geneid | 3998 |
---|---|
ensemblid | ENSG00000074695.6 |
hgncid | 6631 |
symbol | LMAN1 |
name | lectin, mannose binding 1 |
refseq_nuc | NM_005570.4 |
refseq_prot | NP_005561.1 |
ensembl_nuc | ENST00000251047.6 |
ensembl_prot | ENSP00000251047.4 |
mane_status | MANE Select |
chr | chr18 |
start | 59327823 |
end | 59359265 |
strand | - |
ver | v1.2 |
region | chr18:59327823-59359265 |
region5000 | chr18:59322823-59364265 |
regionname0 | LMAN1_chr18_59327823_59359265 |
regionname5000 | LMAN1_chr18_59322823_59364265 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 510 | 312 | 60 | 61 | 155 | 8 | 26 | 124 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002 | 0/0 | 510 | 44 | 1 | 11 | 28 | 2 | 2 | 21 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003 | 0/0 | 510 | 24 | 16 | 3 | 0 | 3 | 2 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0004 | 0/0 | 510 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0005 | 0/0 | 114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0006 | 0/0 | 510 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0007 | 0/0 | 510 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1533 | 291 | 58 | 48 | 153 | 8 | 23 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0002 | 0/0 | 1533 | 44 | 1 | 11 | 28 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0003 | 0/1 | 1533 | 20 | 1 | 13 | 2 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0004 | 0/0 | 1533 | 18 | 11 | 3 | 0 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0005 | 0/0 | 1533 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0006 | 0/0 | 1533 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0007 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0008 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0009 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0010 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
c0011 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3292 | 175 | 34 | 40 | 76 | 8 | 15 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0002 | 0/0 | 3292 | 139 | 17 | 24 | 81 | 3 | 14 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0003 | 0/0 | 3292 | 18 | 0 | 0 | 17 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0004 | 0/0 | 3292 | 10 | 2 | 3 | 0 | 3 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0005 | 0/0 | 3292 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0006 | 0/0 | 3292 | 8 | 0 | 5 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0007 | 0/0 | 3292 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0008 | 0/0 | 3292 | 4 | 0 | 1 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0009 | 0/0 | 3273 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0010 | 0/0 | 3292 | 3 | 2 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0011 | 0/0 | 3292 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0012 | 0/0 | 3292 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0013 | 0/0 | 3292 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0014 | 0/0 | 3292 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0015 | 0/0 | 3292 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0016 | 0/0 | 3292 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0017 | 0/0 | 3292 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0018 | 0/0 | 3292 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0019 | 0/0 | 3292 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
t0020 | 0/0 | 3292 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 26 | 2 | 5 | 15 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0002 | 0/0 | 12 | 1 | 1 | 8 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0003 | 0/0 | 12 | 1 | 2 | 6 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0004 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0005 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0006 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0007 | 0/0 | 5 | 1 | 1 | 0 | 2 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0010 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0019 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1533 | 291 | 58 | 48 | 153 | 8 | 23 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0003 | 0/1 | 1533 | 20 | 1 | 13 | 2 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0010 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002c0002 | 0/0 | 1533 | 44 | 1 | 11 | 28 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0004 | 0/0 | 1533 | 18 | 11 | 3 | 0 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0005 | 0/0 | 1533 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0007 | 0/0 | 1533 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0004c0006 | 0/0 | 1533 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0005c0011 | 0/0 | 1516 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0006c0009 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0007c0008 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4824 | 123 | 31 | 23 | 53 | 6 | 9 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0002 | 0/0 | 4824 | 134 | 16 | 23 | 80 | 2 | 13 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0003 | 0/0 | 4824 | 18 | 0 | 0 | 17 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0009 | 0/0 | 4805 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0010 | 0/0 | 4824 | 3 | 2 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0011 | 0/0 | 4824 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0012 | 0/0 | 4824 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0014 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0015 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0016 | 0/0 | 4824 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0017 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0018 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0001t0019 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0003t0001 | 0/1 | 4824 | 20 | 1 | 13 | 2 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0001c0010t0001 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002c0002t0001 | 0/0 | 4824 | 30 | 1 | 4 | 21 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002c0002t0006 | 0/0 | 4824 | 8 | 0 | 5 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002c0002t0008 | 0/0 | 4824 | 4 | 0 | 1 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002c0002t0013 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0002c0002t0020 | 0/0 | 4824 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0004t0004 | 0/0 | 4824 | 9 | 2 | 3 | 0 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0004t0005 | 0/0 | 4824 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0005t0007 | 0/0 | 4824 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0003c0007t0004 | 0/0 | 4824 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0004c0006t0002 | 0/0 | 4824 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0005c0011t0001 | 0/0 | 4807 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0006c0009t0002 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
a0007c0008t0002 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | copy fasta | chr18 | 59322823 | 59364265 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 26 | 2 | 5 | 15 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0006 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0002 | 0/0 | 12 | 1 | 1 | 8 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0003 | 0/0 | 12 | 1 | 2 | 6 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0005 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0010g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0014g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0015g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0016g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0018g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0001t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0001c0010t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0004 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0006g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0006g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0008g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0013g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0002c0002t0020g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0004g0007 | 0/0 | 5 | 1 | 1 | 0 | 2 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0004t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0005t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0005t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0005t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0005t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0005t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0003c0007t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0004c0006t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0004c0006t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0004c0006t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0005c0011t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0006c0009t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
a0007c0008t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0006 | t0002 | g0054 | EUR | GBR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00099 | hp2 | a0003 | c0004 | t0004 | g0007 | EUR | GBR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0094 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00639 | hp2 | a0002 | c0002 | t0006 | g0026 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00735 | hp2 | a0001 | c0001 | t0010 | g0234 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG00741 | hp2 | a0003 | c0004 | t0004 | g0007 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0093 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01192 | hp1 | a0004 | c0006 | t0002 | g0052 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01255 | hp1 | a0003 | c0004 | t0004 | g0065 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01257 | hp1 | a0002 | c0002 | t0006 | g0049 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01258 | hp1 | a0002 | c0002 | t0006 | g0026 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0142 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01517 | hp2 | a0003 | c0004 | t0004 | g0007 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0097 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0203 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01934 | hp1 | a0003 | c0004 | t0004 | g0064 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01943 | hp1 | a0002 | c0002 | t0006 | g0141 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01952 | hp1 | a0001 | c0001 | t0016 | g0168 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01952 | hp2 | a0002 | c0002 | t0020 | g0221 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0078 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01993 | hp2 | a0002 | c0002 | t0006 | g0026 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02055 | hp2 | a0003 | c0004 | t0005 | g0063 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02071 | hp2 | a0002 | c0002 | t0013 | g0223 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0073 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02280 | hp1 | a0003 | c0004 | t0004 | g0061 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0130 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02451 | hp2 | a0003 | c0004 | t0005 | g0056 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0196 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02683 | hp1 | a0003 | c0004 | t0004 | g0007 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02698 | hp2 | a0004 | c0006 | t0002 | g0053 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02717 | hp1 | a0003 | c0004 | t0005 | g0028 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02809 | hp1 | a0003 | c0004 | t0005 | g0060 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02809 | hp2 | a0003 | c0004 | t0004 | g0007 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02818 | hp1 | a0003 | c0004 | t0005 | g0028 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02886 | hp1 | a0003 | c0004 | t0005 | g0059 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02895 | hp2 | a0003 | c0005 | t0007 | g0068 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02897 | hp1 | a0003 | c0005 | t0007 | g0067 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02922 | hp2 | a0003 | c0004 | t0005 | g0057 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02976 | hp2 | a0003 | c0005 | t0007 | g0066 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0074 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03486 | hp2 | a0003 | c0005 | t0007 | g0069 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03491 | hp1 | a0003 | c0004 | t0004 | g0062 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03516 | hp1 | a0001 | c0010 | t0001 | g0194 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03540 | hp1 | a0003 | c0004 | t0005 | g0055 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0202 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03704 | hp2 | a0005 | c0011 | t0001 | g0075 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0081 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0080 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0079 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18612 | hp1 | a0002 | c0002 | t0006 | g0049 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18906 | hp1 | a0003 | c0005 | t0007 | g0070 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18906 | hp2 | a0003 | c0004 | t0005 | g0058 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18945 | hp2 | a0002 | c0002 | t0008 | g0229 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18951 | hp1 | a0001 | c0001 | t0019 | g0176 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18953 | hp2 | a0001 | c0001 | t0018 | g0173 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18975 | hp2 | a0002 | c0002 | t0006 | g0220 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18987 | hp1 | a0002 | c0002 | t0008 | g0144 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19003 | hp1 | a0002 | c0002 | t0006 | g0217 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0195 | AFR | LWK | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0089 | AFR | LWK | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19062 | hp1 | a0001 | c0001 | t0015 | g0201 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19078 | hp1 | a0002 | c0002 | t0008 | g0228 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19085 | hp2 | a0007 | c0008 | t0002 | g0153 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ASW | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20805 | hp2 | a0003 | c0007 | t0004 | g0071 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | GIH | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01123 | hp1 | a0002 | c0002 | t0008 | g0215 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02109 | hp2 | a0006 | c0009 | t0002 | g0135 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | USA | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | USA | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0077 | REF | REF | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0132 | REF | REF | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:59333237
|
T | A | 1 | a0002 | 44 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
missense_variant | MODERATE | c.1228A>T | p.Met410Leu | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/13 | 1249/4824 | 1228/1533 | 410/510 | chr18 | 59333237 | ||
chr18:59338845
|
A | G | 1 | a0007 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1064T>C | p.Ile355Thr | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 9/13 | 1085/4824 | 1064/1533 | 355/510 | chr18 | 59338845 | ||
chr18:59347514
|
G | A | 1 | a0006 | 1 | HG02109.hp2 | missense_variant&splice_region_variant | MODERATE | c.821C>T | p.Pro274Leu | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/13 | 842/4824 | 821/1533 | 274/510 | chr18 | 59347514 | ||
chr18:59354565
|
T | C | 1 | a0005 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.493A>G | p.Ile165Val | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/13 | 514/4824 | 493/1533 | 165/510 | chr18 | 59354565 | ||
chr18:59355523
|
CGACCTCT others(10): Show |
C | 1 | a0005 | 1 | HG03704.hp2 | frameshift_variant | HIGH | c.333_349delAGTGACTG others(9): Show |
p.Val112fs | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 2/13 | 370/4824 | 333/1533 | 111/510 | chr18 | 59355523 | ||
chr18:59359129
|
A | G | 1 | a0003 | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
missense_variant | MODERATE | c.116T>C | p.Val39Ala | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/13 | 137/4824 | 116/1533 | 39/510 | chr18 | 59359129 | ||
chr18:59359204
|
C | T | 1 | a0004 | 3 | HG00099.hp1 HG01192.hp1 HG02698.hp2 |
missense_variant | MODERATE | c.41G>A | p.Arg14Gln | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/13 | 62/4824 | 41/1533 | 14/510 | chr18 | 59359204 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:59338952
|
C | T | 1 | a0003c0005 | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.957G>A | p.Ala319Ala | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 9/13 | 978/4824 | 957/1533 | 319/510 | chr18 | 59338952 | ||
chr18:59349129
|
T | G | 1 | a0001c0010 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.747A>C | p.Ala249Ala | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/13 | 768/4824 | 747/1533 | 249/510 | chr18 | 59349129 | ||
chr18:59355522
|
T | C | 4 | a0001c0003a0003c0004a0003c0005others(1): Show | 44 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(41): Show |
synonymous_variant | LOW | c.351A>G | p.Arg117Arg | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 2/13 | 372/4824 | 351/1533 | 117/510 | chr18 | 59355522 | ||
chr18:59359050
|
G | A | 1 | a0003c0007 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.195C>T | p.Pro65Pro | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/13 | 216/4824 | 195/1533 | 65/510 | chr18 | 59359050 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:59327986
|
A | T | 1 | a0001c0001t0003 | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3107T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 3107 | chr18 | 59327986 | |||||
chr18:59328164
|
A | G | 9 | a0001c0001t0002a0001c0001t0010a0001c0001t0016others(6): Show | 146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*2929T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2929 | chr18 | 59328164 | |||||
chr18:59328200
|
C | T | 1 | a0001c0001t0015 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2893G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2893 | chr18 | 59328200 | |||||
chr18:59328347
|
G | T | 1 | a0001c0001t0014 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2746C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2746 | chr18 | 59328347 | |||||
chr18:59328630
|
G | A | 1 | a0001c0001t0016 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2463 | chr18 | 59328630 | |||||
chr18:59328688
|
G | T | 2 | a0003c0004t0004a0003c0007t0004 | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2405C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2405 | chr18 | 59328688 | |||||
chr18:59328706
|
T | C | 4 | a0003c0004t0004a0003c0004t0005a0003c0005t0007others(1): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2387A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2387 | chr18 | 59328706 | |||||
chr18:59328876
|
C | T | 5 | a0001c0001t0009a0003c0004t0004a0003c0004t0005others(2): Show | 27 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2217G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2217 | chr18 | 59328876 | |||||
chr18:59328897
|
A | G | 1 | a0001c0001t0010 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2196T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2196 | chr18 | 59328897 | |||||
chr18:59328909
|
T | C | 1 | a0003c0005t0007 | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2184A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2184 | chr18 | 59328909 | |||||
chr18:59329030
|
G | C | 4 | a0003c0004t0004a0003c0004t0005a0003c0005t0007others(1): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2063C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2063 | chr18 | 59329030 | |||||
chr18:59329122
|
C | T | 1 | a0002c0002t0013 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1971G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1971 | chr18 | 59329122 | |||||
chr18:59329170
|
T | G | 1 | a0001c0001t0017 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1923A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1923 | chr18 | 59329170 | |||||
chr18:59329271
|
C | A | 2 | a0002c0002t0006a0002c0002t0020 | 9 | HG00639.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1822 | chr18 | 59329271 | |||||
chr18:59329294
|
T | G | 4 | a0003c0004t0004a0003c0004t0005a0003c0005t0007others(1): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1799A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1799 | chr18 | 59329294 | |||||
chr18:59329822
|
T | C | 1 | a0001c0001t0018 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1271 | chr18 | 59329822 | |||||
chr18:59330233
|
A | C | 1 | a0001c0001t0011 | 2 | HG02572.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*860T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 860 | chr18 | 59330233 | |||||
chr18:59330299
|
T | C | 1 | a0001c0001t0019 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 794 | chr18 | 59330299 | |||||
chr18:59330421
|
GAGGAATG others(12): Show |
G | 1 | a0001c0001t0009 | 3 | HG01884.hp1 HG02717.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*653_*671delTGTGGG others(13): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 653 | chr18 | 59330421 | |||||
chr18:59330441
|
A | G | 1 | a0002c0002t0008 | 4 | HG01123.hp1 NA18945.hp2 NA18987.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*652T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 652 | chr18 | 59330441 | |||||
chr18:59330444
|
T | C | 1 | a0002c0002t0020 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*649A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 649 | chr18 | 59330444 | |||||
chr18:59330603
|
G | A | 1 | a0001c0001t0003 | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*490C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 490 | chr18 | 59330603 | |||||
chr18:59330929
|
T | C | 1 | a0001c0001t0012 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*164A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 164 | chr18 | 59330929 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:59331236
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1497-107G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 12/12 | chr18 | 59331236 | ||||||
chr18:59331310
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0009g0031a0001c0001t0009g0097 | 4 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1496+108T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 12/12 | chr18 | 59331310 | ||||||
chr18:59331669
|
C | T | 13 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(10): Show | 17 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-130G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59331669 | ||||||
chr18:59331840
|
A | G | 1 | a0004c0006t0002g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1375-301T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59331840 | ||||||
chr18:59332076
|
C | A | 3 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1375-537G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332076 | ||||||
chr18:59332104
|
C | T | 2 | a0001c0001t0011g0195a0001c0001t0011g0196 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1375-565G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332104 | ||||||
chr18:59332170
|
A | C | 1 | a0001c0001t0003g0210 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1375-631T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332170 | ||||||
chr18:59332245
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(49): Show | 99 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1375-706A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332245 | ||||||
chr18:59332379
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1374+712A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332379 | ||||||
chr18:59332567
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1374+524C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332567 | ||||||
chr18:59332739
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(15): Show | 29 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1374+352A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332739 | ||||||
chr18:59332796
|
T | TTAAGCAA others(2): Show |
5 | a0003c0005t0007g0066a0003c0005t0007g0067a0003c0005t0007g0068others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1374+286_1374+294d others(11): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332796 | ||||||
chr18:59332809
|
G | A | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1374+282C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332809 | ||||||
chr18:59332979
|
A | T | 1 | a0006c0009t0002g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1374+112T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332979 | ||||||
chr18:59333042
|
T | C | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1374+49A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59333042 | ||||||
chr18:59333071
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(65): Show | 126 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1374+20C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59333071 | ||||||
chr18:59333286
|
GT | G | 21 | a0001c0001t0001g0127a0001c0001t0002g0160a0003c0004t0004g0007others(18): Show | 26 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1221-43delA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333286 | ||||||
chr18:59333298
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1221-54G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333298 | ||||||
chr18:59333386
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1221-142C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333386 | ||||||
chr18:59333690
|
A | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0187 | 5 | HG00738.hp2 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-446T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333690 | ||||||
chr18:59333851
|
G | GA | 20 | a0002c0002t0001g0224a0003c0004t0004g0007a0003c0004t0004g0061others(17): Show | 25 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1221-608dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333851 | ||||||
chr18:59333859
|
A | G | 13 | a0001c0001t0003g0020a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1221-615T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333859 | ||||||
chr18:59333945
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0088 | 3 | HG00323.hp1 HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1221-701T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333945 | ||||||
chr18:59334007
|
G | A | 1 | a0002c0002t0013g0223 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1221-763C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334007 | ||||||
chr18:59334083
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1221-839G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334083 | ||||||
chr18:59334106
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(9): Show | 23 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1221-862T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334106 | ||||||
chr18:59334328
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1221-1084T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334328 | ||||||
chr18:59334478
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0098 | 4 | HG02300.hp1 NA18957.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221-1234A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334478 | ||||||
chr18:59334581
|
C | T | 1 | a0004c0006t0002g0052 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1221-1337G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334581 | ||||||
chr18:59334602
|
A | G | 1 | a0002c0002t0001g0225 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1221-1358T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334602 | ||||||
chr18:59334633
|
T | C | 1 | a0001c0003t0001g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1221-1389A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334633 | ||||||
chr18:59334842
|
A | AT | 23 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0002g0016others(20): Show | 26 | HG00408.hp1 HG00609.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1221-1599dupA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334842 | ||||||
chr18:59335124
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1221-1880T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335124 | ||||||
chr18:59335160
|
G | A | 1 | a0001c0003t0001g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1221-1916C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335160 | ||||||
chr18:59335173
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(9): Show | 23 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1221-1929G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335173 | ||||||
chr18:59335206
|
C | G | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1221-1962G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335206 | ||||||
chr18:59335229
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1221-1985A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335229 | ||||||
chr18:59335231
|
C | T | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1221-1987G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335231 | ||||||
chr18:59335237
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1221-1993G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335237 | ||||||
chr18:59335373
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1221-2129G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335373 | ||||||
chr18:59335491
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0190 | 3 | HG02145.hp1 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1221-2247A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335491 | ||||||
chr18:59335708
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1221-2464A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335708 | ||||||
chr18:59335896
|
C | T | 5 | a0003c0005t0007g0066a0003c0005t0007g0067a0003c0005t0007g0068others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-2652G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335896 | ||||||
chr18:59335911
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1220+2646A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335911 | ||||||
chr18:59335933
|
A | G | 3 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0179 | 3 | HG00597.hp2 NA19072.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1220+2624T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335933 | ||||||
chr18:59336202
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1220+2355G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336202 | ||||||
chr18:59336238
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1220+2319A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336238 | ||||||
chr18:59336387
|
T | C | 6 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(3): Show | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1220+2170A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336387 | ||||||
chr18:59336472
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0190 | 3 | HG02145.hp1 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1220+2085C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336472 | ||||||
chr18:59336482
|
G | C | 8 | a0003c0004t0005g0028a0003c0004t0005g0055a0003c0004t0005g0056others(5): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1220+2075C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336482 | ||||||
chr18:59336600
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1220+1957C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336600 | ||||||
chr18:59336657
|
G | A | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220+1900C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336657 | ||||||
chr18:59336767
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1220+1790G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336767 | ||||||
chr18:59336920
|
T | TA | 33 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(30): Show | 50 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1220+1636dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336920 | ||||||
chr18:59337041
|
T | C | 1 | a0001c0001t0003g0209 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1220+1516A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337041 | ||||||
chr18:59337123
|
A | G | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220+1434T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337123 | ||||||
chr18:59337167
|
T | C | 5 | a0003c0004t0005g0055a0003c0004t0005g0057a0003c0004t0005g0059others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+1390A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337167 | ||||||
chr18:59337198
|
A | G | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1220+1359T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337198 | ||||||
chr18:59337367
|
C | T | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220+1190G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337367 | ||||||
chr18:59337500
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(120): Show | 204 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1220+1057T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337500 | ||||||
chr18:59337531
|
T | C | 22 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0234others(19): Show | 27 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1220+1026A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337531 | ||||||
chr18:59337915
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0112 | 5 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+642T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337915 | ||||||
chr18:59338296
|
C | A | 1 | a0001c0001t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1220+261G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338296 | ||||||
chr18:59338423
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(52): Show | 102 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1220+134A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338423 | ||||||
chr18:59338507
|
T | A | 6 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(3): Show | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1220+50A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338507 | ||||||
chr18:59338538
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1220+19C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338538 | ||||||
chr18:59338690
|
T | C | 1 | a0001c0001t0002g0037 | 2 | NA18942.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1150-63A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 9/12 | chr18 | 59338690 | ||||||
chr18:59339266
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.956-313G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339266 | ||||||
chr18:59339341
|
A | G | 1 | a0004c0006t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.956-388T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339341 | ||||||
chr18:59339650
|
T | A | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.956-697A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339650 | ||||||
chr18:59339713
|
G | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0121 | 3 | NA18967.hp1 NA18984.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.956-760C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339713 | ||||||
chr18:59339879
|
C | T | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.956-926G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339879 | ||||||
chr18:59340025
|
T | C | 1 | a0001c0001t0011g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.956-1072A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340025 | ||||||
chr18:59340222
|
G | A | 3 | a0002c0002t0001g0143a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | HG02083.hp2 NA18986.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.956-1269C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340222 | ||||||
chr18:59340337
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(228): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.956-1384C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340337 | ||||||
chr18:59340421
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(15): Show | 29 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.956-1468A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340421 | ||||||
chr18:59340641
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.956-1688C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340641 | ||||||
chr18:59340696
|
A | G | 6 | a0001c0001t0001g0032a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 7 | NA18940.hp1 NA18946.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-1743T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340696 | ||||||
chr18:59340702
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.956-1749T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340702 | ||||||
chr18:59340759
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0145 | 3 | HG02559.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.956-1806A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340759 | ||||||
chr18:59340848
|
T | C | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-1895A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340848 | ||||||
chr18:59340903
|
T | C | 8 | a0003c0004t0005g0028a0003c0004t0005g0055a0003c0004t0005g0056others(5): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-1950A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340903 | ||||||
chr18:59341020
|
T | C | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-2067A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341020 | ||||||
chr18:59341097
|
AAAAAG | A | 8 | a0003c0004t0005g0028a0003c0004t0005g0055a0003c0004t0005g0056others(5): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-2149_956-2145d others(7): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341097 | ||||||
chr18:59341604
|
T | C | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.956-2651A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341604 | ||||||
chr18:59341768
|
T | C | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-2815A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341768 | ||||||
chr18:59341852
|
T | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.956-2899A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341852 | ||||||
chr18:59342075
|
T | C | 4 | a0003c0005t0007g0067a0003c0005t0007g0068a0003c0005t0007g0069others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-3122A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342075 | ||||||
chr18:59342224
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(142): Show | 239 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.956-3271G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342224 | ||||||
chr18:59342250
|
T | C | 1 | a0001c0001t0001g0015 | 4 | NA18947.hp2 NA18998.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-3297A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342250 | ||||||
chr18:59342329
|
A | G | 1 | a0002c0002t0001g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.956-3376T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342329 | ||||||
chr18:59342537
|
T | C | 29 | a0001c0001t0009g0031a0001c0001t0009g0097a0002c0002t0001g0004others(26): Show | 47 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.955+3382A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342537 | ||||||
chr18:59342738
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0125 | 3 | HG01081.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.955+3181T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342738 | ||||||
chr18:59342750
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.955+3169G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342750 | ||||||
chr18:59342889
|
A | G | 26 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(23): Show | 39 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.955+3030T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342889 | ||||||
chr18:59342985
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(143): Show | 240 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.955+2934C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342985 | ||||||
chr18:59343054
|
T | TA | 78 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(75): Show | 140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.955+2864dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343054 | ||||||
chr18:59343054
|
T | TAA | 5 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0001t0001g0121others(2): Show | 6 | HG02257.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+2863_955+2864d others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343054 | ||||||
chr18:59343143
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.955+2776A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343143 | ||||||
chr18:59343221
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(130): Show | 222 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.955+2698A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343221 | ||||||
chr18:59343274
|
T | A | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+2645A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343274 | ||||||
chr18:59343289
|
G | GA | 13 | a0001c0001t0001g0111a0001c0001t0003g0020a0001c0001t0003g0045others(10): Show | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.955+2629dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343289 | ||||||
chr18:59343345
|
C | T | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+2574G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343345 | ||||||
chr18:59343484
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(143): Show | 240 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.955+2435C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343484 | ||||||
chr18:59343563
|
T | C | 27 | a0002c0002t0001g0004a0002c0002t0001g0011a0002c0002t0001g0047others(24): Show | 44 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.955+2356A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343563 | ||||||
chr18:59343578
|
A | T | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+2341T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343578 | ||||||
chr18:59343646
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.955+2273A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343646 | ||||||
chr18:59343732
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.955+2187A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343732 | ||||||
chr18:59343817
|
G | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+2102C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343817 | ||||||
chr18:59343960
|
C | T | 1 | a0003c0004t0005g0028 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.955+1959G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343960 | ||||||
chr18:59343988
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.955+1931T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343988 | ||||||
chr18:59344069
|
T | C | 3 | a0002c0002t0001g0143a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | HG02083.hp2 NA18986.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.955+1850A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344069 | ||||||
chr18:59344072
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.955+1847T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344072 | ||||||
chr18:59344147
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.955+1772C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344147 | ||||||
chr18:59344489
|
G | C | 3 | a0002c0002t0001g0139a0002c0002t0001g0142a0002c0002t0001g0227 | 3 | HG00642.hp1 HG00735.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.955+1430C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344489 | ||||||
chr18:59344617
|
G | GACAAATG others(26): Show |
1 | a0001c0001t0001g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955+1269_955+1301d others(35): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344617 | ||||||
chr18:59344654
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0044others(5): Show | 18 | HG00738.hp2 HG01109.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.955+1265T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344654 | ||||||
chr18:59344666
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.955+1253C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344666 | ||||||
chr18:59344700
|
G | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(142): Show | 239 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.955+1219C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344700 | ||||||
chr18:59344798
|
A | C | 29 | a0001c0001t0002g0218a0001c0001t0002g0219a0002c0002t0001g0004others(26): Show | 46 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.955+1121T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344798 | ||||||
chr18:59344828
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.955+1091A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344828 | ||||||
chr18:59344989
|
C | A | 8 | a0003c0004t0005g0028a0003c0004t0005g0055a0003c0004t0005g0056others(5): Show | 9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+930G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344989 | ||||||
chr18:59345013
|
C | T | 5 | a0003c0005t0007g0066a0003c0005t0007g0067a0003c0005t0007g0068others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+906G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345013 | ||||||
chr18:59345096
|
G | GT | 3 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.955+822dupA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345096 | ||||||
chr18:59345118
|
G | C | 1 | a0001c0001t0012g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.955+801C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345118 | ||||||
chr18:59345129
|
A | G | 1 | a0001c0003t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.955+790T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345129 | ||||||
chr18:59345344
|
C | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(142): Show | 239 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.955+575G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345344 | ||||||
chr18:59345657
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.955+262A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345657 | ||||||
chr18:59345747
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.955+172T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345747 | ||||||
chr18:59346209
|
C | CT | 33 | a0001c0001t0001g0127a0001c0001t0002g0030a0001c0001t0002g0035others(30): Show | 39 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.823-159dupA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346209
|
C | CTT | 12 | a0001c0001t0002g0158a0001c0001t0002g0161a0001c0001t0002g0166others(9): Show | 16 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-160_823-159dup others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346209
|
CT | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(64): Show | 126 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.823-159delA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346209
|
CTT | C | 10 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0123others(7): Show | 12 | HG01167.hp1 HG01257.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.823-160_823-159del others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346209
|
CTTT | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(9): Show | 23 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.823-161_823-159del others(3): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346209
|
CTTTTTTT | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0122others(5): Show | 12 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.823-165_823-159del others(7): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346209
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0050 | 2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.823-171_823-159del others(13): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | ||||||
chr18:59346236
|
T | A | 1 | a0001c0001t0002g0157 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.823-185A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346236 | ||||||
chr18:59346236
|
T | TA | 4 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0094others(1): Show | 7 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-186dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346236 | ||||||
chr18:59346250
|
G | A | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-199C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346250 | ||||||
chr18:59346377
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0044others(33): Show | 51 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.823-326A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346377 | ||||||
chr18:59346466
|
G | C | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.823-415C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346466 | ||||||
chr18:59346542
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.823-491T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346542 | ||||||
chr18:59346547
|
C | G | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-496G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346547 | ||||||
chr18:59346675
|
C | G | 1 | a0001c0001t0002g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.823-624G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346675 | ||||||
chr18:59346787
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+726A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346787 | ||||||
chr18:59346815
|
C | T | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.822+698G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346815 | ||||||
chr18:59346946
|
C | G | 1 | a0002c0002t0001g0047 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.822+567G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346946 | ||||||
chr18:59346953
|
G | A | 1 | a0001c0001t0001g0034 | 2 | NA18944.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.822+560C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346953 | ||||||
chr18:59347046
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0095 | 3 | HG02257.hp2 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.822+467A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347046 | ||||||
chr18:59347076
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.822+437T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347076 | ||||||
chr18:59347115
|
C | T | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.822+398G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347115 | ||||||
chr18:59347149
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+364C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347149 | ||||||
chr18:59347264
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(228): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.822+249T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347264 | ||||||
chr18:59347269
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(228): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.822+244T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347269 | ||||||
chr18:59347302
|
CAG | C | 3 | a0003c0005t0007g0067a0003c0005t0007g0068a0003c0005t0007g0070 | 3 | HG02895.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.822+209_822+210del others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347302 | ||||||
chr18:59347304
|
G | C | 12 | a0001c0001t0002g0017a0001c0001t0002g0025a0001c0001t0002g0037others(9): Show | 20 | HG00621.hp1 HG02056.hp2 HG03834.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+209C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347304 | ||||||
chr18:59347320
|
CA | C | 10 | a0001c0001t0002g0023a0001c0001t0002g0025a0001c0001t0002g0086others(7): Show | 14 | HG00642.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.822+192delT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAA | C | 15 | a0001c0001t0002g0030a0001c0001t0002g0041a0001c0001t0002g0042others(12): Show | 18 | HG00609.hp1 HG01099.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.822+191_822+192del others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAA | C | 13 | a0001c0001t0002g0003a0001c0001t0002g0038a0001c0001t0002g0039others(10): Show | 27 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.822+190_822+192del others(3): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAA | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0024others(20): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.822+189_822+192del others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAA | C | 10 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0076others(7): Show | 17 | HG01168.hp2 HG02074.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.822+188_822+192del others(5): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0090a0003c0004t0004g0061a0003c0004t0004g0064others(6): Show | 10 | HG01934.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+183_822+192del others(10): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(4): Show |
C | 4 | a0003c0004t0004g0007a0003c0004t0004g0062a0003c0004t0004g0065others(1): Show | 8 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+182_822+192del others(11): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(5): Show |
C | 1 | a0003c0005t0007g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.822+181_822+192del others(12): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0200a0003c0005t0007g0066a0003c0005t0007g0067others(2): Show | 5 | HG02723.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+180_822+192del others(13): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0125 | 3 | HG02486.hp1 HG03688.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.822+178_822+192del others(15): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(9): Show |
C | 13 | a0001c0001t0001g0100a0001c0001t0001g0115a0001c0001t0001g0116others(10): Show | 13 | HG00621.hp2 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+177_822+192del others(16): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(10): Show |
C | 62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(59): Show | 121 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.822+176_822+192del others(17): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(11): Show |
C | 14 | a0001c0001t0001g0186a0001c0001t0003g0020a0001c0001t0003g0045others(11): Show | 22 | HG01106.hp2 HG01123.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.822+175_822+192del others(18): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(12): Show |
C | 35 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0009g0031others(32): Show | 57 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.822+174_822+192del others(19): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(13): Show |
C | 2 | a0002c0002t0001g0216a0002c0002t0006g0217 | 2 | HG02132.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.822+173_822+192del others(20): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0002g0149 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.822+171_822+192del others(22): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347320
|
CAAAAAAA others(18): Show |
C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.822+168_822+192del others(25): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | ||||||
chr18:59347472
|
A | AAACC | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.822+40_822+41insGG others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347472 | ||||||
chr18:59347481
|
G | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(16): Show | 30 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+32C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347481 | ||||||
chr18:59347580
|
T | TA | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.764-10dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347580 | ||||||
chr18:59347657
|
T | C | 26 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(23): Show | 39 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.764-86A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347657 | ||||||
chr18:59347677
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0123a0001c0001t0001g0124 | 5 | HG00408.hp2 NA18961.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-106A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347677 | ||||||
chr18:59347681
|
G | A | 5 | a0003c0005t0007g0066a0003c0005t0007g0067a0003c0005t0007g0068others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-110C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347681 | ||||||
chr18:59347970
|
G | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-399C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347970 | ||||||
chr18:59347979
|
T | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG00408.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.764-408A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347979 | ||||||
chr18:59348044
|
C | T | 14 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(11): Show | 19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.764-473G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348044 | ||||||
chr18:59348116
|
T | C | 1 | a0003c0005t0007g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.764-545A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348116 | ||||||
chr18:59348276
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02258.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-705G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348276 | ||||||
chr18:59348291
|
T | C | 6 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(3): Show | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.764-720A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348291 | ||||||
chr18:59348453
|
C | T | 13 | a0001c0001t0003g0020a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.763+660G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348453 | ||||||
chr18:59348530
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.763+583A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348530 | ||||||
chr18:59348568
|
T | A | 29 | a0001c0001t0002g0218a0001c0001t0002g0219a0002c0002t0001g0004others(26): Show | 46 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.763+545A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348568 | ||||||
chr18:59348803
|
C | T | 1 | a0003c0005t0007g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.763+310G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348803 | ||||||
chr18:59349378
|
T | C | 26 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(23): Show | 39 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.640-142A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349378 | ||||||
chr18:59349442
|
G | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(11): Show | 25 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.640-206C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349442 | ||||||
chr18:59349835
|
T | C | 26 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(23): Show | 39 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.640-599A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349835 | ||||||
chr18:59349840
|
A | C | 1 | a0002c0002t0008g0215 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.640-604T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349840 | ||||||
chr18:59349841
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.640-605A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349841 | ||||||
chr18:59350155
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.640-919A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350155 | ||||||
chr18:59350222
|
A | G | 13 | a0001c0001t0003g0020a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.640-986T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350222 | ||||||
chr18:59350466
|
T | A | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.640-1230A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350466 | ||||||
chr18:59350479
|
G | T | 1 | a0001c0001t0003g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.640-1243C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350479 | ||||||
chr18:59350526
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.640-1290C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350526 | ||||||
chr18:59350534
|
G | A | 3 | a0002c0002t0008g0144a0002c0002t0008g0228a0002c0002t0008g0229 | 3 | NA18945.hp2 NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.640-1298C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350534 | ||||||
chr18:59350686
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.640-1450C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350686 | ||||||
chr18:59350759
|
T | C | 1 | a0001c0003t0001g0233 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.640-1523A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350759 | ||||||
chr18:59350790
|
C | T | 6 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(3): Show | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-1554G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350790 | ||||||
chr18:59351001
|
G | A | 26 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(23): Show | 39 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.640-1765C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351001 | ||||||
chr18:59351006
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.640-1770C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351006 | ||||||
chr18:59351023
|
C | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.640-1787G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351023 | ||||||
chr18:59351490
|
G | C | 13 | a0001c0001t0003g0020a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.639+1712C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351490 | ||||||
chr18:59351513
|
T | C | 1 | a0001c0003t0001g0083 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.639+1689A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351513 | ||||||
chr18:59351665
|
T | C | 1 | a0001c0001t0003g0214 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.639+1537A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351665 | ||||||
chr18:59351690
|
G | A | 26 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(23): Show | 39 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.639+1512C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351690 | ||||||
chr18:59351807
|
G | A | 1 | a0004c0006t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.639+1395C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351807 | ||||||
chr18:59351889
|
T | C | 4 | a0003c0005t0007g0067a0003c0005t0007g0068a0003c0005t0007g0069others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+1313A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351889 | ||||||
chr18:59351916
|
C | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | NA18940.hp1 NA18946.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+1286G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351916 | ||||||
chr18:59352042
|
T | G | 6 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(3): Show | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.639+1160A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352042 | ||||||
chr18:59352429
|
C | T | 5 | a0003c0005t0007g0066a0003c0005t0007g0067a0003c0005t0007g0068others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+773G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352429 | ||||||
chr18:59352442
|
T | C | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.639+760A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352442 | ||||||
chr18:59352475
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.639+727G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352475 | ||||||
chr18:59352528
|
A | G | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.639+674T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352528 | ||||||
chr18:59352547
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.639+655G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352547 | ||||||
chr18:59352586
|
C | T | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.639+616G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352586 | ||||||
chr18:59352593
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.639+609G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352593 | ||||||
chr18:59352801
|
T | C | 4 | a0001c0001t0002g0023a0001c0001t0002g0133a0001c0001t0002g0134others(1): Show | 6 | HG00642.hp2 HG00733.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+401A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352801 | ||||||
chr18:59352905
|
GTCTA | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(45): Show | 95 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.639+293_639+296del others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352905 | ||||||
chr18:59353074
|
T | C | 13 | a0001c0001t0003g0020a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.639+128A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59353074 | ||||||
chr18:59353545
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0098 | 4 | HG02300.hp1 NA18957.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-244T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353545 | ||||||
chr18:59353647
|
C | T | 2 | a0001c0001t0009g0031a0001c0001t0009g0097 | 3 | HG01884.hp1 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.540-346G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353647 | ||||||
chr18:59353708
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.540-407G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353708 | ||||||
chr18:59353924
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.539+595A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353924 | ||||||
chr18:59353974
|
T | C | 29 | a0001c0001t0002g0218a0001c0001t0002g0219a0002c0002t0001g0004others(26): Show | 46 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.539+545A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353974 | ||||||
chr18:59354048
|
C | T | 3 | a0003c0005t0007g0067a0003c0005t0007g0068a0003c0005t0007g0070 | 3 | HG02895.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539+471G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354048 | ||||||
chr18:59354093
|
A | G | 31 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(28): Show | 44 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.539+426T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354093 | ||||||
chr18:59354191
|
A | C | 1 | a0003c0005t0007g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.539+328T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354191 | ||||||
chr18:59354246
|
A | T | 6 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(3): Show | 10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.539+273T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354246 | ||||||
chr18:59354262
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.539+257G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354262 | ||||||
chr18:59354317
|
G | T | 31 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(28): Show | 44 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.539+202C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354317 | ||||||
chr18:59354341
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539+178A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354341 | ||||||
chr18:59354506
|
AAC | A | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.539+11_539+12delGT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354506 | ||||||
chr18:59354595
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.478-15T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354595 | ||||||
chr18:59354597
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0095 | 3 | HG02257.hp2 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.478-17G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354597 | ||||||
chr18:59354726
|
A | G | 3 | a0001c0001t0010g0202a0001c0001t0010g0203a0001c0001t0010g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.478-146T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354726 | ||||||
chr18:59354971
|
G | C | 73 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0010others(70): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.477+342C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354971 | ||||||
chr18:59354975
|
G | A | 2 | a0001c0001t0011g0195a0001c0001t0011g0196 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.477+338C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354975 | ||||||
chr18:59355165
|
A | G | 1 | a0001c0003t0001g0077 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.477+148T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355165 | ||||||
chr18:59355197
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.477+116A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355197 | ||||||
chr18:59355205
|
T | A | 2 | a0003c0004t0005g0060a0003c0004t0005g0063 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.477+108A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355205 | ||||||
chr18:59355266
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.477+47C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355266 | ||||||
chr18:59355308
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.477+5A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355308 | ||||||
chr18:59355921
|
ACTAT | A | 5 | a0003c0005t0007g0066a0003c0005t0007g0067a0003c0005t0007g0068others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-267_215-264del others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59355921 | ||||||
chr18:59356405
|
G | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0043others(15): Show | 29 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.215-747C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356405 | ||||||
chr18:59356469
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.215-811C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356469 | ||||||
chr18:59356503
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.215-845C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356503 | ||||||
chr18:59356623
|
T | G | 1 | a0001c0001t0002g0198 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.215-965A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356623 | ||||||
chr18:59356639
|
T | G | 1 | a0001c0001t0014g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215-981A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356639 | ||||||
chr18:59356670
|
TG | T | 12 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0029others(9): Show | 20 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-1013delC | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356670 | ||||||
chr18:59356864
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.215-1206C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356864 | ||||||
chr18:59356990
|
G | T | 1 | a0001c0001t0002g0092 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.215-1332C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356990 | ||||||
chr18:59357012
|
G | T | 1 | a0001c0001t0002g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.215-1354C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357012 | ||||||
chr18:59357019
|
A | C | 1 | a0001c0001t0010g0202 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.215-1361T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357019 | ||||||
chr18:59357022
|
T | C | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1364A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357022 | ||||||
chr18:59357023
|
T | A | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1365A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357023 | ||||||
chr18:59357025
|
T | G | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1367A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357025 | ||||||
chr18:59357026
|
C | A | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1368G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357026 | ||||||
chr18:59357027
|
T | C | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1369A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357027 | ||||||
chr18:59357030
|
T | G | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1372A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357030 | ||||||
chr18:59357031
|
T | A | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1373A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357031 | ||||||
chr18:59357032
|
T | C | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1374A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357032 | ||||||
chr18:59357033
|
T | G | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1375A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357033 | ||||||
chr18:59357034
|
T | A | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1376A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357034 | ||||||
chr18:59357036
|
T | G | 1 | a0003c0004t0004g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1378A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357036 | ||||||
chr18:59357037
|
T | A | 18 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(15): Show | 23 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.215-1379A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357037 | ||||||
chr18:59357086
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.215-1428A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357086 | ||||||
chr18:59357129
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-1471C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357129 | ||||||
chr18:59357386
|
T | C | 1 | a0001c0001t0014g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214+1645A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357386 | ||||||
chr18:59357882
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+1149T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357882 | ||||||
chr18:59357892
|
C | A | 1 | a0001c0001t0015g0201 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.214+1139G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357892 | ||||||
chr18:59357917
|
T | C | 4 | a0003c0004t0004g0061a0003c0004t0004g0064a0003c0004t0004g0065others(1): Show | 4 | HG01255.hp1 HG01934.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1114A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357917 | ||||||
chr18:59357933
|
C | A | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1098G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357933 | ||||||
chr18:59357934
|
G | C | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1097C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357934 | ||||||
chr18:59357935
|
T | TATAAAAC others(10): Show |
1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1095_214+1096i others(19): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357935 | ||||||
chr18:59357937
|
G | C | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1094C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357937 | ||||||
chr18:59357939
|
G | A | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1092C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357939 | ||||||
chr18:59357940
|
C | A | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1091G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357940 | ||||||
chr18:59357950
|
C | G | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1081G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357950 | ||||||
chr18:59357958
|
T | A | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1073A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357958 | ||||||
chr18:59357959
|
A | G | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1072T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357959 | ||||||
chr18:59357962
|
G | C | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1069C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357962 | ||||||
chr18:59357963
|
T | TA | 39 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(36): Show | 61 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.214+1067dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357963 | ||||||
chr18:59357963
|
TA | T | 25 | a0001c0001t0001g0088a0001c0001t0002g0076a0001c0001t0002g0084others(22): Show | 33 | HG00423.hp2 HG01123.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.214+1067delT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357963 | ||||||
chr18:59357963
|
TAAA | T | 10 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0005g0028others(7): Show | 15 | HG00099.hp2 HG00741.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+1065_214+1067d others(5): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357963 | ||||||
chr18:59357969
|
A | T | 1 | a0005c0011t0001g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1062T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357969 | ||||||
chr18:59358191
|
A | G | 2 | a0001c0001t0012g0073a0001c0001t0012g0074 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.214+840T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358191 | ||||||
chr18:59358204
|
T | C | 3 | a0001c0001t0002g0051a0001c0001t0002g0230a0001c0001t0002g0231 | 4 | HG00423.hp1 HG02080.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+827A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358204 | ||||||
chr18:59358380
|
C | T | 15 | a0001c0001t0010g0234a0003c0004t0004g0007a0003c0004t0004g0061others(12): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+651G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358380 | ||||||
chr18:59358730
|
G | C | 1 | a0001c0001t0002g0232 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214+301C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358730 | ||||||
chr18:59358846
|
G | C | 1 | a0001c0003t0001g0233 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.214+185C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358846 | ||||||
chr18:59358863
|
C | T | 19 | a0003c0004t0004g0007a0003c0004t0004g0061a0003c0004t0004g0062others(16): Show | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.214+168G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358863 | ||||||
chr18:59358866
|
G | A | 1 | a0001c0001t0010g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.214+165C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358866 | ||||||
chr18:59358937
|
G | A | 1 | a0003c0005t0007g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214+94C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358937 | ||||||
chr18:59358993
|
G | T | 1 | a0001c0001t0002g0072 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214+38C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358993 | ||||||
chr18:59359024
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0235 | 4 | HG00544.hp1 NA19055.hp1 NA19076.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.214+7C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59359024 |