geneid | 10982 |
---|---|
ensemblid | ENSG00000166974.13 |
hgncid | 6891 |
symbol | MAPRE2 |
name | microtubule associated protein RP/EB family member 2 |
refseq_nuc | NM_014268.4 |
refseq_prot | NP_055083.1 |
ensembl_nuc | ENST00000300249.10 |
ensembl_prot | ENSP00000300249.4 |
mane_status | MANE Select |
chr | chr18 |
start | 35041413 |
end | 35143470 |
strand | + |
ver | v1.2 |
region | chr18:35041413-35143470 |
region5000 | chr18:35036413-35148470 |
regionname0 | MAPRE2_chr18_35041413_35143470 |
regionname5000 | MAPRE2_chr18_35036413_35148470 |
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 | 327 | 369 | 86 | 64 | 176 | 8 | 33 | 136 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0002 | 0/0 | 327 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 984 | 367 | 86 | 63 | 175 | 8 | 33 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
c0002 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
c0003 | 0/0 | 984 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
c0004 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3230 | 91 | 6 | 16 | 55 | 2 | 12 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0002 | 0/1 | 3228 | 48 | 25 | 3 | 14 | 0 | 5 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0003 | 1/0 | 3229 | 45 | 2 | 14 | 22 | 2 | 4 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0004 | 0/0 | 3227 | 42 | 0 | 5 | 34 | 0 | 3 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0005 | 0/0 | 3225 | 29 | 1 | 8 | 15 | 0 | 5 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0006 | 0/0 | 3225 | 19 | 0 | 1 | 18 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0007 | 0/0 | 3229 | 14 | 10 | 0 | 3 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0008 | 0/0 | 3221 | 9 | 1 | 4 | 0 | 2 | 2 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0009 | 0/0 | 3221 | 9 | 7 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0010 | 0/0 | 3229 | 6 | 0 | 0 | 5 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0011 | 0/0 | 3227 | 5 | 4 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0012 | 0/0 | 3231 | 5 | 5 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0013 | 0/0 | 3232 | 4 | 4 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0014 | 0/0 | 3230 | 3 | 0 | 3 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0015 | 0/0 | 3229 | 3 | 3 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0016 | 0/0 | 3228 | 3 | 0 | 2 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0017 | 0/0 | 3226 | 3 | 3 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0018 | 0/0 | 3230 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0019 | 0/0 | 3230 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0020 | 0/0 | 3230 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0021 | 0/0 | 3230 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0022 | 0/0 | 3228 | 2 | 0 | 1 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0023 | 0/0 | 3224 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0024 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0025 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0026 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0027 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0028 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0029 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0030 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0031 | 0/0 | 3227 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0032 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0033 | 0/0 | 3233 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0034 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0035 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0036 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0037 | 0/0 | 3220 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0038 | 0/0 | 3221 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0039 | 0/0 | 3221 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0040 | 0/0 | 3224 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0041 | 0/0 | 3224 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
t0042 | 0/0 | 3224 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 984 | 367 | 86 | 63 | 175 | 8 | 33 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0002 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0004 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0002c0003 | 0/0 | 984 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4213 | 90 | 6 | 16 | 55 | 2 | 11 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0002 | 0/1 | 4211 | 47 | 25 | 3 | 13 | 0 | 5 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0003 | 1/0 | 4212 | 45 | 2 | 14 | 22 | 2 | 4 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0004 | 0/0 | 4210 | 41 | 0 | 4 | 34 | 0 | 3 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0005 | 0/0 | 4208 | 29 | 1 | 8 | 15 | 0 | 5 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0006 | 0/0 | 4208 | 19 | 0 | 1 | 18 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0007 | 0/0 | 4212 | 14 | 10 | 0 | 3 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0008 | 0/0 | 4204 | 9 | 1 | 4 | 0 | 2 | 2 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0009 | 0/0 | 4204 | 9 | 7 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0010 | 0/0 | 4212 | 6 | 0 | 0 | 5 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0011 | 0/0 | 4210 | 5 | 4 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0012 | 0/0 | 4214 | 5 | 5 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0013 | 0/0 | 4215 | 4 | 4 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0014 | 0/0 | 4213 | 3 | 0 | 3 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0015 | 0/0 | 4212 | 3 | 3 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0016 | 0/0 | 4211 | 3 | 0 | 2 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0017 | 0/0 | 4209 | 3 | 3 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0018 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0019 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0020 | 0/0 | 4213 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0021 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0022 | 0/0 | 4211 | 2 | 0 | 1 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0023 | 0/0 | 4207 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0024 | 0/0 | 4208 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0025 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0026 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0027 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0028 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0029 | 0/0 | 4212 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0030 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0031 | 0/0 | 4210 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0032 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0033 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0034 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0035 | 0/0 | 4214 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0036 | 0/0 | 4205 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0037 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0038 | 0/0 | 4204 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0039 | 0/0 | 4204 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0040 | 0/0 | 4207 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0041 | 0/0 | 4207 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0001t0042 | 0/0 | 4207 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0002t0002 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0001c0004t0004 | 0/0 | 4210 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
a0002c0003t0001 | 0/0 | 4213 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | copy fasta | chr18 | 35036413 | 35148470 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0008g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0010g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0010g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0010g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0011g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0011g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0012g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0014g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0014g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0014g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0016g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0016g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0017g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0017g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0018g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0020g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0020g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0021g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0021g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0022g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0022g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0023g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0023g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0024g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0024g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0025g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0026g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0027g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0028g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0029g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0030g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0031g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0032g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0033g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0036g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0037g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0038g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0039g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0040g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0041g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0001t0042g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0001c0004t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0029 | g0144 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00280 | hp2 | a0001 | c0001 | t0008 | g0114 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0138 | EUR | FIN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00408 | hp1 | a0001 | c0001 | t0040 | g0185 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00621 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | CHS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0149 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0248 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01069 | hp2 | a0001 | c0001 | t0016 | g0277 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01070 | hp2 | a0001 | c0001 | t0037 | g0331 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01081 | hp1 | a0001 | c0001 | t0020 | g0319 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01106 | hp1 | a0001 | c0001 | t0020 | g0317 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01167 | hp1 | a0001 | c0001 | t0022 | g0061 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0259 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01255 | hp2 | a0001 | c0001 | t0011 | g0038 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01346 | hp1 | a0001 | c0004 | t0004 | g0089 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0286 | EUR | IBS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0008 | EUR | IBS | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0054 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01928 | hp1 | a0001 | c0001 | t0014 | g0320 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0173 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01934 | hp2 | a0001 | c0001 | t0014 | g0318 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01943 | hp1 | a0001 | c0001 | t0026 | g0340 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0197 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0123 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0175 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02015 | hp1 | a0001 | c0001 | t0027 | g0029 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02040 | hp1 | a0001 | c0001 | t0030 | g0299 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | CDX | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02258 | hp1 | a0001 | c0001 | t0042 | g0109 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0224 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0210 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02300 | hp2 | a0001 | c0001 | t0014 | g0323 | AMR | PEL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02523 | hp2 | a0001 | c0001 | t0032 | g0121 | EAS | KHV | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02615 | hp2 | a0001 | c0001 | t0018 | g0253 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0053 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0261 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02630 | hp1 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02647 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02717 | hp1 | a0001 | c0001 | t0019 | g0207 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0212 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0202 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0148 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0231 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0150 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0230 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0242 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02922 | hp2 | a0001 | c0001 | t0015 | g0262 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02965 | hp2 | a0001 | c0001 | t0021 | g0102 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0243 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03041 | hp1 | a0001 | c0001 | t0039 | g0250 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03041 | hp2 | a0001 | c0001 | t0017 | g0181 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0351 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03098 | hp2 | a0001 | c0001 | t0017 | g0203 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03130 | hp1 | a0001 | c0001 | t0035 | g0208 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0232 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0179 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0216 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03209 | hp1 | a0001 | c0001 | t0024 | g0238 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03209 | hp2 | a0001 | c0001 | t0028 | g0260 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03225 | hp1 | a0001 | c0001 | t0033 | g0218 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03239 | hp2 | a0001 | c0001 | t0038 | g0338 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0229 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03486 | hp1 | a0001 | c0001 | t0018 | g0247 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0206 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0052 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0226 | AFR | ESN | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03579 | hp2 | a0001 | c0001 | t0013 | g0205 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0063 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0133 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03942 | hp2 | a0001 | c0001 | t0007 | g0032 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0167 | SAS | BEB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0309 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04204 | hp1 | a0001 | c0001 | t0036 | g0122 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | STU | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18522 | hp1 | a0001 | c0001 | t0015 | g0240 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | CHB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18906 | hp1 | a0001 | c0001 | t0019 | g0215 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0244 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18957 | hp1 | a0001 | c0001 | t0016 | g0146 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0284 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18959 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18960 | hp1 | a0001 | c0001 | t0041 | g0157 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18963 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18967 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18969 | hp1 | a0001 | c0001 | t0010 | g0294 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18969 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18987 | hp2 | a0001 | c0001 | t0010 | g0274 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18988 | hp2 | a0001 | c0001 | t0022 | g0131 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18997 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA18999 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19001 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19002 | hp2 | a0001 | c0001 | t0031 | g0077 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19004 | hp2 | a0001 | c0001 | t0010 | g0314 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0246 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0211 | AFR | LWK | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19055 | hp1 | a0001 | c0001 | t0023 | g0012 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19058 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19060 | hp2 | a0001 | c0001 | t0010 | g0311 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19070 | hp2 | a0001 | c0001 | t0023 | g0170 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19076 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19079 | hp1 | a0001 | c0001 | t0006 | g0263 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19084 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19091 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19240 | hp1 | a0001 | c0001 | t0021 | g0057 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA20129 | hp1 | a0001 | c0001 | t0024 | g0239 | AFR | ASW | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ASW | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0124 | EUR | TSI | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0156 | SAS | GIH | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | GIH | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG01123 | hp2 | a0001 | c0001 | t0016 | g0128 | AMR | CLM | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02109 | hp1 | a0001 | c0001 | t0025 | g0020 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0119 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0249 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0209 | AFR | MSL | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0222 | REF | REF | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0154 | REF | REF | MAPRE2_chr18_35036413_35148470 | MAPRE2 | chr18 | 35036413 | 35148470 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35132062
|
G | A | 1 | a0002 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.781G>A | p.Val261Met | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/7 | 908/4212 | 781/984 | 261/327 | chr18 | 35132062 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35102038
|
T | C | 1 | a0001c0002 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.489T>C | p.Asp163Asp | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/7 | 616/4212 | 489/984 | 163/327 | chr18 | 35102038 | ||
chr18:35140351
|
G | A | 1 | a0001c0004 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.966G>A | p.Pro322Pro | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1093/4212 | 966/984 | 322/327 | chr18 | 35140351 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35140395
|
C | T | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(11): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 26 | chr18 | 35140395 | |||||
chr18:35140412
|
G | A | 1 | a0001c0001t0025 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 43 | chr18 | 35140412 | |||||
chr18:35140578
|
G | A | 4 | a0001c0001t0008a0001c0001t0036a0001c0001t0037others(1): Show | 12 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*209G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 209 | chr18 | 35140578 | |||||
chr18:35140889
|
G | A | 1 | a0001c0001t0018 | 2 | HG02615.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 520 | chr18 | 35140889 | |||||
chr18:35141114
|
C | T | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(11): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*745C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 745 | chr18 | 35141114 | |||||
chr18:35141134
|
C | G | 6 | a0001c0001t0012a0001c0001t0013a0001c0001t0025others(3): Show | 13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*765C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 765 | chr18 | 35141134 | |||||
chr18:35141149
|
G | T | 1 | a0001c0001t0032 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*780G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 780 | chr18 | 35141149 | |||||
chr18:35141226
|
G | A | 6 | a0001c0001t0012a0001c0001t0013a0001c0001t0025others(3): Show | 13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*857G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 857 | chr18 | 35141226 | |||||
chr18:35141362
|
A | T | 6 | a0001c0001t0012a0001c0001t0013a0001c0001t0025others(3): Show | 13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*993A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 993 | chr18 | 35141362 | |||||
chr18:35141438
|
G | A | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(10): Show | 79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1069 | chr18 | 35141438 | |||||
chr18:35141564
|
A | C | 1 | a0001c0001t0031 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1195A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1195 | chr18 | 35141564 | |||||
chr18:35141627
|
T | TTTC | 6 | a0001c0001t0012a0001c0001t0013a0001c0001t0025others(3): Show | 13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1261_*1263dupCTT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1264 | INFO_REALIGN_3_PRIME | chr18 | 35141627 | ||||
chr18:35141661
|
TTTTC | T | 6 | a0001c0001t0008a0001c0001t0009a0001c0001t0036others(3): Show | 22 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1296_*1299delCTTT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1296 | INFO_REALIGN_3_PRIME | chr18 | 35141661 | ||||
chr18:35141759
|
T | G | 1 | a0001c0001t0019 | 2 | HG02717.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1390T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1390 | chr18 | 35141759 | |||||
chr18:35141797
|
T | C | 2 | a0001c0001t0006a0001c0001t0023 | 21 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1428T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1428 | chr18 | 35141797 | |||||
chr18:35141942
|
AAAAT | A | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(11): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1578_*1581delAAAT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1578 | INFO_REALIGN_3_PRIME | chr18 | 35141942 | ||||
chr18:35141987
|
A | T | 4 | a0001c0001t0004a0001c0001t0022a0001c0001t0031others(1): Show | 45 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1618A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1618 | chr18 | 35141987 | |||||
chr18:35142069
|
C | A | 1 | a0001c0001t0020 | 2 | HG01081.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1700 | chr18 | 35142069 | |||||
chr18:35142118
|
G | A | 2 | a0001c0001t0014a0001c0001t0026 | 4 | HG01928.hp1 HG01934.hp2 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1749 | chr18 | 35142118 | |||||
chr18:35142148
|
T | C | 1 | a0001c0001t0039 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1779 | chr18 | 35142148 | |||||
chr18:35142190
|
C | A | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(11): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1821C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 1821 | chr18 | 35142190 | |||||
chr18:35142697
|
C | T | 1 | a0001c0001t0035 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2328C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2328 | chr18 | 35142697 | |||||
chr18:35142849
|
G | C | 32 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(29): Show | 212 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2480G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2480 | chr18 | 35142849 | |||||
chr18:35142904
|
A | G | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 319 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*2535A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2535 | chr18 | 35142904 | |||||
chr18:35142905
|
T | G | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 319 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*2536T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2536 | chr18 | 35142905 | |||||
chr18:35142953
|
A | C | 16 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(13): Show | 84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2584A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2584 | chr18 | 35142953 | |||||
chr18:35142959
|
C | G | 1 | a0001c0001t0038 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2590C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2590 | chr18 | 35142959 | |||||
chr18:35143071
|
G | GA | 10 | a0001c0001t0001a0001c0001t0014a0001c0001t0017others(7): Show | 107 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2720dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2721 | INFO_REALIGN_3_PRIME | chr18 | 35143071 | ||||
chr18:35143071
|
GA | G | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(13): Show | 109 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2720delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2720 | INFO_REALIGN_3_PRIME | chr18 | 35143071 | ||||
chr18:35143086
|
A | G | 2 | a0001c0001t0024a0001c0001t0042 | 3 | HG02258.hp1 HG03209.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2717A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 2717 | chr18 | 35143086 | |||||
chr18:35143377
|
A | G | 1 | a0001c0001t0029 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3008A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 3008 | chr18 | 35143377 | |||||
chr18:35143447
|
TA | T | 8 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(5): Show | 57 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3088delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 7/7 | 3088 | INFO_REALIGN_3_PRIME | chr18 | 35143447 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35041922
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.122+261G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35041922 | ||||||
chr18:35042204
|
G | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(38): Show | 44 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.122+543G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042204 | ||||||
chr18:35042230
|
T | G | 48 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(45): Show | 50 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.122+569T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042230 | ||||||
chr18:35042400
|
G | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18945.hp1 NA18977.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+739G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042400 | ||||||
chr18:35042485
|
A | G | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122+824A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042485 | ||||||
chr18:35042730
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122+1069C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042730 | ||||||
chr18:35042824
|
G | A | 1 | a0001c0001t0021g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122+1163G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042824 | ||||||
chr18:35042879
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+1218C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35042879 | ||||||
chr18:35042924
|
CA | C | 257 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(254): Show | 264 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.122+1276delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35042924 | |||||
chr18:35042924
|
CAA | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(35): Show | 41 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.122+1275_122+1276d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35042924 | |||||
chr18:35043008
|
A | G | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.122+1347A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043008 | ||||||
chr18:35043017
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0002g0101 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.122+1356C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043017 | ||||||
chr18:35043380
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(249): Show | 260 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.122+1719C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043380 | ||||||
chr18:35043491
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.122+1830T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043491 | ||||||
chr18:35043600
|
A | G | 1 | a0001c0001t0001g0350 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.122+1939A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043600 | ||||||
chr18:35043635
|
G | T | 96 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 97 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(94): Show |
intron_variant | MODIFIER | c.122+1974G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35043635 | ||||||
chr18:35044090
|
G | T | 1 | a0001c0001t0006g0263 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.122+2429G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044090 | ||||||
chr18:35044176
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0002g0101 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.122+2515G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044176 | ||||||
chr18:35044239
|
T | C | 1 | a0001c0001t0003g0108 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+2578T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044239 | ||||||
chr18:35044294
|
A | C | 4 | a0001c0001t0009g0259a0001c0001t0015g0261a0001c0001t0015g0262others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+2633A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044294 | ||||||
chr18:35044597
|
T | C | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122+2936T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044597 | ||||||
chr18:35044703
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(295): Show | 308 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.122+3042A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044703 | ||||||
chr18:35044845
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(84): Show | 92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.122+3184T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044845 | ||||||
chr18:35044865
|
A | C | 27 | a0001c0001t0001g0255a0001c0001t0002g0014a0001c0001t0002g0237others(24): Show | 28 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+3204A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044865 | ||||||
chr18:35044895
|
C | G | 4 | a0001c0001t0001g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+3234C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044895 | ||||||
chr18:35044962
|
T | C | 77 | a0001c0001t0001g0172a0001c0001t0001g0255a0001c0001t0002g0014others(74): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.122+3301T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35044962 | ||||||
chr18:35045197
|
C | T | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.122+3536C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045197 | ||||||
chr18:35045433
|
T | G | 3 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112 | 3 | NA18987.hp1 NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.122+3772T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045433 | ||||||
chr18:35045443
|
T | TA | 87 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(84): Show | 92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.122+3782_122+3783i others(3): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045443 | ||||||
chr18:35045444
|
T | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(84): Show | 92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.122+3783T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045444 | ||||||
chr18:35045444
|
T | TA | 117 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(114): Show | 119 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.122+3794dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35045444 | |||||
chr18:35045542
|
G | C | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122+3881G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045542 | ||||||
chr18:35045650
|
G | A | 3 | a0001c0001t0007g0019a0001c0001t0013g0018a0001c0001t0025g0020 | 3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+3989G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045650 | ||||||
chr18:35045752
|
A | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0221a0001c0001t0002g0222 | 4 | HG00642.hp1 HG01099.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+4091A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045752 | ||||||
chr18:35045919
|
C | A | 1 | a0001c0001t0006g0161 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.122+4258C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35045919 | ||||||
chr18:35046618
|
A | G | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.122+4957A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046618 | ||||||
chr18:35046682
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(39): Show | 45 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.122+5021A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046682 | ||||||
chr18:35046770
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.122+5109G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046770 | ||||||
chr18:35046860
|
C | A | 2 | a0001c0001t0001g0223a0001c0001t0007g0224 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.122+5199C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35046860 | ||||||
chr18:35047002
|
G | A | 3 | a0001c0001t0007g0019a0001c0001t0013g0018a0001c0001t0025g0020 | 3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+5341G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047002 | ||||||
chr18:35047013
|
T | C | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+5352T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047013 | ||||||
chr18:35047030
|
T | C | 3 | a0001c0001t0007g0019a0001c0001t0013g0018a0001c0001t0025g0020 | 3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+5369T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047030 | ||||||
chr18:35047050
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(194): Show | 203 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.122+5389G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047050 | ||||||
chr18:35047126
|
A | T | 44 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0002g0101others(41): Show | 46 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.122+5465A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047126 | ||||||
chr18:35047415
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(79): Show | 87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.122+5754T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047415 | ||||||
chr18:35047524
|
A | G | 119 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(116): Show | 121 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.122+5863A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047524 | ||||||
chr18:35047621
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+5960A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047621 | ||||||
chr18:35047716
|
T | TA | 110 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(107): Show | 116 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.122+6071dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35047716 | |||||
chr18:35047716
|
T | TAA | 94 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(91): Show | 95 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(92): Show |
intron_variant | MODIFIER | c.122+6070_122+6071d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35047716 | |||||
chr18:35047902
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.122+6241A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35047902 | ||||||
chr18:35048095
|
C | G | 2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+6434C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048095 | ||||||
chr18:35048147
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122+6486C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048147 | ||||||
chr18:35048148
|
G | A | 3 | a0001c0001t0007g0019a0001c0001t0013g0018a0001c0001t0025g0020 | 3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+6487G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048148 | ||||||
chr18:35048428
|
G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+6767G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048428 | ||||||
chr18:35048514
|
A | G | 3 | a0001c0001t0007g0019a0001c0001t0013g0018a0001c0001t0025g0020 | 3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+6853A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048514 | ||||||
chr18:35048555
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(37): Show | 43 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.122+6894A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048555 | ||||||
chr18:35048603
|
T | C | 352 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(349): Show | 369 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.122+6942T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048603 | ||||||
chr18:35048671
|
A | C | 1 | a0001c0001t0003g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.122+7010A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048671 | ||||||
chr18:35048681
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(23): Show | 29 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.122+7020G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048681 | ||||||
chr18:35048699
|
A | G | 44 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0002g0101others(41): Show | 46 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.122+7038A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35048699 | ||||||
chr18:35049325
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.122+7664G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049325 | ||||||
chr18:35049628
|
C | G | 3 | a0001c0001t0033g0218a0001c0001t0034g0219a0001c0001t0035g0208 | 3 | HG02630.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+7967C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049628 | ||||||
chr18:35049633
|
C | T | 3 | a0001c0001t0005g0217a0001c0001t0009g0216a0001c0001t0019g0215 | 3 | HG03195.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.122+7972C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049633 | ||||||
chr18:35049809
|
G | A | 3 | a0001c0001t0033g0218a0001c0001t0034g0219a0001c0001t0035g0208 | 3 | HG02630.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+8148G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049809 | ||||||
chr18:35049858
|
C | T | 109 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0099others(106): Show | 110 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.122+8197C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049858 | ||||||
chr18:35049865
|
A | C | 6 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(3): Show | 6 | HG02080.hp1 NA18944.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+8204A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049865 | ||||||
chr18:35049939
|
C | T | 1 | a0001c0001t0037g0331 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.122+8278C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35049939 | ||||||
chr18:35050121
|
G | A | 1 | a0001c0001t0008g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.122+8460G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050121 | ||||||
chr18:35050380
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+8719A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050380 | ||||||
chr18:35050429
|
C | T | 27 | a0001c0001t0001g0255a0001c0001t0002g0014a0001c0001t0002g0237others(24): Show | 28 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+8768C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050429 | ||||||
chr18:35050500
|
T | C | 45 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0002g0101others(42): Show | 47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.122+8839T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050500 | ||||||
chr18:35050663
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.122+9002G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050663 | ||||||
chr18:35050796
|
C | G | 1 | a0001c0001t0002g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122+9135C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35050796 | ||||||
chr18:35051013
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.122+9352C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051013 | ||||||
chr18:35051606
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122+9945A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051606 | ||||||
chr18:35051658
|
G | A | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+9997G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051658 | ||||||
chr18:35051752
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(228): Show | 239 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.122+10091C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051752 | ||||||
chr18:35051859
|
C | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+10198C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051859 | ||||||
chr18:35051860
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.122+10199G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051860 | ||||||
chr18:35051891
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(228): Show | 239 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.122+10230A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051891 | ||||||
chr18:35051909
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(228): Show | 239 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.122+10248G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051909 | ||||||
chr18:35051916
|
G | A | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+10255G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35051916 | ||||||
chr18:35052035
|
A | G | 6 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+10374A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052035 | ||||||
chr18:35052057
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(235): Show | 246 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.122+10396C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052057 | ||||||
chr18:35052236
|
T | C | 45 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0002g0101others(42): Show | 47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.122+10575T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052236 | ||||||
chr18:35052279
|
A | G | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+10618A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052279 | ||||||
chr18:35052296
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.122+10635A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052296 | ||||||
chr18:35052379
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.122+10718A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052379 | ||||||
chr18:35052609
|
G | A | 78 | a0001c0001t0001g0172a0001c0001t0001g0255a0001c0001t0002g0014others(75): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+10948G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052609 | ||||||
chr18:35052782
|
A | G | 85 | a0001c0001t0001g0015a0001c0001t0001g0172a0001c0001t0001g0255others(82): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.122+11121A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052782 | ||||||
chr18:35052826
|
C | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 147 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.122+11165C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35052826 | ||||||
chr18:35053008
|
C | CCA | 55 | a0001c0001t0001g0015a0001c0001t0001g0172a0001c0001t0001g0344others(52): Show | 58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.122+11360_122+1136 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053008 | |||||
chr18:35053008
|
CCA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(134): Show | 141 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.122+11360_122+1136 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053008 | |||||
chr18:35053009
|
CA | C | 4 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0002g0222others(1): Show | 4 | HG03831.hp2 NA18975.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+11349delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053009 | ||||||
chr18:35053010
|
A | C | 3 | a0001c0001t0002g0252a0001c0001t0007g0224a0001c0001t0018g0253 | 3 | HG02258.hp2 HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.122+11349A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053010 | ||||||
chr18:35053012
|
A | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(134): Show | 141 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.122+11351A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053012 | ||||||
chr18:35053012
|
A | G | 1 | a0001c0001t0005g0156 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.122+11351A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053012 | ||||||
chr18:35053014
|
A | C | 99 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0099others(96): Show | 100 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.122+11353A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053014 | ||||||
chr18:35053107
|
A | G | 1 | a0001c0001t0001g0001 | 3 | NA18952.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.122+11446A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053107 | ||||||
chr18:35053588
|
A | G | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+11927A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053588 | ||||||
chr18:35053611
|
G | GT | 4 | a0001c0001t0002g0022a0001c0001t0002g0042a0001c0001t0002g0043others(1): Show | 4 | HG02735.hp2 HG03492.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+11951dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053611 | |||||
chr18:35053634
|
A | G | 1 | a0001c0001t0012g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.122+11973A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053634 | ||||||
chr18:35053797
|
T | TA | 3 | a0001c0001t0007g0019a0001c0001t0013g0018a0001c0001t0025g0020 | 3 | HG02109.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.122+12137dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35053797 | |||||
chr18:35053921
|
T | C | 1 | a0001c0001t0005g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.122+12260T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35053921 | ||||||
chr18:35054032
|
C | T | 3 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0342 | 3 | NA18997.hp1 NA19076.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.122+12371C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054032 | ||||||
chr18:35054051
|
C | A | 1 | a0001c0001t0004g0059 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.122+12390C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054051 | ||||||
chr18:35054191
|
A | T | 1 | a0001c0001t0003g0152 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.122+12530A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054191 | ||||||
chr18:35054336
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122+12675A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054336 | ||||||
chr18:35054449
|
T | G | 3 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236 | 3 | HG02886.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.122+12788T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054449 | ||||||
chr18:35054613
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+12952C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054613 | ||||||
chr18:35054670
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(288): Show | 301 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.122+13009A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054670 | ||||||
chr18:35054877
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+13216G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35054877 | ||||||
chr18:35055108
|
G | A | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+13447G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055108 | ||||||
chr18:35055162
|
C | T | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122+13501C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055162 | ||||||
chr18:35055362
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.122+13701C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055362 | ||||||
chr18:35055537
|
C | CTCTG | 4 | a0001c0001t0002g0103a0001c0001t0013g0205a0001c0001t0013g0206others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+13877_122+1387 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTCTGTGT others(7): Show |
1 | a0001c0001t0022g0061 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.122+13877_122+1387 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTG | 5 | a0001c0001t0007g0229a0001c0001t0008g0148a0001c0001t0008g0149others(2): Show | 5 | HG00735.hp1 HG02258.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+13902_122+1390 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTG | 5 | a0001c0001t0002g0009a0001c0001t0007g0230a0001c0001t0012g0231others(2): Show | 6 | HG02559.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+13900_122+1390 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTG | 4 | a0001c0001t0001g0270a0001c0001t0004g0062a0001c0001t0004g0063others(1): Show | 4 | HG01433.hp2 HG03927.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+13898_122+1390 others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(1): Show |
12 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0332others(9): Show | 12 | HG02080.hp1 HG03139.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+13896_122+1390 others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(3): Show |
108 | a0001c0001t0001g0015a0001c0001t0001g0104a0001c0001t0001g0158others(105): Show | 112 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.122+13894_122+1390 others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(5): Show |
72 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0098others(69): Show | 75 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.122+13892_122+1390 others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(7): Show |
11 | a0001c0001t0001g0322a0001c0001t0003g0321a0001c0001t0004g0097others(8): Show | 11 | HG01081.hp1 HG01106.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+13890_122+1390 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(9): Show |
5 | a0001c0001t0003g0324a0001c0001t0005g0204a0001c0001t0009g0245others(2): Show | 5 | HG02300.hp2 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+13888_122+1390 others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(11): Show |
5 | a0001c0001t0009g0246a0001c0001t0009g0248a0001c0001t0009g0249others(2): Show | 5 | HG00735.hp2 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+13886_122+1390 others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(13): Show |
1 | a0001c0001t0039g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+13884_122+1390 others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055537
|
C | CTGTGTGT others(19): Show |
1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.122+13878_122+1390 others(30): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055537 | |||||
chr18:35055539
|
G | C | 3 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0033g0218 | 3 | HG02280.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.122+13878G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055539 | ||||||
chr18:35055563
|
G | GTGTA | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | |||||
chr18:35055563
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0002g0023a0001c0001t0007g0024 | 2 | NA18948.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.122+13903_122+1390 others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | |||||
chr18:35055563
|
G | GTGTGTGT others(5): Show |
15 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(12): Show | 15 | HG00423.hp1 HG02040.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | |||||
chr18:35055563
|
G | GTGTGTGT others(7): Show |
4 | a0001c0001t0001g0316a0001c0001t0002g0027a0001c0001t0007g0019others(1): Show | 4 | HG02109.hp1 HG03540.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | |||||
chr18:35055563
|
G | GTGTGTGT others(9): Show |
27 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(24): Show | 30 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.122+13903_122+1390 others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | |||||
chr18:35055563
|
G | GTGTGTGT others(11): Show |
2 | a0001c0001t0002g0022a0001c0001t0002g0041 | 2 | HG02056.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.122+13903_122+1390 others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055563 | |||||
chr18:35055565
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(70): Show | 76 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.122+13904A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055565 | ||||||
chr18:35055690
|
C | T | 4 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(1): Show | 4 | HG02280.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+14029C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055690 | ||||||
chr18:35055901
|
G | T | 2 | a0001c0001t0004g0067a0001c0001t0004g0096 | 2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.122+14240G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35055901 | ||||||
chr18:35055955
|
C | CA | 43 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(40): Show | 47 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.123-14224dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35055955 | |||||
chr18:35056078
|
AT | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(82): Show | 90 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.123-14110delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35056078 | |||||
chr18:35056213
|
A | C | 1 | a0001c0001t0009g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-13982A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056213 | ||||||
chr18:35056254
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.123-13941A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056254 | ||||||
chr18:35056444
|
A | G | 9 | a0001c0001t0002g0103a0001c0001t0012g0209a0001c0001t0012g0210others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-13751A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056444 | ||||||
chr18:35056528
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(89): Show | 98 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.123-13667C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056528 | ||||||
chr18:35056621
|
ATCTAC | A | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-13569_123-1356 others(9): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35056621 | |||||
chr18:35056734
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(87): Show | 96 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.123-13461T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056734 | ||||||
chr18:35056781
|
G | T | 1 | a0001c0001t0009g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.123-13414G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056781 | ||||||
chr18:35056895
|
G | A | 1 | a0001c0001t0012g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123-13300G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35056895 | ||||||
chr18:35057063
|
G | T | 2 | a0001c0001t0001g0223a0001c0001t0007g0224 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.123-13132G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057063 | ||||||
chr18:35057073
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(264): Show | 277 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.123-13122G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057073 | ||||||
chr18:35057102
|
C | T | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-13093C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057102 | ||||||
chr18:35057171
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(274): Show | 287 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.123-13024T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057171 | ||||||
chr18:35057305
|
A | C | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.123-12890A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057305 | ||||||
chr18:35057334
|
G | T | 9 | a0001c0001t0002g0103a0001c0001t0012g0209a0001c0001t0012g0210others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-12861G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057334 | ||||||
chr18:35057507
|
C | CGT | 9 | a0001c0001t0001g0273a0001c0001t0002g0220a0001c0001t0002g0234others(6): Show | 9 | HG01109.hp1 HG02615.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-12665_123-1266 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGT | 64 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0172others(61): Show | 64 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.123-12667_123-1266 others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGT | 50 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(47): Show | 50 | HG00323.hp1 HG01070.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.123-12669_123-1266 others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(1): Show |
30 | a0001c0001t0002g0014a0001c0001t0002g0103a0001c0001t0002g0225others(27): Show | 33 | HG00735.hp2 HG01255.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.123-12671_123-1266 others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(3): Show |
42 | a0001c0001t0001g0028a0001c0001t0002g0013a0001c0001t0002g0221others(39): Show | 43 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.123-12673_123-1266 others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(5): Show |
19 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0344others(16): Show | 20 | HG01099.hp2 HG01496.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-12675_123-1266 others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(7): Show |
27 | a0001c0001t0001g0100a0001c0001t0001g0159a0001c0001t0001g0349others(24): Show | 28 | HG00558.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-12677_123-1266 others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(9): Show |
10 | a0001c0001t0001g0160a0001c0001t0002g0043a0001c0001t0002g0044others(7): Show | 10 | HG01168.hp2 HG01255.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-12679_123-1266 others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(11): Show |
9 | a0001c0001t0001g0098a0001c0001t0002g0050a0001c0001t0002g0056others(6): Show | 9 | HG00558.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-12681_123-1266 others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(13): Show |
8 | a0001c0001t0001g0001a0001c0001t0004g0062a0001c0001t0004g0063others(5): Show | 10 | HG02155.hp2 HG03927.hp2 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-12683_123-1266 others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(15): Show |
24 | a0001c0001t0004g0002a0001c0001t0004g0059a0001c0001t0004g0060others(21): Show | 26 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.123-12685_123-1266 others(26): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(17): Show |
1 | a0001c0001t0004g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.123-12687_123-1266 others(28): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
C | CGTGTGTG others(19): Show |
1 | a0001c0001t0004g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.123-12664_123-1266 others(30): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057507
|
CGT | C | 4 | a0001c0001t0003g0115a0001c0001t0003g0151a0001c0001t0003g0152others(1): Show | 4 | HG01074.hp2 HG01433.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12665_123-1266 others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35057507 | |||||
chr18:35057654
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-12541A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057654 | ||||||
chr18:35057672
|
G | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-12523G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057672 | ||||||
chr18:35057827
|
C | T | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(1): Show | 4 | HG02080.hp1 NA18944.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12368C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057827 | ||||||
chr18:35057837
|
C | T | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-12358C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057837 | ||||||
chr18:35057975
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(264): Show | 277 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.123-12220G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35057975 | ||||||
chr18:35058080
|
A | G | 1 | a0001c0001t0006g0198 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.123-12115A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058080 | ||||||
chr18:35058144
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.123-12051A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058144 | ||||||
chr18:35058269
|
C | A | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-11926C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058269 | ||||||
chr18:35058373
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123-11822C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058373 | ||||||
chr18:35058395
|
G | T | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-11800G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058395 | ||||||
chr18:35058397
|
G | A | 3 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0342 | 3 | NA18997.hp1 NA19076.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.123-11798G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058397 | ||||||
chr18:35058555
|
G | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-11640G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058555 | ||||||
chr18:35058564
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(298): Show | 312 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.123-11631T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058564 | ||||||
chr18:35058797
|
CT | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(264): Show | 277 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.123-11395delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35058797 | |||||
chr18:35058830
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123-11365G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058830 | ||||||
chr18:35058866
|
A | G | 10 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-11329A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058866 | ||||||
chr18:35058888
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(264): Show | 277 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.123-11307C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35058888 | ||||||
chr18:35059042
|
GATTAA | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(79): Show | 87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.123-11146_123-1114 others(9): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35059042 | |||||
chr18:35059075
|
A | G | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-11120A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059075 | ||||||
chr18:35059109
|
T | C | 9 | a0001c0001t0002g0103a0001c0001t0012g0209a0001c0001t0012g0210others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-11086T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059109 | ||||||
chr18:35059323
|
TA | T | 20 | a0001c0001t0001g0313a0001c0001t0001g0315a0001c0001t0001g0326others(17): Show | 20 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-10859delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35059323 | |||||
chr18:35059396
|
A | G | 1 | a0001c0001t0003g0321 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.123-10799A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059396 | ||||||
chr18:35059407
|
G | C | 4 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336others(1): Show | 4 | HG02080.hp1 NA18944.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-10788G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059407 | ||||||
chr18:35059541
|
A | G | 1 | a0001c0001t0012g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.123-10654A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059541 | ||||||
chr18:35059687
|
T | G | 1 | a0001c0001t0004g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.123-10508T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059687 | ||||||
chr18:35059689
|
A | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-10506A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059689 | ||||||
chr18:35059749
|
A | T | 1 | a0001c0001t0039g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123-10446A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059749 | ||||||
chr18:35059766
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123-10429A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059766 | ||||||
chr18:35059801
|
G | A | 1 | a0001c0001t0004g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.123-10394G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059801 | ||||||
chr18:35059810
|
C | T | 1 | a0001c0001t0004g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.123-10385C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059810 | ||||||
chr18:35059911
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.123-10284A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059911 | ||||||
chr18:35059943
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(78): Show | 86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.123-10252A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35059943 | ||||||
chr18:35060023
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-10172G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060023 | ||||||
chr18:35060049
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(273): Show | 286 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(283): Show |
intron_variant | MODIFIER | c.123-10146G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060049 | ||||||
chr18:35060219
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123-9976C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060219 | ||||||
chr18:35060302
|
A | AG | 18 | a0001c0001t0001g0271a0001c0001t0001g0313a0001c0001t0001g0334others(15): Show | 18 | HG00735.hp2 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.123-9888dupG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35060302 | |||||
chr18:35060320
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0098others(78): Show | 86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.123-9875T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060320 | ||||||
chr18:35060841
|
G | C | 91 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0099others(88): Show | 91 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.123-9354G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35060841 | ||||||
chr18:35061001
|
A | C | 9 | a0001c0001t0002g0103a0001c0001t0012g0209a0001c0001t0012g0210others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-9194A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061001 | ||||||
chr18:35061095
|
TC | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(263): Show | 276 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.123-9099delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061095 | ||||||
chr18:35061302
|
T | G | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-8893T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061302 | ||||||
chr18:35061416
|
A | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(349): Show | 369 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.123-8779A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061416 | ||||||
chr18:35061479
|
C | T | 1 | a0001c0001t0005g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-8716C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061479 | ||||||
chr18:35061537
|
A | G | 6 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(3): Show | 6 | HG02280.hp1 HG02723.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-8658A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061537 | ||||||
chr18:35061623
|
T | TGGAGACA others(8): Show |
1 | a0001c0001t0009g0245 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.123-8571_123-8570i others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35061623 | |||||
chr18:35061714
|
C | G | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-8481C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061714 | ||||||
chr18:35061900
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123-8295G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35061900 | ||||||
chr18:35062272
|
A | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0221a0001c0001t0002g0222others(3): Show | 7 | HG00642.hp1 HG01099.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-7923A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062272 | ||||||
chr18:35062473
|
G | A | 1 | a0001c0001t0007g0037 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.123-7722G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062473 | ||||||
chr18:35062488
|
T | C | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-7707T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062488 | ||||||
chr18:35062868
|
A | G | 1 | a0001c0001t0031g0077 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.123-7327A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35062868 | ||||||
chr18:35063080
|
G | A | 3 | a0001c0001t0003g0118a0001c0001t0021g0057a0001c0001t0021g0102 | 3 | HG01106.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-7115G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063080 | ||||||
chr18:35063116
|
T | C | 4 | a0001c0001t0006g0012a0001c0001t0006g0168a0001c0001t0006g0178others(1): Show | 4 | NA18968.hp2 NA19000.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-7079T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063116 | ||||||
chr18:35063125
|
A | T | 1 | a0001c0001t0001g0343 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.123-7070A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063125 | ||||||
chr18:35063143
|
G | T | 70 | a0001c0001t0002g0014a0001c0001t0002g0237a0001c0001t0002g0241others(67): Show | 73 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.123-7052G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063143 | ||||||
chr18:35063165
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(164): Show | 176 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.123-7030G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063165 | ||||||
chr18:35063205
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.123-6990G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063205 | ||||||
chr18:35063251
|
A | C | 78 | a0001c0001t0002g0014a0001c0001t0002g0237a0001c0001t0002g0241others(75): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.123-6944A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063251 | ||||||
chr18:35063253
|
A | G | 78 | a0001c0001t0002g0014a0001c0001t0002g0237a0001c0001t0002g0241others(75): Show | 81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.123-6942A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063253 | ||||||
chr18:35063257
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.123-6938C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063257 | ||||||
chr18:35063260
|
C | T | 2 | a0001c0001t0004g0068a0001c0004t0004g0089 | 2 | HG01168.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.123-6935C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063260 | ||||||
chr18:35063261
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123-6934G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063261 | ||||||
chr18:35063296
|
A | G | 1 | a0001c0001t0005g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123-6899A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063296 | ||||||
chr18:35063297
|
T | C | 4 | a0001c0001t0005g0214a0001c0001t0006g0180a0001c0001t0007g0019others(1): Show | 4 | HG02647.hp1 HG02683.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-6898T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063297 | ||||||
chr18:35063309
|
G | A | 2 | a0001c0001t0017g0181a0001c0001t0017g0203 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.123-6886G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063309 | ||||||
chr18:35063328
|
T | C | 28 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0002g0005others(25): Show | 29 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-6867T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063328 | ||||||
chr18:35063343
|
G | A | 26 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(23): Show | 27 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.123-6852G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063343 | ||||||
chr18:35063360
|
T | A | 1 | a0001c0001t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-6835T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063360 | ||||||
chr18:35063360
|
T | G | 154 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(151): Show | 158 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.123-6835T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063360 | ||||||
chr18:35063386
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-6809C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063386 | ||||||
chr18:35063396
|
T | C | 6 | a0001c0001t0009g0259a0001c0001t0015g0240a0001c0001t0015g0261others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-6799T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063396 | ||||||
chr18:35063402
|
C | T | 5 | a0001c0001t0009g0259a0001c0001t0015g0240a0001c0001t0015g0261others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6793C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063402 | ||||||
chr18:35063428
|
A | G | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-6767A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063428 | ||||||
chr18:35063478
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-6717G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063478 | ||||||
chr18:35063484
|
TA | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(170): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.123-6697delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35063484 | |||||
chr18:35063513
|
C | T | 9 | a0001c0001t0008g0006a0001c0001t0008g0114a0001c0001t0008g0123others(6): Show | 10 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-6682C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063513 | ||||||
chr18:35063525
|
A | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-6670A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063525 | ||||||
chr18:35063616
|
A | G | 9 | a0001c0001t0007g0019a0001c0001t0007g0226a0001c0001t0007g0227others(6): Show | 9 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-6579A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063616 | ||||||
chr18:35063705
|
A | C | 4 | a0001c0001t0004g0059a0001c0001t0004g0066a0001c0001t0004g0070others(1): Show | 4 | NA18956.hp1 NA19066.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-6490A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063705 | ||||||
chr18:35063847
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.123-6348A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063847 | ||||||
chr18:35063856
|
G | C | 2 | a0001c0001t0002g0237a0001c0001t0002g0254 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.123-6339G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063856 | ||||||
chr18:35063980
|
C | G | 3 | a0001c0001t0009g0216a0001c0001t0019g0207a0001c0001t0019g0215 | 3 | HG02717.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.123-6215C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063980 | ||||||
chr18:35063980
|
C | T | 17 | a0001c0001t0002g0005a0001c0001t0002g0023a0001c0001t0002g0025others(14): Show | 18 | HG00558.hp1 HG02027.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-6215C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063980 | ||||||
chr18:35063997
|
CT | C | 4 | a0001c0001t0009g0243a0001c0001t0009g0259a0001c0001t0017g0181others(1): Show | 4 | HG01243.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-6195delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35063997 | |||||
chr18:35063999
|
T | TA | 22 | a0001c0001t0005g0011a0001c0001t0005g0177a0001c0001t0005g0186others(19): Show | 23 | HG00408.hp1 HG00544.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(3): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAA | 27 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0003g0166others(24): Show | 29 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAA | 5 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0001g0347others(2): Show | 5 | HG02647.hp1 HG03540.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAA | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0005g0173 | 3 | HG00642.hp1 HG01928.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.123-6196_123-6195i others(7): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0002g0256 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.123-6196_123-6195i others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0002g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.123-6196_123-6195i others(13): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0344 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.123-6196_123-6195i others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAAAA others(7): Show |
4 | a0001c0001t0002g0014a0001c0001t0002g0237a0001c0001t0002g0241others(1): Show | 5 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6196_123-6195i others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0349a0001c0001t0002g0254 | 2 | HG02451.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.123-6196_123-6195i others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-6196_123-6195i others(19): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTA | T | 14 | a0001c0001t0009g0242a0001c0001t0009g0244a0001c0001t0009g0245others(11): Show | 14 | HG02258.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-6195_123-6194d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTAAAAAA others(1): Show |
T | 14 | a0001c0001t0002g0025a0001c0001t0002g0033a0001c0001t0002g0040others(11): Show | 14 | HG00621.hp2 HG01168.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-6195_123-6188d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTAAAAAA others(2): Show |
T | 64 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(61): Show | 69 | HG00408.hp2 HG00558.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.123-6195_123-6187d others(11): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTAAAAAA others(3): Show |
T | 2 | a0001c0001t0004g0088a0001c0001t0004g0094 | 2 | HG00639.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.123-6195_123-6186d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTAAAAAA others(7): Show |
T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-6195_123-6182d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTAAAAAA others(10): Show |
T | 5 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0009g0216others(2): Show | 5 | HG02717.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-6195_123-6179d others(19): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35063999
|
TTAAAAAA others(11): Show |
T | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123-6195_123-6178d others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35063999 | ||||||
chr18:35064000
|
T | A | 73 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0344others(70): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.123-6195T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064000 | ||||||
chr18:35064000
|
T | TA | 26 | a0001c0001t0001g0159a0001c0001t0001g0223a0001c0001t0001g0325others(23): Show | 29 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-6162dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAA | 13 | a0001c0001t0001g0098a0001c0001t0001g0213a0001c0001t0001g0255others(10): Show | 14 | HG00558.hp2 HG02559.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-6163_123-6162d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAA | 16 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(13): Show | 16 | HG01123.hp1 HG02074.hp2 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.123-6164_123-6162d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(1): Show |
7 | a0001c0001t0001g0266a0001c0001t0001g0283a0001c0001t0001g0310others(4): Show | 7 | HG01168.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-6169_123-6162d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(2): Show |
8 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0281others(5): Show | 8 | HG01192.hp1 HG01243.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-6170_123-6162d others(11): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0280a0001c0001t0001g0333 | 2 | HG03669.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.123-6172_123-6162d others(13): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(5): Show |
10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0270others(7): Show | 10 | HG01167.hp2 HG01433.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-6173_123-6162d others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(6): Show |
13 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0276others(10): Show | 13 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-6174_123-6162d others(15): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(7): Show |
4 | a0001c0001t0001g0172a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG01109.hp2 HG02683.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-6175_123-6162d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(8): Show |
5 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0288others(2): Show | 5 | HG01081.hp1 HG01106.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-6176_123-6162d others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123-6177_123-6162d others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0275 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.123-6178_123-6162d others(19): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.123-6179_123-6162d others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0298a0001c0001t0030g0299 | 2 | HG02040.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.123-6180_123-6162d others(21): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0001g0297 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.123-6181_123-6162d others(22): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0272 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.123-6182_123-6162d others(23): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0337 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123-6184_123-6162d others(25): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
T | TAAAAAAA others(17): Show |
1 | a0001c0001t0001g0296 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.123-6185_123-6162d others(26): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
TA | T | 8 | a0001c0001t0003g0145a0001c0001t0003g0155a0001c0001t0007g0227others(5): Show | 8 | HG01993.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-6162delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
TAAAA | T | 8 | a0001c0001t0002g0103a0001c0001t0003g0286a0001c0001t0012g0209others(5): Show | 8 | HG01517.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-6165_123-6162d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064000
|
TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.123-6175_123-6162d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064000 | |||||
chr18:35064033
|
A | T | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-6162A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064033 | ||||||
chr18:35064150
|
C | T | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-6045C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064150 | ||||||
chr18:35064197
|
CA | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(183): Show | 196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.123-5985delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064197 | |||||
chr18:35064217
|
T | C | 1 | a0001c0001t0003g0007 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.123-5978T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064217 | ||||||
chr18:35064292
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(294): Show | 308 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.123-5903C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064292 | ||||||
chr18:35064361
|
G | C | 14 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(11): Show | 16 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.123-5834G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064361 | ||||||
chr18:35064372
|
G | GA | 179 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(176): Show | 189 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.123-5821dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35064372 | |||||
chr18:35064430
|
G | A | 3 | a0001c0001t0004g0060a0001c0001t0004g0075a0001c0001t0004g0092 | 3 | NA18983.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.123-5765G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064430 | ||||||
chr18:35064496
|
A | G | 1 | a0001c0001t0003g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-5699A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064496 | ||||||
chr18:35064527
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(176): Show | 189 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.123-5668A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064527 | ||||||
chr18:35064562
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(176): Show | 189 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.123-5633A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064562 | ||||||
chr18:35064624
|
C | T | 347 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(344): Show | 364 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(361): Show |
intron_variant | MODIFIER | c.123-5571C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35064624 | ||||||
chr18:35065222
|
A | G | 1 | a0001c0001t0029g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.123-4973A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065222 | ||||||
chr18:35065276
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0041g0157 | 2 | HG02922.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.123-4919C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065276 | ||||||
chr18:35065350
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-4845T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065350 | ||||||
chr18:35065768
|
G | A | 13 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(10): Show | 15 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.123-4427G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065768 | ||||||
chr18:35065774
|
G | A | 1 | a0001c0001t0005g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.123-4421G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065774 | ||||||
chr18:35065890
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(175): Show | 188 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.123-4305T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065890 | ||||||
chr18:35065946
|
G | T | 1 | a0001c0001t0030g0299 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.123-4249G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065946 | ||||||
chr18:35065948
|
A | C | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123-4247A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065948 | ||||||
chr18:35065981
|
G | A | 1 | a0001c0001t0002g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.123-4214G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35065981 | ||||||
chr18:35066213
|
G | A | 67 | a0001c0001t0003g0166a0001c0001t0003g0339a0001c0001t0005g0010others(64): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.123-3982G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066213 | ||||||
chr18:35066313
|
G | A | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(9): Show | 14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-3882G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066313 | ||||||
chr18:35066365
|
T | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(80): Show | 88 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.123-3830T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066365 | ||||||
chr18:35066379
|
C | T | 1 | a0001c0001t0009g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-3816C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066379 | ||||||
chr18:35066468
|
C | T | 27 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0002g0005others(24): Show | 28 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.123-3727C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066468 | ||||||
chr18:35066768
|
T | C | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG01884.hp2 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.123-3427T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066768 | ||||||
chr18:35066816
|
T | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(187): Show | 199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.123-3379T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35066816 | ||||||
chr18:35067003
|
T | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-3192T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067003 | ||||||
chr18:35067114
|
A | G | 1 | a0001c0001t0006g0197 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.123-3081A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067114 | ||||||
chr18:35067137
|
T | G | 7 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-3058T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067137 | ||||||
chr18:35067171
|
G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-3024G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067171 | ||||||
chr18:35067399
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(184): Show | 196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.123-2796C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067399 | ||||||
chr18:35067515
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-2680G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067515 | ||||||
chr18:35067601
|
T | A | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123-2594T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067601 | ||||||
chr18:35067621
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.123-2574A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067621 | ||||||
chr18:35067635
|
T | G | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-2560T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067635 | ||||||
chr18:35067685
|
G | A | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.123-2510G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067685 | ||||||
chr18:35067974
|
C | T | 1 | a0001c0001t0005g0193 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.123-2221C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067974 | ||||||
chr18:35067984
|
T | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(184): Show | 196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.123-2211T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35067984 | ||||||
chr18:35068091
|
C | T | 1 | a0001c0001t0012g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123-2104C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068091 | ||||||
chr18:35068220
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(167): Show | 179 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.123-1975A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068220 | ||||||
chr18:35068326
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(81): Show | 89 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.123-1869G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068326 | ||||||
chr18:35068462
|
G | T | 5 | a0001c0001t0009g0259a0001c0001t0015g0240a0001c0001t0015g0261others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-1733G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068462 | ||||||
chr18:35068506
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0159others(168): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.123-1689A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068506 | ||||||
chr18:35068581
|
C | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-1614C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068581 | ||||||
chr18:35068840
|
C | T | 1 | a0001c0001t0003g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-1355C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068840 | ||||||
chr18:35068887
|
C | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.123-1308C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068887 | ||||||
chr18:35068929
|
C | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-1266C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35068929 | ||||||
chr18:35069226
|
A | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0004g0002others(40): Show | 47 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.123-969A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069226 | ||||||
chr18:35069273
|
T | C | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.123-922T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069273 | ||||||
chr18:35069381
|
G | GT | 10 | a0001c0001t0002g0103a0001c0001t0012g0209a0001c0001t0012g0210others(7): Show | 10 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-806dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35069381 | |||||
chr18:35069388
|
T | TA | 138 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(135): Show | 145 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.123-807_123-806ins others(1): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069388 | ||||||
chr18:35069389
|
T | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0300others(139): Show | 149 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.123-806T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069389 | ||||||
chr18:35069389
|
T | TA | 37 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(34): Show | 39 | HG00642.hp1 HG00735.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.123-801dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35069389 | |||||
chr18:35069425
|
T | C | 13 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(10): Show | 15 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.123-770T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069425 | ||||||
chr18:35069469
|
G | A | 3 | a0001c0001t0004g0002a0001c0001t0004g0065a0001c0001t0004g0076 | 5 | HG00408.hp2 NA18964.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-726G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069469 | ||||||
chr18:35069531
|
A | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(165): Show | 177 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.123-664A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069531 | ||||||
chr18:35069542
|
T | C | 1 | a0001c0001t0008g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-653T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069542 | ||||||
chr18:35069662
|
A | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(172): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.123-533A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069662 | ||||||
chr18:35069754
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.123-441C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069754 | ||||||
chr18:35069802
|
C | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-393C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069802 | ||||||
chr18:35069870
|
G | GCTA | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-323_123-321dup others(3): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr18 | 35069870 | |||||
chr18:35069901
|
C | T | 2 | a0001c0001t0005g0191a0001c0001t0005g0192 | 2 | NA18981.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.123-294C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35069901 | ||||||
chr18:35070092
|
T | C | 1 | a0001c0001t0004g0062 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.123-103T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35070092 | ||||||
chr18:35070128
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0350 | 2 | NA18612.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.123-67G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35070128 | ||||||
chr18:35070181
|
T | C | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-14T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 1/6 | chr18 | 35070181 | ||||||
chr18:35070330
|
A | T | 7 | a0001c0001t0004g0069a0001c0001t0004g0087a0001c0001t0004g0091others(4): Show | 7 | NA18939.hp2 NA18975.hp2 NA19001.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.250+8A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070330 | ||||||
chr18:35070332
|
AT | A | 7 | a0001c0001t0004g0069a0001c0001t0004g0087a0001c0001t0004g0091others(4): Show | 7 | NA18939.hp2 NA18975.hp2 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+12delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35070332 | |||||
chr18:35070363
|
G | C | 2 | a0001c0001t0013g0205a0001c0001t0013g0206 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.250+41G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070363 | ||||||
chr18:35070377
|
A | G | 101 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(98): Show | 102 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.250+55A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070377 | ||||||
chr18:35070585
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+263C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070585 | ||||||
chr18:35070685
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0033g0218a0001c0001t0034g0219 | 3 | HG02630.hp1 HG03225.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.250+363C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070685 | ||||||
chr18:35070842
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+520C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35070842 | ||||||
chr18:35071003
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(165): Show | 177 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.250+681A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071003 | ||||||
chr18:35071095
|
T | C | 4 | a0001c0001t0001g0099a0001c0001t0001g0213a0001c0001t0001g0273others(1): Show | 4 | HG01123.hp1 HG03239.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+773T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071095 | ||||||
chr18:35071124
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02074.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.250+802G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071124 | ||||||
chr18:35071299
|
TG | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(165): Show | 177 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.250+978delG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071299 | ||||||
chr18:35071607
|
G | A | 10 | a0001c0001t0002g0103a0001c0001t0012g0209a0001c0001t0012g0210others(7): Show | 10 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.250+1285G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071607 | ||||||
chr18:35071756
|
C | G | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+1434C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071756 | ||||||
chr18:35071832
|
C | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(173): Show | 186 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.250+1510C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071832 | ||||||
chr18:35071834
|
C | A | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250+1512C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071834 | ||||||
chr18:35071993
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250+1671G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35071993 | ||||||
chr18:35072021
|
A | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+1699A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072021 | ||||||
chr18:35072087
|
C | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+1765C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072087 | ||||||
chr18:35072102
|
A | G | 1 | a0001c0001t0003g0143 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.250+1780A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072102 | ||||||
chr18:35072346
|
G | A | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+2024G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072346 | ||||||
chr18:35072415
|
T | G | 86 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(83): Show | 90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.250+2093T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072415 | ||||||
chr18:35072697
|
A | T | 1 | a0001c0001t0002g0025 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.250+2375A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072697 | ||||||
chr18:35072761
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+2439G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072761 | ||||||
chr18:35072816
|
A | G | 1 | a0001c0001t0004g0074 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.250+2494A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072816 | ||||||
chr18:35072925
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.250+2603A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072925 | ||||||
chr18:35072934
|
G | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+2612G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072934 | ||||||
chr18:35072959
|
CTCCATAG others(3): Show |
C | 1 | a0001c0001t0002g0025 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.250+2638_250+2647d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35072959 | ||||||
chr18:35073029
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0028others(180): Show | 193 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.250+2707T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073029 | ||||||
chr18:35073057
|
A | G | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+2735A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073057 | ||||||
chr18:35073083
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(165): Show | 177 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.250+2761G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073083 | ||||||
chr18:35073153
|
T | G | 1 | a0001c0001t0001g0325 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.250+2831T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073153 | ||||||
chr18:35073184
|
A | T | 1 | a0001c0001t0003g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.250+2862A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073184 | ||||||
chr18:35073243
|
C | G | 1 | a0001c0001t0010g0311 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.250+2921C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073243 | ||||||
chr18:35073244
|
T | C | 2 | a0001c0001t0013g0205a0001c0001t0013g0206 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.250+2922T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073244 | ||||||
chr18:35073285
|
T | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250+2963T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073285 | ||||||
chr18:35073320
|
C | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250+2998C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073320 | ||||||
chr18:35073445
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+3123G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073445 | ||||||
chr18:35073526
|
A | C | 1 | a0001c0001t0023g0170 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.250+3204A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073526 | ||||||
chr18:35073565
|
T | G | 25 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(22): Show | 26 | HG00558.hp1 HG01255.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.250+3243T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073565 | ||||||
chr18:35073954
|
A | G | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.250+3632A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35073954 | ||||||
chr18:35074273
|
A | G | 1 | a0001c0001t0017g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250+3951A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074273 | ||||||
chr18:35074279
|
G | T | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.250+3957G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074279 | ||||||
chr18:35074289
|
A | AT | 8 | a0001c0001t0001g0342a0001c0001t0007g0226a0001c0001t0007g0227others(5): Show | 8 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+3976dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35074289 | |||||
chr18:35074472
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.250+4150G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074472 | ||||||
chr18:35074576
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+4254G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074576 | ||||||
chr18:35074590
|
A | G | 1 | a0001c0001t0006g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.250+4268A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074590 | ||||||
chr18:35074783
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.250+4461G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35074783 | ||||||
chr18:35074865
|
ACTGTCAC others(3): Show |
A | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+4553_250+4562d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35074865 | |||||
chr18:35075003
|
A | G | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.250+4681A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075003 | ||||||
chr18:35075218
|
A | T | 1 | a0001c0001t0008g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.250+4896A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075218 | ||||||
chr18:35075249
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(152): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+4927G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075249 | ||||||
chr18:35075602
|
A | G | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+5280A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075602 | ||||||
chr18:35075620
|
T | G | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250+5298T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075620 | ||||||
chr18:35075727
|
A | G | 2 | a0001c0001t0004g0071a0001c0001t0004g0073 | 2 | NA18989.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.250+5405A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075727 | ||||||
chr18:35075914
|
TC | T | 67 | a0001c0001t0003g0166a0001c0001t0003g0339a0001c0001t0005g0010others(64): Show | 69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.250+5595delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35075914 | |||||
chr18:35075921
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(154): Show | 164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+5599A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075921 | ||||||
chr18:35075966
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+5644G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35075966 | ||||||
chr18:35076026
|
T | C | 2 | a0001c0001t0009g0245a0001c0001t0009g0246 | 2 | HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.250+5704T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076026 | ||||||
chr18:35076111
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(154): Show | 164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+5789A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076111 | ||||||
chr18:35076140
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(153): Show | 163 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.250+5818C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076140 | ||||||
chr18:35076226
|
C | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+5904C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076226 | ||||||
chr18:35076539
|
G | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6217G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076539 | ||||||
chr18:35076561
|
C | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6239C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076561 | ||||||
chr18:35076768
|
C | T | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(9): Show | 14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+6446C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076768 | ||||||
chr18:35076793
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.250+6471T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076793 | ||||||
chr18:35076825
|
C | T | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(9): Show | 14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+6503C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076825 | ||||||
chr18:35076971
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(181): Show | 193 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.250+6649T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35076971 | ||||||
chr18:35077024
|
C | T | 38 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(35): Show | 39 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.250+6702C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077024 | ||||||
chr18:35077238
|
CGT | C | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6918_250+6919d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077238 | |||||
chr18:35077239
|
G | A | 1 | a0001c0001t0013g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.250+6917G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077239 | ||||||
chr18:35077240
|
TGC | T | 62 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0158others(59): Show | 62 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.250+6927_250+6928d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077240 | |||||
chr18:35077243
|
G | A | 4 | a0001c0001t0004g0059a0001c0001t0004g0066a0001c0001t0004g0070others(1): Show | 4 | NA18956.hp1 NA19066.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+6921G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077243 | ||||||
chr18:35077244
|
C | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6922C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077244 | ||||||
chr18:35077245
|
GCGCGCAC others(5): Show |
G | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.250+6925_250+6936d others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077245 | |||||
chr18:35077247
|
GCGCA | G | 22 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(19): Show | 23 | HG01884.hp1 HG01891.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.250+6927_250+6930d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | |||||
chr18:35077247
|
GCGCACA | G | 24 | a0001c0001t0002g0013a0001c0001t0002g0221a0001c0001t0002g0222others(21): Show | 25 | HG00642.hp1 HG01099.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.250+6927_250+6932d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | |||||
chr18:35077247
|
GCGCACAC others(7): Show |
G | 1 | a0001c0001t0005g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.250+6927_250+6940d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | |||||
chr18:35077247
|
GCGCACAC others(9): Show |
G | 72 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0344others(69): Show | 75 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.250+6927_250+6942d others(18): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | |||||
chr18:35077247
|
GCGCACAC others(11): Show |
G | 6 | a0001c0001t0006g0178a0001c0001t0006g0188a0001c0001t0007g0019others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+6927_250+6944d others(20): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | |||||
chr18:35077247
|
GCGCACAC others(15): Show |
G | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.250+6927_250+6948d others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077247 | |||||
chr18:35077249
|
G | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0098a0001c0001t0001g0099others(67): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.250+6927G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077249 | ||||||
chr18:35077251
|
A | G | 3 | a0001c0001t0002g0103a0001c0001t0011g0054a0001c0001t0035g0208 | 3 | HG01884.hp2 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.250+6929A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077251 | ||||||
chr18:35077258
|
CACACACA others(7): Show |
C | 2 | a0001c0001t0002g0103a0001c0001t0035g0208 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.250+6950_250+6963d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077258 | |||||
chr18:35077260
|
CACACACA others(5): Show |
C | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250+6950_250+6961d others(14): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077260 | |||||
chr18:35077262
|
CACACACA others(3): Show |
C | 7 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6950_250+6959d others(12): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077262 | |||||
chr18:35077264
|
CACACACA others(1): Show |
C | 3 | a0001c0001t0002g0220a0001c0001t0004g0082a0001c0001t0004g0093 | 3 | HG01109.hp1 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.250+6950_250+6957d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077264 | |||||
chr18:35077266
|
CACACAT | C | 40 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0023others(37): Show | 41 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.250+6950_250+6955d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077266 | |||||
chr18:35077268
|
CACAT | C | 26 | a0001c0001t0002g0022a0001c0001t0002g0041a0001c0001t0002g0043others(23): Show | 28 | HG01167.hp1 HG01168.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.250+6950_250+6953d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077268 | |||||
chr18:35077270
|
CAT | C | 3 | a0001c0001t0001g0001a0001c0001t0004g0065a0001c0001t0031g0077 | 5 | HG00408.hp2 NA18952.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+6950_250+6951d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077270 | |||||
chr18:35077272
|
T | C | 82 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0344others(79): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.250+6950T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077272 | ||||||
chr18:35077272
|
TAC | T | 8 | a0001c0001t0002g0225a0001c0001t0007g0226a0001c0001t0007g0227others(5): Show | 8 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+6968_250+6969d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35077272 | |||||
chr18:35077275
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0004g0064a0001c0001t0004g0074 | 3 | HG02155.hp2 NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.250+6953A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077275 | ||||||
chr18:35077292
|
A | G | 2 | a0001c0001t0007g0229a0001c0001t0007g0232 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.250+6970A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077292 | ||||||
chr18:35077303
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.250+6981G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077303 | ||||||
chr18:35077315
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+6993G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077315 | ||||||
chr18:35077578
|
T | C | 4 | a0001c0001t0003g0118a0001c0001t0003g0130a0001c0001t0003g0135others(1): Show | 4 | HG01106.hp2 HG01346.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+7256T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077578 | ||||||
chr18:35077622
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+7300A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077622 | ||||||
chr18:35077652
|
A | G | 8 | a0001c0001t0001g0223a0001c0001t0002g0233a0001c0001t0002g0234others(5): Show | 8 | HG02257.hp2 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+7330A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077652 | ||||||
chr18:35077676
|
G | A | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.250+7354G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35077676 | ||||||
chr18:35078052
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250+7730G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078052 | ||||||
chr18:35078064
|
A | C | 1 | a0001c0001t0001g0336 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.250+7742A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078064 | ||||||
chr18:35078286
|
T | G | 1 | a0001c0001t0006g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.250+7964T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078286 | ||||||
chr18:35078629
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250+8307G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078629 | ||||||
chr18:35078630
|
G | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(81): Show | 89 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.250+8308G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078630 | ||||||
chr18:35078640
|
A | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(154): Show | 164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+8318A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078640 | ||||||
chr18:35078671
|
A | T | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+8349A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078671 | ||||||
chr18:35078729
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.250+8407C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078729 | ||||||
chr18:35078751
|
C | CT | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+8432dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35078751 | |||||
chr18:35078760
|
C | T | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.250+8438C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078760 | ||||||
chr18:35078819
|
G | C | 2 | a0001c0001t0005g0156a0001c0001t0005g0214 | 2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.250+8497G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078819 | ||||||
chr18:35078920
|
T | G | 1 | a0001c0001t0027g0029 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.250+8598T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078920 | ||||||
chr18:35078952
|
T | A | 4 | a0001c0001t0002g0234a0001c0001t0005g0156a0001c0001t0005g0214others(1): Show | 4 | HG02615.hp1 HG02683.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+8630T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35078952 | ||||||
chr18:35078965
|
TC | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+8645delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35078965 | |||||
chr18:35079254
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(81): Show | 89 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.250+8932A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079254 | ||||||
chr18:35079305
|
C | T | 3 | a0001c0001t0002g0013a0001c0001t0002g0221a0001c0001t0002g0222 | 4 | HG00642.hp1 HG01099.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+8983C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079305 | ||||||
chr18:35079385
|
T | C | 1 | a0001c0001t0036g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250+9063T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079385 | ||||||
chr18:35079456
|
C | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+9134C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079456 | ||||||
chr18:35079496
|
C | T | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+9174C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079496 | ||||||
chr18:35079736
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0007g0224a0001c0001t0013g0150 | 3 | HG02257.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.250+9414C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079736 | ||||||
chr18:35079747
|
A | G | 2 | a0001c0001t0037g0331a0001c0001t0038g0338 | 2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.250+9425A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079747 | ||||||
chr18:35079851
|
A | C | 11 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(8): Show | 13 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.250+9529A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079851 | ||||||
chr18:35079902
|
T | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+9580T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079902 | ||||||
chr18:35079976
|
A | G | 1 | a0001c0001t0005g0169 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.250+9654A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35079976 | ||||||
chr18:35080000
|
C | A | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+9678C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080000 | ||||||
chr18:35080025
|
C | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+9703C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080025 | ||||||
chr18:35080065
|
CCAAA | C | 3 | a0001c0001t0024g0238a0001c0001t0024g0239a0001c0001t0028g0260 | 3 | HG03209.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.250+9746_250+9749d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35080065 | |||||
chr18:35080212
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250+9890A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080212 | ||||||
chr18:35080228
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(181): Show | 193 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.250+9906A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080228 | ||||||
chr18:35080785
|
C | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+10463C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080785 | ||||||
chr18:35080812
|
GC | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(156): Show | 166 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250+10491delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080812 | ||||||
chr18:35080813
|
C | G | 3 | a0001c0001t0005g0167a0001c0001t0005g0199a0001c0001t0005g0202 | 3 | HG02735.hp1 HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.250+10491C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080813 | ||||||
chr18:35080815
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(156): Show | 166 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250+10493T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080815 | ||||||
chr18:35080880
|
C | G | 1 | a0001c0001t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250+10558C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080880 | ||||||
chr18:35080980
|
T | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+10658T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35080980 | ||||||
chr18:35081042
|
T | C | 1 | a0001c0001t0018g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250+10720T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081042 | ||||||
chr18:35081055
|
A | T | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+10733A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081055 | ||||||
chr18:35081213
|
T | C | 3 | a0001c0001t0001g0223a0001c0001t0007g0224a0001c0001t0013g0150 | 3 | HG02257.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.250+10891T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081213 | ||||||
chr18:35081291
|
A | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0223others(192): Show | 204 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.250+10969A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081291 | ||||||
chr18:35081453
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(152): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+11131T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081453 | ||||||
chr18:35081507
|
C | T | 4 | a0001c0001t0005g0183a0001c0001t0005g0184a0001c0001t0005g0186others(1): Show | 4 | HG00423.hp2 HG02071.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+11185C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081507 | ||||||
chr18:35081517
|
G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+11195G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081517 | ||||||
chr18:35081537
|
C | T | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250+11215C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081537 | ||||||
chr18:35081654
|
C | A | 3 | a0001c0001t0001g0264a0001c0001t0001g0291a0001c0001t0001g0295 | 3 | HG01167.hp2 HG01361.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.250+11332C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081654 | ||||||
chr18:35081737
|
C | T | 1 | a0001c0001t0013g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.250+11415C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081737 | ||||||
chr18:35081858
|
A | G | 2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.250+11536A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35081858 | ||||||
chr18:35081990
|
TAAAAATA others(310): Show |
T | 187 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(184): Show | 196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.250+11687_250+1200 others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35081990 | |||||
chr18:35082146
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250+11824C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082146 | ||||||
chr18:35082182
|
T | C | 1 | a0001c0001t0003g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250+11860T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082182 | ||||||
chr18:35082183
|
G | C | 1 | a0001c0001t0003g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250+11861G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082183 | ||||||
chr18:35082215
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250+11893G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082215 | ||||||
chr18:35082246
|
C | T | 1 | a0001c0001t0003g0116 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.250+11924C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082246 | ||||||
chr18:35082289
|
C | CA | 18 | a0001c0001t0001g0104a0001c0001t0001g0223a0001c0001t0001g0276others(15): Show | 18 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.250+11990dupA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35082289 | |||||
chr18:35082289
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0233a0001c0001t0007g0251 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.250+11978_250+1199 others(17): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35082289 | |||||
chr18:35082289
|
CA | C | 6 | a0001c0001t0001g0328a0001c0001t0001g0342a0001c0001t0003g0137others(3): Show | 6 | HG01070.hp2 HG02015.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+11990delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35082289 | |||||
chr18:35082320
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+11998G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082320 | ||||||
chr18:35082382
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.250+12060T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082382 | ||||||
chr18:35082385
|
G | A | 2 | a0001c0001t0002g0237a0001c0001t0002g0254 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.250+12063G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082385 | ||||||
chr18:35082399
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.250+12077T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082399 | ||||||
chr18:35082587
|
A | G | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+12265A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082587 | ||||||
chr18:35082632
|
T | G | 1 | a0001c0001t0007g0230 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.250+12310T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082632 | ||||||
chr18:35082789
|
TG | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0033a0001c0001t0007g0021others(1): Show | 5 | NA18939.hp1 NA18951.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+12468delG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082789 | ||||||
chr18:35082851
|
T | G | 1 | a0001c0001t0011g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.250+12529T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082851 | ||||||
chr18:35082859
|
T | C | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(9): Show | 14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.250+12537T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082859 | ||||||
chr18:35082901
|
T | C | 1 | a0001c0001t0006g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.250+12579T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35082901 | ||||||
chr18:35083007
|
T | G | 1 | a0001c0001t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250+12685T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083007 | ||||||
chr18:35083254
|
G | A | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+12932G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083254 | ||||||
chr18:35083563
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.250+13241G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083563 | ||||||
chr18:35083564
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(152): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+13242C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083564 | ||||||
chr18:35083601
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250+13279A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083601 | ||||||
chr18:35083724
|
A | G | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+13402A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083724 | ||||||
chr18:35083764
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(152): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.250+13442C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083764 | ||||||
chr18:35083765
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0292a0001c0001t0001g0307others(7): Show | 11 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.250+13443G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083765 | ||||||
chr18:35083775
|
C | A | 1 | a0001c0001t0002g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250+13453C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083775 | ||||||
chr18:35083957
|
TG | T | 22 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0103others(19): Show | 24 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.251-13488delG | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35083957 | ||||||
chr18:35084302
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.251-13144A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084302 | ||||||
chr18:35084341
|
G | C | 1 | a0001c0001t0004g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.251-13105G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084341 | ||||||
chr18:35084374
|
C | T | 2 | a0001c0001t0004g0062a0001c0001t0004g0063 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.251-13072C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084374 | ||||||
chr18:35084804
|
A | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-12642A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084804 | ||||||
chr18:35084890
|
G | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(159): Show | 169 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.251-12556G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35084890 | ||||||
chr18:35085060
|
A | G | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(9): Show | 14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.251-12386A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085060 | ||||||
chr18:35085075
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.251-12371A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085075 | ||||||
chr18:35085205
|
T | C | 2 | a0001c0001t0002g0237a0001c0001t0002g0254 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-12241T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085205 | ||||||
chr18:35085347
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(152): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.251-12099G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085347 | ||||||
chr18:35085386
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.251-12060C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085386 | ||||||
chr18:35085457
|
T | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(79): Show | 87 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-11989T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085457 | ||||||
chr18:35085797
|
C | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(294): Show | 308 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.251-11649C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35085797 | ||||||
chr18:35086215
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(152): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.251-11231A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086215 | ||||||
chr18:35086549
|
T | C | 7 | a0001c0001t0001g0223a0001c0001t0002g0234a0001c0001t0005g0156others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-10897T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086549 | ||||||
chr18:35086581
|
T | A | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-10865T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086581 | ||||||
chr18:35086847
|
A | G | 1 | a0001c0001t0012g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.251-10599A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086847 | ||||||
chr18:35086896
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(190): Show | 202 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.251-10550T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35086896 | ||||||
chr18:35087254
|
GT | G | 9 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-10186delT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35087254 | |||||
chr18:35087285
|
T | G | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02735.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.251-10161T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087285 | ||||||
chr18:35087388
|
A | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-10058A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087388 | ||||||
chr18:35087634
|
T | G | 2 | a0001c0001t0024g0238a0001c0001t0024g0239 | 2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.251-9812T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087634 | ||||||
chr18:35087816
|
T | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-9630T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35087816 | ||||||
chr18:35088184
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(155): Show | 165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.251-9262A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088184 | ||||||
chr18:35088209
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(184): Show | 196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.251-9237T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088209 | ||||||
chr18:35088242
|
G | A | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-9204G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088242 | ||||||
chr18:35088357
|
T | C | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-9089T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088357 | ||||||
chr18:35088431
|
G | T | 1 | a0001c0001t0005g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.251-9015G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088431 | ||||||
chr18:35088500
|
G | A | 3 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244 | 3 | HG02896.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.251-8946G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35088500 | ||||||
chr18:35089161
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0007g0224 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.251-8285A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089161 | ||||||
chr18:35089248
|
G | A | 98 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0022others(95): Show | 101 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.251-8198G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089248 | ||||||
chr18:35089298
|
T | C | 1 | a0001c0001t0021g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.251-8148T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089298 | ||||||
chr18:35089349
|
C | A | 1 | a0001c0001t0017g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.251-8097C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089349 | ||||||
chr18:35089476
|
T | A | 91 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0022others(88): Show | 94 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.251-7970T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089476 | ||||||
chr18:35089533
|
GC | G | 91 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0022others(88): Show | 94 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.251-7911delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35089533 | |||||
chr18:35089648
|
A | G | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-7798A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089648 | ||||||
chr18:35089674
|
C | A | 3 | a0001c0001t0003g0129a0001c0001t0003g0134a0001c0001t0016g0128 | 3 | HG00642.hp2 HG01123.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.251-7772C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089674 | ||||||
chr18:35089676
|
C | T | 1 | a0001c0001t0004g0097 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.251-7770C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089676 | ||||||
chr18:35089804
|
T | C | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-7642T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089804 | ||||||
chr18:35089847
|
G | T | 7 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(4): Show | 7 | HG02109.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-7599G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089847 | ||||||
chr18:35089917
|
G | A | 49 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0003g0166others(46): Show | 51 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.251-7529G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089917 | ||||||
chr18:35089977
|
A | G | 1 | a0002c0003t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.251-7469A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35089977 | ||||||
chr18:35090050
|
A | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-7396A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090050 | ||||||
chr18:35090057
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(305): Show | 320 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.251-7389T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090057 | ||||||
chr18:35090173
|
G | GT | 6 | a0001c0001t0003g0110a0001c0001t0003g0126a0001c0001t0003g0129others(3): Show | 6 | HG00642.hp2 HG03098.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-7264dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090173 | |||||
chr18:35090324
|
A | G | 2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.251-7122A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090324 | ||||||
chr18:35090533
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0004g0064a0001c0001t0004g0074 | 3 | HG02155.hp2 NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.251-6913A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090533 | ||||||
chr18:35090570
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0013others(52): Show | 61 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.251-6876A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090570 | ||||||
chr18:35090577
|
C | T | 39 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0022others(36): Show | 40 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-6869C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090577 | ||||||
chr18:35090591
|
T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(183): Show | 195 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.251-6855T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090591 | ||||||
chr18:35090731
|
CA | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(322): Show | 342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.251-6700delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090731 | |||||
chr18:35090731
|
CAA | C | 14 | a0001c0001t0001g0223a0001c0001t0001g0270a0001c0001t0001g0334others(11): Show | 14 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-6701_251-6700d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090731 | |||||
chr18:35090733
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.251-6707_251-6694d others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35090733 | |||||
chr18:35090839
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.251-6607A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090839 | ||||||
chr18:35090886
|
G | A | 1 | a0001c0001t0004g0069 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.251-6560G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35090886 | ||||||
chr18:35091152
|
C | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.251-6294C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091152 | ||||||
chr18:35091363
|
T | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-6083T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091363 | ||||||
chr18:35091497
|
C | CTA | 39 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0022others(36): Show | 40 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-5946_251-5945d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35091497 | |||||
chr18:35091624
|
A | G | 1 | a0001c0001t0010g0314 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.251-5822A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091624 | ||||||
chr18:35091641
|
G | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0083 | 2 | HG01975.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.251-5805G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091641 | ||||||
chr18:35091691
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.251-5755A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091691 | ||||||
chr18:35091716
|
C | T | 8 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-5730C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091716 | ||||||
chr18:35091867
|
G | T | 39 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0022others(36): Show | 40 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-5579G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091867 | ||||||
chr18:35091903
|
G | T | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-5543G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091903 | ||||||
chr18:35091984
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.251-5462A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35091984 | ||||||
chr18:35092030
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0100others(193): Show | 205 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.251-5416A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092030 | ||||||
chr18:35092058
|
C | T | 1 | a0001c0001t0039g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.251-5388C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092058 | ||||||
chr18:35092205
|
G | T | 4 | a0001c0001t0009g0248a0001c0001t0018g0247a0001c0001t0018g0253others(1): Show | 4 | HG00735.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-5241G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092205 | ||||||
chr18:35092572
|
A | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.251-4874A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092572 | ||||||
chr18:35092590
|
A | G | 5 | a0001c0001t0009g0259a0001c0001t0015g0240a0001c0001t0015g0261others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-4856A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092590 | ||||||
chr18:35092810
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.251-4636C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092810 | ||||||
chr18:35092872
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(305): Show | 320 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.251-4574G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092872 | ||||||
chr18:35092904
|
G | C | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.251-4542G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092904 | ||||||
chr18:35092938
|
G | A | 38 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(35): Show | 39 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.251-4508G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35092938 | ||||||
chr18:35093005
|
A | G | 1 | a0001c0001t0012g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.251-4441A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093005 | ||||||
chr18:35093211
|
CA | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(174): Show | 187 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.251-4208delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35093211 | |||||
chr18:35093211
|
CAA | C | 107 | a0001c0001t0001g0293a0001c0001t0002g0022a0001c0001t0002g0023others(104): Show | 109 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.251-4209_251-4208d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35093211 | |||||
chr18:35093238
|
A | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0315others(6): Show | 10 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-4208A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093238 | ||||||
chr18:35093334
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.251-4112C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093334 | ||||||
chr18:35093379
|
A | T | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-4067A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093379 | ||||||
chr18:35093464
|
C | G | 2 | a0001c0001t0003g0120a0001c0001t0003g0125 | 2 | HG04115.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.251-3982C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093464 | ||||||
chr18:35093537
|
T | C | 1 | a0001c0001t0004g0072 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.251-3909T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093537 | ||||||
chr18:35093647
|
C | T | 38 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(35): Show | 39 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.251-3799C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093647 | ||||||
chr18:35093770
|
A | G | 1 | a0001c0001t0018g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.251-3676A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35093770 | ||||||
chr18:35094101
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0002g0254 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-3345C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094101 | ||||||
chr18:35094102
|
G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-3344G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094102 | ||||||
chr18:35094201
|
A | G | 4 | a0001c0001t0002g0005a0001c0001t0002g0033a0001c0001t0007g0021others(1): Show | 5 | NA18939.hp1 NA18951.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-3245A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094201 | ||||||
chr18:35094386
|
A | G | 1 | a0001c0001t0003g0321 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.251-3060A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094386 | ||||||
chr18:35094444
|
A | G | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-3002A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094444 | ||||||
chr18:35094469
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0005others(180): Show | 192 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.251-2977A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094469 | ||||||
chr18:35094956
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.251-2490C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094956 | ||||||
chr18:35094965
|
G | C | 1 | a0001c0001t0002g0036 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.251-2481G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35094965 | ||||||
chr18:35095278
|
T | G | 1 | a0001c0001t0003g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.251-2168T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095278 | ||||||
chr18:35095363
|
T | TAC | 64 | a0001c0001t0001g0008a0001c0001t0001g0099a0001c0001t0001g0105others(61): Show | 70 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.251-2046_251-2045d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | |||||
chr18:35095363
|
T | TACAC | 48 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 49 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.251-2048_251-2045d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | |||||
chr18:35095363
|
T | TACACAC | 12 | a0001c0001t0001g0273a0001c0001t0001g0322a0001c0001t0001g0334others(9): Show | 12 | HG00323.hp2 HG01099.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-2050_251-2045d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | |||||
chr18:35095363
|
T | TATAC | 8 | a0001c0001t0002g0225a0001c0001t0002g0237a0001c0001t0002g0254others(5): Show | 8 | HG02080.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-2082_251-2081i others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | |||||
chr18:35095363
|
T | TATACAC | 39 | a0001c0001t0001g0001a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 45 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.251-2082_251-2081i others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | |||||
chr18:35095363
|
TAC | T | 4 | a0001c0001t0001g0295a0001c0001t0003g0141a0001c0001t0003g0142others(1): Show | 4 | HG01081.hp2 HG02083.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-2046_251-2045d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095363 | |||||
chr18:35095365
|
C | T | 8 | a0001c0001t0001g0028a0001c0001t0004g0064a0001c0001t0004g0065others(5): Show | 8 | HG00408.hp2 HG01346.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-2081C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095365 | ||||||
chr18:35095386
|
A | G | 1 | a0001c0001t0004g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.251-2060A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095386 | ||||||
chr18:35095390
|
A | G | 1 | a0001c0001t0033g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.251-2056A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095390 | ||||||
chr18:35095392
|
A | ACACACG | 13 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.251-2049_251-2048i others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095392 | |||||
chr18:35095392
|
A | G | 64 | a0001c0001t0001g0341a0001c0001t0005g0010a0001c0001t0005g0011others(61): Show | 66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.251-2054A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095392 | ||||||
chr18:35095394
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0002g0013a0001c0001t0002g0014others(54): Show | 63 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.251-2052A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095394 | ||||||
chr18:35095396
|
A | ACG | 7 | a0001c0001t0001g0223a0001c0001t0002g0022a0001c0001t0002g0101others(4): Show | 7 | HG01109.hp1 HG02132.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-2049_251-2048i others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095396 | |||||
chr18:35095396
|
A | G | 39 | a0001c0001t0002g0005a0001c0001t0002g0023a0001c0001t0002g0025others(36): Show | 40 | HG00558.hp1 HG01255.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.251-2050A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095396 | ||||||
chr18:35095396
|
ACACACG | A | 63 | a0001c0001t0001g0341a0001c0001t0005g0010a0001c0001t0005g0011others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.251-2044_251-2039d others(8): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095396 | |||||
chr18:35095398
|
A | G | 2 | a0001c0001t0007g0019a0001c0001t0013g0018 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.251-2048A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095398 | ||||||
chr18:35095398
|
ACACG | A | 8 | a0001c0001t0003g0166a0001c0001t0003g0339a0001c0001t0005g0162others(5): Show | 8 | HG02818.hp1 HG03041.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-2044_251-2041d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095398 | |||||
chr18:35095400
|
ACG | A | 9 | a0001c0001t0002g0040a0001c0001t0002g0103a0001c0001t0002g0233others(6): Show | 9 | HG02280.hp2 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-2044_251-2043d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095400 | |||||
chr18:35095402
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0223a0001c0001t0002g0005others(104): Show | 114 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.251-2044G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095402 | ||||||
chr18:35095402
|
G | GCACACAC others(1): Show |
9 | a0001c0001t0001g0028a0001c0001t0004g0064a0001c0001t0004g0065others(6): Show | 9 | HG00408.hp2 HG01346.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-2040_251-2033d others(10): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095402 | |||||
chr18:35095456
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.251-1990C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095456 | ||||||
chr18:35095457
|
G | A | 1 | a0001c0001t0008g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.251-1989G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095457 | ||||||
chr18:35095483
|
G | C | 2 | a0001c0001t0002g0237a0001c0001t0002g0254 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-1963G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095483 | ||||||
chr18:35095523
|
G | GT | 72 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0341others(69): Show | 80 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.251-1909dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095523 | |||||
chr18:35095523
|
G | GTT | 110 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(107): Show | 112 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.251-1910_251-1909d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095523 | |||||
chr18:35095523
|
G | GTTT | 13 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0167others(10): Show | 13 | HG01884.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-1911_251-1909d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35095523 | |||||
chr18:35095590
|
G | C | 1 | a0001c0001t0004g0065 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.251-1856G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095590 | ||||||
chr18:35095627
|
A | G | 1 | a0001c0001t0007g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.251-1819A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095627 | ||||||
chr18:35095682
|
G | A | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.251-1764G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095682 | ||||||
chr18:35095858
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0013others(66): Show | 75 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.251-1588G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35095858 | ||||||
chr18:35096046
|
T | G | 2 | a0001c0001t0006g0182a0001c0001t0040g0185 | 2 | HG00408.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.251-1400T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096046 | ||||||
chr18:35096109
|
G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-1337G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096109 | ||||||
chr18:35096181
|
G | A | 1 | a0001c0001t0024g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.251-1265G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096181 | ||||||
chr18:35096526
|
A | G | 1 | a0001c0001t0005g0164 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.251-920A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096526 | ||||||
chr18:35096589
|
G | GACTC | 86 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(83): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.251-856_251-853dup others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35096589 | |||||
chr18:35096789
|
TATAAGTA others(14): Show |
T | 84 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(81): Show | 87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-639_251-619del others(21): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35096789 | |||||
chr18:35096813
|
A | AAGTAATA others(17): Show |
1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.251-618_251-595dup others(24): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr18 | 35096813 | |||||
chr18:35096863
|
A | G | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.251-583A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096863 | ||||||
chr18:35096941
|
A | G | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-505A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35096941 | ||||||
chr18:35097017
|
G | A | 84 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(81): Show | 87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-429G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097017 | ||||||
chr18:35097056
|
T | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0221a0001c0001t0002g0222others(1): Show | 5 | HG00642.hp1 HG01099.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-390T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097056 | ||||||
chr18:35097190
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.251-256A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097190 | ||||||
chr18:35097211
|
A | ATGCATAT others(4): Show |
1 | a0001c0001t0005g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251-235_251-234ins others(11): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097211 | ||||||
chr18:35097214
|
A | G | 1 | a0001c0001t0005g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251-232A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 2/6 | chr18 | 35097214 | ||||||
chr18:35097669
|
G | A | 45 | a0001c0001t0001g0028a0001c0001t0002g0225a0001c0001t0004g0002others(42): Show | 47 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.396+78G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35097669 | ||||||
chr18:35097737
|
C | A | 1 | a0001c0001t0004g0075 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.396+146C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35097737 | ||||||
chr18:35098250
|
T | C | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.396+659T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098250 | ||||||
chr18:35098393
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.396+802A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098393 | ||||||
chr18:35098445
|
G | A | 1 | a0001c0001t0008g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.396+854G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098445 | ||||||
chr18:35098693
|
C | A | 1 | a0001c0001t0001g0269 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.396+1102C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098693 | ||||||
chr18:35098734
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396+1143A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098734 | ||||||
chr18:35098812
|
C | T | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.396+1221C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35098812 | ||||||
chr18:35099155
|
A | G | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.396+1564A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099155 | ||||||
chr18:35099177
|
C | T | 1 | a0001c0001t0012g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396+1586C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099177 | ||||||
chr18:35099259
|
A | G | 2 | a0001c0001t0003g0112a0001c0001t0010g0274 | 2 | NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.396+1668A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099259 | ||||||
chr18:35099600
|
G | A | 1 | a0001c0001t0014g0320 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.396+2009G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099600 | ||||||
chr18:35099686
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396+2095A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099686 | ||||||
chr18:35099822
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397-2124T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35099822 | ||||||
chr18:35100069
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397-1877G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100069 | ||||||
chr18:35100091
|
A | G | 1 | a0001c0001t0027g0029 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.397-1855A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100091 | ||||||
chr18:35100117
|
A | T | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.397-1829A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100117 | ||||||
chr18:35100162
|
C | T | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.397-1784C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100162 | ||||||
chr18:35100407
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.397-1539C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100407 | ||||||
chr18:35100576
|
A | T | 20 | a0001c0001t0001g0159a0001c0001t0001g0265a0001c0001t0001g0269others(17): Show | 20 | HG00423.hp1 HG02040.hp1 NA18943.hp1 others(17): Show |
intron_variant | MODIFIER | c.397-1370A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100576 | ||||||
chr18:35100611
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.397-1335C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100611 | ||||||
chr18:35100741
|
A | G | 3 | a0001c0001t0004g0060a0001c0001t0004g0075a0001c0001t0004g0092 | 3 | NA18983.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.397-1205A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100741 | ||||||
chr18:35100796
|
T | A | 1 | a0001c0001t0002g0022 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.397-1150T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100796 | ||||||
chr18:35100869
|
G | A | 2 | a0001c0001t0013g0150a0001c0001t0033g0218 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.397-1077G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100869 | ||||||
chr18:35100906
|
G | A | 40 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(37): Show | 41 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.397-1040G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100906 | ||||||
chr18:35100930
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0002g0013others(68): Show | 77 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.397-1016T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35100930 | ||||||
chr18:35101017
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.397-929C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101017 | ||||||
chr18:35101022
|
A | G | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.397-924A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101022 | ||||||
chr18:35101024
|
A | G | 1 | a0001c0001t0004g0072 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.397-922A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101024 | ||||||
chr18:35101317
|
T | C | 1 | a0001c0001t0011g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.397-629T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101317 | ||||||
chr18:35101783
|
A | G | 1 | a0001c0001t0005g0169 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.397-163A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 3/6 | chr18 | 35101783 | ||||||
chr18:35102185
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.610+26G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102185 | ||||||
chr18:35102373
|
C | T | 13 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+214C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102373 | ||||||
chr18:35102405
|
C | T | 351 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(348): Show | 368 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(365): Show |
intron_variant | MODIFIER | c.610+246C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102405 | ||||||
chr18:35102569
|
T | C | 13 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(10): Show | 13 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.610+410T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102569 | ||||||
chr18:35102753
|
C | A | 4 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0231others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+594C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102753 | ||||||
chr18:35102889
|
T | C | 1 | a0001c0001t0007g0228 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610+730T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35102889 | ||||||
chr18:35103019
|
G | GTGGTAAG others(9): Show |
2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610+860_610+861ins others(16): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103019 | ||||||
chr18:35103021
|
C | T | 2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610+862C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103021 | ||||||
chr18:35103264
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.610+1105A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103264 | ||||||
chr18:35103437
|
A | G | 78 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0162others(75): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.610+1278A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103437 | ||||||
chr18:35103583
|
T | C | 2 | a0001c0001t0033g0218a0001c0001t0034g0219 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610+1424T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103583 | ||||||
chr18:35103597
|
A | G | 1 | a0001c0001t0004g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.610+1438A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103597 | ||||||
chr18:35103725
|
A | G | 1 | a0001c0001t0013g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610+1566A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103725 | ||||||
chr18:35103834
|
A | G | 1 | a0001c0001t0013g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610+1675A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103834 | ||||||
chr18:35103869
|
G | A | 1 | a0001c0001t0003g0324 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.610+1710G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103869 | ||||||
chr18:35103972
|
A | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0233 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.610+1813A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35103972 | ||||||
chr18:35104051
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0002g0005a0001c0001t0002g0013others(90): Show | 100 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.610+1892A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104051 | ||||||
chr18:35104161
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+2002C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104161 | ||||||
chr18:35104220
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+2061T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104220 | ||||||
chr18:35104238
|
T | A | 90 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(87): Show | 93 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.610+2079T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104238 | ||||||
chr18:35104288
|
A | G | 2 | a0001c0001t0019g0207a0001c0001t0019g0215 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.610+2129A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104288 | ||||||
chr18:35104363
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0004g0002a0001c0001t0004g0058others(41): Show | 48 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.610+2204T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104363 | ||||||
chr18:35104369
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.610+2210C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104369 | ||||||
chr18:35104559
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.610+2400C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104559 | ||||||
chr18:35104736
|
G | A | 8 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0212others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+2577G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104736 | ||||||
chr18:35104769
|
G | A | 4 | a0001c0001t0015g0240a0001c0001t0015g0261a0001c0001t0015g0262others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+2610G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35104769 | ||||||
chr18:35105436
|
A | T | 3 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0321 | 3 | HG01257.hp2 NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.610+3277A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105436 | ||||||
chr18:35105526
|
A | G | 78 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0162others(75): Show | 81 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.610+3367A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105526 | ||||||
chr18:35105669
|
A | G | 3 | a0001c0001t0008g0309a0001c0001t0037g0331a0001c0001t0038g0338 | 3 | HG01070.hp2 HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.610+3510A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105669 | ||||||
chr18:35105729
|
A | G | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.610+3570A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35105729 | ||||||
chr18:35106308
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+4149G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106308 | ||||||
chr18:35106357
|
T | TGC | 200 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0223others(197): Show | 210 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.610+4198_610+4199i others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106357 | ||||||
chr18:35106528
|
A | G | 9 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(6): Show | 9 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.610+4369A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106528 | ||||||
chr18:35106591
|
G | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610+4432G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106591 | ||||||
chr18:35106598
|
G | C | 84 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(81): Show | 87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.610+4439G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35106598 | ||||||
chr18:35106856
|
TAC | T | 50 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0162others(47): Show | 52 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.610+4701_610+4702d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35106856 | |||||
chr18:35107038
|
G | T | 1 | a0001c0001t0033g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610+4879G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107038 | ||||||
chr18:35107089
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0308 | 2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.610+4930C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107089 | ||||||
chr18:35107296
|
A | G | 2 | a0001c0001t0005g0156a0001c0001t0005g0214 | 2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.610+5137A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107296 | ||||||
chr18:35107308
|
G | A | 88 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(85): Show | 91 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.610+5149G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107308 | ||||||
chr18:35107487
|
CCTT | C | 45 | a0001c0001t0001g0001a0001c0001t0002g0225a0001c0001t0004g0002others(42): Show | 49 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.610+5332_610+5334d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35107487 | |||||
chr18:35107585
|
G | T | 1 | a0001c0001t0013g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610+5426G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107585 | ||||||
chr18:35107644
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.610+5485C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107644 | ||||||
chr18:35107655
|
C | T | 6 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0173others(3): Show | 8 | HG01255.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.610+5496C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107655 | ||||||
chr18:35107820
|
G | C | 1 | a0001c0001t0003g0141 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.610+5661G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35107820 | ||||||
chr18:35108026
|
G | A | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.610+5867G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108026 | ||||||
chr18:35108074
|
A | G | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.610+5915A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108074 | ||||||
chr18:35108122
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0344others(4): Show | 8 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.610+5963C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108122 | ||||||
chr18:35108288
|
A | G | 2 | a0001c0001t0006g0034a0001c0001t0006g0035 | 2 | NA18944.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.610+6129A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108288 | ||||||
chr18:35108363
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0233 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.610+6204G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108363 | ||||||
chr18:35108607
|
A | G | 1 | a0001c0001t0010g0311 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.610+6448A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108607 | ||||||
chr18:35108635
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.610+6476T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108635 | ||||||
chr18:35108876
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+6717C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108876 | ||||||
chr18:35108995
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0002g0013a0001c0001t0002g0014others(54): Show | 63 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.610+6836A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35108995 | ||||||
chr18:35109316
|
A | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+7157A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35109316 | ||||||
chr18:35109824
|
T | A | 93 | a0001c0001t0001g0001a0001c0001t0002g0005a0001c0001t0002g0013others(90): Show | 100 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.610+7665T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35109824 | ||||||
chr18:35110204
|
C | T | 1 | a0001c0001t0004g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.610+8045C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110204 | ||||||
chr18:35110350
|
T | C | 9 | a0001c0001t0005g0164a0001c0001t0005g0183a0001c0001t0005g0184others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.610+8191T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110350 | ||||||
chr18:35110377
|
C | T | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.610+8218C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110377 | ||||||
chr18:35110411
|
T | C | 3 | a0001c0001t0009g0245a0001c0001t0009g0246a0001c0001t0009g0259 | 3 | HG01243.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.610+8252T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110411 | ||||||
chr18:35110427
|
A | G | 1 | a0001c0001t0005g0175 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.610+8268A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110427 | ||||||
chr18:35110562
|
A | T | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.610+8403A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110562 | ||||||
chr18:35110779
|
G | A | 1 | a0001c0001t0029g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.610+8620G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110779 | ||||||
chr18:35110792
|
A | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(100): Show | 106 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.610+8633A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110792 | ||||||
chr18:35110818
|
A | G | 6 | a0001c0001t0004g0059a0001c0001t0004g0066a0001c0001t0004g0070others(3): Show | 6 | NA18956.hp1 NA18988.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.610+8659A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110818 | ||||||
chr18:35110903
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610+8744C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110903 | ||||||
chr18:35110908
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.610+8749A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35110908 | ||||||
chr18:35111543
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.610+9384T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35111543 | ||||||
chr18:35111952
|
A | G | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | NA18977.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.610+9793A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35111952 | ||||||
chr18:35112166
|
T | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0205a0001c0001t0013g0206 | 3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.610+10007T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112166 | ||||||
chr18:35112184
|
C | CT | 16 | a0001c0001t0003g0324a0001c0001t0007g0230a0001c0001t0012g0209others(13): Show | 16 | HG01123.hp2 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.610+10040dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35112184 | |||||
chr18:35112450
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.610+10291C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112450 | ||||||
chr18:35112510
|
C | T | 3 | a0001c0001t0005g0217a0001c0001t0024g0238a0001c0001t0024g0239 | 3 | HG03209.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.610+10351C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112510 | ||||||
chr18:35112512
|
T | C | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+10353T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112512 | ||||||
chr18:35112626
|
C | A | 1 | a0001c0001t0033g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610+10467C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112626 | ||||||
chr18:35112686
|
T | C | 1 | a0001c0001t0002g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.610+10527T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112686 | ||||||
chr18:35112806
|
A | C | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610+10647A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112806 | ||||||
chr18:35112846
|
C | T | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+10687C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112846 | ||||||
chr18:35112877
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0292a0001c0001t0001g0307others(6): Show | 10 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.610+10718G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35112877 | ||||||
chr18:35113054
|
C | T | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+10895C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113054 | ||||||
chr18:35113339
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(294): Show | 308 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.610+11180A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113339 | ||||||
chr18:35113393
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.610+11234C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113393 | ||||||
chr18:35113460
|
T | G | 1 | a0001c0001t0002g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.610+11301T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113460 | ||||||
chr18:35113467
|
TA | T | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+11317delA | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35113467 | |||||
chr18:35113468
|
A | T | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(9): Show | 14 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.610+11309A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113468 | ||||||
chr18:35113670
|
A | T | 4 | a0001c0001t0001g0313a0001c0001t0001g0315a0001c0001t0001g0346others(1): Show | 4 | NA18988.hp1 NA18998.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+11511A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113670 | ||||||
chr18:35113763
|
C | T | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610+11604C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113763 | ||||||
chr18:35113961
|
A | G | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+11802A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113961 | ||||||
chr18:35113988
|
A | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0233a0001c0001t0005g0156others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+11829A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35113988 | ||||||
chr18:35114166
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.610+12007C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114166 | ||||||
chr18:35114221
|
A | G | 1 | a0001c0001t0006g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.610+12062A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114221 | ||||||
chr18:35114259
|
A | C | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.610+12100A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114259 | ||||||
chr18:35114467
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610+12308G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114467 | ||||||
chr18:35114528
|
G | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610+12369G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35114528 | ||||||
chr18:35115209
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.611-11739A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115209 | ||||||
chr18:35115330
|
T | C | 44 | a0001c0001t0001g0001a0001c0001t0004g0002a0001c0001t0004g0058others(41): Show | 48 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.611-11618T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115330 | ||||||
chr18:35115370
|
T | A | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-11578T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115370 | ||||||
chr18:35115429
|
G | A | 10 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.611-11519G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115429 | ||||||
chr18:35115517
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.611-11431G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115517 | ||||||
chr18:35115520
|
C | G | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-11428C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115520 | ||||||
chr18:35115560
|
T | C | 1 | a0001c0001t0006g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.611-11388T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115560 | ||||||
chr18:35115716
|
G | A | 1 | a0001c0001t0039g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-11232G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115716 | ||||||
chr18:35115719
|
G | T | 9 | a0001c0001t0005g0164a0001c0001t0005g0183a0001c0001t0005g0184others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-11229G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115719 | ||||||
chr18:35115731
|
G | A | 200 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0013others(197): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.611-11217G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115731 | ||||||
chr18:35115824
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0002g0225a0001c0001t0004g0002others(42): Show | 49 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.611-11124A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35115824 | ||||||
chr18:35116089
|
G | T | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.611-10859G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116089 | ||||||
chr18:35116219
|
G | A | 1 | a0001c0001t0016g0128 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.611-10729G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116219 | ||||||
chr18:35116301
|
T | C | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.611-10647T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116301 | ||||||
chr18:35116572
|
C | T | 1 | a0001c0001t0004g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.611-10376C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116572 | ||||||
chr18:35116782
|
T | C | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.611-10166T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116782 | ||||||
chr18:35116812
|
C | T | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.611-10136C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116812 | ||||||
chr18:35116848
|
C | A | 1 | a0001c0001t0003g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.611-10100C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35116848 | ||||||
chr18:35117243
|
A | C | 7 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(4): Show | 7 | HG02451.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-9705A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117243 | ||||||
chr18:35117259
|
C | T | 6 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-9689C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117259 | ||||||
chr18:35117301
|
C | T | 1 | a0001c0001t0004g0074 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.611-9647C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117301 | ||||||
chr18:35117714
|
C | G | 80 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(77): Show | 83 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.611-9234C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117714 | ||||||
chr18:35117800
|
A | G | 1 | a0001c0001t0005g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.611-9148A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117800 | ||||||
chr18:35117879
|
C | A | 44 | a0001c0001t0002g0225a0001c0001t0004g0002a0001c0001t0004g0058others(41): Show | 46 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.611-9069C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117879 | ||||||
chr18:35117928
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.611-9020G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35117928 | ||||||
chr18:35118162
|
C | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.611-8786C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118162 | ||||||
chr18:35118291
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.611-8657A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118291 | ||||||
chr18:35118380
|
A | G | 1 | a0001c0001t0013g0206 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.611-8568A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118380 | ||||||
chr18:35118390
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0267a0001c0001t0001g0308 | 3 | HG02040.hp2 NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.611-8558C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35118390 | ||||||
chr18:35119031
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.611-7917A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119031 | ||||||
chr18:35119110
|
C | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0014others(89): Show | 97 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.611-7838C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119110 | ||||||
chr18:35119138
|
C | T | 10 | a0001c0001t0009g0216a0001c0001t0009g0242a0001c0001t0009g0243others(7): Show | 10 | HG00735.hp2 HG01243.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.611-7810C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119138 | ||||||
chr18:35119404
|
T | C | 1 | a0001c0001t0003g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.611-7544T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119404 | ||||||
chr18:35119546
|
A | G | 1 | a0001c0001t0010g0314 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.611-7402A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119546 | ||||||
chr18:35119650
|
T | A | 2 | a0001c0001t0005g0162a0001c0001t0005g0177 | 2 | NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.611-7298T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119650 | ||||||
chr18:35119661
|
G | T | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.611-7287G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119661 | ||||||
chr18:35119741
|
C | A | 3 | a0001c0001t0002g0009a0001c0001t0002g0103a0001c0001t0002g0233 | 4 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-7207C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119741 | ||||||
chr18:35119786
|
G | T | 47 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0162others(44): Show | 49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.611-7162G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119786 | ||||||
chr18:35119838
|
C | A | 11 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(8): Show | 11 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.611-7110C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119838 | ||||||
chr18:35119960
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.611-6988G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35119960 | ||||||
chr18:35120283
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.611-6665C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120283 | ||||||
chr18:35120490
|
G | A | 1 | a0001c0001t0010g0294 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.611-6458G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120490 | ||||||
chr18:35120514
|
G | A | 76 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(73): Show | 79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.611-6434G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120514 | ||||||
chr18:35120721
|
C | G | 1 | a0001c0001t0016g0146 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.611-6227C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120721 | ||||||
chr18:35120863
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0308 | 2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.611-6085G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120863 | ||||||
chr18:35120874
|
T | C | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-6074T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120874 | ||||||
chr18:35120880
|
A | G | 4 | a0001c0001t0015g0240a0001c0001t0015g0261a0001c0001t0015g0262others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.611-6068A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120880 | ||||||
chr18:35120976
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.611-5972G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35120976 | ||||||
chr18:35121576
|
C | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0014others(89): Show | 97 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.611-5372C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35121576 | ||||||
chr18:35121708
|
A | G | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.611-5240A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35121708 | ||||||
chr18:35121878
|
G | C | 1 | a0001c0001t0006g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.611-5070G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35121878 | ||||||
chr18:35121890
|
C | CAT | 4 | a0001c0001t0002g0014a0001c0001t0002g0241a0001c0001t0002g0252others(1): Show | 5 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-5056_611-5055d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35121890 | |||||
chr18:35121961
|
C | CTAG | 1 | a0001c0001t0001g0001 | 3 | NA18952.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.611-4985_611-4983d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35121961 | |||||
chr18:35122034
|
G | A | 1 | a0001c0001t0012g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.611-4914G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122034 | ||||||
chr18:35122162
|
G | A | 1 | a0001c0001t0004g0097 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.611-4786G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122162 | ||||||
chr18:35122207
|
A | G | 1 | a0001c0001t0003g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.611-4741A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122207 | ||||||
chr18:35122305
|
CTG | C | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-4641_611-4640d others(4): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr18 | 35122305 | |||||
chr18:35122543
|
T | G | 1 | a0001c0001t0006g0034 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.611-4405T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122543 | ||||||
chr18:35122951
|
A | C | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-3997A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122951 | ||||||
chr18:35122963
|
C | T | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.611-3985C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35122963 | ||||||
chr18:35123035
|
G | A | 86 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(83): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.611-3913G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123035 | ||||||
chr18:35123202
|
T | G | 1 | a0001c0001t0002g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.611-3746T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123202 | ||||||
chr18:35123380
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.611-3568C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123380 | ||||||
chr18:35123432
|
G | A | 200 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0013others(197): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.611-3516G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123432 | ||||||
chr18:35123584
|
A | G | 91 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0005g0010others(88): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.611-3364A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123584 | ||||||
chr18:35123627
|
C | T | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-3321C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123627 | ||||||
chr18:35123962
|
C | A | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.611-2986C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35123962 | ||||||
chr18:35124331
|
G | A | 1 | a0001c0001t0039g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.611-2617G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124331 | ||||||
chr18:35124367
|
G | A | 1 | a0001c0001t0013g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.611-2581G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124367 | ||||||
chr18:35124381
|
A | G | 2 | a0001c0001t0020g0317a0001c0001t0020g0319 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.611-2567A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124381 | ||||||
chr18:35124401
|
A | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0103a0001c0001t0002g0233others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.611-2547A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124401 | ||||||
chr18:35124533
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.611-2415C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124533 | ||||||
chr18:35124604
|
C | A | 1 | a0001c0001t0004g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.611-2344C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124604 | ||||||
chr18:35124605
|
A | T | 1 | a0001c0001t0004g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.611-2343A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124605 | ||||||
chr18:35124606
|
T | G | 1 | a0001c0001t0004g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.611-2342T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124606 | ||||||
chr18:35124913
|
A | G | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.611-2035A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35124913 | ||||||
chr18:35125084
|
A | C | 2 | a0001c0001t0008g0148a0001c0001t0008g0149 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.611-1864A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125084 | ||||||
chr18:35125320
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.611-1628C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125320 | ||||||
chr18:35125477
|
G | A | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.611-1471G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125477 | ||||||
chr18:35125491
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.611-1457A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125491 | ||||||
chr18:35125750
|
C | T | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044 | 3 | HG02735.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.611-1198C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125750 | ||||||
chr18:35125751
|
G | A | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.611-1197G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125751 | ||||||
chr18:35125818
|
A | G | 1 | a0001c0001t0013g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.611-1130A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125818 | ||||||
chr18:35125833
|
T | C | 2 | a0001c0001t0018g0247a0001c0001t0018g0253 | 2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.611-1115T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125833 | ||||||
chr18:35125982
|
G | A | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-966G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35125982 | ||||||
chr18:35126138
|
T | C | 1 | a0001c0001t0008g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.611-810T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126138 | ||||||
chr18:35126228
|
A | G | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.611-720A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126228 | ||||||
chr18:35126555
|
T | C | 1 | a0001c0001t0003g0139 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.611-393T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126555 | ||||||
chr18:35126717
|
T | C | 1 | a0001c0001t0002g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.611-231T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126717 | ||||||
chr18:35126852
|
G | A | 2 | a0001c0001t0004g0062a0001c0001t0004g0063 | 2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.611-96G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 4/6 | chr18 | 35126852 | ||||||
chr18:35127246
|
A | T | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+159A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127246 | ||||||
chr18:35127335
|
C | T | 1 | a0001c0001t0011g0351 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.750+248C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127335 | ||||||
chr18:35127368
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0002g0005a0001c0001t0002g0009others(197): Show | 211 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.750+281C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127368 | ||||||
chr18:35127678
|
A | G | 6 | a0001c0001t0004g0059a0001c0001t0004g0066a0001c0001t0004g0070others(3): Show | 6 | NA18956.hp1 NA18988.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+591A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127678 | ||||||
chr18:35127807
|
T | C | 3 | a0001c0001t0003g0118a0001c0001t0003g0130a0001c0001t0003g0135 | 3 | HG01106.hp2 HG01981.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.750+720T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127807 | ||||||
chr18:35127829
|
C | G | 6 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+742C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127829 | ||||||
chr18:35127836
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.750+749C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127836 | ||||||
chr18:35127943
|
G | C | 1 | a0001c0001t0007g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.750+856G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35127943 | ||||||
chr18:35128020
|
G | A | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.750+933G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128020 | ||||||
chr18:35128036
|
G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0251a0001c0001t0021g0057others(1): Show | 4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+949G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128036 | ||||||
chr18:35128203
|
C | A | 1 | a0001c0001t0002g0023 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.750+1116C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128203 | ||||||
chr18:35128682
|
A | G | 3 | a0001c0001t0013g0018a0001c0001t0013g0205a0001c0001t0013g0206 | 3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.750+1595A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128682 | ||||||
chr18:35128686
|
G | A | 2 | a0001c0001t0003g0126a0001c0001t0003g0127 | 2 | HG01361.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.750+1599G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128686 | ||||||
chr18:35128765
|
T | C | 8 | a0001c0001t0002g0014a0001c0001t0002g0237a0001c0001t0002g0241others(5): Show | 9 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1678T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128765 | ||||||
chr18:35128831
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0002g0005a0001c0001t0002g0013others(90): Show | 100 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.750+1744C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128831 | ||||||
chr18:35128833
|
A | G | 1 | a0001c0001t0021g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.750+1746A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128833 | ||||||
chr18:35128845
|
C | T | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.750+1758C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128845 | ||||||
chr18:35128874
|
A | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG01884.hp2 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.750+1787A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128874 | ||||||
chr18:35128905
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.750+1818C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128905 | ||||||
chr18:35128907
|
T | C | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.750+1820T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35128907 | ||||||
chr18:35129002
|
T | C | 11 | a0001c0001t0008g0006a0001c0001t0008g0114a0001c0001t0008g0119others(8): Show | 12 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.750+1915T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129002 | ||||||
chr18:35129039
|
GAAGA | G | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1953_750+1956d others(6): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129039 | ||||||
chr18:35129076
|
T | C | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.750+1989T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129076 | ||||||
chr18:35129257
|
T | G | 1 | a0001c0001t0004g0070 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.750+2170T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129257 | ||||||
chr18:35129261
|
C | T | 1 | a0001c0001t0005g0202 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.750+2174C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129261 | ||||||
chr18:35129353
|
C | T | 1 | a0001c0001t0005g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.750+2266C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129353 | ||||||
chr18:35129400
|
T | C | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.750+2313T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129400 | ||||||
chr18:35129463
|
A | T | 1 | a0001c0001t0005g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.750+2376A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129463 | ||||||
chr18:35129529
|
G | C | 2 | a0001c0001t0005g0186a0001c0001t0005g0187 | 2 | HG02523.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.750+2442G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129529 | ||||||
chr18:35129748
|
G | A | 1 | a0001c0001t0004g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.751-2284G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129748 | ||||||
chr18:35129755
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.751-2277A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129755 | ||||||
chr18:35129792
|
G | A | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.751-2240G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35129792 | ||||||
chr18:35130056
|
C | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0251a0001c0001t0021g0057others(1): Show | 4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.751-1976C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130056 | ||||||
chr18:35130115
|
G | A | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1917G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130115 | ||||||
chr18:35130153
|
G | T | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-1879G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130153 | ||||||
chr18:35130326
|
T | C | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1706T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130326 | ||||||
chr18:35130332
|
A | G | 1 | a0001c0001t0003g0145 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.751-1700A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130332 | ||||||
chr18:35130393
|
A | G | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.751-1639A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130393 | ||||||
chr18:35130544
|
A | G | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.751-1488A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130544 | ||||||
chr18:35130587
|
T | G | 3 | a0001c0001t0017g0179a0001c0001t0017g0181a0001c0001t0017g0203 | 3 | HG03041.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.751-1445T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130587 | ||||||
chr18:35130720
|
C | T | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.751-1312C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130720 | ||||||
chr18:35130876
|
G | A | 1 | a0001c0001t0040g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.751-1156G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130876 | ||||||
chr18:35130979
|
G | A | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-1053G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35130979 | ||||||
chr18:35131039
|
T | C | 1 | a0001c0001t0003g0138 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.751-993T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131039 | ||||||
chr18:35131053
|
C | T | 1 | a0001c0001t0003g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.751-979C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131053 | ||||||
chr18:35131129
|
T | C | 3 | a0001c0001t0001g0322a0001c0001t0021g0057a0001c0001t0021g0102 | 3 | HG02965.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.751-903T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131129 | ||||||
chr18:35131161
|
G | A | 77 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(74): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.751-871G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131161 | ||||||
chr18:35131400
|
A | G | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-632A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131400 | ||||||
chr18:35131433
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.751-599A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131433 | ||||||
chr18:35131441
|
G | C | 81 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(78): Show | 84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.751-591G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131441 | ||||||
chr18:35131485
|
T | C | 18 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(15): Show | 18 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.751-547T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131485 | ||||||
chr18:35131494
|
G | A | 1 | a0001c0001t0003g0321 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.751-538G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131494 | ||||||
chr18:35131727
|
T | A | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-305T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131727 | ||||||
chr18:35131810
|
C | T | 77 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(74): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.751-222C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131810 | ||||||
chr18:35131929
|
T | TTC | 3 | a0001c0001t0007g0019a0001c0001t0021g0057a0001c0001t0021g0102 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.751-87_751-86dupCT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr18 | 35131929 | |||||
chr18:35131989
|
A | G | 1 | a0001c0001t0001g0001 | 3 | NA18952.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.751-43A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | chr18 | 35131989 | ||||||
chr18:35132001
|
G | GT | 98 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0002g0005others(95): Show | 105 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.751-23dupT | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr18 | 35132001 | |||||
chr18:35132334
|
A | C | 9 | a0001c0001t0001g0265a0001c0001t0001g0269a0001c0001t0001g0271others(6): Show | 9 | NA18956.hp2 NA18957.hp2 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+144A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132334 | ||||||
chr18:35132618
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.909+428C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132618 | ||||||
chr18:35132865
|
C | A | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.909+675C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132865 | ||||||
chr18:35132875
|
AC | A | 9 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.909+686delC | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35132875 | ||||||
chr18:35133027
|
G | A | 76 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(73): Show | 79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.909+837G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133027 | ||||||
chr18:35133380
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.909+1190G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133380 | ||||||
chr18:35133483
|
C | G | 6 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+1293C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133483 | ||||||
chr18:35133508
|
G | A | 2 | a0001c0001t0006g0163a0001c0001t0006g0201 | 2 | NA18967.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.909+1318G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133508 | ||||||
chr18:35133561
|
G | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0014others(89): Show | 97 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.909+1371G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133561 | ||||||
chr18:35133768
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0308 | 2 | NA18971.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.909+1578G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133768 | ||||||
chr18:35133889
|
T | C | 3 | a0001c0001t0004g0002a0001c0001t0004g0065a0001c0001t0004g0076 | 5 | HG00408.hp2 NA18964.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+1699T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35133889 | ||||||
chr18:35134129
|
T | G | 1 | a0001c0001t0030g0299 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+1939T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134129 | ||||||
chr18:35134430
|
G | A | 1 | a0001c0001t0027g0029 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.909+2240G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134430 | ||||||
chr18:35134482
|
G | A | 77 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(74): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.909+2292G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134482 | ||||||
chr18:35134616
|
G | A | 2 | a0001c0001t0005g0156a0001c0001t0005g0214 | 2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.909+2426G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134616 | ||||||
chr18:35134775
|
C | T | 1 | a0001c0001t0011g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.909+2585C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134775 | ||||||
chr18:35134889
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.909+2699G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134889 | ||||||
chr18:35134907
|
C | A | 22 | a0001c0001t0007g0019a0001c0001t0007g0226a0001c0001t0007g0227others(19): Show | 22 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.909+2717C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35134907 | ||||||
chr18:35135193
|
T | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0103a0001c0001t0002g0233others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+3003T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135193 | ||||||
chr18:35135247
|
C | T | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.909+3057C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135247 | ||||||
chr18:35135290
|
G | A | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.909+3100G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135290 | ||||||
chr18:35135338
|
A | T | 5 | a0001c0001t0002g0009a0001c0001t0002g0103a0001c0001t0002g0233others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+3148A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135338 | ||||||
chr18:35135426
|
A | G | 3 | a0001c0001t0013g0018a0001c0001t0013g0205a0001c0001t0013g0206 | 3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.909+3236A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135426 | ||||||
chr18:35135449
|
A | G | 1 | a0001c0001t0004g0070 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.909+3259A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135449 | ||||||
chr18:35135451
|
G | A | 12 | a0001c0001t0012g0209a0001c0001t0012g0210a0001c0001t0012g0211others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+3261G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135451 | ||||||
chr18:35135473
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.909+3283A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135473 | ||||||
chr18:35135475
|
A | T | 3 | a0001c0001t0007g0019a0001c0001t0021g0057a0001c0001t0021g0102 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.909+3285A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135475 | ||||||
chr18:35135717
|
C | T | 77 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(74): Show | 80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.909+3527C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135717 | ||||||
chr18:35135827
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+3637G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35135827 | ||||||
chr18:35136151
|
A | G | 3 | a0001c0001t0013g0018a0001c0001t0013g0205a0001c0001t0013g0206 | 3 | HG02647.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.909+3961A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136151 | ||||||
chr18:35136173
|
A | G | 1 | a0001c0001t0025g0020 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.909+3983A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136173 | ||||||
chr18:35136203
|
G | A | 1 | a0001c0001t0007g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.909+4013G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136203 | ||||||
chr18:35136290
|
C | T | 1 | a0001c0001t0004g0072 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.910-4005C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136290 | ||||||
chr18:35136415
|
G | A | 1 | a0001c0001t0007g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.910-3880G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136415 | ||||||
chr18:35136478
|
G | A | 201 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0013others(198): Show | 210 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.910-3817G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136478 | ||||||
chr18:35136529
|
C | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(33): Show | 37 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.910-3766C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136529 | ||||||
chr18:35136583
|
G | A | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.910-3712G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136583 | ||||||
chr18:35136854
|
A | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0103a0001c0001t0002g0233others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-3441A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136854 | ||||||
chr18:35136869
|
T | C | 1 | a0001c0001t0042g0109 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.910-3426T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136869 | ||||||
chr18:35136885
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.910-3410G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136885 | ||||||
chr18:35136908
|
C | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0251a0001c0001t0021g0057others(1): Show | 4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3387C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35136908 | ||||||
chr18:35137133
|
T | C | 4 | a0001c0001t0007g0019a0001c0001t0007g0251a0001c0001t0021g0057others(1): Show | 4 | HG02486.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-3162T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137133 | ||||||
chr18:35137274
|
T | C | 2 | a0001c0001t0002g0235a0001c0001t0002g0236 | 2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.910-3021T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137274 | ||||||
chr18:35137545
|
ATCT | A | 3 | a0001c0001t0001g0255a0001c0001t0021g0057a0001c0001t0021g0102 | 3 | HG02922.hp1 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.910-2745_910-2743d others(5): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr18 | 35137545 | |||||
chr18:35137632
|
A | G | 1 | a0001c0001t0004g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.910-2663A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137632 | ||||||
chr18:35137666
|
A | G | 1 | a0001c0001t0006g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.910-2629A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137666 | ||||||
chr18:35137710
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.910-2585C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137710 | ||||||
chr18:35137838
|
A | C | 6 | a0001c0001t0007g0226a0001c0001t0007g0227a0001c0001t0007g0228others(3): Show | 6 | HG02451.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-2457A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137838 | ||||||
chr18:35137858
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.910-2437G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35137858 | ||||||
chr18:35138057
|
G | A | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.910-2238G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138057 | ||||||
chr18:35138182
|
C | T | 36 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0023others(33): Show | 37 | HG00558.hp1 HG01109.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.910-2113C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138182 | ||||||
chr18:35138188
|
G | C | 60 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0221others(57): Show | 64 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.910-2107G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138188 | ||||||
chr18:35138279
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0002g0005others(118): Show | 128 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.910-2016T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138279 | ||||||
chr18:35138386
|
C | G | 1 | a0001c0001t0007g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.910-1909C>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138386 | ||||||
chr18:35138447
|
T | C | 1 | a0001c0001t0003g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.910-1848T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138447 | ||||||
chr18:35138522
|
A | T | 1 | a0001c0001t0005g0195 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.910-1773A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138522 | ||||||
chr18:35138633
|
T | A | 200 | a0001c0001t0001g0100a0001c0001t0002g0005a0001c0001t0002g0009others(197): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.910-1662T>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138633 | ||||||
chr18:35138701
|
G | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0102 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.910-1594G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138701 | ||||||
chr18:35138747
|
G | T | 1 | a0001c0001t0002g0009 | 2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.910-1548G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138747 | ||||||
chr18:35138800
|
C | A | 21 | a0001c0001t0008g0006a0001c0001t0008g0114a0001c0001t0008g0119others(18): Show | 22 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.910-1495C>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138800 | ||||||
chr18:35138836
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0307a0001c0001t0001g0315others(5): Show | 9 | HG01099.hp2 HG01496.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.910-1459A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138836 | ||||||
chr18:35138914
|
T | G | 1 | a0001c0001t0003g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-1381T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138914 | ||||||
chr18:35138917
|
G | T | 4 | a0001c0001t0015g0240a0001c0001t0015g0261a0001c0001t0015g0262others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1378G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138917 | ||||||
chr18:35138923
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0002g0005a0001c0001t0002g0013others(90): Show | 100 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.910-1372C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138923 | ||||||
chr18:35138960
|
G | A | 200 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0013others(197): Show | 209 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.910-1335G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35138960 | ||||||
chr18:35139006
|
G | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0002g0005others(193): Show | 207 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.910-1289G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139006 | ||||||
chr18:35139043
|
G | C | 1 | a0001c0001t0034g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.910-1252G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139043 | ||||||
chr18:35139221
|
G | A | 1 | a0001c0001t0039g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.910-1074G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139221 | ||||||
chr18:35139230
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.910-1065G>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139230 | ||||||
chr18:35139235
|
C | T | 1 | a0001c0001t0003g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.910-1060C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139235 | ||||||
chr18:35139270
|
A | C | 3 | a0001c0001t0002g0013a0001c0001t0002g0221a0001c0001t0002g0222 | 4 | HG00642.hp1 HG01099.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1025A>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139270 | ||||||
chr18:35139285
|
A | G | 47 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0162others(44): Show | 49 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.910-1010A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139285 | ||||||
chr18:35139392
|
T | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0002g0005others(99): Show | 110 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.910-903T>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139392 | ||||||
chr18:35139492
|
A | T | 1 | a0001c0001t0007g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.910-803A>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139492 | ||||||
chr18:35139572
|
G | A | 1 | a0001c0001t0035g0208 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.910-723G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139572 | ||||||
chr18:35139618
|
C | T | 76 | a0001c0001t0005g0010a0001c0001t0005g0011a0001c0001t0005g0156others(73): Show | 79 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.910-677C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139618 | ||||||
chr18:35139758
|
T | C | 1 | a0001c0001t0004g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.910-537T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139758 | ||||||
chr18:35139795
|
G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0123 | 3 | HG01192.hp2 HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.910-500G>A | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139795 | ||||||
chr18:35139853
|
T | C | 1 | a0001c0001t0015g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-442T>C | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139853 | ||||||
chr18:35139911
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.910-384C>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35139911 | ||||||
chr18:35140031
|
A | G | 1 | a0001c0001t0007g0019 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.910-264A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140031 | ||||||
chr18:35140040
|
A | G | 1 | a0001c0001t0012g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-255A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140040 | ||||||
chr18:35140111
|
G | T | 1 | a0002c0003t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.910-184G>T | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140111 | ||||||
chr18:35140112
|
G | GTGATCAT others(6): Show |
1 | a0002c0003t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.910-183_910-182ins others(13): Show |
MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140112 | ||||||
chr18:35140225
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(102): Show | 108 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.910-70A>G | MAPRE2 | ENSG00000166974.13 | transcript | ENST00000300249.10 | protein_coding | 6/6 | chr18 | 35140225 |