geneid | 4125 |
---|---|
ensemblid | ENSG00000104774.13 |
hgncid | 6826 |
symbol | MAN2B1 |
name | mannosidase alpha class 2B member 1 |
refseq_nuc | NM_000528.4 |
refseq_prot | NP_000519.2 |
ensembl_nuc | ENST00000456935.7 |
ensembl_prot | ENSP00000395473.2 |
mane_status | MANE Select |
chr | chr19 |
start | 12646512 |
end | 12666742 |
strand | - |
ver | v1.2 |
region | chr19:12646512-12666742 |
region5000 | chr19:12641512-12671742 |
regionname0 | MAN2B1_chr19_12646512_12666742 |
regionname5000 | MAN2B1_chr19_12641512_12671742 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1011 | 221 | 30 | 28 | 127 | 4 | 31 | 103 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002 | 0/0 | 1011 | 28 | 1 | 12 | 7 | 4 | 4 | 6 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003 | 0/0 | 1011 | 26 | 3 | 10 | 6 | 4 | 3 | 5 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004 | 0/0 | 1011 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0005 | 0/0 | 1011 | 18 | 2 | 9 | 2 | 1 | 4 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0006 | 0/0 | 1011 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0007 | 0/0 | 1011 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0008 | 0/0 | 1011 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0009 | 0/0 | 1011 | 8 | 0 | 3 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0010 | 0/0 | 1011 | 6 | 0 | 4 | 2 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0011 | 0/0 | 1011 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0012 | 0/0 | 1011 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0013 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0014 | 0/0 | 1011 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0015 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0016 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0017 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0018 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0019 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0020 | 0/1 | 1011 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0021 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0022 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0023 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3036 | 207 | 20 | 27 | 127 | 4 | 28 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0002 | 0/0 | 3036 | 24 | 1 | 10 | 5 | 4 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0003 | 0/0 | 3036 | 22 | 3 | 8 | 5 | 4 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0004 | 0/0 | 3036 | 18 | 2 | 9 | 2 | 1 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0005 | 0/0 | 3036 | 14 | 14 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0006 | 0/0 | 3036 | 9 | 9 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0007 | 0/0 | 3036 | 8 | 0 | 3 | 0 | 5 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0008 | 0/0 | 3036 | 7 | 7 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0009 | 0/0 | 3036 | 6 | 0 | 4 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0010 | 0/0 | 3036 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0011 | 0/0 | 3036 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0012 | 0/0 | 3036 | 5 | 4 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0013 | 0/0 | 3036 | 4 | 3 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0014 | 0/0 | 3036 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0015 | 0/0 | 3036 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0016 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0017 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0018 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0019 | 0/0 | 3036 | 3 | 2 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0020 | 0/0 | 3036 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0021 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0022 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0023 | 0/0 | 3036 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0024 | 0/0 | 3036 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0025 | 0/0 | 3036 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0026 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0027 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0028 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0029 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0030 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0031 | 0/1 | 3036 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0032 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0033 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0034 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0035 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0036 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0037 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
c0038 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 3 | 9 | 0 | 3 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0002 | 0/0 | 9 | 0 | 4 | 1 | 3 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0003 | 0/0 | 8 | 0 | 4 | 1 | 1 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0012 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3036 | 207 | 20 | 27 | 127 | 4 | 28 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0010 | 0/0 | 3036 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0015 | 0/0 | 3036 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0024 | 0/0 | 3036 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0029 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0030 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002c0002 | 0/0 | 3036 | 24 | 1 | 10 | 5 | 4 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002c0022 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002c0025 | 0/0 | 3036 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0003 | 0/0 | 3036 | 22 | 3 | 8 | 5 | 4 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0021 | 0/0 | 3036 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0037 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0038 | 0/0 | 3036 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004c0005 | 0/0 | 3036 | 14 | 14 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004c0019 | 0/0 | 3036 | 3 | 2 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004c0023 | 0/0 | 3036 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0005c0004 | 0/0 | 3036 | 18 | 2 | 9 | 2 | 1 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0006c0006 | 0/0 | 3036 | 9 | 9 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0006c0014 | 0/0 | 3036 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0007c0008 | 0/0 | 3036 | 7 | 7 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0007c0018 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0008c0012 | 0/0 | 3036 | 5 | 4 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0008c0016 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0009c0007 | 0/0 | 3036 | 8 | 0 | 3 | 0 | 5 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0010c0009 | 0/0 | 3036 | 6 | 0 | 4 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0011c0011 | 0/0 | 3036 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0012c0013 | 0/0 | 3036 | 4 | 3 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0013c0017 | 0/0 | 3036 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0014c0020 | 0/0 | 3036 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0015c0027 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0016c0036 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0017c0028 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0018c0035 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0019c0032 | 0/0 | 3036 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0020c0031 | 0/1 | 3036 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0021c0034 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0022c0033 | 0/0 | 3036 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0023c0026 | 0/0 | 3036 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3185 | 205 | 20 | 27 | 125 | 4 | 28 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0001t0002 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0010t0001 | 0/0 | 3185 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0015t0001 | 0/0 | 3185 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0024t0001 | 0/0 | 3185 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0029t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0001c0030t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002c0002t0001 | 0/0 | 3185 | 24 | 1 | 10 | 5 | 4 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002c0022t0001 | 0/0 | 3185 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0002c0025t0001 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0003t0001 | 0/0 | 3185 | 22 | 3 | 8 | 5 | 4 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0021t0001 | 0/0 | 3185 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0037t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0003c0038t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004c0005t0001 | 0/0 | 3185 | 14 | 14 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004c0019t0001 | 0/0 | 3185 | 3 | 2 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0004c0023t0001 | 0/0 | 3185 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0005c0004t0001 | 0/0 | 3185 | 18 | 2 | 9 | 2 | 1 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0006c0006t0001 | 0/0 | 3185 | 9 | 9 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0006c0014t0001 | 0/0 | 3185 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0007c0008t0001 | 0/0 | 3185 | 7 | 7 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0007c0018t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0008c0012t0001 | 0/0 | 3185 | 5 | 4 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0008c0016t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0009c0007t0001 | 0/0 | 3185 | 8 | 0 | 3 | 0 | 5 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0010c0009t0001 | 0/0 | 3185 | 6 | 0 | 4 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0011c0011t0001 | 0/0 | 3185 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0012c0013t0001 | 0/0 | 3185 | 4 | 3 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0013c0017t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0014c0020t0001 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0015c0027t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0016c0036t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0017c0028t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0018c0035t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0019c0032t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0020c0031t0001 | 0/1 | 3185 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0021c0034t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0022c0033t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
a0023c0026t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | copy fasta | chr19 | 12641512 | 12671742 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 0 | 3 | 9 | 0 | 3 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0010t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0010t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0010t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0010t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0015t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0015t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0015t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0015t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0024t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0024t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0029t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0001c0030t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0002 | 0/0 | 9 | 0 | 4 | 1 | 3 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0022t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0022t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0025t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0002c0025t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0003 | 0/0 | 8 | 0 | 4 | 1 | 1 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0021t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0037t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0003c0038t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0019t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0019t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0023t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0004c0023t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0005c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0006t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0014t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0014t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0014t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0006c0014t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0008t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0018t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0018t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0007c0018t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0012t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0012t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0012t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0012t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0016t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0016t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0008c0016t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0009c0007t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0010c0009t0001g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0010c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0010c0009t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0011c0011t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0011c0011t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0011c0011t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0011c0011t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0012c0013t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0012c0013t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0013c0017t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0013c0017t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0014c0020t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0014c0020t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0015c0027t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0016c0036t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0017c0028t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0018c0035t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0019c0032t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0020c0031t0001g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0021c0034t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0022c0033t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
a0023c0026t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0001 | g0181 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00280 | hp1 | a0009 | c0007 | t0001 | g0145 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0203 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00544 | hp2 | a0010 | c0009 | t0001 | g0007 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00558 | hp1 | a0015 | c0027 | t0001 | g0044 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00609 | hp2 | a0011 | c0011 | t0001 | g0218 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00621 | hp2 | a0014 | c0020 | t0001 | g0133 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0031 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00642 | hp1 | a0009 | c0007 | t0001 | g0147 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00733 | hp1 | a0009 | c0007 | t0001 | g0146 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0260 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01070 | hp1 | a0005 | c0004 | t0001 | g0188 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0166 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01074 | hp2 | a0009 | c0007 | t0001 | g0149 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01081 | hp1 | a0003 | c0021 | t0001 | g0032 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0275 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01099 | hp2 | a0005 | c0004 | t0001 | g0193 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01106 | hp1 | a0010 | c0009 | t0001 | g0143 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01109 | hp1 | a0012 | c0013 | t0001 | g0176 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01168 | hp2 | a0005 | c0004 | t0001 | g0024 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01243 | hp1 | a0003 | c0021 | t0001 | g0032 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01258 | hp2 | a0002 | c0022 | t0001 | g0273 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01261 | hp1 | a0005 | c0004 | t0001 | g0015 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01261 | hp2 | a0010 | c0009 | t0001 | g0007 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01346 | hp2 | a0019 | c0032 | t0001 | g0165 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01358 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01358 | hp2 | a0010 | c0009 | t0001 | g0007 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01361 | hp2 | a0005 | c0004 | t0001 | g0191 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01515 | hp2 | a0009 | c0007 | t0001 | g0097 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01516 | hp1 | a0009 | c0007 | t0001 | g0148 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0262 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0261 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01517 | hp2 | a0009 | c0007 | t0001 | g0098 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01884 | hp1 | a0012 | c0013 | t0001 | g0014 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01884 | hp2 | a0007 | c0008 | t0001 | g0186 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01891 | hp1 | a0006 | c0006 | t0001 | g0023 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01928 | hp1 | a0005 | c0004 | t0001 | g0025 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01934 | hp2 | a0004 | c0023 | t0001 | g0048 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01943 | hp1 | a0005 | c0004 | t0001 | g0025 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01952 | hp2 | a0008 | c0012 | t0001 | g0233 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01975 | hp1 | a0001 | c0029 | t0001 | g0117 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01975 | hp2 | a0002 | c0022 | t0001 | g0276 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01993 | hp1 | a0010 | c0009 | t0001 | g0007 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02055 | hp2 | a0004 | c0005 | t0001 | g0216 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02080 | hp1 | a0002 | c0025 | t0001 | g0297 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02129 | hp2 | a0005 | c0004 | t0001 | g0266 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02145 | hp2 | a0008 | c0012 | t0001 | g0028 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0182 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02257 | hp2 | a0006 | c0006 | t0001 | g0281 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02273 | hp2 | a0005 | c0004 | t0001 | g0190 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02280 | hp1 | a0004 | c0005 | t0001 | g0210 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02280 | hp2 | a0006 | c0014 | t0001 | g0039 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02293 | hp2 | a0005 | c0004 | t0001 | g0189 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02300 | hp2 | a0017 | c0028 | t0001 | g0051 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02451 | hp1 | a0004 | c0023 | t0001 | g0047 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02451 | hp2 | a0004 | c0005 | t0001 | g0206 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02615 | hp1 | a0004 | c0019 | t0001 | g0029 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02615 | hp2 | a0021 | c0034 | t0001 | g0199 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02622 | hp2 | a0004 | c0005 | t0001 | g0211 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02630 | hp1 | a0008 | c0016 | t0001 | g0177 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02630 | hp2 | a0004 | c0005 | t0001 | g0207 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02647 | hp1 | a0016 | c0036 | t0001 | g0284 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02647 | hp2 | a0007 | c0008 | t0001 | g0038 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02717 | hp1 | a0006 | c0006 | t0001 | g0280 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02717 | hp2 | a0008 | c0012 | t0001 | g0232 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02809 | hp1 | a0008 | c0016 | t0001 | g0288 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02809 | hp2 | a0004 | c0005 | t0001 | g0214 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02818 | hp1 | a0004 | c0005 | t0001 | g0205 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02818 | hp2 | a0004 | c0005 | t0001 | g0217 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02886 | hp1 | a0003 | c0003 | t0001 | g0046 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02886 | hp2 | a0007 | c0008 | t0001 | g0289 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02895 | hp1 | a0004 | c0005 | t0001 | g0213 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02895 | hp2 | a0012 | c0013 | t0001 | g0014 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02896 | hp1 | a0004 | c0005 | t0001 | g0208 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02896 | hp2 | a0001 | c0010 | t0001 | g0229 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02897 | hp1 | a0001 | c0010 | t0001 | g0225 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02897 | hp2 | a0004 | c0005 | t0001 | g0212 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02965 | hp1 | a0013 | c0017 | t0001 | g0026 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0293 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02970 | hp1 | a0022 | c0033 | t0001 | g0201 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02970 | hp2 | a0001 | c0015 | t0001 | g0222 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02976 | hp1 | a0005 | c0004 | t0001 | g0194 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02976 | hp2 | a0007 | c0018 | t0001 | g0234 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03041 | hp2 | a0001 | c0015 | t0001 | g0221 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03098 | hp1 | a0006 | c0006 | t0001 | g0283 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03098 | hp2 | a0008 | c0012 | t0001 | g0231 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03130 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03130 | hp2 | a0007 | c0018 | t0001 | g0236 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03139 | hp2 | a0006 | c0006 | t0001 | g0184 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03195 | hp2 | a0013 | c0017 | t0001 | g0026 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03209 | hp1 | a0006 | c0006 | t0001 | g0264 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03209 | hp2 | a0006 | c0006 | t0001 | g0282 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03453 | hp2 | a0001 | c0015 | t0001 | g0227 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03486 | hp1 | a0001 | c0010 | t0001 | g0228 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0267 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03492 | hp2 | a0001 | c0024 | t0001 | g0286 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03516 | hp1 | a0005 | c0004 | t0001 | g0195 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03516 | hp2 | a0004 | c0019 | t0001 | g0029 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03540 | hp2 | a0001 | c0015 | t0001 | g0226 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03579 | hp1 | a0006 | c0014 | t0001 | g0040 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03579 | hp2 | a0012 | c0013 | t0001 | g0014 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03654 | hp2 | a0005 | c0004 | t0001 | g0034 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03669 | hp2 | a0005 | c0004 | t0001 | g0192 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0271 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03704 | hp1 | a0001 | c0024 | t0001 | g0285 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03704 | hp2 | a0005 | c0004 | t0001 | g0034 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03831 | hp2 | a0001 | c0030 | t0001 | g0122 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03834 | hp1 | a0005 | c0004 | t0001 | g0015 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04228 | hp1 | a0003 | c0038 | t0001 | g0298 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18522 | hp1 | a0006 | c0014 | t0001 | g0042 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18522 | hp2 | a0013 | c0017 | t0001 | g0187 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18612 | hp1 | a0014 | c0020 | t0001 | g0116 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18906 | hp1 | a0007 | c0008 | t0001 | g0290 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18941 | hp2 | a0011 | c0011 | t0001 | g0220 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18948 | hp2 | a0005 | c0004 | t0001 | g0015 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18953 | hp2 | a0002 | c0025 | t0001 | g0296 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18960 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18966 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18970 | hp2 | a0011 | c0011 | t0001 | g0027 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18971 | hp1 | a0011 | c0011 | t0001 | g0219 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18977 | hp1 | a0023 | c0026 | t0001 | g0043 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18983 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18986 | hp2 | a0018 | c0035 | t0001 | g0277 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18991 | hp2 | a0003 | c0037 | t0001 | g0295 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19030 | hp2 | a0007 | c0008 | t0001 | g0198 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19043 | hp1 | a0007 | c0008 | t0001 | g0197 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19067 | hp1 | a0011 | c0011 | t0001 | g0027 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19067 | hp2 | a0010 | c0009 | t0001 | g0131 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19240 | hp1 | a0006 | c0006 | t0001 | g0023 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA19240 | hp2 | a0001 | c0010 | t0001 | g0223 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20129 | hp1 | a0008 | c0016 | t0001 | g0183 | AFR | ASW | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20129 | hp2 | a0004 | c0005 | t0001 | g0215 | AFR | ASW | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20752 | hp1 | a0009 | c0007 | t0001 | g0092 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20752 | hp2 | a0005 | c0004 | t0001 | g0024 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01123 | hp1 | a0004 | c0019 | t0001 | g0237 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02109 | hp1 | a0007 | c0018 | t0001 | g0235 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02486 | hp1 | a0004 | c0005 | t0001 | g0209 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02486 | hp2 | a0001 | c0010 | t0001 | g0230 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG02559 | hp2 | a0008 | c0012 | t0001 | g0028 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03471 | hp1 | a0001 | c0010 | t0001 | g0224 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
HG03471 | hp2 | a0007 | c0008 | t0001 | g0200 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20300 | hp1 | a0004 | c0005 | t0001 | g0196 | AFR | USA | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA21309 | hp1 | a0006 | c0006 | t0001 | g0265 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
NA21309 | hp2 | a0006 | c0014 | t0001 | g0041 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
homoSapiens_chm13v2 | hp1 | a0020 | c0031 | t0001 | g0255 | REF | REF | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:12646663
|
C | T | 1 | a0014 | 2 | HG00621.hp2 NA18612.hp1 |
missense_variant | MODERATE | c.2993G>A | p.Arg998His | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 24/24 | 3034/3185 | 2993/3036 | 998/1011 | chr19 | 12646663 | ||
chr19:12649959
|
C | T | 2 | a0012a0021 | 5 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
missense_variant | MODERATE | c.2221G>A | p.Gly741Arg | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/24 | 2262/3185 | 2221/3036 | 741/1011 | chr19 | 12649959 | ||
chr19:12650013
|
C | T | 1 | a0020 | 1 | homoSapiens_chm13v2.hp1 | missense_variant&splice_region_variant | MODERATE | c.2167G>A | p.Asp723Asn | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/24 | 2208/3185 | 2167/3036 | 723/1011 | chr19 | 12650013 | ||
chr19:12652193
|
G | A | 1 | a0010 | 6 | HG00544.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
missense_variant | MODERATE | c.2006C>T | p.Pro669Leu | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/24 | 2047/3185 | 2006/3036 | 669/1011 | chr19 | 12652193 | ||
chr19:12652385
|
G | A | 1 | a0022 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1906C>T | p.Pro636Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 15/24 | 1947/3185 | 1906/3036 | 636/1011 | chr19 | 12652385 | ||
chr19:12655780
|
G | C | 1 | a0013 | 3 | HG02965.hp1 HG03195.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.1744C>G | p.Gln582Glu | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/24 | 1785/3185 | 1744/3036 | 582/1011 | chr19 | 12655780 | ||
chr19:12657035
|
C | A | 4 | a0007a0008a0012others(1): Show | 23 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
missense_variant | MODERATE | c.1441G>T | p.Ala481Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 12/24 | 1482/3185 | 1441/3036 | 481/1011 | chr19 | 12657035 | ||
chr19:12658134
|
T | C | 1 | a0009 | 8 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(5): Show |
missense_variant | MODERATE | c.1238A>G | p.Asn413Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/24 | 1279/3185 | 1238/3036 | 413/1011 | chr19 | 12658134 | ||
chr19:12661276
|
C | T | 7 | a0002a0003a0007others(4): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
missense_variant | MODERATE | c.1010G>A | p.Arg337Gln | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/24 | 1051/3185 | 1010/3036 | 337/1011 | chr19 | 12661276 | ||
chr19:12661351
|
G | A | 10 | a0002a0003a0004others(7): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
missense_variant | MODERATE | c.935C>T | p.Thr312Ile | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/24 | 976/3185 | 935/3036 | 312/1011 | chr19 | 12661351 | ||
chr19:12661364
|
G | A | 1 | a0019 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.922C>T | p.Arg308Cys | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/24 | 963/3185 | 922/3036 | 308/1011 | chr19 | 12661364 | ||
chr19:12663394
|
G | C | 7 | a0002a0004a0005others(4): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
missense_variant | MODERATE | c.832C>G | p.Leu278Val | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/24 | 873/3185 | 832/3036 | 278/1011 | chr19 | 12663394 | ||
chr19:12663706
|
T | C | 1 | a0018 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.760A>G | p.Thr254Ala | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 801/3185 | 760/3036 | 254/1011 | chr19 | 12663706 | ||
chr19:12663718
|
C | A | 1 | a0011 | 5 | HG00609.hp2 NA18941.hp2 NA18970.hp2 others(2): Show |
missense_variant | MODERATE | c.748G>T | p.Ala250Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 789/3185 | 748/3036 | 250/1011 | chr19 | 12663718 | ||
chr19:12663780
|
C | T | 1 | a0017 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.686G>A | p.Arg229Gln | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 727/3185 | 686/3036 | 229/1011 | chr19 | 12663780 | ||
chr19:12664813
|
C | A | 1 | a0016 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.609G>T | p.Glu203Asp | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/24 | 650/3185 | 609/3036 | 203/1011 | chr19 | 12664813 | ||
chr19:12665433
|
C | T | 1 | a0015 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.355G>A | p.Val119Met | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/24 | 396/3185 | 355/3036 | 119/1011 | chr19 | 12665433 | ||
chr19:12665502
|
C | T | 1 | a0023 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.286G>A | p.Gly96Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/24 | 327/3185 | 286/3036 | 96/1011 | chr19 | 12665502 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:12648277
|
G | C | 1 | a0006c0014 | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
synonymous_variant | LOW | c.2562C>G | p.Ala854Ala | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/24 | 2603/3185 | 2562/3036 | 854/1011 | chr19 | 12648277 | ||
chr19:12648352
|
T | G | 1 | a0001c0030 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.2487A>C | p.Leu829Leu | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/24 | 2528/3185 | 2487/3036 | 829/1011 | chr19 | 12648352 | ||
chr19:12649386
|
G | A | 1 | a0006c0006 | 9 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.2310C>T | p.Pro770Pro | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 19/24 | 2351/3185 | 2310/3036 | 770/1011 | chr19 | 12649386 | ||
chr19:12649413
|
G | A | 1 | a0004c0023 | 2 | HG01934.hp2 HG02451.hp1 |
synonymous_variant | LOW | c.2283C>T | p.Pro761Pro | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 19/24 | 2324/3185 | 2283/3036 | 761/1011 | chr19 | 12649413 | ||
chr19:12652264
|
G | A | 1 | a0001c0010 | 6 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.1935C>T | p.Asn645Asn | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/24 | 1976/3185 | 1935/3036 | 645/1011 | chr19 | 12652264 | ||
chr19:12655742
|
C | T | 1 | a0001c0029 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.1782G>A | p.Gln594Gln | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/24 | 1823/3185 | 1782/3036 | 594/1011 | chr19 | 12655742 | ||
chr19:12658469
|
G | C | 2 | a0002c0022a0003c0021 | 4 | HG01081.hp1 HG01243.hp1 HG01258.hp2 others(1): Show |
synonymous_variant | LOW | c.1068C>G | p.Pro356Pro | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 8/24 | 1109/3185 | 1068/3036 | 356/1011 | chr19 | 12658469 | ||
chr19:12663719
|
G | A | 5 | a0001c0010a0001c0015a0004c0019others(2): Show | 21 | HG01123.hp1 HG01952.hp2 HG02109.hp1 others(18): Show |
synonymous_variant | LOW | c.747C>T | p.Thr249Thr | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 788/3185 | 747/3036 | 249/1011 | chr19 | 12663719 | ||
chr19:12664828
|
G | A | 1 | a0001c0024 | 2 | HG03492.hp2 HG03704.hp1 |
synonymous_variant | LOW | c.594C>T | p.Phe198Phe | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/24 | 635/3185 | 594/3036 | 198/1011 | chr19 | 12664828 | ||
chr19:12666567
|
G | A | 2 | a0002c0025a0003c0037 | 3 | HG02080.hp1 NA18953.hp2 NA18991.hp2 |
synonymous_variant | LOW | c.135C>T | p.Ala45Ala | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/24 | 176/3185 | 135/3036 | 45/1011 | chr19 | 12666567 | ||
chr19:12666663
|
G | C | 1 | a0003c0038 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.39C>G | p.Arg13Arg | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/24 | 80/3185 | 39/3036 | 13/1011 | chr19 | 12666663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:12646529
|
G | A | 1 | a0001c0001t0002 | 2 | NA18945.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*91C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 24/24 | 91 | chr19 | 12646529 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:12646811
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2924-79C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12646811 | ||||||
chr19:12646882
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2924-150C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12646882 | ||||||
chr19:12646884
|
C | T | 25 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(22): Show | 28 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.2924-152G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12646884 | ||||||
chr19:12647136
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2923+97A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12647136 | ||||||
chr19:12647140
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2923+93C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12647140 | ||||||
chr19:12647183
|
C | T | 4 | a0001c0015t0001g0221a0001c0015t0001g0222a0001c0015t0001g0226others(1): Show | 4 | HG02970.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2923+50G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12647183 | ||||||
chr19:12647629
|
G | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2665-31C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647629 | ||||||
chr19:12647672
|
C | A | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2665-74G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647672 | ||||||
chr19:12647717
|
G | T | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2665-119C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647717 | ||||||
chr19:12647843
|
T | C | 1 | a0022c0033t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2665-245A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647843 | ||||||
chr19:12647909
|
A | G | 34 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(31): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.2664+266T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647909 | ||||||
chr19:12648001
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0240a0001c0001t0001g0241 | 8 | HG00438.hp2 NA18941.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2664+174C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12648001 | ||||||
chr19:12648025
|
G | T | 1 | a0006c0006t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2664+150C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12648025 | ||||||
chr19:12648060
|
T | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0139a0001c0001t0001g0141 | 3 | HG03239.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2664+115A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12648060 | ||||||
chr19:12648505
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2437-103C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648505 | ||||||
chr19:12648509
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2437-107C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648509 | ||||||
chr19:12648766
|
G | GC | 20 | a0003c0003t0001g0046a0004c0005t0001g0196a0004c0005t0001g0205others(17): Show | 22 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2437-365_2437-364i others(3): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648766 | ||||||
chr19:12648785
|
A | C | 1 | a0009c0007t0001g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2436+351T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648785 | ||||||
chr19:12648803
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2436+333A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648803 | ||||||
chr19:12648822
|
C | G | 10 | a0007c0008t0001g0038a0007c0008t0001g0197a0007c0008t0001g0198others(7): Show | 11 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+314G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648822 | ||||||
chr19:12648893
|
G | A | 9 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(6): Show | 9 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2436+243C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648893 | ||||||
chr19:12648951
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0123 | 2 | NA18950.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2436+185A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648951 | ||||||
chr19:12649017
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2436+119G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12649017 | ||||||
chr19:12649291
|
G | T | 1 | a0002c0002t0001g0278 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2355+50C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 19/23 | chr19 | 12649291 | ||||||
chr19:12649473
|
A | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(82): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.2268-45T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649473 | ||||||
chr19:12649477
|
C | CT | 22 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0093others(19): Show | 22 | HG00621.hp2 HG01346.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.2268-50dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(2): Show |
26 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0088others(23): Show | 30 | HG00733.hp2 HG01361.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.2268-58_2268-50dup others(9): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(3): Show |
43 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0036others(40): Show | 51 | HG00423.hp1 HG00621.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.2268-59_2268-50dup others(10): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(4): Show |
12 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0091others(9): Show | 12 | HG00438.hp1 HG02257.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.2268-60_2268-50dup others(11): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0170a0001c0001t0001g0249others(1): Show | 4 | HG00558.hp1 HG02071.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2268-61_2268-50dup others(12): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0050a0004c0005t0001g0212others(1): Show | 4 | HG02809.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268-62_2268-50dup others(13): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(7): Show |
9 | a0001c0001t0001g0053a0001c0001t0001g0057a0004c0005t0001g0213others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2268-63_2268-50dup others(14): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(8): Show |
30 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0035others(27): Show | 33 | HG00140.hp1 HG00323.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.2268-64_2268-50dup others(15): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(9): Show |
15 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0080others(12): Show | 22 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.2268-65_2268-50dup others(16): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(10): Show |
4 | a0001c0001t0001g0104a0005c0004t0001g0188a0005c0004t0001g0190others(1): Show | 4 | HG00280.hp1 HG01070.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.2268-66_2268-50dup others(17): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0100a0005c0004t0001g0189 | 2 | HG02293.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.2268-67_2268-50dup others(18): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
C | CTTTTTTT others(16): Show |
1 | a0009c0007t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2268-50_2268-49ins others(23): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
CT | C | 36 | a0001c0001t0001g0125a0002c0002t0001g0002a0002c0002t0001g0033others(33): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.2268-50delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649477
|
CTTTTT | C | 4 | a0001c0010t0001g0224a0012c0013t0001g0014a0012c0013t0001g0176others(1): Show | 6 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2268-54_2268-50del others(5): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | ||||||
chr19:12649575
|
G | A | 3 | a0001c0001t0001g0126a0004c0023t0001g0047a0004c0023t0001g0048 | 3 | HG01934.hp2 HG02451.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2268-147C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649575 | ||||||
chr19:12649631
|
G | A | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268-203C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649631 | ||||||
chr19:12649697
|
T | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(108): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2267+216A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649697 | ||||||
chr19:12649810
|
G | A | 1 | a0018c0035t0001g0277 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2267+103C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649810 | ||||||
chr19:12649850
|
T | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(134): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.2267+63A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649850 | ||||||
chr19:12649910
|
C | G | 10 | a0007c0008t0001g0038a0007c0008t0001g0197a0007c0008t0001g0198others(7): Show | 11 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.2267+3G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649910 | ||||||
chr19:12650262
|
G | C | 1 | a0002c0002t0001g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2047-40C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650262 | ||||||
chr19:12650357
|
C | CT | 9 | a0001c0001t0001g0056a0001c0001t0001g0071a0001c0001t0001g0086others(6): Show | 9 | HG01515.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2047-136dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650357 | ||||||
chr19:12650357
|
CT | C | 55 | a0001c0001t0001g0154a0001c0001t0001g0245a0001c0001t0001g0249others(52): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.2047-136delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650357 | ||||||
chr19:12650361
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2047-139A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650361 | ||||||
chr19:12650430
|
C | T | 9 | a0004c0005t0001g0196a0004c0005t0001g0205a0004c0005t0001g0206others(6): Show | 9 | HG01934.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2047-208G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650430 | ||||||
chr19:12650519
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2047-297G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650519 | ||||||
chr19:12650544
|
G | A | 2 | a0006c0006t0001g0023a0006c0006t0001g0184 | 3 | HG01891.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2047-322C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650544 | ||||||
chr19:12650568
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2047-346T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650568 | ||||||
chr19:12650604
|
C | T | 1 | a0001c0030t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2047-382G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650604 | ||||||
chr19:12650622
|
T | G | 1 | a0002c0002t0001g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2047-400A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650622 | ||||||
chr19:12650650
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0052others(18): Show | 28 | HG00423.hp1 HG00621.hp1 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.2047-428C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650650 | ||||||
chr19:12650674
|
C | CT | 5 | a0001c0001t0001g0020a0001c0001t0001g0103a0001c0001t0001g0119others(2): Show | 6 | HG03139.hp2 NA18945.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.2047-453dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650674 | ||||||
chr19:12650869
|
TCCATGTT others(2): Show |
T | 20 | a0003c0003t0001g0046a0004c0005t0001g0196a0004c0005t0001g0205others(17): Show | 22 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2047-656_2047-648d others(11): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650869 | ||||||
chr19:12650952
|
G | A | 1 | a0007c0008t0001g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2047-730C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650952 | ||||||
chr19:12650973
|
C | CT | 25 | a0001c0001t0001g0022a0001c0001t0001g0083a0001c0001t0001g0109others(22): Show | 27 | HG00323.hp2 HG01167.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.2047-752dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650973 | ||||||
chr19:12650973
|
C | CTT | 12 | a0004c0005t0001g0196a0004c0005t0001g0205a0004c0005t0001g0206others(9): Show | 13 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2047-753_2047-752d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650973 | ||||||
chr19:12650973
|
CT | C | 39 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0088others(36): Show | 43 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2047-752delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650973 | ||||||
chr19:12651109
|
G | T | 2 | a0003c0003t0001g0261a0003c0003t0001g0262 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2047-887C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651109 | ||||||
chr19:12651156
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2047-934G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651156 | ||||||
chr19:12651424
|
A | G | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2046+729T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651424 | ||||||
chr19:12651640
|
TGA | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0077others(19): Show | 25 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2046+511_2046+512d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651640 | ||||||
chr19:12651740
|
C | G | 1 | a0003c0003t0001g0046 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2046+413G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651740 | ||||||
chr19:12651853
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0251 | 3 | HG02080.hp2 NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2046+300A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651853 | ||||||
chr19:12651881
|
A | G | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2046+272T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651881 | ||||||
chr19:12651959
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0155a0001c0001t0001g0287 | 3 | HG00323.hp1 HG01978.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2046+194A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651959 | ||||||
chr19:12651969
|
T | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(134): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.2046+184A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651969 | ||||||
chr19:12652477
|
C | T | 1 | a0022c0033t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1831-17G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652477 | ||||||
chr19:12652536
|
C | CT | 123 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(120): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1831-77dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652536 | ||||||
chr19:12652536
|
C | CTT | 9 | a0001c0001t0001g0082a0001c0001t0001g0243a0006c0014t0001g0039others(6): Show | 9 | HG02280.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1831-78_1831-77dup others(2): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652536 | ||||||
chr19:12652618
|
A | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(82): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1831-158T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652618 | ||||||
chr19:12652619
|
C | G | 1 | a0003c0003t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1831-159G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652619 | ||||||
chr19:12652625
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1831-165C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652625 | ||||||
chr19:12652840
|
A | AT | 7 | a0001c0001t0001g0119a0004c0005t0001g0212a0004c0005t0001g0213others(4): Show | 7 | HG01361.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1831-381dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652840 | ||||||
chr19:12652840
|
AT | A | 127 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(124): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1831-381delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652840 | ||||||
chr19:12653035
|
T | C | 1 | a0002c0002t0001g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1831-575A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653035 | ||||||
chr19:12653087
|
GC | G | 10 | a0001c0010t0001g0223a0001c0010t0001g0224a0001c0010t0001g0225others(7): Show | 10 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1831-628delG | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653087 | ||||||
chr19:12653144
|
G | GT | 25 | a0001c0001t0001g0052a0001c0001t0001g0077a0001c0001t0001g0093others(22): Show | 25 | HG00423.hp2 HG00733.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1831-685dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653144 | ||||||
chr19:12653144
|
GT | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(95): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1831-685delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653144 | ||||||
chr19:12653149
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1831-689A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653149 | ||||||
chr19:12653388
|
A | AC | 49 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(46): Show | 58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1831-929dupG | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653388 | ||||||
chr19:12653388
|
AC | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 210 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.1831-929delG | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653388 | ||||||
chr19:12653393
|
C | CA | 34 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(31): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.1831-934_1831-933i others(3): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653393 | ||||||
chr19:12653394
|
C | G | 1 | a0006c0014t0001g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1831-934G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653394 | ||||||
chr19:12653395
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0241 | 7 | NA18941.hp1 NA18943.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-935G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653395 | ||||||
chr19:12653496
|
C | T | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1831-1036G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653496 | ||||||
chr19:12653602
|
A | T | 2 | a0008c0012t0001g0028a0008c0012t0001g0233 | 3 | HG01952.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1831-1142T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653602 | ||||||
chr19:12653615
|
T | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1831-1155A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653615 | ||||||
chr19:12653637
|
G | A | 1 | a0003c0003t0001g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1831-1177C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653637 | ||||||
chr19:12653835
|
C | T | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1831-1375G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653835 | ||||||
chr19:12653950
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1831-1490G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653950 | ||||||
chr19:12654008
|
C | T | 16 | a0007c0008t0001g0038a0007c0008t0001g0186a0007c0008t0001g0197others(13): Show | 19 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1831-1548G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654008 | ||||||
chr19:12654094
|
A | G | 1 | a0003c0003t0001g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1830+1600T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654094 | ||||||
chr19:12654155
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0075others(20): Show | 26 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1830+1539C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654155 | ||||||
chr19:12654260
|
T | C | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+1434A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654260 | ||||||
chr19:12654264
|
C | G | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+1430G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654264 | ||||||
chr19:12654338
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1830+1356C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654338 | ||||||
chr19:12654409
|
T | C | 2 | a0001c0001t0001g0291a0023c0026t0001g0043 | 2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1830+1285A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654409 | ||||||
chr19:12654470
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1830+1224T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654470 | ||||||
chr19:12654998
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1830+696G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654998 | ||||||
chr19:12655121
|
T | A | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1830+573A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655121 | ||||||
chr19:12655208
|
C | T | 2 | a0006c0014t0001g0041a0006c0014t0001g0042 | 2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1830+486G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655208 | ||||||
chr19:12655264
|
G | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+430C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655264 | ||||||
chr19:12655278
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1830+416G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655278 | ||||||
chr19:12655296
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0292 | 2 | HG00423.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1830+398A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655296 | ||||||
chr19:12655335
|
C | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+359G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655335 | ||||||
chr19:12655478
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1830+216A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655478 | ||||||
chr19:12655556
|
G | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(81): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1830+138C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655556 | ||||||
chr19:12656074
|
G | T | 10 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0113others(7): Show | 10 | HG00621.hp2 NA18612.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-195C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656074 | ||||||
chr19:12656099
|
G | A | 7 | a0004c0005t0001g0196a0004c0005t0001g0205a0004c0005t0001g0206others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1645-220C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656099 | ||||||
chr19:12656142
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1645-263C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656142 | ||||||
chr19:12656190
|
G | A | 3 | a0002c0002t0001g0204a0004c0023t0001g0047a0004c0023t0001g0048 | 3 | HG01934.hp2 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1645-311C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656190 | ||||||
chr19:12656215
|
T | G | 20 | a0003c0003t0001g0046a0004c0005t0001g0196a0004c0005t0001g0205others(17): Show | 22 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1645-336A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656215 | ||||||
chr19:12656356
|
C | CA | 15 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0108others(12): Show | 17 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1644+214dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656356 | ||||||
chr19:12656525
|
C | G | 1 | a0001c0001t0001g0111 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1644+46G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656525 | ||||||
chr19:12657096
|
C | G | 8 | a0006c0006t0001g0023a0006c0006t0001g0184a0006c0006t0001g0264others(5): Show | 9 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420-40G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657096 | ||||||
chr19:12657298
|
T | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0157 | 3 | HG02132.hp2 HG02165.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1419+148A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657298 | ||||||
chr19:12657336
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1419+110G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657336 | ||||||
chr19:12657417
|
C | T | 5 | a0007c0008t0001g0038a0007c0008t0001g0289a0007c0008t0001g0290others(2): Show | 5 | HG02647.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+29G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657417 | ||||||
chr19:12657430
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1419+16C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657430 | ||||||
chr19:12657577
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(79): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1310-22C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657577 | ||||||
chr19:12657611
|
G | A | 9 | a0007c0008t0001g0197a0007c0008t0001g0198a0007c0018t0001g0234others(6): Show | 10 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1310-56C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657611 | ||||||
chr19:12657918
|
G | A | 1 | a0010c0009t0001g0131 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1309+145C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657918 | ||||||
chr19:12657954
|
C | CA | 53 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0045others(50): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1309+108dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | ||||||
chr19:12657954
|
CA | C | 27 | a0001c0001t0001g0019a0001c0001t0001g0109a0001c0001t0001g0110others(24): Show | 31 | HG01123.hp1 HG01891.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.1309+108delT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | ||||||
chr19:12657954
|
CAA | C | 11 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 11 | HG00741.hp2 HG01981.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+107_1309+108d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | ||||||
chr19:12657954
|
CAAA | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(83): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1309+106_1309+108d others(5): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | ||||||
chr19:12657954
|
CAAAA | C | 8 | a0001c0001t0001g0100a0007c0008t0001g0197a0007c0018t0001g0234others(5): Show | 9 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309+105_1309+108d others(6): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | ||||||
chr19:12658029
|
G | T | 36 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(33): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.1309+34C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12658029 | ||||||
chr19:12658215
|
C | G | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1230+9G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 9/23 | chr19 | 12658215 | ||||||
chr19:12658359
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0251 | 3 | HG02080.hp2 NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1110-15C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 8/23 | chr19 | 12658359 | ||||||
chr19:12658580
|
T | C | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-70A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658580 | ||||||
chr19:12658619
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1027-109T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658619 | ||||||
chr19:12658662
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1027-152C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658662 | ||||||
chr19:12658690
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1027-180G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658690 | ||||||
chr19:12658850
|
C | A | 19 | a0004c0005t0001g0196a0004c0005t0001g0205a0004c0005t0001g0206others(16): Show | 21 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1027-340G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658850 | ||||||
chr19:12658872
|
T | C | 1 | a0006c0006t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1027-362A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658872 | ||||||
chr19:12658874
|
T | G | 1 | a0022c0033t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1027-364A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658874 | ||||||
chr19:12658888
|
A | T | 1 | a0006c0006t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1027-378T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658888 | ||||||
chr19:12659018
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1027-508C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659018 | ||||||
chr19:12659020
|
C | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0151others(4): Show | 9 | HG02129.hp1 HG02135.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027-510G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659020 | ||||||
chr19:12659171
|
A | G | 2 | a0009c0007t0001g0097a0009c0007t0001g0098 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1027-661T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659171 | ||||||
chr19:12659268
|
C | G | 9 | a0007c0008t0001g0197a0007c0008t0001g0198a0007c0018t0001g0234others(6): Show | 10 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-758G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659268 | ||||||
chr19:12659297
|
C | CT | 9 | a0001c0001t0001g0066a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 9 | HG01243.hp2 HG02135.hp2 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027-788dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | ||||||
chr19:12659297
|
CT | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0059others(20): Show | 28 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1027-788delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | ||||||
chr19:12659297
|
CTT | C | 60 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(57): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.1027-789_1027-788d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | ||||||
chr19:12659297
|
CTTT | C | 8 | a0002c0002t0001g0204a0002c0002t0001g0267a0003c0003t0001g0293others(5): Show | 9 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027-790_1027-788d others(5): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | ||||||
chr19:12659298
|
T | A | 4 | a0004c0005t0001g0213a0004c0005t0001g0214a0004c0005t0001g0215others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-788A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659298 | ||||||
chr19:12659328
|
G | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1027-818C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659328 | ||||||
chr19:12659492
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1027-982T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659492 | ||||||
chr19:12659745
|
G | C | 10 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(7): Show | 10 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-1235C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659745 | ||||||
chr19:12659812
|
CT | C | 88 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(85): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1027-1303delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659812 | ||||||
chr19:12659849
|
A | G | 5 | a0007c0008t0001g0038a0007c0008t0001g0289a0007c0008t0001g0290others(2): Show | 5 | HG02647.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-1339T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659849 | ||||||
chr19:12659920
|
G | T | 2 | a0001c0001t0001g0291a0023c0026t0001g0043 | 2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1026+1340C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659920 | ||||||
chr19:12659946
|
T | C | 3 | a0007c0008t0001g0289a0007c0008t0001g0290a0008c0016t0001g0288 | 3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1026+1314A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659946 | ||||||
chr19:12660273
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1026+987T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660273 | ||||||
chr19:12660276
|
G | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1026+984C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660276 | ||||||
chr19:12660301
|
C | G | 2 | a0004c0005t0001g0205a0004c0005t0001g0206 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1026+959G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660301 | ||||||
chr19:12660406
|
A | G | 88 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(85): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1026+854T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660406 | ||||||
chr19:12660450
|
C | G | 36 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(33): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.1026+810G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660450 | ||||||
chr19:12660481
|
G | A | 3 | a0002c0002t0001g0274a0004c0023t0001g0047a0004c0023t0001g0048 | 3 | HG01934.hp2 HG01981.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1026+779C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660481 | ||||||
chr19:12660496
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1026+764G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660496 | ||||||
chr19:12660752
|
A | AT | 40 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0052others(37): Show | 42 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1026+507dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | ||||||
chr19:12660752
|
A | ATTTTT | 7 | a0001c0001t0001g0049a0004c0005t0001g0212a0004c0005t0001g0213others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+503_1026+507d others(7): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | ||||||
chr19:12660752
|
AT | A | 73 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0068others(70): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1026+507delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | ||||||
chr19:12660752
|
ATT | A | 9 | a0002c0002t0001g0204a0002c0002t0001g0275a0002c0022t0001g0276others(6): Show | 10 | HG01081.hp2 HG01891.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026+506_1026+507d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | ||||||
chr19:12660935
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0162a0019c0032t0001g0165 | 4 | HG00323.hp2 HG01346.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+325A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660935 | ||||||
chr19:12660978
|
C | T | 6 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+282G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660978 | ||||||
chr19:12660999
|
T | C | 12 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(9): Show | 12 | HG01934.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1026+261A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660999 | ||||||
chr19:12661009
|
A | G | 89 | a0001c0001t0001g0081a0002c0002t0001g0002a0002c0002t0001g0033others(86): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1026+251T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661009 | ||||||
chr19:12661060
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1026+200A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661060 | ||||||
chr19:12661152
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0080 | 2 | HG00642.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1026+108T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661152 | ||||||
chr19:12661158
|
C | A | 4 | a0005c0004t0001g0194a0005c0004t0001g0195a0013c0017t0001g0026others(1): Show | 5 | HG02965.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+102G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661158 | ||||||
chr19:12661176
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1026+84C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661176 | ||||||
chr19:12661210
|
G | A | 1 | a0002c0002t0001g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026+50C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661210 | ||||||
chr19:12661449
|
T | C | 76 | a0002c0002t0001g0002a0002c0002t0001g0033a0002c0002t0001g0202others(73): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.910-73A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661449 | ||||||
chr19:12661505
|
C | A | 1 | a0002c0002t0001g0203 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.910-129G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661505 | ||||||
chr19:12661550
|
C | A | 10 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(7): Show | 10 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.910-174G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661550 | ||||||
chr19:12661628
|
A | G | 6 | a0001c0001t0001g0045a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-252T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661628 | ||||||
chr19:12661760
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910-384C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661760 | ||||||
chr19:12661824
|
G | GA | 10 | a0001c0001t0001g0052a0001c0001t0001g0168a0006c0006t0001g0023others(7): Show | 11 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-449dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661824 | ||||||
chr19:12661824
|
GA | G | 9 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(6): Show | 9 | HG01070.hp1 HG02698.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.910-449delT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661824 | ||||||
chr19:12661838
|
A | G | 1 | a0007c0008t0001g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.910-462T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661838 | ||||||
chr19:12661855
|
T | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.910-479A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661855 | ||||||
chr19:12661910
|
T | TCTCGGCT others(6): Show |
1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.910-547_910-535dup others(13): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661910 | ||||||
chr19:12661913
|
C | T | 1 | a0001c0001t0001g0017 | 2 | NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.910-537G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661913 | ||||||
chr19:12662017
|
G | A | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-641C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662017 | ||||||
chr19:12662159
|
A | G | 1 | a0005c0004t0001g0024 | 2 | HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.910-783T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662159 | ||||||
chr19:12662293
|
T | C | 2 | a0001c0001t0001g0291a0023c0026t0001g0043 | 2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.910-917A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662293 | ||||||
chr19:12662319
|
A | G | 15 | a0007c0008t0001g0186a0007c0008t0001g0197a0007c0008t0001g0198others(12): Show | 18 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.910-943T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662319 | ||||||
chr19:12662357
|
G | A | 8 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+960C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662357 | ||||||
chr19:12662486
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0066others(4): Show | 13 | HG00438.hp2 HG02155.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.909+831G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662486 | ||||||
chr19:12662654
|
A | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0052others(14): Show | 24 | HG00423.hp1 HG00621.hp1 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+663T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662654 | ||||||
chr19:12662744
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.909+573T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662744 | ||||||
chr19:12662855
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.909+462A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662855 | ||||||
chr19:12662863
|
G | A | 18 | a0002c0002t0001g0204a0004c0005t0001g0196a0004c0005t0001g0205others(15): Show | 20 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.909+454C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662863 | ||||||
chr19:12662863
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.909+454C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662863 | ||||||
chr19:12662937
|
C | CA | 95 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0169others(92): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.909+379dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662937 | ||||||
chr19:12662948
|
A | T | 9 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0002g0060others(6): Show | 10 | HG00609.hp2 NA18522.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.909+369T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662948 | ||||||
chr19:12662949
|
A | T | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.909+368T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662949 | ||||||
chr19:12662951
|
T | A | 12 | a0001c0001t0001g0052a0001c0001t0001g0057a0004c0023t0001g0047others(9): Show | 13 | HG01891.hp1 HG01934.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+366A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662951 | ||||||
chr19:12662952
|
A | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.909+365T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662952 | ||||||
chr19:12662953
|
A | T | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.909+364T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662953 | ||||||
chr19:12662954
|
T | A | 2 | a0004c0023t0001g0047a0004c0023t0001g0048 | 2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.909+363A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662954 | ||||||
chr19:12662966
|
A | G | 1 | a0007c0008t0001g0186 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.909+351T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662966 | ||||||
chr19:12663151
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.909+166A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12663151 | ||||||
chr19:12663169
|
G | A | 6 | a0004c0005t0001g0212a0004c0005t0001g0213a0004c0005t0001g0214others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+148C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12663169 | ||||||
chr19:12663235
|
C | G | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(4): Show | 7 | HG02109.hp2 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+82G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12663235 | ||||||
chr19:12663484
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-22T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663484 | ||||||
chr19:12663488
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-26C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663488 | ||||||
chr19:12663495
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-33T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663495 | ||||||
chr19:12663510
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-48G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663510 | ||||||
chr19:12663512
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-50A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663512 | ||||||
chr19:12663520
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-58T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663520 | ||||||
chr19:12663566
|
A | AGATGCAA others(15): Show |
1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-105_764-104ins others(22): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663566 | ||||||
chr19:12663582
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-120G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663582 | ||||||
chr19:12663583
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+120T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663583 | ||||||
chr19:12663584
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+119C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663584 | ||||||
chr19:12663587
|
C | G | 1 | a0002c0002t0001g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.763+116G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663587 | ||||||
chr19:12663606
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+97C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663606 | ||||||
chr19:12663607
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+96C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663607 | ||||||
chr19:12663608
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+95T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663608 | ||||||
chr19:12663929
|
G | C | 5 | a0004c0023t0001g0047a0004c0023t0001g0048a0007c0008t0001g0289others(2): Show | 5 | HG01934.hp2 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-94C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12663929 | ||||||
chr19:12664018
|
A | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.631-183T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664018 | ||||||
chr19:12664035
|
G | A | 1 | a0007c0008t0001g0290 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.631-200C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664035 | ||||||
chr19:12664048
|
G | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0030others(58): Show | 88 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.631-213C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664048 | ||||||
chr19:12664087
|
G | A | 1 | a0002c0002t0001g0278 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.631-252C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664087 | ||||||
chr19:12664274
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.631-439A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664274 | ||||||
chr19:12664460
|
C | T | 5 | a0004c0023t0001g0047a0004c0023t0001g0048a0007c0008t0001g0289others(2): Show | 5 | HG01934.hp2 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+332G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664460 | ||||||
chr19:12664471
|
G | A | 4 | a0006c0006t0001g0280a0006c0006t0001g0281a0006c0006t0001g0282others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+321C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664471 | ||||||
chr19:12664763
|
G | A | 1 | a0005c0004t0001g0034 | 2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.630+29C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664763 | ||||||
chr19:12664791
|
C | G | 1 | a0003c0003t0001g0046 | 1 | HG02886.hp1 | splice_donor_variant&intron_variant | HIGH | c.630+1G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664791 | ||||||
chr19:12665022
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.437-37C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665022 | ||||||
chr19:12665185
|
G | T | 1 | a0001c0001t0001g0045 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.436+167C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665185 | ||||||
chr19:12665208
|
G | C | 3 | a0007c0008t0001g0289a0007c0008t0001g0290a0008c0016t0001g0288 | 3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.436+144C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665208 | ||||||
chr19:12665318
|
G | A | 2 | a0001c0001t0001g0291a0023c0026t0001g0043 | 2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.436+34C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665318 | ||||||
chr19:12665638
|
C | G | 4 | a0006c0014t0001g0039a0006c0014t0001g0040a0006c0014t0001g0041others(1): Show | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+65G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 2/23 | chr19 | 12665638 | ||||||
chr19:12665984
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.160-179A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12665984 | ||||||
chr19:12666040
|
T | A | 1 | a0003c0003t0001g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-235A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666040 | ||||||
chr19:12666082
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.160-277C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666082 | ||||||
chr19:12666177
|
C | T | 1 | a0007c0008t0001g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.159+366G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666177 | ||||||
chr19:12666352
|
A | C | 1 | a0001c0001t0001g0037 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.159+191T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666352 | ||||||
chr19:12666452
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.159+91T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666452 | ||||||
chr19:12666472
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.159+71G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666472 |