | C | 1 | a0001c0001t0006g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-56-5663T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295545 | ||||||
chr20:37295895
|
T | C | 1 | a0001c0001t0006g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-56-5313T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295895 | ||||||
chr20:37295981
|
T | A | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-5227T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295981 | ||||||
chr20:37296013
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-56-5195C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296013 | ||||||
chr20:37296049
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-5159C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296049 | ||||||
chr20:37296315
|
T | C | 1 | a0001c0001t0011g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-56-4893T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296315 | ||||||
chr20:37296429
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-56-4779G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296429 | ||||||
chr20:37296526
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-56-4682C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296526 | ||||||
chr20:37296640
|
G | T | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-4568G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296640 | ||||||
chr20:37296817
|
G | A | 1 | a0001c0001t0006g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-56-4391G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296817 | ||||||
chr20:37296893
|
G | A | 47 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(44): Show | 104 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-56-4315G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296893 | ||||||
chr20:37296927
|
C | T | 1 | a0001c0001t0014g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-56-4281C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296927 | ||||||
chr20:37297334
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-56-3874G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297334 | ||||||
chr20:37297542
|
C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-3666C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297542 | ||||||
chr20:37297803
|
C | T | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-3405C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297803 | ||||||
chr20:37297804
|
G | A | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-56-3404G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297804 | ||||||
chr20:37298449
|
T | G | 35 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0006others(32): Show | 88 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-56-2759T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298449 | ||||||
chr20:37298523
|
A | T | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-2685A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298523 | ||||||
chr20:37298542
|
T | C | 1 | a0001c0001t0019g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-56-2666T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298542 | ||||||
chr20:37298548
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-56-2660C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298548 | ||||||
chr20:37298660
|
C | T | 1 | a0001c0001t0004g0017 | 3 | HG00642.hp2 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-56-2548C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298660 | ||||||
chr20:37298741
|
AT | A | 3 | a0001c0001t0001g0007a0001c0001t0002g0052a0001c0001t0007g0007 | 5 | HG01069.hp1 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-2452delT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37298741 | |||||
chr20:37298776
|
G | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(37): Show | 95 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-56-2432G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298776 | ||||||
chr20:37299084
|
G | T | 1 | a0001c0001t0021g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-56-2124G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299084 | ||||||
chr20:37299294
|
G | T | 1 | a0001c0001t0016g0090 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-56-1914G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299294 | ||||||
chr20:37299467
|
G | A | 3 | a0001c0001t0007g0025a0001c0001t0007g0043a0001c0001t0007g0065 | 4 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1741G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299467 | ||||||
chr20:37299608
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-56-1600G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299608 | ||||||
chr20:37299735
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-1473C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299735 | ||||||
chr20:37299762
|
A | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-1446A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299762 | ||||||
chr20:37299939
|
A | G | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-1269A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299939 | ||||||
chr20:37299972
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-56-1236G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299972 | ||||||
chr20:37300041
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-56-1167C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300041 | ||||||
chr20:37300136
|
A | C | 2 | a0001c0001t0002g0012a0001c0001t0002g0052 | 4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1072A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300136 | ||||||
chr20:37300190
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-1018C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300190 | ||||||
chr20:37300229
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-979C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300229 | ||||||
chr20:37300310
|
C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-898C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300310 | ||||||
chr20:37300958
|
C | A | 1 | a0001c0001t0002g0054 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-56-250C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300958 | ||||||
chr20:37300981
|
A | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0051a0001c0001t0030g0023 | 3 | HG02155.hp2 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-56-227A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300981 | ||||||
chr20:37301004
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-56-204G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37301004 | ||||||
chr20:37301006
|
G | A | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-202G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37301006 | ||||||
chr20:37301059
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-149C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37301059 | ||||||
chr20:37301135
|
C | CATAA | 3 | a0001c0001t0002g0055a0001c0001t0002g0096a0001c0001t0008g0110 | 3 | HG01192.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-56-46_-56-43dupAA others(2): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37301135 | |||||
chr20:37301135
|
C | CATAAATA others(5): Show |
2 | a0001c0001t0004g0017a0001c0001t0011g0100 | 4 | HG00642.hp2 HG01167.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-54_-56-43dupAA others(10): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37301135 | |||||
chr20:37301135
|
CATAA | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 8 | HG01106.hp1 HG01109.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-46_-56-43delAA others(2): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37301135 | |||||
chr20:37301881
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.150+468A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37301881 | ||||||
chr20:37302046
|
A | G | 1 | a0001c0001t0004g0017 | 3 | HG00642.hp2 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.150+633A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302046 | ||||||
chr20:37302181
|
C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+768C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302181 | ||||||
chr20:37302226
|
T | G | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+813T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302226 | ||||||
chr20:37302419
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+1006T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302419 | ||||||
chr20:37302668
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+1255G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302668 | ||||||
chr20:37302766
|
G | GT | 17 | a0001c0001t0002g0032a0001c0001t0003g0029a0001c0001t0003g0030others(14): Show | 22 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.150+1365dupT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37302766 | |||||
chr20:37303055
|
G | A | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+1642G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303055 | ||||||
chr20:37303300
|
CTA | C | 3 | a0001c0001t0007g0025a0001c0001t0007g0043a0001c0001t0007g0065 | 4 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+1888_150+1889d others(4): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303300 | ||||||
chr20:37303325
|
A | G | 1 | a0001c0001t0002g0096 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.150+1912A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303325 | ||||||
chr20:37303583
|
G | A | 1 | a0001c0001t0006g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.150+2170G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303583 | ||||||
chr20:37304145
|
G | T | 1 | a0001c0001t0014g0063 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+2732G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304145 | ||||||
chr20:37304200
|
A | G | 1 | a0001c0001t0005g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.150+2787A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304200 | ||||||
chr20:37304228
|
G | A | 1 | a0001c0001t0005g0020 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.150+2815G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304228 | ||||||
chr20:37304295
|
A | G | 19 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0022others(16): Show | 49 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.150+2882A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304295 | ||||||
chr20:37304506
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.150+3093G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304506 | ||||||
chr20:37304533
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150+3120C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304533 | ||||||
chr20:37304597
|
C | T | 1 | a0001c0001t0013g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.150+3184C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304597 | ||||||
chr20:37304879
|
A | C | 1 | a0001c0001t0014g0063 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+3466A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304879 | ||||||
chr20:37304967
|
C | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+3554C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304967 | ||||||
chr20:37304977
|
G | GC | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(132): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.150+3565dupC | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37304977 | |||||
chr20:37305122
|
T | C | 1 | a0001c0001t0003g0011 | 3 | HG01361.hp1 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.150+3709T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305122 | ||||||
chr20:37305123
|
T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+3710T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305123 | ||||||
chr20:37305127
|
G | A | 1 | a0001c0001t0001g0014 | 3 | HG01074.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.150+3714G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305127 | ||||||
chr20:37305213
|
G | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+3800G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305213 | ||||||
chr20:37305358
|
T | C | 10 | a0001c0001t0002g0024a0001c0001t0002g0062a0001c0001t0002g0092others(7): Show | 15 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.150+3945T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305358 | ||||||
chr20:37305588
|
C | T | 1 | a0001c0001t0021g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.150+4175C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305588 | ||||||
chr20:37305679
|
C | CT | 5 | a0001c0001t0004g0081a0001c0001t0007g0025a0001c0001t0007g0043others(2): Show | 6 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+4283dupT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37305679 | |||||
chr20:37305679
|
CT | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0069others(2): Show | 7 | HG00639.hp2 HG01433.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+4283delT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37305679 | |||||
chr20:37305686
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0034 | 3 | HG00408.hp2 NA19058.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.150+4273T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305686 | ||||||
chr20:37305696
|
T | A | 1 | a0001c0001t0002g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.150+4283T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305696 | ||||||
chr20:37305707
|
T | C | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+4294T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305707 | ||||||
chr20:37305801
|
C | T | 2 | a0001c0001t0011g0100a0001c0001t0018g0115 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.150+4388C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305801 | ||||||
chr20:37306004
|
A | G | 2 | a0001c0001t0002g0012a0001c0001t0002g0052 | 4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4591A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306004 | ||||||
chr20:37306079
|
G | C | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+4666G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306079 | ||||||
chr20:37306114
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0015 | 10 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.150+4701G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306114 | ||||||
chr20:37306688
|
T | A | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.150+5275T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306688 | ||||||
chr20:37306793
|
T | C | 1 | a0001c0001t0031g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.150+5380T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306793 | ||||||
chr20:37306836
|
C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+5423C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306836 | ||||||
chr20:37307212
|
C | T | 1 | a0001c0001t0012g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.150+5799C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307212 | ||||||
chr20:37307229
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0019g0039 | 3 | HG02145.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150+5816G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307229 | ||||||
chr20:37307396
|
G | A | 1 | a0001c0001t0006g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.150+5983G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307396 | ||||||
chr20:37307415
|
T | C | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+6002T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307415 | ||||||
chr20:37307531
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.150+6118C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307531 | ||||||
chr20:37307590
|
C | A | 1 | a0001c0001t0003g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.150+6177C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307590 | ||||||
chr20:37307756
|
C | CA | 5 | a0001c0001t0002g0022a0001c0001t0002g0097a0001c0001t0007g0025others(2): Show | 7 | HG01261.hp2 HG02074.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+6357dupA | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37307756 | |||||
chr20:37307786
|
A | G | 1 | a0001c0001t0007g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.150+6373A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307786 | ||||||
chr20:37307787
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+6374C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307787 | ||||||
chr20:37307968
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150+6555C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307968 | ||||||
chr20:37307969
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.150+6556G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307969 | ||||||
chr20:37307996
|
C | T | 1 | a0001c0001t0003g0106 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.150+6583C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307996 | ||||||
chr20:37308068
|
C | T | 1 | a0001c0001t0004g0080 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.150+6655C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308068 | ||||||
chr20:37308666
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150+7253G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308666 | ||||||
chr20:37308698
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.150+7285T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308698 | ||||||
chr20:37308794
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+7381A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308794 | ||||||
chr20:37308909
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-7399A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308909 | ||||||
chr20:37309152
|
G | GTC | 6 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0036others(3): Show | 8 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-7145_151-7144d others(4): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37309152 | |||||
chr20:37309190
|
C | T | 3 | a0001c0001t0007g0025a0001c0001t0007g0043a0001c0001t0007g0065 | 4 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-7118C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309190 | ||||||
chr20:37309496
|
C | T | 3 | a0001c0001t0003g0030a0001c0001t0003g0105a0001c0001t0025g0030 | 3 | HG00323.hp2 HG00735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.151-6812C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309496 | ||||||
chr20:37309578
|
C | G | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-6730C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309578 | ||||||
chr20:37309616
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-6692G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309616 | ||||||
chr20:37309650
|
A | G | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-6658A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309650 | ||||||
chr20:37309799
|
G | A | 1 | a0001c0001t0012g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.151-6509G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309799 | ||||||
chr20:37309976
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.151-6332G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309976 | ||||||
chr20:37310127
|
G | A | 1 | a0001c0001t0002g0021 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.151-6181G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310127 | ||||||
chr20:37310211
|
G | A | 19 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0012others(16): Show | 42 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.151-6097G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310211 | ||||||
chr20:37310289
|
G | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0109 | 2 | HG01175.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.151-6019G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310289 | ||||||
chr20:37310362
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0010g0010a0001c0001t0011g0100others(1): Show | 8 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-5946A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310362 | ||||||
chr20:37310432
|
C | T | 1 | a0001c0001t0004g0017 | 3 | HG00642.hp2 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.151-5876C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310432 | ||||||
chr20:37310737
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.151-5571C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310737 | ||||||
chr20:37310958
|
T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-5350T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310958 | ||||||
chr20:37311132
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-5176C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311132 | ||||||
chr20:37311169
|
G | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(53): Show | 118 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.151-5139G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311169 | ||||||
chr20:37311290
|
T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-5018T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311290 | ||||||
chr20:37311499
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.151-4809G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311499 | ||||||
chr20:37311612
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(56): Show | 122 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.151-4696T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311612 | ||||||
chr20:37311753
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-4555C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311753 | ||||||
chr20:37311810
|
C | A | 1 | a0001c0001t0017g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-4498C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311810 | ||||||
chr20:37311834
|
A | G | 5 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0036others(2): Show | 7 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-4474A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311834 | ||||||
chr20:37311835
|
ACT | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-4470_151-4469d others(4): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37311835 | |||||
chr20:37311846
|
C | T | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-4462C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311846 | ||||||
chr20:37311996
|
A | AC | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-4310dupC | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37311996 | |||||
chr20:37312006
|
C | T | 1 | a0001c0001t0002g0021 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.151-4302C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312006 | ||||||
chr20:37312044
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-4264A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312044 | ||||||
chr20:37312209
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.151-4099G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312209 | ||||||
chr20:37312480
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3828A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312480 | ||||||
chr20:37312671
|
G | C | 1 | a0001c0001t0002g0058 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.151-3637G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312671 | ||||||
chr20:37312705
|
A | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3603A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312705 | ||||||
chr20:37312808
|
G | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3500G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312808 | ||||||
chr20:37312990
|
CTTTCA | C | 3 | a0001c0001t0002g0023a0001c0001t0002g0051a0001c0001t0030g0023 | 3 | HG02155.hp2 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.151-3310_151-3306d others(7): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37312990 | |||||
chr20:37313147
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3161A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313147 | ||||||
chr20:37313149
|
C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3159C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313149 | ||||||
chr20:37313161
|
G | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3147G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313161 | ||||||
chr20:37313174
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.151-3134C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313174 | ||||||
chr20:37313194
|
T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3114T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313194 | ||||||
chr20:37313210
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3098C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313210 | ||||||
chr20:37313252
|
C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3056C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313252 | ||||||
chr20:37313281
|
G | C | 1 | a0001c0002t0001g0073 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.151-3027G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313281 | ||||||
chr20:37313288
|
A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3020A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313288 | ||||||
chr20:37313319
|
C | T | 1 | a0001c0001t0020g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.151-2989C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313319 | ||||||
chr20:37313430
|
C | T | 1 | a0001c0001t0009g0077 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.151-2878C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313430 | ||||||
chr20:37313440
|
C | CA | 2 | a0001c0001t0007g0025a0001c0001t0007g0065 | 3 | HG01261.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.151-2867dupA | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37313440 | |||||
chr20:37313566
|
C | T | 2 | a0001c0001t0003g0037a0001c0001t0004g0081 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151-2742C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313566 | ||||||
chr20:37313638
|
G | A | 1 | a0001c0001t0011g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151-2670G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313638 | ||||||
chr20:37313680
|
TG | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-2625delG | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37313680 | |||||
chr20:37313699
|
T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-2609T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313699 | ||||||
chr20:37313737
|
G | C | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-2571G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313737 | ||||||
chr20:37313751
|
G | A | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-2557G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313751 | ||||||
chr20:37313769
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.151-2539G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313769 | ||||||
chr20:37314234
|
C | T | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-2074C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314234 | ||||||
chr20:37314289
|
C | T | 6 | a0001c0001t0006g0067a0001c0001t0006g0093a0001c0001t0007g0025others(3): Show | 9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-2019C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314289 | ||||||
chr20:37314315
|
T | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0022others(18): Show | 53 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.151-1993T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314315 | ||||||
chr20:37314376
|
T | G | 61 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(58): Show | 126 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.151-1932T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314376 | ||||||
chr20:37314401
|
T | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0022others(19): Show | 54 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.151-1907T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314401 | ||||||
chr20:37314425
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151-1883C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314425 | ||||||
chr20:37314479
|
G | T | 6 | a0001c0001t0006g0067a0001c0001t0006g0093a0001c0001t0007g0025others(3): Show | 9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1829G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314479 | ||||||
chr20:37314492
|
G | A | 6 | a0001c0001t0006g0067a0001c0001t0006g0093a0001c0001t0007g0025others(3): Show | 9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1816G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314492 | ||||||
chr20:37314616
|
G | T | 1 | a0001c0001t0017g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-1692G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314616 | ||||||
chr20:37314888
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1420C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314888 | ||||||
chr20:37314993
|
C | T | 6 | a0001c0001t0006g0067a0001c0001t0006g0093a0001c0001t0007g0025others(3): Show | 9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1315C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314993 | ||||||
chr20:37314994
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0102 | 2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-1314C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314994 | ||||||
chr20:37315034
|
CA | C | 6 | a0001c0001t0006g0067a0001c0001t0006g0093a0001c0001t0007g0025others(3): Show | 9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1272delA | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37315034 | |||||
chr20:37315151
|
A | G | 5 | a0001c0001t0006g0067a0001c0001t0006g0093a0001c0001t0007g0025others(2): Show | 6 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-1157A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315151 | ||||||
chr20:37315378
|
C | G | 1 | a0001c0001t0006g0084 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151-930C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315378 | ||||||
chr20:37315648
|
G | A | 1 | a0001c0001t0013g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.151-660G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315648 | ||||||
chr20:37315681
|
C | G | 2 | a0001c0001t0004g0017a0001c0001t0018g0115 | 4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-627C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315681 | ||||||
chr20:37315851
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0075 | 2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.151-457G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315851 | ||||||
chr20:37315988
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.151-320A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315988 |