geneid | 5241 |
---|---|
ensemblid | ENSG00000082175.16 |
hgncid | 8910 |
symbol | PGR |
name | progesterone receptor |
refseq_nuc | NM_000926.4 |
refseq_prot | NP_000917.3 |
ensembl_nuc | ENST00000325455.10 |
ensembl_prot | ENSP00000325120.5 |
mane_status | MANE Select |
chr | chr11 |
start | 101029624 |
end | 101129813 |
strand | - |
ver | v1.2 |
region | chr11:101029624-101129813 |
region5000 | chr11:101024624-101134813 |
regionname0 | PGR_chr11_101029624_101129813 |
regionname5000 | PGR_chr11_101024624_101134813 |
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 | 933 | 202 | 54 | 48 | 57 | 13 | 28 | 42 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002 | 0/0 | 933 | 17 | 1 | 10 | 1 | 3 | 2 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003 | 0/0 | 933 | 15 | 14 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004 | 0/0 | 933 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0005 | 0/0 | 933 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0006 | 0/0 | 933 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0007 | 0/0 | 933 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0008 | 0/0 | 933 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0009 | 0/0 | 431 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0010 | 0/0 | 933 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0011 | 0/0 | 933 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2802 | 101 | 31 | 19 | 28 | 3 | 19 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0002 | 0/0 | 2802 | 58 | 18 | 9 | 26 | 2 | 3 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0003 | 0/1 | 2802 | 38 | 4 | 18 | 2 | 7 | 6 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0004 | 0/0 | 2802 | 14 | 1 | 9 | 0 | 3 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0005 | 0/0 | 2802 | 14 | 13 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0006 | 0/0 | 2802 | 8 | 7 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0007 | 0/0 | 2802 | 3 | 0 | 2 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0008 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0009 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0010 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0011 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0012 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0013 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0014 | 0/0 | 2802 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0015 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0016 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0017 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0018 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0019 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0020 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0021 | 0/0 | 2802 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0022 | 0/0 | 2780 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0023 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
c0024 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
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 | 10240 | 30 | 6 | 4 | 15 | 2 | 3 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0002 | 0/0 | 10237 | 29 | 3 | 14 | 2 | 4 | 6 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0003 | 0/0 | 10237 | 25 | 0 | 4 | 16 | 1 | 4 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0004 | 0/0 | 10237 | 21 | 14 | 4 | 0 | 1 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0005 | 0/0 | 10240 | 8 | 2 | 4 | 1 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0006 | 0/0 | 10240 | 6 | 5 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0007 | 0/0 | 10237 | 6 | 0 | 2 | 0 | 2 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0008 | 0/0 | 10237 | 5 | 2 | 0 | 3 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0009 | 0/0 | 10240 | 5 | 3 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0010 | 0/0 | 10237 | 5 | 3 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0011 | 0/0 | 10235 | 4 | 3 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0012 | 0/0 | 10237 | 4 | 0 | 0 | 2 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0013 | 0/0 | 10237 | 4 | 4 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0014 | 0/0 | 10239 | 4 | 0 | 0 | 0 | 0 | 4 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0015 | 0/0 | 10240 | 3 | 0 | 2 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0016 | 0/0 | 10240 | 3 | 0 | 0 | 3 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0017 | 0/0 | 10237 | 3 | 0 | 1 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0018 | 0/0 | 10240 | 2 | 0 | 0 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0019 | 0/0 | 10240 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0020 | 0/0 | 10240 | 2 | 0 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0021 | 0/0 | 10241 | 2 | 0 | 0 | 0 | 2 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0022 | 0/0 | 10240 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0023 | 0/0 | 10240 | 2 | 1 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0024 | 0/0 | 10240 | 2 | 0 | 0 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0025 | 0/0 | 10240 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0026 | 0/0 | 10240 | 2 | 1 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0027 | 0/0 | 10237 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0028 | 0/1 | 10237 | 2 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0029 | 0/0 | 10237 | 2 | 0 | 0 | 0 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0030 | 0/0 | 10237 | 2 | 0 | 0 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0031 | 0/0 | 10237 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0032 | 0/0 | 10240 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0033 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0034 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0035 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0036 | 0/0 | 10238 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0037 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0038 | 0/0 | 10235 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0039 | 0/0 | 10230 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0040 | 0/0 | 10235 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0041 | 0/0 | 10235 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0042 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0043 | 0/0 | 10240 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0044 | 0/0 | 10240 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0045 | 0/0 | 10240 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0046 | 0/0 | 10240 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0047 | 0/0 | 10240 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0048 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0049 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0050 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0051 | 0/0 | 10240 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0052 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0053 | 0/0 | 10235 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0054 | 0/0 | 10240 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0055 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0056 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0057 | 0/0 | 10240 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0058 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0059 | 0/0 | 10240 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0060 | 0/0 | 10240 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0061 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0062 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0063 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0064 | 0/0 | 10232 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0065 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0066 | 0/0 | 10237 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0067 | 0/0 | 10237 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0068 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0069 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0070 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0071 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0072 | 0/0 | 10237 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0073 | 0/0 | 10237 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0074 | 0/0 | 10237 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0075 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0076 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0077 | 0/0 | 10238 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0078 | 0/0 | 10237 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0079 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0080 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0081 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0082 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0083 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0084 | 0/0 | 10225 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0085 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0086 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0087 | 0/0 | 10237 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0088 | 0/0 | 10237 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0089 | 0/0 | 10238 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0090 | 0/0 | 10237 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
t0091 | 1/0 | 10236 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
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 | 2 | 0 | 0 | 0 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2802 | 101 | 31 | 19 | 28 | 3 | 19 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002 | 0/0 | 2802 | 58 | 18 | 9 | 26 | 2 | 3 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003 | 0/1 | 2802 | 38 | 4 | 18 | 2 | 7 | 6 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0007 | 0/0 | 2802 | 3 | 0 | 2 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0019 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0024 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004 | 0/0 | 2802 | 14 | 1 | 9 | 0 | 3 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0014 | 0/0 | 2802 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0015 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0016 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005 | 0/0 | 2802 | 14 | 13 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0020 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0006 | 0/0 | 2802 | 8 | 7 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0017 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0018 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0005c0008 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0005c0012 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0006c0010 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0006c0011 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0007c0023 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0008c0021 | 0/0 | 2802 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0009c0022 | 0/0 | 2780 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0010c0013 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0011c0009 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 13038 | 2 | 0 | 0 | 0 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0003 | 0/0 | 13038 | 20 | 0 | 2 | 15 | 0 | 3 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0004 | 0/0 | 13038 | 20 | 13 | 4 | 0 | 1 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0007 | 0/0 | 13038 | 6 | 0 | 2 | 0 | 2 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0008 | 0/0 | 13038 | 5 | 2 | 0 | 3 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0010 | 0/0 | 13038 | 5 | 3 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0012 | 0/0 | 13038 | 4 | 0 | 0 | 2 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0013 | 0/0 | 13038 | 4 | 4 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0014 | 0/0 | 13040 | 3 | 0 | 0 | 0 | 0 | 3 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0017 | 0/0 | 13038 | 3 | 0 | 1 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0027 | 0/0 | 13038 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0029 | 0/0 | 13038 | 2 | 0 | 0 | 0 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0030 | 0/0 | 13038 | 2 | 0 | 0 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0033 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0034 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0035 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0036 | 0/0 | 13039 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0037 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0062 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0063 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0065 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0066 | 0/0 | 13038 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0072 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0073 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0074 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0076 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0078 | 0/0 | 13038 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0079 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0082 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0085 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0086 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0087 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0088 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0089 | 0/0 | 13039 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0090 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0001t0091 | 1/0 | 13037 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0001 | 0/0 | 13041 | 30 | 6 | 4 | 15 | 2 | 3 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0009 | 0/0 | 13041 | 4 | 2 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0016 | 0/0 | 13041 | 3 | 0 | 0 | 3 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0018 | 0/0 | 13041 | 2 | 0 | 0 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0022 | 0/0 | 13041 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0023 | 0/0 | 13041 | 2 | 1 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0024 | 0/0 | 13041 | 2 | 0 | 0 | 2 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0026 | 0/0 | 13041 | 2 | 1 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0032 | 0/0 | 13041 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0046 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0048 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0049 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0050 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0051 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0056 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0057 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0060 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0002t0084 | 0/0 | 13026 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0002 | 0/0 | 13038 | 24 | 2 | 12 | 2 | 4 | 4 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0003 | 0/0 | 13038 | 2 | 0 | 0 | 0 | 1 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0014 | 0/0 | 13040 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0028 | 0/1 | 13038 | 2 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0061 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0067 | 0/0 | 13038 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0068 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0069 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0070 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0071 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0080 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0081 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0003t0083 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0007t0003 | 0/0 | 13038 | 3 | 0 | 2 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0019t0075 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0001c0024t0077 | 0/0 | 13039 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0005 | 0/0 | 13041 | 5 | 1 | 3 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0015 | 0/0 | 13041 | 2 | 0 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0020 | 0/0 | 13041 | 2 | 0 | 2 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0021 | 0/0 | 13042 | 2 | 0 | 0 | 0 | 2 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0043 | 0/0 | 13041 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0044 | 0/0 | 13041 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0004t0045 | 0/0 | 13041 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0014t0002 | 0/0 | 13038 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0015t0054 | 0/0 | 13041 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0002c0016t0005 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0006 | 0/0 | 13041 | 6 | 5 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0019 | 0/0 | 13041 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0025 | 0/0 | 13041 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0052 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0053 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0055 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0005t0059 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0003c0020t0064 | 0/0 | 13033 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0006t0011 | 0/0 | 13036 | 4 | 3 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0006t0038 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0006t0039 | 0/0 | 13031 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0006t0040 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0006t0041 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0017t0002 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0004c0018t0042 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0005c0008t0031 | 0/0 | 13038 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0005c0012t0058 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0006c0010t0004 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0006c0011t0009 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0007c0023t0005 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0008c0021t0005 | 0/0 | 13041 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0009c0022t0002 | 0/0 | 13016 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0010c0013t0015 | 0/0 | 13041 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
a0011c0009t0047 | 0/0 | 13041 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | copy fasta | chr11 | 101024624 | 101134813 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0010g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0010g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0012g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0014g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0014g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0014g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0017g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0017g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0027g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0027g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0029g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0029g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0030g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0030g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0033g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0034g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0035g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0036g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0037g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0062g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0063g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0065g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0066g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0072g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0073g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0074g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0076g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0078g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0079g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0082g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0085g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0086g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0087g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0088g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0089g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0090g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0001t0091g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0016g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0016g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0016g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0018g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0018g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0022g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0023g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0023g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0024g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0024g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0026g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0026g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0032g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0032g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0046g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0048g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0049g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0050g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0051g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0056g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0057g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0060g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0002t0084g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0014g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0028g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0028g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0061g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0067g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0068g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0069g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0070g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0071g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0080g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0081g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0003t0083g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0007t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0007t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0007t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0019t0075g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0001c0024t0077g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0015g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0015g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0020g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0020g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0021g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0021g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0043g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0044g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0004t0045g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0014t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0015t0054g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0002c0016t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0019g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0025g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0025g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0052g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0053g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0055g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0005t0059g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0003c0020t0064g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0011g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0038g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0039g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0040g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0006t0041g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0017t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0004c0018t0042g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0005c0008t0031g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0005c0008t0031g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0005c0012t0058g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0006c0010t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0006c0011t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0007c0023t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0008c0021t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0009c0022t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0010c0013t0015g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
a0011c0009t0047g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0004 | t0045 | g0035 | EUR | GBR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0180 | EUR | GBR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00140 | hp1 | a0001 | c0024 | t0077 | g0210 | EUR | GBR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00140 | hp2 | a0001 | c0003 | t0028 | g0194 | EUR | GBR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0052 | EUR | FIN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00323 | hp2 | a0001 | c0003 | t0003 | g0203 | EUR | FIN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00423 | hp1 | a0002 | c0016 | t0005 | g0030 | EAS | CHS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00423 | hp2 | a0001 | c0001 | t0030 | g0099 | EAS | CHS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00597 | hp1 | a0001 | c0002 | t0024 | g0129 | EAS | CHS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00597 | hp2 | a0001 | c0001 | t0017 | g0078 | EAS | CHS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00621 | hp1 | a0001 | c0002 | t0057 | g0122 | EAS | CHS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00621 | hp2 | a0001 | c0003 | t0002 | g0207 | EAS | CHS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00639 | hp2 | a0001 | c0003 | t0068 | g0190 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00642 | hp2 | a0001 | c0001 | t0076 | g0064 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00733 | hp1 | a0001 | c0002 | t0026 | g0042 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00733 | hp2 | a0001 | c0003 | t0002 | g0193 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00735 | hp1 | a0001 | c0001 | t0086 | g0226 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00735 | hp2 | a0002 | c0014 | t0002 | g0034 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00738 | hp1 | a0001 | c0003 | t0002 | g0170 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00738 | hp2 | a0001 | c0002 | t0009 | g0227 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0181 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01069 | hp1 | a0009 | c0022 | t0002 | g0208 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01070 | hp2 | a0001 | c0003 | t0071 | g0191 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01074 | hp1 | a0002 | c0004 | t0044 | g0028 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0051 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01081 | hp2 | a0001 | c0003 | t0080 | g0183 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01099 | hp1 | a0001 | c0002 | t0009 | g0228 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01099 | hp2 | a0001 | c0003 | t0002 | g0177 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01106 | hp1 | a0002 | c0004 | t0043 | g0032 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0220 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01109 | hp2 | a0001 | c0001 | t0034 | g0005 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01167 | hp1 | a0001 | c0007 | t0003 | g0096 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0200 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0189 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01168 | hp2 | a0001 | c0001 | t0087 | g0240 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01175 | hp1 | a0001 | c0003 | t0069 | g0172 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01175 | hp2 | a0002 | c0004 | t0005 | g0027 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01192 | hp2 | a0002 | c0004 | t0005 | g0026 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01243 | hp1 | a0003 | c0005 | t0006 | g0162 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01243 | hp2 | a0004 | c0006 | t0011 | g0012 | AMR | PUR | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01255 | hp1 | a0001 | c0003 | t0081 | g0192 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01256 | hp1 | a0002 | c0004 | t0020 | g0024 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01256 | hp2 | a0001 | c0001 | t0037 | g0006 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01257 | hp1 | a0001 | c0003 | t0002 | g0187 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01258 | hp1 | a0002 | c0004 | t0020 | g0029 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0186 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0175 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01261 | hp2 | a0002 | c0004 | t0005 | g0025 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01346 | hp1 | a0001 | c0002 | t0023 | g0147 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01346 | hp2 | a0001 | c0001 | t0035 | g0004 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01433 | hp1 | a0001 | c0002 | t0084 | g0216 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0054 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01515 | hp1 | a0001 | c0003 | t0067 | g0182 | EUR | IBS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01515 | hp2 | a0002 | c0004 | t0021 | g0036 | EUR | IBS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0150 | EUR | IBS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0178 | EUR | IBS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0149 | EUR | IBS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01517 | hp2 | a0002 | c0004 | t0021 | g0037 | EUR | IBS | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0151 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01884 | hp2 | a0001 | c0003 | t0083 | g0211 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0075 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01891 | hp2 | a0002 | c0004 | t0005 | g0031 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01934 | hp1 | a0002 | c0004 | t0015 | g0021 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01934 | hp2 | a0001 | c0003 | t0002 | g0188 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01981 | hp1 | a0001 | c0007 | t0003 | g0069 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01981 | hp2 | a0008 | c0021 | t0005 | g0205 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01993 | hp1 | a0001 | c0003 | t0002 | g0199 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01993 | hp2 | a0002 | c0004 | t0015 | g0022 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02015 | hp2 | a0001 | c0001 | t0073 | g0086 | EAS | KHV | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02055 | hp1 | a0003 | c0005 | t0025 | g0160 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02055 | hp2 | a0004 | c0006 | t0038 | g0017 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02145 | hp1 | a0003 | c0020 | t0064 | g0168 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02145 | hp2 | a0007 | c0023 | t0005 | g0209 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | CDX | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | CDX | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02165 | hp1 | a0001 | c0003 | t0002 | g0179 | EAS | CDX | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CDX | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0174 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02257 | hp2 | a0003 | c0005 | t0055 | g0167 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02258 | hp1 | a0004 | c0006 | t0011 | g0016 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02258 | hp2 | a0001 | c0002 | t0048 | g0079 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02273 | hp1 | a0001 | c0001 | t0033 | g0003 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02273 | hp2 | a0001 | c0003 | t0070 | g0201 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02280 | hp1 | a0001 | c0001 | t0089 | g0235 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02280 | hp2 | a0001 | c0002 | t0009 | g0232 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0202 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02300 | hp2 | a0001 | c0001 | t0085 | g0231 | AMR | PEL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02451 | hp1 | a0005 | c0012 | t0058 | g0019 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0223 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02572 | hp2 | a0001 | c0001 | t0013 | g0090 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0089 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02630 | hp1 | a0005 | c0008 | t0031 | g0154 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02647 | hp1 | a0003 | c0005 | t0052 | g0169 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02698 | hp1 | a0001 | c0003 | t0002 | g0173 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02698 | hp2 | a0001 | c0003 | t0014 | g0206 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02717 | hp2 | a0001 | c0002 | t0026 | g0044 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02735 | hp2 | a0001 | c0001 | t0012 | g0082 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02738 | hp1 | a0010 | c0013 | t0015 | g0020 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02818 | hp2 | a0001 | c0019 | t0075 | g0156 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02886 | hp1 | a0004 | c0017 | t0002 | g0038 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02895 | hp2 | a0001 | c0002 | t0022 | g0055 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02896 | hp1 | a0001 | c0001 | t0062 | g0058 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02896 | hp2 | a0004 | c0006 | t0011 | g0015 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02897 | hp2 | a0004 | c0006 | t0011 | g0014 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02922 | hp1 | a0001 | c0002 | t0032 | g0215 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02922 | hp2 | a0001 | c0002 | t0022 | g0043 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0251 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0084 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02976 | hp1 | a0001 | c0002 | t0032 | g0214 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02976 | hp2 | a0001 | c0002 | t0049 | g0080 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03041 | hp1 | a0003 | c0005 | t0025 | g0159 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03041 | hp2 | a0003 | c0005 | t0006 | g0163 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03098 | hp1 | a0001 | c0001 | t0063 | g0060 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03130 | hp1 | a0001 | c0001 | t0082 | g0107 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03130 | hp2 | a0003 | c0005 | t0006 | g0161 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03139 | hp1 | a0001 | c0001 | t0013 | g0074 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03195 | hp2 | a0001 | c0001 | t0090 | g0233 | AFR | ESN | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03209 | hp1 | a0003 | c0005 | t0006 | g0164 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03209 | hp2 | a0001 | c0002 | t0023 | g0146 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03225 | hp1 | a0004 | c0006 | t0041 | g0013 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03225 | hp2 | a0006 | c0010 | t0004 | g0213 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03239 | hp1 | a0001 | c0003 | t0003 | g0204 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03239 | hp2 | a0001 | c0001 | t0014 | g0050 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03453 | hp1 | a0001 | c0002 | t0056 | g0142 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03453 | hp2 | a0003 | c0005 | t0053 | g0166 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03486 | hp1 | a0004 | c0018 | t0042 | g0039 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03486 | hp2 | a0003 | c0005 | t0019 | g0002 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0045 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03490 | hp2 | a0002 | c0004 | t0005 | g0033 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0048 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03579 | hp2 | a0001 | c0002 | t0050 | g0141 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03654 | hp1 | a0001 | c0001 | t0078 | g0046 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03654 | hp2 | a0001 | c0001 | t0029 | g0062 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03669 | hp1 | a0001 | c0001 | t0066 | g0077 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03688 | hp1 | a0001 | c0003 | t0002 | g0176 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03688 | hp2 | a0001 | c0001 | t0029 | g0104 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0249 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03710 | hp2 | a0001 | c0001 | t0014 | g0047 | SAS | PJL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03927 | hp1 | a0001 | c0001 | t0036 | g0007 | SAS | BEB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03927 | hp2 | a0002 | c0015 | t0054 | g0023 | SAS | BEB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04115 | hp1 | a0001 | c0001 | t0012 | g0153 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04115 | hp2 | a0001 | c0003 | t0002 | g0198 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0184 | SAS | BEB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | BEB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04199 | hp2 | a0001 | c0001 | t0014 | g0053 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04204 | hp1 | a0011 | c0009 | t0047 | g0018 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | YRI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | YRI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | CHB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18946 | hp1 | a0001 | c0002 | t0016 | g0138 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18947 | hp2 | a0001 | c0002 | t0016 | g0140 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18949 | hp1 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18953 | hp1 | a0001 | c0001 | t0088 | g0243 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18959 | hp1 | a0001 | c0001 | t0008 | g0081 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18960 | hp1 | a0001 | c0002 | t0018 | g0009 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18960 | hp2 | a0001 | c0001 | t0017 | g0083 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18968 | hp2 | a0001 | c0002 | t0024 | g0137 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18971 | hp1 | a0001 | c0002 | t0060 | g0130 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18971 | hp2 | a0001 | c0002 | t0046 | g0101 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18974 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18974 | hp2 | a0001 | c0007 | t0003 | g0152 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18977 | hp2 | a0001 | c0002 | t0016 | g0120 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18984 | hp1 | a0001 | c0001 | t0030 | g0100 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19009 | hp2 | a0001 | c0002 | t0018 | g0008 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19030 | hp1 | a0005 | c0008 | t0031 | g0155 | AFR | LWK | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0196 | AFR | LWK | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19043 | hp1 | a0001 | c0003 | t0061 | g0171 | AFR | LWK | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19043 | hp2 | a0006 | c0011 | t0009 | g0212 | AFR | LWK | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19060 | hp1 | a0001 | c0001 | t0074 | g0102 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19085 | hp1 | a0001 | c0001 | t0072 | g0061 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19090 | hp1 | a0001 | c0002 | t0051 | g0135 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19240 | hp1 | a0003 | c0005 | t0059 | g0158 | AFR | YRI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA19240 | hp2 | a0003 | c0005 | t0006 | g0157 | AFR | YRI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0247 | EUR | TSI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0197 | EUR | TSI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA20805 | hp1 | a0001 | c0003 | t0002 | g0195 | EUR | TSI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0049 | EUR | TSI | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0248 | SAS | GIH | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0250 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG01123 | hp2 | a0001 | c0001 | t0017 | g0094 | AMR | CLM | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02109 | hp1 | a0003 | c0005 | t0006 | g0165 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02109 | hp2 | a0001 | c0002 | t0009 | g0229 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG02559 | hp2 | a0001 | c0001 | t0027 | g0059 | AFR | ACB | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03471 | hp1 | a0001 | c0001 | t0079 | g0040 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG03471 | hp2 | a0003 | c0005 | t0019 | g0002 | AFR | MSL | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG06807 | hp1 | a0004 | c0006 | t0039 | g0011 | AFR | USA | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | USA | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA21309 | hp1 | a0001 | c0001 | t0065 | g0108 | AFR | LWK | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
NA21309 | hp2 | a0004 | c0006 | t0040 | g0010 | AFR | LWK | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0028 | g0185 | REF | REF | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0091 | g0252 | REF | REF | PGR_chr11_101024624_101134813 | PGR | chr11 | 101024624 | 101134813 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101062681
|
C | A | 4 | a0002a0007a0008others(1): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
missense_variant | MODERATE | c.1978G>T | p.Val660Leu | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/8 | 2721/13037 | 1978/2802 | 660/933 | chr11 | 101062681 | ||
chr11:101127464
|
T | G | 1 | a0005 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1607A>C | p.Gln536Pro | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 2350/13037 | 1607/2802 | 536/933 | chr11 | 101127464 | ||
chr11:101127741
|
C | A | 2 | a0003a0011 | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
missense_variant | MODERATE | c.1330G>T | p.Ala444Ser | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 2073/13037 | 1330/2802 | 444/933 | chr11 | 101127741 | ||
chr11:101127900
|
CCTCCTCC others(27): Show |
C | 1 | a0009 | 1 | HG01069.hp1 | frameshift_variant | HIGH | c.1137_1170delCTTCCA others(28): Show |
p.Asp379fs | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1913/13037 | 1137/2802 | 379/933 | chr11 | 101127900 | ||
chr11:101128031
|
C | G | 1 | a0004 | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
missense_variant | MODERATE | c.1040G>C | p.Cys347Ser | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1783/13037 | 1040/2802 | 347/933 | chr11 | 101128031 | ||
chr11:101128040
|
C | G | 3 | a0002a0007a0010 | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
missense_variant | MODERATE | c.1031G>C | p.Ser344Thr | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1774/13037 | 1031/2802 | 344/933 | chr11 | 101128040 | ||
chr11:101128045
|
C | CGCTAAGA others(5): Show |
1 | a0009 | 1 | HG01069.hp1 | disruptive_inframe_insertion | MODERATE | c.1025_1026insTCCTTT others(6): Show |
p.Pro342_Arg343insPr others(10): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1768/13037 | 1025/2802 | 342/933 | chr11 | 101128045 | ||
chr11:101128053
|
C | G | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1018G>C | p.Ala340Pro | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1761/13037 | 1018/2802 | 340/933 | chr11 | 101128053 | ||
chr11:101128056
|
A | G | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1015T>C | p.Phe339Leu | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1758/13037 | 1015/2802 | 339/933 | chr11 | 101128056 | ||
chr11:101128058
|
G | T | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1013C>A | p.Ala338Asp | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1756/13037 | 1013/2802 | 338/933 | chr11 | 101128058 | ||
chr11:101128070
|
C | G | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1001G>C | p.Gly334Ala | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1744/13037 | 1001/2802 | 334/933 | chr11 | 101128070 | ||
chr11:101128073
|
G | C | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.998C>G | p.Ala333Gly | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1741/13037 | 998/2802 | 333/933 | chr11 | 101128073 | ||
chr11:101128074
|
C | T | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.997G>A | p.Ala333Thr | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1740/13037 | 997/2802 | 333/933 | chr11 | 101128074 | ||
chr11:101128095
|
C | G | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.976G>C | p.Asp326His | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1719/13037 | 976/2802 | 326/933 | chr11 | 101128095 | ||
chr11:101128213
|
G | C | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.858C>G | p.Asp286Glu | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1601/13037 | 858/2802 | 286/933 | chr11 | 101128213 | ||
chr11:101128214
|
T | G | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.857A>C | p.Asp286Ala | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1600/13037 | 857/2802 | 286/933 | chr11 | 101128214 | ||
chr11:101128224
|
C | G | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.847G>C | p.Val283Leu | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1590/13037 | 847/2802 | 283/933 | chr11 | 101128224 | ||
chr11:101128226
|
A | C | 1 | a0009 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.845T>G | p.Leu282Arg | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1588/13037 | 845/2802 | 282/933 | chr11 | 101128226 | ||
chr11:101128514
|
G | A | 1 | a0007 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.557C>T | p.Pro186Leu | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1300/13037 | 557/2802 | 186/933 | chr11 | 101128514 | ||
chr11:101128769
|
G | T | 1 | a0010 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.302C>A | p.Ser101Tyr | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1045/13037 | 302/2802 | 101/933 | chr11 | 101128769 | ||
chr11:101128919
|
A | G | 1 | a0006 | 2 | HG03225.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.152T>C | p.Ile51Thr | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 895/13037 | 152/2802 | 51/933 | chr11 | 101128919 | ||
chr11:101128923
|
C | T | 1 | a0011 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.148G>A | p.Ala50Thr | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 891/13037 | 148/2802 | 50/933 | chr11 | 101128923 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101039260
|
T | C | 12 | a0001c0002a0002c0004a0002c0015others(9): Show | 95 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(92): Show |
synonymous_variant | LOW | c.2658A>G | p.Gln886Gln | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3401/13037 | 2658/2802 | 886/933 | chr11 | 101039260 | ||
chr11:101051471
|
G | A | 5 | a0002c0004a0002c0016a0007c0023others(2): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
synonymous_variant | LOW | c.2310C>T | p.His770His | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/8 | 3053/13037 | 2310/2802 | 770/933 | chr11 | 101051471 | ||
chr11:101062655
|
G | A | 1 | a0002c0016 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.2004C>T | p.Ala668Ala | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/8 | 2747/13037 | 2004/2802 | 668/933 | chr11 | 101062655 | ||
chr11:101091797
|
G | T | 1 | a0001c0007 | 3 | HG01167.hp1 HG01981.hp1 NA18974.hp2 |
synonymous_variant | LOW | c.1869C>A | p.Arg623Arg | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/8 | 2612/13037 | 1869/2802 | 623/933 | chr11 | 101091797 | ||
chr11:101127715
|
G | A | 1 | a0001c0019 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.1356C>T | p.Ser452Ser | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 2099/13037 | 1356/2802 | 452/933 | chr11 | 101127715 | ||
chr11:101127892
|
G | A | 3 | a0001c0003a0008c0021a0009c0022 | 40 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(37): Show |
synonymous_variant | LOW | c.1179C>T | p.Gly393Gly | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1922/13037 | 1179/2802 | 393/933 | chr11 | 101127892 | ||
chr11:101128051
|
G | A | 1 | a0009c0022 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.1020C>T | p.Ala340Ala | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1763/13037 | 1020/2802 | 340/933 | chr11 | 101128051 | ||
chr11:101128201
|
C | G | 1 | a0009c0022 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.870G>C | p.Ala290Ala | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1613/13037 | 870/2802 | 290/933 | chr11 | 101128201 | ||
chr11:101128227
|
G | A | 1 | a0009c0022 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.844C>T | p.Leu282Leu | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1587/13037 | 844/2802 | 282/933 | chr11 | 101128227 | ||
chr11:101128459
|
G | A | 1 | a0004c0006 | 8 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
synonymous_variant | LOW | c.612C>T | p.His204His | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1355/13037 | 612/2802 | 204/933 | chr11 | 101128459 | ||
chr11:101128522
|
T | C | 1 | a0001c0024 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.549A>G | p.Lys183Lys | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 1292/13037 | 549/2802 | 183/933 | chr11 | 101128522 | ||
chr11:101128915
|
A | T | 1 | a0005c0012 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.156T>A | p.Pro52Pro | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 899/13037 | 156/2802 | 52/933 | chr11 | 101128915 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101029705
|
T | C | 1 | a0004c0006t0040 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9411A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 9411 | chr11 | 101029705 | |||||
chr11:101029711
|
G | A | 1 | a0002c0004t0044 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9405C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 9405 | chr11 | 101029711 | |||||
chr11:101029985
|
T | C | 33 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(30): Show | 74 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*9131A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 9131 | chr11 | 101029985 | |||||
chr11:101030035
|
A | G | 11 | a0001c0003t0071a0002c0004t0005a0002c0004t0015others(8): Show | 18 | HG00099.hp1 HG00423.hp1 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*9081T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 9081 | chr11 | 101030035 | |||||
chr11:101030102
|
A | C | 33 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(30): Show | 74 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*9014T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 9014 | chr11 | 101030102 | |||||
chr11:101030247
|
C | T | 22 | a0001c0001t0003a0001c0001t0008a0001c0001t0017others(19): Show | 52 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8869G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8869 | chr11 | 101030247 | |||||
chr11:101030258
|
A | T | 1 | a0003c0005t0052 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8858T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8858 | chr11 | 101030258 | |||||
chr11:101030599
|
CAGGCATA others(8): Show |
C | 1 | a0001c0002t0084 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8502_*8516delCAGA others(11): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8502 | chr11 | 101030599 | |||||
chr11:101030737
|
G | A | 1 | a0001c0001t0078 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8379C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8379 | chr11 | 101030737 | |||||
chr11:101030742
|
A | G | 11 | a0001c0001t0002a0001c0003t0002a0001c0003t0067others(8): Show | 35 | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*8374T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8374 | chr11 | 101030742 | |||||
chr11:101030858
|
G | A | 1 | a0002c0015t0054 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8258C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8258 | chr11 | 101030858 | |||||
chr11:101030868
|
G | A | 14 | a0001c0001t0003a0001c0001t0030a0001c0001t0033others(11): Show | 37 | HG00323.hp2 HG00423.hp2 HG00642.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*8248C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8248 | chr11 | 101030868 | |||||
chr11:101031017
|
A | T | 2 | a0001c0001t0010a0001c0002t0049 | 6 | HG01109.hp1 HG01123.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8099T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 8099 | chr11 | 101031017 | |||||
chr11:101031266
|
ACGGGG | A | 3 | a0003c0005t0053a0003c0020t0064a0004c0006t0039 | 3 | HG02145.hp1 HG03453.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7845_*7849delCCCC others(1): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7845 | chr11 | 101031266 | |||||
chr11:101031284
|
G | A | 1 | a0002c0015t0054 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7832C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7832 | chr11 | 101031284 | |||||
chr11:101031322
|
C | A | 31 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(28): Show | 71 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*7794G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7794 | chr11 | 101031322 | |||||
chr11:101031590
|
C | CT | 4 | a0001c0001t0036a0001c0001t0089a0001c0024t0077others(1): Show | 5 | HG00140.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7525dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7525 | chr11 | 101031590 | |||||
chr11:101031678
|
T | A | 2 | a0001c0001t0062a0001c0001t0063 | 2 | HG02896.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7438A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7438 | chr11 | 101031678 | |||||
chr11:101031722
|
T | C | 1 | a0001c0001t0074 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7394A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7394 | chr11 | 101031722 | |||||
chr11:101031920
|
C | A | 3 | a0001c0002t0050a0001c0002t0056a0003c0005t0055 | 3 | HG02257.hp2 HG03453.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7196G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7196 | chr11 | 101031920 | |||||
chr11:101032010
|
A | G | 1 | a0002c0004t0020 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7106T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 7106 | chr11 | 101032010 | |||||
chr11:101032263
|
T | C | 89 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(86): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*6853A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 6853 | chr11 | 101032263 | |||||
chr11:101032614
|
C | T | 22 | a0001c0001t0003a0001c0001t0008a0001c0001t0017others(19): Show | 52 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*6502G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 6502 | chr11 | 101032614 | |||||
chr11:101033201
|
G | A | 1 | a0001c0001t0072 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5915C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 5915 | chr11 | 101033201 | |||||
chr11:101033319
|
A | G | 3 | a0001c0001t0062a0001c0001t0079a0001c0002t0032 | 4 | HG02896.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5797T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 5797 | chr11 | 101033319 | |||||
chr11:101033504
|
C | T | 22 | a0001c0001t0003a0001c0001t0008a0001c0001t0017others(19): Show | 52 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*5612G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 5612 | chr11 | 101033504 | |||||
chr11:101033827
|
C | T | 1 | a0001c0001t0029 | 2 | HG03654.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5289G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 5289 | chr11 | 101033827 | |||||
chr11:101034022
|
C | T | 1 | a0001c0002t0016 | 3 | NA18946.hp1 NA18947.hp2 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5094G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 5094 | chr11 | 101034022 | |||||
chr11:101034060
|
C | T | 1 | a0001c0001t0073 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5056G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 5056 | chr11 | 101034060 | |||||
chr11:101034325
|
C | T | 19 | a0001c0001t0003a0001c0001t0008a0001c0001t0017others(16): Show | 49 | HG00323.hp2 HG00597.hp2 HG01109.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4791G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4791 | chr11 | 101034325 | |||||
chr11:101034541
|
G | T | 1 | a0003c0005t0059 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4575C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4575 | chr11 | 101034541 | |||||
chr11:101034566
|
G | A | 84 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(81): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*4550C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4550 | chr11 | 101034566 | |||||
chr11:101034569
|
C | T | 1 | a0001c0003t0061 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4547G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4547 | chr11 | 101034569 | |||||
chr11:101034747
|
T | G | 1 | a0001c0002t0056 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4369A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4369 | chr11 | 101034747 | |||||
chr11:101034782
|
A | T | 2 | a0001c0002t0048a0001c0002t0049 | 2 | HG02258.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4334T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4334 | chr11 | 101034782 | |||||
chr11:101034799
|
T | C | 1 | a0001c0002t0057 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4317A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4317 | chr11 | 101034799 | |||||
chr11:101034908
|
A | T | 1 | a0011c0009t0047 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4208T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4208 | chr11 | 101034908 | |||||
chr11:101034978
|
T | G | 40 | a0001c0001t0076a0001c0002t0001a0001c0002t0009others(37): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*4138A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4138 | chr11 | 101034978 | |||||
chr11:101035002
|
A | T | 38 | a0001c0002t0001a0001c0002t0009a0001c0002t0016others(35): Show | 87 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*4114T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 4114 | chr11 | 101035002 | |||||
chr11:101035197
|
T | G | 1 | a0003c0005t0025 | 2 | HG02055.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3919A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3919 | chr11 | 101035197 | |||||
chr11:101035296
|
T | TAA | 2 | a0001c0001t0014a0001c0003t0014 | 4 | HG02698.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3818_*3819dupTT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3819 | chr11 | 101035296 | |||||
chr11:101035320
|
T | C | 1 | a0002c0004t0045 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3796A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3796 | chr11 | 101035320 | |||||
chr11:101035371
|
C | T | 1 | a0001c0001t0065 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3745G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3745 | chr11 | 101035371 | |||||
chr11:101035656
|
G | A | 1 | a0001c0001t0082 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3460C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3460 | chr11 | 101035656 | |||||
chr11:101035937
|
A | G | 2 | a0004c0006t0011a0004c0006t0041 | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3179T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3179 | chr11 | 101035937 | |||||
chr11:101035943
|
A | G | 1 | a0001c0001t0033 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3173 | chr11 | 101035943 | |||||
chr11:101035962
|
C | T | 4 | a0001c0002t0022a0001c0002t0026a0003c0005t0019others(1): Show | 7 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3154G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3154 | chr11 | 101035962 | |||||
chr11:101036060
|
T | G | 1 | a0002c0004t0021 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3056A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3056 | chr11 | 101036060 | |||||
chr11:101036079
|
G | T | 1 | a0001c0002t0046 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3037C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 3037 | chr11 | 101036079 | |||||
chr11:101036132
|
T | A | 1 | a0001c0002t0060 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2984A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2984 | chr11 | 101036132 | |||||
chr11:101036156
|
T | C | 2 | a0001c0002t0024a0001c0002t0060 | 3 | HG00597.hp1 NA18968.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2960A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2960 | chr11 | 101036156 | |||||
chr11:101036167
|
T | C | 1 | a0003c0005t0019 | 2 | HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2949A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2949 | chr11 | 101036167 | |||||
chr11:101036246
|
T | A | 1 | a0001c0001t0037 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2870A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2870 | chr11 | 101036246 | |||||
chr11:101036720
|
G | A | 5 | a0003c0020t0064a0004c0006t0011a0004c0006t0039others(2): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2396C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2396 | chr11 | 101036720 | |||||
chr11:101036814
|
T | A | 2 | a0004c0006t0011a0004c0006t0041 | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2302A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2302 | chr11 | 101036814 | |||||
chr11:101036953
|
A | G | 1 | a0001c0003t0068 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2163T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 2163 | chr11 | 101036953 | |||||
chr11:101037143
|
A | G | 14 | a0001c0001t0002a0001c0003t0002a0001c0003t0028others(11): Show | 39 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1973T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1973 | chr11 | 101037143 | |||||
chr11:101037267
|
C | T | 90 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(87): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1849G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1849 | chr11 | 101037267 | |||||
chr11:101037352
|
T | TA | 41 | a0001c0002t0001a0001c0002t0009a0001c0002t0016others(38): Show | 95 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1763_*1764insT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1763 | chr11 | 101037352 | |||||
chr11:101037353
|
G | A | 1 | a0003c0005t0025 | 2 | HG02055.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1763C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1763 | chr11 | 101037353 | |||||
chr11:101037771
|
C | A | 1 | a0001c0001t0017 | 3 | HG00597.hp2 HG01123.hp2 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1345G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1345 | chr11 | 101037771 | |||||
chr11:101037779
|
T | C | 1 | a0001c0001t0065 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1337A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1337 | chr11 | 101037779 | |||||
chr11:101037846
|
C | T | 2 | a0003c0005t0019a0004c0018t0042 | 3 | HG03471.hp2 HG03486.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1270 | chr11 | 101037846 | |||||
chr11:101037856
|
T | C | 1 | a0001c0003t0080 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1260 | chr11 | 101037856 | |||||
chr11:101037901
|
T | C | 1 | a0001c0001t0065 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1215A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1215 | chr11 | 101037901 | |||||
chr11:101037909
|
T | C | 2 | a0001c0002t0022a0001c0002t0026 | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1207A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1207 | chr11 | 101037909 | |||||
chr11:101037939
|
A | C | 1 | a0001c0001t0010 | 5 | HG01109.hp1 HG01123.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1177T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1177 | chr11 | 101037939 | |||||
chr11:101038005
|
A | C | 1 | a0001c0003t0067 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1111T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 1111 | chr11 | 101038005 | |||||
chr11:101038158
|
T | C | 1 | a0001c0003t0081 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*958A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 958 | chr11 | 101038158 | |||||
chr11:101038195
|
C | T | 1 | a0001c0002t0022 | 2 | HG02895.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*921G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 921 | chr11 | 101038195 | |||||
chr11:101038455
|
C | T | 11 | a0002c0004t0005a0002c0004t0015a0002c0004t0020others(8): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*661G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 661 | chr11 | 101038455 | |||||
chr11:101038817
|
C | T | 2 | a0003c0005t0019a0004c0018t0042 | 3 | HG03471.hp2 HG03486.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 299 | chr11 | 101038817 | |||||
chr11:101038833
|
G | T | 2 | a0001c0001t0085a0001c0001t0086 | 2 | HG00735.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 283 | chr11 | 101038833 | |||||
chr11:101038847
|
A | G | 1 | a0001c0001t0066 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 269 | chr11 | 101038847 | |||||
chr11:101038849
|
G | GAT | 41 | a0001c0002t0001a0001c0002t0009a0001c0002t0016others(38): Show | 95 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*265_*266dupAT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 266 | chr11 | 101038849 | |||||
chr11:101038898
|
C | T | 12 | a0001c0001t0027a0001c0001t0062a0001c0001t0063others(9): Show | 16 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*218G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 218 | chr11 | 101038898 | |||||
chr11:101039011
|
G | A | 1 | a0001c0001t0082 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 105 | chr11 | 101039011 | |||||
chr11:101039078
|
A | G | 41 | a0001c0002t0001a0001c0002t0009a0001c0002t0016others(38): Show | 95 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*38T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 8/8 | 38 | chr11 | 101039078 | |||||
chr11:101129107
|
A | AG | 103 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(100): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
5_prime_UTR_variant | MODIFIER | c.-38dupC | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 38 | chr11 | 101129107 | |||||
chr11:101129341
|
GT | G | 5 | a0004c0006t0011a0004c0006t0038a0004c0006t0039others(2): Show | 8 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-272delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 272 | chr11 | 101129341 | |||||
chr11:101129346
|
GA | G | 5 | a0004c0006t0011a0004c0006t0038a0004c0006t0039others(2): Show | 8 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-277delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 277 | chr11 | 101129346 | |||||
chr11:101129422
|
A | G | 1 | a0001c0002t0018 | 2 | NA18960.hp1 NA19009.hp2 |
5_prime_UTR_variant | MODIFIER | c.-352T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 352 | chr11 | 101129422 | |||||
chr11:101129483
|
C | T | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG01256.hp2 HG03927.hp1 |
5_prime_UTR_variant | MODIFIER | c.-413G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 413 | chr11 | 101129483 | |||||
chr11:101129639
|
C | T | 3 | a0001c0001t0033a0001c0001t0034a0001c0001t0035 | 3 | HG01109.hp2 HG01346.hp2 HG02273.hp1 |
5_prime_UTR_variant | MODIFIER | c.-569G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 569 | chr11 | 101129639 | |||||
chr11:101129751
|
G | A | 1 | a0001c0003t0083 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-681C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 681 | chr11 | 101129751 | |||||
chr11:101129770
|
A | G | 90 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(87): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
5_prime_UTR_variant | MODIFIER | c.-700T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/8 | 700 | chr11 | 101129770 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101039401
|
T | C | 110 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(107): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2647-130A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039401 | ||||||
chr11:101039404
|
T | A | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2647-133A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039404 | ||||||
chr11:101039523
|
G | C | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2647-252C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039523 | ||||||
chr11:101039559
|
GT | G | 84 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(81): Show | 85 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.2647-289delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039559 | ||||||
chr11:101039579
|
A | T | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2647-308T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039579 | ||||||
chr11:101039700
|
G | A | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2647-429C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039700 | ||||||
chr11:101039738
|
G | A | 84 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(81): Show | 85 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.2647-467C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039738 | ||||||
chr11:101039875
|
T | C | 1 | a0001c0019t0075g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2647-604A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039875 | ||||||
chr11:101039970
|
A | G | 3 | a0001c0001t0082g0107a0003c0005t0059g0158a0005c0012t0058g0019 | 3 | HG02451.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2647-699T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039970 | ||||||
chr11:101039993
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2647-722A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101039993 | ||||||
chr11:101040068
|
AT | A | 11 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2647-798delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040068 | ||||||
chr11:101040069
|
T | A | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2647-798A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040069 | ||||||
chr11:101040188
|
T | C | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2647-917A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040188 | ||||||
chr11:101040264
|
T | C | 87 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(84): Show | 88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.2647-993A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040264 | ||||||
chr11:101040445
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2647-1174A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040445 | ||||||
chr11:101040638
|
C | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2646+1307G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040638 | ||||||
chr11:101040777
|
T | C | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+1168A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040777 | ||||||
chr11:101040817
|
A | T | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+1128T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040817 | ||||||
chr11:101040822
|
T | C | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2646+1123A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040822 | ||||||
chr11:101040921
|
T | A | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2646+1024A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101040921 | ||||||
chr11:101041048
|
T | TAAAAATG others(313): Show |
12 | a0002c0004t0005g0026a0002c0004t0005g0033a0002c0004t0015g0022others(9): Show | 12 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2646+896_2646+897i others(322): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041048 | ||||||
chr11:101041048
|
T | TAAAAATG others(314): Show |
5 | a0002c0004t0005g0025a0002c0004t0005g0027a0002c0004t0015g0021others(2): Show | 5 | HG01175.hp2 HG01261.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2646+896_2646+897i others(323): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041048 | ||||||
chr11:101041048
|
T | TAAAAATG others(315): Show |
1 | a0002c0004t0005g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2646+896_2646+897i others(324): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041048 | ||||||
chr11:101041124
|
G | C | 3 | a0001c0001t0065g0108a0001c0003t0061g0171a0004c0006t0038g0017 | 3 | HG02055.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2646+821C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041124 | ||||||
chr11:101041175
|
T | G | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2646+770A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041175 | ||||||
chr11:101041177
|
C | T | 67 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(64): Show | 67 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2646+768G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041177 | ||||||
chr11:101041229
|
C | G | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2646+716G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041229 | ||||||
chr11:101041284
|
G | T | 2 | a0001c0002t0046g0101a0011c0009t0047g0018 | 2 | HG04204.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2646+661C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041284 | ||||||
chr11:101041285
|
C | A | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+660G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041285 | ||||||
chr11:101041415
|
C | G | 2 | a0001c0003t0002g0188a0001c0003t0081g0192 | 2 | HG01255.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.2646+530G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041415 | ||||||
chr11:101041499
|
T | C | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+446A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041499 | ||||||
chr11:101041504
|
A | G | 38 | a0001c0001t0002g0001a0001c0003t0002g0170a0001c0003t0002g0173others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2646+441T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041504 | ||||||
chr11:101041521
|
A | T | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+424T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041521 | ||||||
chr11:101041665
|
C | T | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2646+280G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041665 | ||||||
chr11:101041723
|
C | T | 2 | a0001c0002t0048g0079a0001c0002t0049g0080 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2646+222G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041723 | ||||||
chr11:101041733
|
A | G | 1 | a0001c0003t0083g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2646+212T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041733 | ||||||
chr11:101041779
|
G | GA | 70 | a0001c0001t0027g0151a0001c0002t0001g0109a0001c0002t0001g0110others(67): Show | 70 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.2646+165dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041779 | ||||||
chr11:101041779
|
G | GAA | 21 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0044others(18): Show | 21 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2646+164_2646+165d others(4): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041779 | ||||||
chr11:101041789
|
C | A | 20 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(17): Show | 20 | HG00738.hp2 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2646+156G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041789 | ||||||
chr11:101041796
|
A | C | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+149T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041796 | ||||||
chr11:101041804
|
G | C | 1 | a0001c0001t0012g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2646+141C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041804 | ||||||
chr11:101041822
|
A | G | 1 | a0001c0003t0070g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2646+123T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041822 | ||||||
chr11:101041823
|
CTT | C | 3 | a0003c0005t0019g0002a0004c0018t0042g0039a0005c0012t0058g0019 | 4 | HG02451.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2646+120_2646+121d others(4): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041823 | ||||||
chr11:101041826
|
T | C | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2646+119A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041826 | ||||||
chr11:101041830
|
C | A | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2646+115G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041830 | ||||||
chr11:101041894
|
T | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2646+51A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041894 | ||||||
chr11:101041938
|
T | G | 1 | a0001c0001t0013g0074 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.2646+7A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 7/7 | chr11 | 101041938 | ||||||
chr11:101042252
|
A | T | 1 | a0001c0001t0008g0081 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2489-150T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042252 | ||||||
chr11:101042422
|
T | C | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2489-320A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042422 | ||||||
chr11:101042434
|
G | A | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2489-332C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042434 | ||||||
chr11:101042550
|
C | A | 20 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(17): Show | 20 | HG00738.hp2 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2489-448G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042550 | ||||||
chr11:101042627
|
C | A | 2 | a0001c0002t0046g0101a0011c0009t0047g0018 | 2 | HG04204.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2489-525G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042627 | ||||||
chr11:101042717
|
G | A | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2489-615C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042717 | ||||||
chr11:101042734
|
C | T | 58 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2489-632G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042734 | ||||||
chr11:101042817
|
T | C | 110 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(107): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2489-715A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042817 | ||||||
chr11:101042920
|
C | T | 41 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(38): Show | 41 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2489-818G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042920 | ||||||
chr11:101042986
|
G | C | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2489-884C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101042986 | ||||||
chr11:101043118
|
A | T | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2489-1016T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043118 | ||||||
chr11:101043129
|
A | G | 67 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(64): Show | 67 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2489-1027T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043129 | ||||||
chr11:101043141
|
TC | T | 3 | a0001c0007t0003g0069a0001c0007t0003g0096a0001c0007t0003g0152 | 3 | HG01167.hp1 HG01981.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2489-1040delG | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043141 | ||||||
chr11:101043167
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2489-1065A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043167 | ||||||
chr11:101043170
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2489-1068A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043170 | ||||||
chr11:101043335
|
C | T | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2489-1233G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043335 | ||||||
chr11:101043398
|
T | C | 110 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(107): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2489-1296A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043398 | ||||||
chr11:101043464
|
A | T | 7 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(4): Show | 8 | HG00733.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2489-1362T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043464 | ||||||
chr11:101043798
|
T | C | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2489-1696A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043798 | ||||||
chr11:101043834
|
G | T | 1 | a0001c0001t0033g0003 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2489-1732C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043834 | ||||||
chr11:101043916
|
C | T | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2489-1814G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043916 | ||||||
chr11:101043985
|
A | T | 2 | a0001c0003t0002g0180a0001c0003t0002g0181 | 2 | HG00099.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2489-1883T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101043985 | ||||||
chr11:101044220
|
G | A | 2 | a0005c0008t0031g0154a0005c0008t0031g0155 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2489-2118C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044220 | ||||||
chr11:101044418
|
T | C | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2489-2316A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044418 | ||||||
chr11:101044465
|
G | A | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2489-2363C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044465 | ||||||
chr11:101044498
|
G | T | 1 | a0001c0002t0048g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2489-2396C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044498 | ||||||
chr11:101044700
|
C | CT | 18 | a0001c0001t0004g0218a0001c0001t0004g0225a0001c0001t0004g0230others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2489-2599dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044700 | ||||||
chr11:101044700
|
CT | C | 101 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.2489-2599delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044700 | ||||||
chr11:101044700
|
CTT | C | 50 | a0001c0001t0003g0091a0001c0002t0001g0109a0001c0002t0001g0110others(47): Show | 50 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.2489-2600_2489-259 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044700 | ||||||
chr11:101044700
|
CTTT | C | 28 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0009g0227others(25): Show | 29 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.2489-2601_2489-259 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044700 | ||||||
chr11:101044792
|
C | T | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2489-2690G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044792 | ||||||
chr11:101044825
|
G | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2489-2723C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044825 | ||||||
chr11:101044911
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2489-2809A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044911 | ||||||
chr11:101044950
|
G | A | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2489-2848C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044950 | ||||||
chr11:101044982
|
C | T | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2489-2880G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101044982 | ||||||
chr11:101045101
|
T | C | 1 | a0001c0001t0008g0081 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2489-2999A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045101 | ||||||
chr11:101045137
|
T | C | 1 | a0001c0001t0003g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2489-3035A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045137 | ||||||
chr11:101045163
|
T | C | 43 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2489-3061A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045163 | ||||||
chr11:101045293
|
T | C | 2 | a0005c0008t0031g0154a0005c0008t0031g0155 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2489-3191A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045293 | ||||||
chr11:101045294
|
A | G | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2489-3192T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045294 | ||||||
chr11:101045393
|
T | A | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2489-3291A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045393 | ||||||
chr11:101045429
|
A | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2489-3327T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045429 | ||||||
chr11:101045646
|
T | G | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2489-3544A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045646 | ||||||
chr11:101045665
|
T | TTG | 8 | a0001c0001t0004g0245a0001c0001t0082g0107a0001c0002t0001g0124others(5): Show | 8 | HG01257.hp2 HG02258.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2489-3565_2489-356 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
T | TTGTG | 4 | a0001c0002t0001g0136a0003c0005t0055g0167a0003c0020t0064g0168others(1): Show | 4 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489-3567_2489-356 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
T | TTGTGTG | 38 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.2489-3569_2489-356 others(10): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
T | TTGTGTGT others(1): Show |
5 | a0001c0002t0001g0115a0001c0002t0001g0119a0001c0002t0001g0143others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2489-3571_2489-356 others(12): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
TTG | T | 93 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(90): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.2489-3565_2489-356 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
TTGTG | T | 18 | a0001c0001t0065g0108a0002c0004t0005g0025a0002c0004t0005g0026others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2489-3567_2489-356 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
TTGTGTGT others(1): Show |
T | 7 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(4): Show | 8 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489-3571_2489-356 others(12): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045665
|
TTGTGTGT others(3): Show |
T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489-3573_2489-356 others(14): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045665 | ||||||
chr11:101045796
|
G | T | 5 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2489-3694C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045796 | ||||||
chr11:101045838
|
C | A | 86 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(83): Show | 87 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2489-3736G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045838 | ||||||
chr11:101045895
|
T | A | 1 | a0001c0001t0004g0246 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2489-3793A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045895 | ||||||
chr11:101045918
|
A | G | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2489-3816T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045918 | ||||||
chr11:101045952
|
G | A | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2489-3850C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101045952 | ||||||
chr11:101046052
|
C | G | 3 | a0001c0002t0001g0114a0001c0002t0001g0125a0001c0002t0001g0126 | 3 | HG01070.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2488+3877G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046052 | ||||||
chr11:101046100
|
GTAATT | G | 2 | a0003c0005t0019g0002a0004c0018t0042g0039 | 3 | HG03471.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2488+3824_2488+382 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046100 | ||||||
chr11:101046113
|
TTTTA | T | 92 | a0001c0001t0079g0040a0001c0002t0001g0109a0001c0002t0001g0110others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2488+3812_2488+381 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046113 | ||||||
chr11:101046150
|
T | C | 2 | a0001c0002t0022g0043a0001c0002t0022g0055 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2488+3779A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046150 | ||||||
chr11:101046271
|
A | C | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2488+3658T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046271 | ||||||
chr11:101046292
|
A | AT | 7 | a0001c0001t0004g0234a0001c0001t0004g0241a0001c0001t0004g0246others(4): Show | 7 | HG00738.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2488+3636dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
A | ATTTTTTT others(6): Show |
2 | a0001c0003t0070g0201a0002c0014t0002g0034 | 2 | HG00735.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2488+3624_2488+363 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
A | ATTTTTTT others(10): Show |
1 | a0001c0003t0002g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2488+3620_2488+363 others(21): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
A | ATTTTTTT others(12): Show |
1 | a0001c0003t0002g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2488+3618_2488+363 others(23): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
AT | A | 11 | a0001c0001t0004g0224a0001c0001t0004g0230a0001c0001t0004g0236others(8): Show | 11 | HG01081.hp1 HG01433.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2488+3636delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATT | A | 8 | a0001c0001t0007g0045a0001c0001t0007g0048a0001c0001t0007g0051others(5): Show | 8 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.2488+3635_2488+363 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTT | A | 7 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0002t0016g0120others(4): Show | 7 | HG02559.hp2 HG02896.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2488+3632_2488+363 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT | A | 7 | a0001c0002t0046g0101a0001c0002t0048g0079a0001c0002t0049g0080others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2488+3630_2488+363 others(11): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0079g0040a0001c0002t0001g0112a0001c0002t0001g0113others(9): Show | 12 | HG00621.hp1 HG01243.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2488+3629_2488+363 others(12): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(2): Show |
A | 13 | a0001c0001t0010g0223a0001c0002t0001g0123a0001c0002t0001g0127others(10): Show | 13 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.2488+3628_2488+363 others(13): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(3): Show |
A | 19 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0115others(16): Show | 19 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.2488+3627_2488+363 others(14): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(4): Show |
A | 5 | a0001c0001t0003g0103a0001c0002t0001g0111a0001c0002t0001g0114others(2): Show | 5 | HG01070.hp1 HG02735.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2488+3626_2488+363 others(15): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0002t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2488+3624_2488+363 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(7): Show |
A | 12 | a0001c0001t0003g0097a0001c0001t0008g0063a0001c0001t0008g0075others(9): Show | 12 | HG01167.hp1 HG01891.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2488+3623_2488+363 others(18): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(8): Show |
A | 43 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(40): Show | 43 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2488+3622_2488+363 others(19): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(9): Show |
A | 6 | a0001c0001t0003g0088a0001c0001t0004g0225a0001c0001t0004g0242others(3): Show | 6 | HG00323.hp2 HG02055.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.2488+3621_2488+363 others(20): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(10): Show |
A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+3620_2488+363 others(21): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(11): Show |
A | 4 | a0001c0003t0002g0184a0001c0003t0069g0172a0003c0005t0019g0002others(1): Show | 5 | HG01175.hp1 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488+3619_2488+363 others(22): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(12): Show |
A | 27 | a0001c0001t0002g0001a0001c0003t0002g0173a0001c0003t0002g0174others(24): Show | 28 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.2488+3618_2488+363 others(23): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(13): Show |
A | 9 | a0001c0003t0002g0177a0001c0003t0071g0191a0004c0006t0011g0012others(6): Show | 9 | HG01070.hp2 HG01099.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+3617_2488+363 others(24): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(14): Show |
A | 1 | a0002c0004t0005g0027 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2488+3616_2488+363 others(25): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(15): Show |
A | 17 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0031others(14): Show | 17 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2488+3615_2488+363 others(26): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046292
|
ATTTTTTT others(18): Show |
A | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2488+3612_2488+363 others(29): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046292 | ||||||
chr11:101046328
|
T | A | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2488+3601A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046328 | ||||||
chr11:101046342
|
C | T | 73 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(70): Show | 74 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.2488+3587G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046342 | ||||||
chr11:101046400
|
A | G | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2488+3529T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046400 | ||||||
chr11:101046493
|
ACCTACTG others(6): Show |
A | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2488+3423_2488+343 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046493 | ||||||
chr11:101046524
|
T | C | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2488+3405A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046524 | ||||||
chr11:101046582
|
A | G | 1 | a0003c0005t0025g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2488+3347T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046582 | ||||||
chr11:101046638
|
T | G | 104 | a0001c0001t0065g0108a0001c0002t0001g0109a0001c0002t0001g0110others(101): Show | 105 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.2488+3291A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046638 | ||||||
chr11:101046869
|
C | T | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2488+3060G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046869 | ||||||
chr11:101046879
|
G | C | 92 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(89): Show | 93 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2488+3050C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046879 | ||||||
chr11:101046893
|
C | T | 104 | a0001c0001t0065g0108a0001c0002t0001g0109a0001c0002t0001g0110others(101): Show | 105 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.2488+3036G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101046893 | ||||||
chr11:101047061
|
TTC | T | 7 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.2488+2866_2488+286 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047061 | ||||||
chr11:101047524
|
T | C | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2488+2405A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047524 | ||||||
chr11:101047702
|
G | C | 86 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(83): Show | 87 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2488+2227C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047702 | ||||||
chr11:101047800
|
T | A | 12 | a0001c0001t0065g0108a0001c0003t0061g0171a0003c0020t0064g0168others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2488+2129A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047800 | ||||||
chr11:101047867
|
A | C | 6 | a0003c0005t0006g0157a0003c0005t0006g0161a0003c0005t0006g0162others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2488+2062T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047867 | ||||||
chr11:101047916
|
G | A | 1 | a0001c0002t0026g0042 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2488+2013C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047916 | ||||||
chr11:101047942
|
C | A | 2 | a0001c0003t0061g0171a0004c0006t0038g0017 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2488+1987G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101047942 | ||||||
chr11:101048018
|
T | C | 3 | a0001c0003t0002g0174a0001c0003t0002g0175a0001c0003t0002g0176 | 3 | HG01261.hp1 HG02257.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2488+1911A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048018 | ||||||
chr11:101048335
|
T | C | 20 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(17): Show | 20 | HG00738.hp2 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2488+1594A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048335 | ||||||
chr11:101048415
|
C | T | 110 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(107): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2488+1514G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048415 | ||||||
chr11:101048551
|
A | T | 1 | a0001c0001t0004g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2488+1378T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048551 | ||||||
chr11:101048625
|
G | A | 2 | a0003c0005t0019g0002a0004c0018t0042g0039 | 3 | HG03471.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2488+1304C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048625 | ||||||
chr11:101048669
|
G | C | 34 | a0001c0001t0002g0001a0001c0003t0002g0170a0001c0003t0002g0174others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2488+1260C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048669 | ||||||
chr11:101048670
|
C | T | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2488+1259G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048670 | ||||||
chr11:101048819
|
C | T | 1 | a0001c0001t0062g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2488+1110G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048819 | ||||||
chr11:101048838
|
A | G | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2488+1091T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048838 | ||||||
chr11:101048904
|
T | C | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2488+1025A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048904 | ||||||
chr11:101048995
|
C | T | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2488+934G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101048995 | ||||||
chr11:101049114
|
T | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2488+815A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049114 | ||||||
chr11:101049243
|
C | T | 1 | a0001c0003t0061g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2488+686G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049243 | ||||||
chr11:101049306
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2488+623C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049306 | ||||||
chr11:101049379
|
C | T | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2488+550G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049379 | ||||||
chr11:101049515
|
A | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+414T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049515 | ||||||
chr11:101049764
|
C | T | 2 | a0003c0005t0019g0002a0004c0018t0042g0039 | 3 | HG03471.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2488+165G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049764 | ||||||
chr11:101049830
|
C | T | 3 | a0001c0002t0016g0120a0001c0002t0016g0138a0001c0002t0016g0140 | 3 | NA18946.hp1 NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2488+99G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049830 | ||||||
chr11:101049844
|
A | T | 86 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(83): Show | 87 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2488+85T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 6/7 | chr11 | 101049844 | ||||||
chr11:101050118
|
C | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2358-59G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050118 | ||||||
chr11:101050137
|
A | G | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2358-78T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050137 | ||||||
chr11:101050166
|
A | C | 1 | a0004c0006t0038g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2358-107T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050166 | ||||||
chr11:101050185
|
C | T | 2 | a0003c0005t0019g0002a0004c0018t0042g0039 | 3 | HG03471.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2358-126G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050185 | ||||||
chr11:101050319
|
G | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2358-260C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050319 | ||||||
chr11:101050348
|
T | C | 3 | a0001c0002t0016g0120a0001c0002t0016g0138a0001c0002t0016g0140 | 3 | NA18946.hp1 NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2358-289A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050348 | ||||||
chr11:101050352
|
T | C | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2358-293A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050352 | ||||||
chr11:101050502
|
A | G | 1 | a0001c0003t0028g0194 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2358-443T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050502 | ||||||
chr11:101050676
|
T | C | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2358-617A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050676 | ||||||
chr11:101050701
|
T | C | 1 | a0001c0003t0083g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2358-642A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050701 | ||||||
chr11:101050934
|
C | A | 84 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(81): Show | 85 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.2357+490G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101050934 | ||||||
chr11:101051010
|
T | C | 1 | a0002c0004t0005g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2357+414A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101051010 | ||||||
chr11:101051069
|
G | T | 5 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2357+355C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101051069 | ||||||
chr11:101051210
|
T | A | 58 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2357+214A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101051210 | ||||||
chr11:101051299
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2357+125C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101051299 | ||||||
chr11:101051381
|
A | G | 43 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2357+43T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101051381 | ||||||
chr11:101051390
|
T | TA | 9 | a0001c0001t0012g0082a0001c0001t0012g0085a0001c0001t0012g0153others(6): Show | 9 | HG02572.hp2 HG02615.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2357+33dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 5/7 | chr11 | 101051390 | ||||||
chr11:101051639
|
T | G | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2213-71A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051639 | ||||||
chr11:101051673
|
A | T | 191 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2213-105T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051673 | ||||||
chr11:101051720
|
T | A | 84 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(81): Show | 85 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.2213-152A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051720 | ||||||
chr11:101051837
|
C | A | 90 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(87): Show | 91 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.2213-269G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051837 | ||||||
chr11:101051889
|
A | G | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2213-321T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051889 | ||||||
chr11:101051892
|
T | A | 19 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0123others(16): Show | 19 | HG00597.hp1 HG00621.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2213-324A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051892 | ||||||
chr11:101051996
|
A | G | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2213-428T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101051996 | ||||||
chr11:101052064
|
G | A | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2213-496C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052064 | ||||||
chr11:101052067
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2213-499G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052067 | ||||||
chr11:101052191
|
G | C | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2213-623C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052191 | ||||||
chr11:101052208
|
G | A | 85 | a0001c0001t0004g0217a0001c0002t0001g0109a0001c0002t0001g0110others(82): Show | 86 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.2213-640C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052208 | ||||||
chr11:101052233
|
G | A | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2213-665C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052233 | ||||||
chr11:101052245
|
C | T | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2213-677G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052245 | ||||||
chr11:101052269
|
C | CTGTG | 3 | a0001c0001t0004g0245a0001c0001t0004g0246a0001c0001t0079g0040 | 3 | HG01257.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2213-705_2213-702d others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTG | C | 3 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0016g0140 | 3 | HG02886.hp2 HG03540.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.2213-703_2213-702d others(4): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTG | C | 19 | a0001c0001t0007g0051a0001c0002t0001g0114a0001c0002t0001g0115others(16): Show | 19 | HG00621.hp1 HG01070.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.2213-705_2213-702d others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTG | C | 22 | a0001c0001t0004g0249a0001c0002t0001g0109a0001c0002t0001g0110others(19): Show | 22 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2213-707_2213-702d others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(1): Show |
C | 23 | a0001c0001t0003g0068a0001c0001t0004g0219a0001c0001t0004g0224others(20): Show | 24 | HG01074.hp1 HG01106.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.2213-709_2213-702d others(10): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(3): Show |
C | 49 | a0001c0001t0004g0218a0001c0001t0004g0221a0001c0001t0004g0225others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.2213-711_2213-702d others(12): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(5): Show |
C | 15 | a0001c0001t0004g0217a0001c0001t0007g0045a0001c0001t0007g0048others(12): Show | 15 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.2213-713_2213-702d others(14): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(7): Show |
C | 64 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(61): Show | 64 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2213-715_2213-702d others(16): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(9): Show |
C | 4 | a0001c0003t0061g0171a0004c0006t0038g0017a0004c0006t0040g0010others(1): Show | 4 | HG02055.hp2 HG02451.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2213-717_2213-702d others(18): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(11): Show |
C | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213-719_2213-702d others(20): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(17): Show |
C | 38 | a0001c0001t0002g0001a0001c0003t0002g0170a0001c0003t0002g0173others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2213-725_2213-702d others(26): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052269
|
CTGTGTGT others(25): Show |
C | 2 | a0001c0001t0004g0241a0001c0001t0004g0242 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2213-733_2213-702d others(34): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052269 | ||||||
chr11:101052317
|
G | A | 10 | a0001c0002t0009g0229a0001c0002t0032g0214a0001c0002t0032g0215others(7): Show | 10 | HG01433.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2213-749C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052317 | ||||||
chr11:101052435
|
C | G | 94 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(91): Show | 95 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2213-867G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052435 | ||||||
chr11:101052475
|
C | A | 12 | a0001c0001t0065g0108a0001c0003t0061g0171a0003c0020t0064g0168others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2213-907G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052475 | ||||||
chr11:101052476
|
C | G | 12 | a0001c0001t0065g0108a0001c0003t0061g0171a0003c0020t0064g0168others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2213-908G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052476 | ||||||
chr11:101052514
|
A | G | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2213-946T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052514 | ||||||
chr11:101052564
|
T | C | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2213-996A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052564 | ||||||
chr11:101052569
|
T | A | 43 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2213-1001A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052569 | ||||||
chr11:101052709
|
A | C | 5 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2213-1141T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052709 | ||||||
chr11:101052790
|
G | T | 5 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2213-1222C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101052790 | ||||||
chr11:101053284
|
G | C | 16 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(13): Show | 16 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2213-1716C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053284 | ||||||
chr11:101053302
|
G | A | 58 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2213-1734C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053302 | ||||||
chr11:101053325
|
G | A | 19 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(16): Show | 20 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.2213-1757C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053325 | ||||||
chr11:101053356
|
A | C | 1 | a0001c0002t0001g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2213-1788T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053356 | ||||||
chr11:101053360
|
GCTACTCT | G | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2213-1799_2213-179 others(11): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053360 | ||||||
chr11:101053505
|
C | CTCCCTCC others(17): Show |
4 | a0001c0002t0048g0079a0001c0002t0049g0080a0003c0005t0052g0169others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2213-1961_2213-193 others(28): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053505 | ||||||
chr11:101053505
|
C | CTCCCTCC others(38): Show |
60 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(57): Show | 61 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.2213-1982_2213-193 others(49): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053505 | ||||||
chr11:101053505
|
C | CTCCCTCC others(83): Show |
1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2213-1938_2213-193 others(94): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053505 | ||||||
chr11:101053505
|
C | CTCCCTCC others(14): Show |
1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2213-1938_2213-193 others(25): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053505 | ||||||
chr11:101053505
|
CTCCCTCC others(59): Show |
C | 10 | a0001c0001t0065g0108a0001c0003t0061g0171a0003c0020t0064g0168others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2213-2003_2213-193 others(70): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053505 | ||||||
chr11:101053519
|
C | CCCTTTCT others(38): Show |
5 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2213-1952_2213-195 others(49): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053519 | ||||||
chr11:101053522
|
T | TCCTTTCT others(59): Show |
2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2213-1955_2213-195 others(70): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053522 | ||||||
chr11:101053543
|
C | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2213-1975G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053543 | ||||||
chr11:101053550
|
T | C | 5 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2213-1982A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053550 | ||||||
chr11:101053571
|
T | C | 6 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2213-2003A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053571 | ||||||
chr11:101053577
|
C | G | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2213-2009G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053577 | ||||||
chr11:101053606
|
CCCTCCTT others(17): Show |
C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2213-2062_2213-203 others(28): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053606 | ||||||
chr11:101053748
|
T | C | 1 | a0004c0006t0038g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2213-2180A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053748 | ||||||
chr11:101053804
|
TCCCTCCT others(9): Show |
T | 10 | a0001c0001t0065g0108a0001c0003t0061g0171a0003c0020t0064g0168others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2213-2252_2213-223 others(20): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053804 | ||||||
chr11:101053914
|
G | C | 3 | a0003c0005t0019g0002a0004c0018t0042g0039a0005c0012t0058g0019 | 4 | HG02451.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2213-2346C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101053914 | ||||||
chr11:101054027
|
T | G | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2213-2459A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054027 | ||||||
chr11:101054153
|
T | G | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2213-2585A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054153 | ||||||
chr11:101054386
|
C | T | 3 | a0001c0001t0079g0040a0001c0002t0023g0146a0001c0002t0023g0147 | 3 | HG01346.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2213-2818G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054386 | ||||||
chr11:101054416
|
C | A | 1 | a0001c0002t0057g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2213-2848G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054416 | ||||||
chr11:101054448
|
A | G | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2213-2880T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054448 | ||||||
chr11:101054505
|
G | C | 1 | a0001c0001t0003g0105 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2213-2937C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054505 | ||||||
chr11:101054507
|
A | T | 17 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(14): Show | 17 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2213-2939T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054507 | ||||||
chr11:101054737
|
A | T | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2213-3169T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054737 | ||||||
chr11:101054779
|
G | C | 1 | a0001c0001t0017g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2213-3211C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054779 | ||||||
chr11:101054897
|
A | G | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2213-3329T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054897 | ||||||
chr11:101054982
|
A | G | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2213-3414T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101054982 | ||||||
chr11:101055031
|
T | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2213-3463A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055031 | ||||||
chr11:101055153
|
G | A | 17 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(14): Show | 17 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2213-3585C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055153 | ||||||
chr11:101055208
|
A | T | 1 | a0001c0002t0009g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2213-3640T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055208 | ||||||
chr11:101055258
|
C | A | 1 | a0001c0003t0002g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2213-3690G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055258 | ||||||
chr11:101055414
|
C | CA | 11 | a0001c0001t0004g0239a0001c0001t0004g0242a0001c0001t0007g0054others(8): Show | 11 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2213-3847dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055414
|
CA | C | 9 | a0001c0001t0010g0251a0001c0001t0027g0151a0001c0001t0062g0058others(6): Show | 9 | HG01346.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2213-3847delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055414
|
CAAA | C | 6 | a0001c0001t0003g0095a0001c0001t0003g0098a0001c0001t0012g0085others(3): Show | 6 | HG03927.hp1 HG04115.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.2213-3849_2213-384 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055414
|
CAAAA | C | 60 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(57): Show | 61 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2213-3850_2213-384 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055414
|
CAAAAA | C | 59 | a0001c0001t0002g0001a0001c0001t0003g0091a0001c0001t0037g0006others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2213-3851_2213-384 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055414
|
CAAAAAA | C | 63 | a0001c0001t0065g0108a0001c0002t0001g0109a0001c0002t0001g0110others(60): Show | 63 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.2213-3852_2213-384 others(10): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055414
|
CAAAAAAA | C | 5 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(2): Show | 5 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2213-3853_2213-384 others(11): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055414 | ||||||
chr11:101055559
|
A | G | 19 | a0001c0001t0004g0217a0001c0001t0004g0218a0001c0001t0004g0219others(16): Show | 19 | HG01081.hp1 HG01243.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2213-3991T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055559 | ||||||
chr11:101055600
|
C | G | 17 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0062g0058others(14): Show | 17 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2213-4032G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055600 | ||||||
chr11:101055614
|
A | G | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2213-4046T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055614 | ||||||
chr11:101055765
|
T | C | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2213-4197A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055765 | ||||||
chr11:101055921
|
T | C | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2213-4353A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101055921 | ||||||
chr11:101056129
|
G | A | 189 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2213-4561C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056129 | ||||||
chr11:101056192
|
G | A | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2213-4624C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056192 | ||||||
chr11:101056211
|
A | C | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2213-4643T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056211 | ||||||
chr11:101056243
|
A | AAAC | 178 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2213-4676_2213-467 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056243 | ||||||
chr11:101056246
|
A | ACT | 11 | a0001c0001t0065g0108a0001c0003t0061g0171a0003c0020t0064g0168others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2213-4680_2213-467 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056246 | ||||||
chr11:101056246
|
A | T | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2213-4678T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056246 | ||||||
chr11:101056349
|
A | T | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2213-4781T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056349 | ||||||
chr11:101056402
|
G | A | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2213-4834C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056402 | ||||||
chr11:101056463
|
A | C | 1 | a0001c0001t0003g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2213-4895T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056463 | ||||||
chr11:101056501
|
C | T | 2 | a0001c0001t0029g0062a0001c0001t0029g0104 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2213-4933G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056501 | ||||||
chr11:101056511
|
G | T | 1 | a0001c0003t0083g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2213-4943C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056511 | ||||||
chr11:101056511
|
GCTGGGGA others(11): Show |
G | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2213-4961_2213-494 others(22): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056511 | ||||||
chr11:101056550
|
C | T | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2213-4982G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056550 | ||||||
chr11:101056551
|
G | A | 140 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2213-4983C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056551 | ||||||
chr11:101056582
|
G | A | 45 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(42): Show | 45 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.2213-5014C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056582 | ||||||
chr11:101056593
|
T | A | 1 | a0001c0001t0004g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2213-5025A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056593 | ||||||
chr11:101056642
|
G | GA | 118 | a0001c0001t0002g0001a0001c0001t0033g0003a0001c0001t0037g0006others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.2213-5075dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056642 | ||||||
chr11:101056642
|
G | GAA | 62 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(59): Show | 62 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2213-5076_2213-507 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056642 | ||||||
chr11:101056642
|
GA | G | 10 | a0001c0001t0065g0108a0001c0001t0082g0107a0001c0003t0061g0171others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2213-5075delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056642 | ||||||
chr11:101056745
|
A | T | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2213-5177T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056745 | ||||||
chr11:101056780
|
T | A | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2213-5212A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056780 | ||||||
chr11:101056866
|
C | T | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2213-5298G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056866 | ||||||
chr11:101056952
|
C | T | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2213-5384G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101056952 | ||||||
chr11:101057176
|
G | C | 1 | a0001c0001t0012g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2212+5271C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101057176 | ||||||
chr11:101057279
|
G | A | 2 | a0001c0001t0008g0063a0001c0001t0087g0240 | 2 | HG01168.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2212+5168C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101057279 | ||||||
chr11:101057362
|
G | A | 1 | a0001c0002t0024g0129 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2212+5085C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101057362 | ||||||
chr11:101057558
|
A | G | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2212+4889T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101057558 | ||||||
chr11:101057789
|
G | A | 1 | a0001c0001t0007g0052 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2212+4658C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101057789 | ||||||
chr11:101057826
|
G | A | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2212+4621C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101057826 | ||||||
chr11:101058031
|
G | A | 3 | a0002c0004t0015g0021a0002c0004t0015g0022a0002c0004t0045g0035 | 3 | HG00099.hp1 HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2212+4416C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058031 | ||||||
chr11:101058104
|
A | G | 183 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2212+4343T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058104 | ||||||
chr11:101058150
|
T | C | 98 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(95): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2212+4297A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058150 | ||||||
chr11:101058314
|
C | G | 2 | a0001c0001t0065g0108a0001c0001t0082g0107 | 2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2212+4133G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058314 | ||||||
chr11:101058456
|
C | T | 43 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.2212+3991G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058456 | ||||||
chr11:101058665
|
C | A | 2 | a0005c0008t0031g0154a0005c0008t0031g0155 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2212+3782G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058665 | ||||||
chr11:101058694
|
C | T | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2212+3753G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058694 | ||||||
chr11:101058775
|
A | G | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2212+3672T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101058775 | ||||||
chr11:101059097
|
T | C | 2 | a0001c0002t0001g0115a0001c0002t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2212+3350A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059097 | ||||||
chr11:101059354
|
T | C | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2212+3093A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059354 | ||||||
chr11:101059432
|
C | T | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2212+3015G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059432 | ||||||
chr11:101059457
|
C | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212+2990G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059457 | ||||||
chr11:101059493
|
T | C | 82 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.2212+2954A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059493 | ||||||
chr11:101059530
|
A | C | 1 | a0001c0001t0078g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2212+2917T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059530 | ||||||
chr11:101059562
|
G | A | 1 | a0001c0003t0002g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2212+2885C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059562 | ||||||
chr11:101059765
|
A | C | 190 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2212+2682T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059765 | ||||||
chr11:101059842
|
C | CA | 13 | a0001c0001t0003g0093a0001c0001t0004g0249a0001c0001t0027g0151others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2212+2604dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059842 | ||||||
chr11:101059842
|
C | CAA | 53 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(50): Show | 53 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.2212+2603_2212+260 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059842 | ||||||
chr11:101059842
|
CA | C | 43 | a0001c0001t0004g0245a0001c0001t0078g0046a0001c0002t0001g0109others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.2212+2604delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059842 | ||||||
chr11:101059842
|
CAA | C | 11 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2212+2603_2212+260 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059842 | ||||||
chr11:101059848
|
A | G | 2 | a0001c0003t0061g0171a0004c0006t0038g0017 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2212+2599T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059848 | ||||||
chr11:101059857
|
A | AAG | 38 | a0001c0001t0002g0001a0001c0003t0002g0173a0001c0003t0002g0174others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.2212+2589_2212+259 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059857 | ||||||
chr11:101059862
|
G | A | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.2212+2585C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059862 | ||||||
chr11:101059863
|
A | AG | 16 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(13): Show | 16 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2212+2583_2212+258 others(5): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059863 | ||||||
chr11:101059863
|
A | G | 2 | a0002c0004t0020g0024a0002c0015t0054g0023 | 2 | HG01256.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2212+2584T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101059863 | ||||||
chr11:101060006
|
G | T | 10 | a0001c0001t0004g0218a0001c0001t0004g0225a0001c0001t0004g0230others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2212+2441C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060006 | ||||||
chr11:101060043
|
C | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2212+2404G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060043 | ||||||
chr11:101060061
|
G | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212+2386C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060061 | ||||||
chr11:101060065
|
G | T | 3 | a0003c0005t0019g0002a0004c0018t0042g0039a0005c0012t0058g0019 | 4 | HG02451.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212+2382C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060065 | ||||||
chr11:101060112
|
A | G | 1 | a0004c0006t0011g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2212+2335T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060112 | ||||||
chr11:101060135
|
G | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2212+2312C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060135 | ||||||
chr11:101060193
|
G | A | 1 | a0011c0009t0047g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2212+2254C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060193 | ||||||
chr11:101060220
|
T | C | 1 | a0001c0001t0034g0005 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2212+2227A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060220 | ||||||
chr11:101060292
|
T | C | 1 | a0001c0001t0004g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2212+2155A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060292 | ||||||
chr11:101060319
|
C | T | 1 | a0001c0003t0002g0197 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2212+2128G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060319 | ||||||
chr11:101060338
|
A | G | 2 | a0001c0003t0061g0171a0004c0006t0038g0017 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2212+2109T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060338 | ||||||
chr11:101060386
|
C | T | 93 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(90): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.2212+2061G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060386 | ||||||
chr11:101060399
|
C | G | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2212+2048G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060399 | ||||||
chr11:101060442
|
G | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212+2005C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060442 | ||||||
chr11:101060527
|
A | G | 1 | a0001c0001t0012g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2212+1920T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060527 | ||||||
chr11:101060625
|
A | G | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2212+1822T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060625 | ||||||
chr11:101060904
|
G | C | 6 | a0003c0005t0006g0157a0003c0005t0006g0161a0003c0005t0006g0162others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2212+1543C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060904 | ||||||
chr11:101060984
|
C | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212+1463G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101060984 | ||||||
chr11:101061064
|
A | G | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2212+1383T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061064 | ||||||
chr11:101061074
|
A | G | 97 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(94): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2212+1373T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061074 | ||||||
chr11:101061171
|
G | A | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2212+1276C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061171 | ||||||
chr11:101061211
|
C | T | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2212+1236G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061211 | ||||||
chr11:101061291
|
G | A | 249 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2212+1156C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061291 | ||||||
chr11:101061331
|
C | A | 1 | a0001c0001t0004g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2212+1116G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061331 | ||||||
chr11:101061430
|
T | C | 2 | a0001c0001t0065g0108a0001c0001t0082g0107 | 2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2212+1017A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061430 | ||||||
chr11:101061448
|
T | C | 4 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212+999A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061448 | ||||||
chr11:101061755
|
A | G | 1 | a0001c0003t0002g0207 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2212+692T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061755 | ||||||
chr11:101061770
|
T | G | 1 | a0001c0002t0057g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2212+677A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061770 | ||||||
chr11:101061808
|
G | A | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2212+639C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061808 | ||||||
chr11:101061872
|
T | C | 63 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(60): Show | 63 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2212+575A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061872 | ||||||
chr11:101061881
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2212+566A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101061881 | ||||||
chr11:101062169
|
G | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212+278C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101062169 | ||||||
chr11:101062298
|
A | G | 1 | a0006c0011t0009g0212 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2212+149T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101062298 | ||||||
chr11:101062394
|
C | A | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2212+53G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 4/7 | chr11 | 101062394 | ||||||
chr11:101062866
|
C | T | 1 | a0004c0006t0039g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1907-114G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101062866 | ||||||
chr11:101062867
|
G | GAATGA | 190 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1907-120_1907-116d others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101062867 | ||||||
chr11:101063047
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1907-295C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063047 | ||||||
chr11:101063099
|
C | T | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1907-347G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063099 | ||||||
chr11:101063100
|
G | T | 55 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(52): Show | 55 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1907-348C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063100 | ||||||
chr11:101063200
|
T | C | 14 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(11): Show | 14 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1907-448A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063200 | ||||||
chr11:101063387
|
C | T | 2 | a0001c0001t0004g0241a0001c0001t0004g0242 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1907-635G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063387 | ||||||
chr11:101063427
|
G | A | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1907-675C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063427 | ||||||
chr11:101063557
|
C | T | 1 | a0001c0003t0061g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1907-805G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063557 | ||||||
chr11:101063558
|
G | A | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1907-806C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063558 | ||||||
chr11:101063583
|
G | C | 198 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1907-831C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063583 | ||||||
chr11:101063636
|
G | A | 92 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1907-884C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063636 | ||||||
chr11:101063857
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1907-1105C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063857 | ||||||
chr11:101063877
|
T | G | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907-1125A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063877 | ||||||
chr11:101063904
|
C | T | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907-1152G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101063904 | ||||||
chr11:101064010
|
A | G | 2 | a0001c0001t0012g0085a0001c0001t0072g0061 | 2 | NA18949.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1907-1258T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064010 | ||||||
chr11:101064160
|
G | A | 1 | a0001c0001t0008g0075 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1907-1408C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064160 | ||||||
chr11:101064190
|
G | A | 1 | a0001c0001t0072g0061 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1907-1438C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064190 | ||||||
chr11:101064230
|
C | T | 25 | a0001c0001t0004g0221a0001c0001t0004g0224a0001c0001t0007g0045others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1907-1478G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064230 | ||||||
chr11:101064331
|
C | CA | 13 | a0001c0001t0004g0219a0001c0001t0004g0221a0001c0001t0004g0244others(10): Show | 13 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1907-1580dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAA | 9 | a0001c0001t0004g0218a0001c0001t0004g0230a0001c0001t0004g0241others(6): Show | 9 | HG01074.hp1 HG01081.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1907-1581_1907-158 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAAA | 10 | a0001c0001t0004g0225a0001c0001t0004g0236a0001c0001t0004g0237others(7): Show | 10 | HG00423.hp1 HG01175.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1907-1582_1907-158 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAAAA | 11 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0088g0243others(8): Show | 11 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1907-1583_1907-158 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAAAAAAA others(4): Show |
2 | a0001c0002t0032g0214a0001c0002t0032g0215 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1907-1590_1907-158 others(15): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAAAAAAA others(5): Show |
3 | a0001c0002t0049g0080a0001c0002t0084g0216a0003c0005t0053g0166 | 3 | HG01433.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1907-1591_1907-158 others(16): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1907-1592_1907-158 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0048g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1907-1593_1907-158 others(18): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CA | C | 31 | a0001c0001t0004g0217a0001c0001t0007g0045a0001c0001t0007g0048others(28): Show | 31 | HG00741.hp2 HG01074.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1907-1580delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAA | C | 31 | a0001c0001t0007g0049a0001c0001t0007g0054a0001c0001t0014g0050others(28): Show | 31 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1907-1581_1907-158 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAA | C | 6 | a0001c0001t0003g0098a0001c0001t0063g0060a0001c0002t0022g0043others(3): Show | 6 | HG02145.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1907-1582_1907-158 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAA | C | 64 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(61): Show | 64 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.1907-1583_1907-158 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAA | C | 29 | a0001c0001t0002g0001a0001c0001t0030g0099a0001c0003t0002g0170others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1907-1584_1907-158 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0046g0101a0011c0009t0047g0018 | 2 | HG04204.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1907-1590_1907-158 others(15): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(5): Show |
C | 2 | a0003c0005t0055g0167a0005c0012t0058g0019 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1907-1591_1907-158 others(16): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0232 | 3 | HG00738.hp2 HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1907-1592_1907-158 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(7): Show |
C | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1907-1593_1907-158 others(18): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0004g0234a0001c0001t0089g0235a0001c0001t0090g0233 | 3 | HG02280.hp1 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1907-1594_1907-158 others(19): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(10): Show |
C | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1907-1596_1907-158 others(21): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(12): Show |
C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1907-1598_1907-158 others(23): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064331
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0002t0001g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1907-1599_1907-158 others(24): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064331 | ||||||
chr11:101064345
|
A | C | 1 | a0001c0001t0066g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1907-1593T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064345 | ||||||
chr11:101064349
|
A | C | 1 | a0001c0001t0003g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1907-1597T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064349 | ||||||
chr11:101064350
|
A | C | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1907-1598T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064350 | ||||||
chr11:101064351
|
A | C | 1 | a0001c0001t0030g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1907-1599T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064351 | ||||||
chr11:101064359
|
A | C | 90 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1907-1607T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064359 | ||||||
chr11:101064360
|
A | C | 1 | a0001c0001t0030g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1907-1608T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064360 | ||||||
chr11:101064361
|
A | C | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1907-1609T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064361 | ||||||
chr11:101064408
|
G | A | 1 | a0001c0001t0004g0245 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1907-1656C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064408 | ||||||
chr11:101064430
|
G | A | 1 | a0001c0003t0061g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1907-1678C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064430 | ||||||
chr11:101064551
|
T | C | 4 | a0001c0001t0012g0082a0001c0001t0012g0085a0001c0001t0012g0153others(1): Show | 4 | HG02735.hp2 HG04115.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907-1799A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064551 | ||||||
chr11:101064557
|
G | A | 8 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907-1805C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064557 | ||||||
chr11:101064573
|
C | G | 11 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(8): Show | 11 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1907-1821G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064573 | ||||||
chr11:101064743
|
C | T | 2 | a0001c0002t0016g0138a0001c0002t0016g0140 | 2 | NA18946.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1907-1991G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064743 | ||||||
chr11:101064764
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1907-2012A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064764 | ||||||
chr11:101064809
|
A | G | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1907-2057T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064809 | ||||||
chr11:101064902
|
A | G | 1 | a0001c0001t0004g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1907-2150T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064902 | ||||||
chr11:101064953
|
G | A | 1 | a0001c0002t0026g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1907-2201C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064953 | ||||||
chr11:101064972
|
A | G | 10 | a0001c0003t0061g0171a0003c0020t0064g0168a0004c0006t0011g0012others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1907-2220T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064972 | ||||||
chr11:101064995
|
G | T | 2 | a0003c0020t0064g0168a0004c0006t0039g0011 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1907-2243C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101064995 | ||||||
chr11:101065049
|
A | G | 138 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(135): Show | 138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1907-2297T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065049 | ||||||
chr11:101065063
|
T | C | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1907-2311A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065063 | ||||||
chr11:101065175
|
T | C | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1907-2423A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065175 | ||||||
chr11:101065198
|
A | G | 55 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(52): Show | 55 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1907-2446T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065198 | ||||||
chr11:101065246
|
C | A | 3 | a0003c0005t0019g0002a0004c0018t0042g0039a0005c0012t0058g0019 | 4 | HG02451.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907-2494G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065246 | ||||||
chr11:101065277
|
G | GTTGT | 83 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(80): Show | 83 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1907-2529_1907-252 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065277 | ||||||
chr11:101065287
|
C | A | 1 | a0006c0010t0004g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1907-2535G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065287 | ||||||
chr11:101065517
|
CAA | C | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1907-2767_1907-276 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065517 | ||||||
chr11:101065549
|
A | T | 1 | a0001c0001t0003g0088 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1907-2797T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065549 | ||||||
chr11:101065615
|
C | A | 20 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(17): Show | 20 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1907-2863G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065615 | ||||||
chr11:101065774
|
C | T | 13 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(10): Show | 14 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1907-3022G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065774 | ||||||
chr11:101065791
|
G | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1907-3039C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065791 | ||||||
chr11:101065968
|
C | T | 2 | a0005c0008t0031g0154a0005c0008t0031g0155 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1907-3216G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101065968 | ||||||
chr11:101066084
|
C | T | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1907-3332G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066084 | ||||||
chr11:101066088
|
C | T | 3 | a0001c0002t0032g0214a0001c0002t0032g0215a0001c0002t0084g0216 | 3 | HG01433.hp1 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1907-3336G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066088 | ||||||
chr11:101066134
|
A | G | 1 | a0003c0005t0055g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1907-3382T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066134 | ||||||
chr11:101066177
|
C | G | 1 | a0001c0003t0002g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1907-3425G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066177 | ||||||
chr11:101066187
|
C | T | 1 | a0002c0004t0005g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1907-3435G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066187 | ||||||
chr11:101066310
|
C | T | 1 | a0001c0003t0070g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1907-3558G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066310 | ||||||
chr11:101066329
|
C | T | 60 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(57): Show | 60 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1907-3577G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066329 | ||||||
chr11:101066355
|
A | G | 1 | a0001c0003t0002g0193 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1907-3603T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066355 | ||||||
chr11:101066498
|
T | C | 1 | a0001c0003t0002g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1907-3746A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066498 | ||||||
chr11:101066545
|
C | T | 3 | a0001c0003t0002g0189a0001c0003t0028g0185a0001c0003t0069g0172 | 3 | HG01168.hp1 HG01175.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1907-3793G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066545 | ||||||
chr11:101066576
|
C | A | 68 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(65): Show | 69 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1907-3824G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066576 | ||||||
chr11:101066665
|
T | C | 2 | a0001c0001t0003g0093a0001c0007t0003g0152 | 2 | NA18955.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1907-3913A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066665 | ||||||
chr11:101066877
|
G | A | 1 | a0004c0017t0002g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1907-4125C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066877 | ||||||
chr11:101066892
|
C | T | 1 | a0007c0023t0005g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1907-4140G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101066892 | ||||||
chr11:101067159
|
A | G | 195 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1907-4407T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067159 | ||||||
chr11:101067225
|
T | C | 4 | a0001c0003t0002g0173a0001c0003t0002g0186a0001c0003t0002g0187others(1): Show | 4 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-4473A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067225 | ||||||
chr11:101067322
|
C | T | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1907-4570G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067322 | ||||||
chr11:101067401
|
A | G | 1 | a0001c0001t0010g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1907-4649T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067401 | ||||||
chr11:101067562
|
C | T | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1907-4810G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067562 | ||||||
chr11:101067590
|
C | T | 2 | a0001c0001t0008g0063a0001c0001t0017g0083 | 2 | NA18960.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1907-4838G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067590 | ||||||
chr11:101067617
|
G | C | 1 | a0001c0001t0029g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1907-4865C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067617 | ||||||
chr11:101067713
|
C | G | 65 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(62): Show | 66 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.1907-4961G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067713 | ||||||
chr11:101067767
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1907-5015A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067767 | ||||||
chr11:101067937
|
C | T | 62 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(59): Show | 63 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1907-5185G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101067937 | ||||||
chr11:101068129
|
G | A | 195 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1907-5377C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068129 | ||||||
chr11:101068564
|
A | G | 1 | a0001c0003t0002g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1907-5812T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068564 | ||||||
chr11:101068648
|
T | A | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1907-5896A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068648 | ||||||
chr11:101068671
|
T | C | 5 | a0001c0003t0002g0173a0001c0003t0002g0186a0001c0003t0002g0187others(2): Show | 5 | HG01070.hp2 HG01081.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1907-5919A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068671 | ||||||
chr11:101068677
|
A | C | 195 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1907-5925T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068677 | ||||||
chr11:101068750
|
C | CAA | 14 | a0001c0001t0082g0107a0001c0002t0022g0043a0001c0002t0022g0055others(11): Show | 15 | HG00733.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1907-6000_1907-599 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068750 | ||||||
chr11:101068750
|
C | CAAA | 52 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(49): Show | 52 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.1907-6001_1907-599 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068750 | ||||||
chr11:101068807
|
C | G | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1907-6055G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068807 | ||||||
chr11:101068825
|
C | T | 1 | a0002c0016t0005g0030 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1907-6073G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068825 | ||||||
chr11:101068847
|
C | T | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1907-6095G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068847 | ||||||
chr11:101068907
|
T | C | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-6155A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101068907 | ||||||
chr11:101069251
|
A | C | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-6499T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069251 | ||||||
chr11:101069252
|
T | G | 51 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1907-6500A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069252 | ||||||
chr11:101069268
|
T | A | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-6516A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069268 | ||||||
chr11:101069288
|
T | G | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1907-6536A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069288 | ||||||
chr11:101069361
|
C | A | 1 | a0001c0001t0029g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1907-6609G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069361 | ||||||
chr11:101069542
|
CAT | C | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1907-6792_1907-679 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069542 | ||||||
chr11:101069672
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1907-6920A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069672 | ||||||
chr11:101069738
|
T | C | 195 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1907-6986A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069738 | ||||||
chr11:101069827
|
A | G | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-7075T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069827 | ||||||
chr11:101069843
|
A | G | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-7091T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069843 | ||||||
chr11:101069969
|
A | G | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1907-7217T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101069969 | ||||||
chr11:101070045
|
T | C | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1907-7293A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070045 | ||||||
chr11:101070060
|
T | C | 2 | a0001c0001t0007g0045a0001c0001t0007g0048 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1907-7308A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070060 | ||||||
chr11:101070076
|
C | T | 4 | a0001c0001t0004g0236a0001c0001t0004g0237a0001c0001t0004g0238others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-7324G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070076 | ||||||
chr11:101070124
|
C | T | 4 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907-7372G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070124 | ||||||
chr11:101070125
|
A | G | 194 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1907-7373T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070125 | ||||||
chr11:101070256
|
T | C | 10 | a0001c0002t0048g0079a0001c0002t0049g0080a0003c0005t0006g0157others(7): Show | 11 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1907-7504A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070256 | ||||||
chr11:101070312
|
A | G | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1907-7560T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070312 | ||||||
chr11:101070455
|
T | A | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1907-7703A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070455 | ||||||
chr11:101070477
|
C | T | 3 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111 | 3 | HG00741.hp2 HG01069.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1907-7725G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070477 | ||||||
chr11:101070510
|
G | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-7758C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070510 | ||||||
chr11:101070572
|
T | C | 10 | a0001c0002t0048g0079a0001c0002t0049g0080a0003c0005t0006g0157others(7): Show | 11 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1907-7820A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070572 | ||||||
chr11:101070574
|
G | A | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1907-7822C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070574 | ||||||
chr11:101070612
|
G | A | 1 | a0001c0003t0002g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1907-7860C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070612 | ||||||
chr11:101070771
|
C | T | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1907-8019G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070771 | ||||||
chr11:101070849
|
C | T | 1 | a0001c0001t0036g0007 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1907-8097G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070849 | ||||||
chr11:101070891
|
G | A | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-8139C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070891 | ||||||
chr11:101070911
|
C | T | 1 | a0001c0003t0002g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1907-8159G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101070911 | ||||||
chr11:101071483
|
A | G | 1 | a0003c0005t0053g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1907-8731T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101071483 | ||||||
chr11:101071485
|
T | C | 6 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0119others(3): Show | 6 | HG01070.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1907-8733A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101071485 | ||||||
chr11:101071905
|
C | T | 2 | a0001c0003t0002g0199a0001c0003t0070g0201 | 2 | HG01993.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1907-9153G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101071905 | ||||||
chr11:101072061
|
T | G | 71 | a0001c0002t0023g0146a0001c0002t0023g0147a0001c0003t0002g0170others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1907-9309A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072061 | ||||||
chr11:101072081
|
A | AG | 194 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1907-9330dupC | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072081 | ||||||
chr11:101072125
|
T | C | 2 | a0001c0002t0001g0121a0006c0011t0009g0212 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1907-9373A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072125 | ||||||
chr11:101072226
|
T | A | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1907-9474A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072226 | ||||||
chr11:101072252
|
A | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1907-9500T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072252 | ||||||
chr11:101072394
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1907-9642G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072394 | ||||||
chr11:101072397
|
T | A | 4 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-9645A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072397 | ||||||
chr11:101072432
|
T | C | 1 | a0002c0004t0045g0035 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1907-9680A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072432 | ||||||
chr11:101072580
|
C | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1907-9828G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072580 | ||||||
chr11:101072646
|
T | C | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-9894A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072646 | ||||||
chr11:101072930
|
T | C | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-10178A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072930 | ||||||
chr11:101072961
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1907-10209C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072961 | ||||||
chr11:101072994
|
T | C | 1 | a0007c0023t0005g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1907-10242A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101072994 | ||||||
chr11:101073003
|
C | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-10251G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073003 | ||||||
chr11:101073188
|
C | A | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1907-10436G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073188 | ||||||
chr11:101073282
|
C | A | 4 | a0001c0002t0048g0079a0001c0002t0049g0080a0003c0005t0052g0169others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-10530G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073282 | ||||||
chr11:101073328
|
T | A | 1 | a0001c0003t0067g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1907-10576A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073328 | ||||||
chr11:101073423
|
C | A | 2 | a0001c0002t0001g0121a0006c0011t0009g0212 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1907-10671G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073423 | ||||||
chr11:101073498
|
T | G | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-10746A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073498 | ||||||
chr11:101073517
|
TA | T | 6 | a0001c0001t0088g0243a0001c0002t0001g0124a0005c0008t0031g0154others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1907-10766delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073517 | ||||||
chr11:101073540
|
C | T | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1907-10788G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073540 | ||||||
chr11:101073614
|
A | G | 1 | a0001c0001t0004g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1907-10862T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073614 | ||||||
chr11:101073644
|
G | T | 66 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0036g0007others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907-10892C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073644 | ||||||
chr11:101073662
|
C | T | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1907-10910G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073662 | ||||||
chr11:101073677
|
C | A | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1907-10925G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073677 | ||||||
chr11:101073739
|
C | T | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1907-10987G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073739 | ||||||
chr11:101073761
|
C | A | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1907-11009G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073761 | ||||||
chr11:101073781
|
G | A | 4 | a0001c0003t0002g0173a0001c0003t0002g0186a0001c0003t0002g0187others(1): Show | 4 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-11029C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073781 | ||||||
chr11:101073820
|
G | A | 1 | a0002c0004t0045g0035 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1907-11068C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073820 | ||||||
chr11:101073829
|
G | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-11077C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073829 | ||||||
chr11:101073994
|
T | C | 2 | a0005c0008t0031g0154a0005c0008t0031g0155 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1907-11242A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101073994 | ||||||
chr11:101074175
|
C | T | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1907-11423G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074175 | ||||||
chr11:101074176
|
G | A | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1907-11424C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074176 | ||||||
chr11:101074179
|
C | A | 61 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(58): Show | 62 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1907-11427G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074179 | ||||||
chr11:101074264
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1907-11512G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074264 | ||||||
chr11:101074363
|
G | T | 134 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0036g0007others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1907-11611C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074363 | ||||||
chr11:101074454
|
A | G | 1 | a0001c0001t0003g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1907-11702T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074454 | ||||||
chr11:101074505
|
C | T | 1 | a0001c0001t0004g0221 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1907-11753G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074505 | ||||||
chr11:101074623
|
G | C | 2 | a0003c0020t0064g0168a0004c0006t0039g0011 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1907-11871C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074623 | ||||||
chr11:101074672
|
A | G | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1907-11920T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074672 | ||||||
chr11:101074748
|
T | C | 1 | a0001c0001t0004g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1907-11996A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074748 | ||||||
chr11:101074786
|
C | T | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1907-12034G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074786 | ||||||
chr11:101074881
|
G | A | 51 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1907-12129C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101074881 | ||||||
chr11:101075074
|
T | C | 1 | a0007c0023t0005g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1907-12322A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075074 | ||||||
chr11:101075099
|
C | T | 61 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(58): Show | 62 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1907-12347G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075099 | ||||||
chr11:101075197
|
T | C | 134 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1907-12445A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075197 | ||||||
chr11:101075330
|
C | T | 61 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(58): Show | 62 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1907-12578G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075330 | ||||||
chr11:101075603
|
A | G | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-12851T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075603 | ||||||
chr11:101075621
|
C | CA | 38 | a0001c0002t0001g0148a0001c0003t0002g0170a0001c0003t0002g0173others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1907-12870dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075621 | ||||||
chr11:101075621
|
CA | C | 19 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060others(16): Show | 20 | HG01346.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1907-12870delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075621 | ||||||
chr11:101075633
|
C | A | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1907-12881G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075633 | ||||||
chr11:101075634
|
A | C | 1 | a0011c0009t0047g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1907-12882T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075634 | ||||||
chr11:101075874
|
T | C | 1 | a0001c0001t0010g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1907-13122A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075874 | ||||||
chr11:101075975
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1907-13223G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101075975 | ||||||
chr11:101076019
|
G | A | 8 | a0001c0001t0007g0049a0001c0001t0007g0054a0001c0001t0014g0047others(5): Show | 8 | HG00140.hp1 HG01433.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1907-13267C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076019 | ||||||
chr11:101076021
|
A | G | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1907-13269T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076021 | ||||||
chr11:101076136
|
C | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1907-13384G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076136 | ||||||
chr11:101076294
|
T | G | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907-13542A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076294 | ||||||
chr11:101076314
|
C | T | 2 | a0001c0002t0048g0079a0001c0002t0049g0080 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1907-13562G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076314 | ||||||
chr11:101076317
|
G | T | 1 | a0001c0003t0014g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1907-13565C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076317 | ||||||
chr11:101076404
|
G | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-13652C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076404 | ||||||
chr11:101076610
|
A | C | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1907-13858T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076610 | ||||||
chr11:101076620
|
T | A | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1907-13868A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076620 | ||||||
chr11:101076671
|
A | G | 51 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1907-13919T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076671 | ||||||
chr11:101076683
|
T | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907-13931A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076683 | ||||||
chr11:101076838
|
C | G | 2 | a0001c0003t0003g0203a0001c0003t0003g0204 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1907-14086G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076838 | ||||||
chr11:101076845
|
A | G | 2 | a0001c0002t0001g0121a0006c0011t0009g0212 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1907-14093T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076845 | ||||||
chr11:101076919
|
A | AT | 45 | a0001c0001t0004g0246a0001c0001t0007g0049a0001c0001t0007g0054others(42): Show | 46 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1907-14168dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
A | ATT | 22 | a0001c0003t0002g0170a0001c0003t0002g0180a0001c0003t0002g0181others(19): Show | 22 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907-14169_1907-14 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
A | ATTT | 11 | a0001c0003t0002g0184a0001c0003t0002g0198a0001c0003t0002g0199others(8): Show | 11 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1907-14170_1907-14 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
A | T | 1 | a0001c0003t0061g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1907-14167T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
AT | A | 12 | a0001c0002t0001g0112a0001c0002t0001g0126a0001c0002t0050g0141others(9): Show | 12 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1907-14168delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
ATT | A | 39 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(36): Show | 39 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1907-14169_1907-14 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
ATTTTTTT others(3): Show |
A | 53 | a0001c0001t0003g0057a0001c0001t0003g0065a0001c0001t0003g0066others(50): Show | 53 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1907-14177_1907-14 others(16): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076919
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0003g0071a0001c0001t0012g0073 | 2 | HG02040.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1907-14178_1907-14 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076919 | ||||||
chr11:101076949
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1907-14197T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076949 | ||||||
chr11:101076990
|
A | T | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1907-14238T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101076990 | ||||||
chr11:101077021
|
C | T | 60 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(57): Show | 61 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1907-14269G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077021 | ||||||
chr11:101077261
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1906+14499C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077261 | ||||||
chr11:101077312
|
C | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1906+14448G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077312 | ||||||
chr11:101077347
|
C | T | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1906+14413G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077347 | ||||||
chr11:101077349
|
G | A | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+14411C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077349 | ||||||
chr11:101077379
|
C | G | 132 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0036g0007others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1906+14381G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077379 | ||||||
chr11:101077637
|
A | G | 1 | a0001c0002t0032g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1906+14123T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077637 | ||||||
chr11:101077816
|
G | A | 1 | a0001c0003t0002g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1906+13944C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077816 | ||||||
chr11:101077995
|
G | A | 2 | a0003c0020t0064g0168a0004c0006t0039g0011 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1906+13765C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101077995 | ||||||
chr11:101078002
|
T | C | 1 | a0003c0005t0055g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1906+13758A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078002 | ||||||
chr11:101078064
|
A | G | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1906+13696T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078064 | ||||||
chr11:101078382
|
T | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1906+13378A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078382 | ||||||
chr11:101078586
|
C | G | 1 | a0001c0002t0057g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1906+13174G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078586 | ||||||
chr11:101078667
|
C | T | 2 | a0002c0004t0005g0027a0008c0021t0005g0205 | 2 | HG01175.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1906+13093G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078667 | ||||||
chr11:101078740
|
G | A | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1906+13020C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078740 | ||||||
chr11:101078776
|
A | T | 1 | a0003c0005t0055g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1906+12984T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078776 | ||||||
chr11:101078790
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1906+12970A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101078790 | ||||||
chr11:101079382
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1906+12378T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079382 | ||||||
chr11:101079383
|
G | A | 2 | a0001c0002t0050g0141a0001c0002t0056g0142 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1906+12377C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079383 | ||||||
chr11:101079410
|
C | T | 1 | a0001c0001t0003g0072 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1906+12350G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079410 | ||||||
chr11:101079421
|
C | CA | 61 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1906+12338dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079421 | ||||||
chr11:101079421
|
CA | C | 43 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1906+12338delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079421 | ||||||
chr11:101079813
|
G | A | 10 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1906+11947C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079813 | ||||||
chr11:101079826
|
C | G | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1906+11934G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101079826 | ||||||
chr11:101080245
|
C | T | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1906+11515G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080245 | ||||||
chr11:101080250
|
T | C | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1906+11510A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080250 | ||||||
chr11:101080275
|
C | T | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1906+11485G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080275 | ||||||
chr11:101080435
|
T | A | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1906+11325A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080435 | ||||||
chr11:101080713
|
G | A | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1906+11047C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080713 | ||||||
chr11:101080728
|
T | C | 251 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1906+11032A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080728 | ||||||
chr11:101080787
|
T | C | 1 | a0001c0019t0075g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1906+10973A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080787 | ||||||
chr11:101080844
|
G | A | 9 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(6): Show | 9 | HG01074.hp1 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1906+10916C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080844 | ||||||
chr11:101080936
|
A | C | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+10824T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101080936 | ||||||
chr11:101081015
|
C | G | 71 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(68): Show | 72 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1906+10745G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081015 | ||||||
chr11:101081179
|
C | T | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+10581G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081179 | ||||||
chr11:101081205
|
G | A | 1 | a0001c0002t0056g0142 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1906+10555C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081205 | ||||||
chr11:101081246
|
G | A | 1 | a0001c0001t0002g0001 | 2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1906+10514C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081246 | ||||||
chr11:101081393
|
C | G | 68 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(65): Show | 69 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1906+10367G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081393 | ||||||
chr11:101081428
|
C | CA | 7 | a0001c0001t0027g0151a0001c0001t0082g0107a0001c0002t0048g0079others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1906+10331dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081428 | ||||||
chr11:101081428
|
CA | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1906+10331delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081428 | ||||||
chr11:101081730
|
C | T | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1906+10030G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081730 | ||||||
chr11:101081859
|
C | T | 1 | a0001c0003t0002g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1906+9901G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081859 | ||||||
chr11:101081993
|
C | A | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1906+9767G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101081993 | ||||||
chr11:101082125
|
A | ACT | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1906+9633_1906+963 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082125 | ||||||
chr11:101082187
|
C | T | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+9573G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082187 | ||||||
chr11:101082236
|
A | G | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1906+9524T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082236 | ||||||
chr11:101082257
|
G | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+9503C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082257 | ||||||
chr11:101082411
|
C | T | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+9349G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082411 | ||||||
chr11:101082577
|
GA | G | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906+9182delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082577 | ||||||
chr11:101082697
|
T | G | 1 | a0001c0002t0049g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1906+9063A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082697 | ||||||
chr11:101082901
|
C | T | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1906+8859G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101082901 | ||||||
chr11:101083002
|
C | T | 1 | a0001c0002t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1906+8758G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083002 | ||||||
chr11:101083003
|
C | G | 46 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(43): Show | 46 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1906+8757G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083003 | ||||||
chr11:101083044
|
T | G | 1 | a0001c0002t0016g0120 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1906+8716A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083044 | ||||||
chr11:101083223
|
T | C | 3 | a0001c0001t0004g0234a0001c0001t0089g0235a0001c0001t0090g0233 | 3 | HG02280.hp1 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1906+8537A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083223 | ||||||
chr11:101083262
|
G | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+8498C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083262 | ||||||
chr11:101083443
|
C | T | 1 | a0001c0007t0003g0069 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1906+8317G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083443 | ||||||
chr11:101083484
|
T | C | 7 | a0003c0005t0006g0157a0003c0005t0006g0161a0003c0005t0006g0162others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1906+8276A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083484 | ||||||
chr11:101083619
|
G | T | 51 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1906+8141C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083619 | ||||||
chr11:101083693
|
G | A | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1906+8067C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101083693 | ||||||
chr11:101084007
|
C | T | 74 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(71): Show | 75 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1906+7753G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084007 | ||||||
chr11:101084088
|
T | C | 1 | a0004c0006t0038g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1906+7672A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084088 | ||||||
chr11:101084097
|
T | C | 40 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1906+7663A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084097 | ||||||
chr11:101084183
|
A | G | 71 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(68): Show | 72 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1906+7577T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084183 | ||||||
chr11:101084199
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1906+7561G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084199 | ||||||
chr11:101084260
|
T | C | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1906+7500A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084260 | ||||||
chr11:101084428
|
C | T | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1906+7332G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084428 | ||||||
chr11:101084429
|
G | A | 3 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0074g0102 | 3 | NA18981.hp2 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1906+7331C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084429 | ||||||
chr11:101084519
|
G | A | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1906+7241C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084519 | ||||||
chr11:101084551
|
C | G | 71 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(68): Show | 72 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1906+7209G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084551 | ||||||
chr11:101084606
|
TGAGATTG others(15): Show |
T | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906+7132_1906+715 others(26): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084606 | ||||||
chr11:101084615
|
G | A | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1906+7145C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084615 | ||||||
chr11:101084656
|
T | TA | 48 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(45): Show | 48 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1906+7103dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084656 | ||||||
chr11:101084656
|
TA | T | 58 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(55): Show | 58 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1906+7103delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084656 | ||||||
chr11:101084887
|
G | A | 51 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1906+6873C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084887 | ||||||
chr11:101084911
|
T | G | 1 | a0001c0002t0001g0118 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1906+6849A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084911 | ||||||
chr11:101084941
|
C | T | 101 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(98): Show | 102 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1906+6819G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084941 | ||||||
chr11:101084988
|
G | A | 38 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1906+6772C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101084988 | ||||||
chr11:101085053
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1906+6707A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085053 | ||||||
chr11:101085080
|
A | G | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1906+6680T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085080 | ||||||
chr11:101085160
|
A | G | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1906+6600T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085160 | ||||||
chr11:101085299
|
A | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1906+6461T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085299 | ||||||
chr11:101085367
|
T | TA | 8 | a0001c0001t0003g0057a0001c0001t0003g0087a0001c0001t0003g0088others(5): Show | 8 | HG01109.hp2 HG01346.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1906+6392dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085367 | ||||||
chr11:101085367
|
TA | T | 145 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0036g0007others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1906+6392delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085367 | ||||||
chr11:101085468
|
A | G | 43 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0002t0001g0109others(40): Show | 43 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1906+6292T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085468 | ||||||
chr11:101085489
|
C | T | 71 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(68): Show | 72 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1906+6271G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085489 | ||||||
chr11:101085525
|
T | TA | 63 | a0001c0001t0003g0057a0001c0001t0003g0065a0001c0001t0003g0067others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1906+6234dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085525 | ||||||
chr11:101085525
|
T | TAA | 14 | a0001c0001t0003g0056a0001c0001t0003g0072a0001c0001t0003g0097others(11): Show | 14 | HG00423.hp2 HG00741.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1906+6233_1906+623 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085525 | ||||||
chr11:101085525
|
T | TAAA | 32 | a0001c0001t0012g0073a0001c0002t0001g0109a0001c0002t0001g0114others(29): Show | 33 | HG00597.hp1 HG00733.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1906+6232_1906+623 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085525 | ||||||
chr11:101085525
|
T | TAAAA | 31 | a0001c0001t0036g0007a0001c0001t0065g0108a0001c0002t0001g0110others(28): Show | 31 | HG00621.hp1 HG00741.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.1906+6231_1906+623 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085525 | ||||||
chr11:101085525
|
TA | T | 29 | a0001c0001t0004g0234a0001c0001t0004g0241a0001c0001t0012g0082others(26): Show | 29 | HG00099.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1906+6234delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085525 | ||||||
chr11:101085917
|
A | G | 6 | a0001c0003t0002g0199a0001c0003t0002g0200a0001c0003t0002g0202others(3): Show | 6 | HG00323.hp2 HG01167.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+5843T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085917 | ||||||
chr11:101085928
|
T | C | 20 | a0001c0001t0012g0073a0002c0004t0005g0025a0002c0004t0005g0026others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+5832A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101085928 | ||||||
chr11:101086037
|
C | T | 1 | a0001c0001t0004g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1906+5723G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086037 | ||||||
chr11:101086152
|
A | G | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1906+5608T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086152 | ||||||
chr11:101086215
|
C | G | 1 | a0004c0006t0011g0012 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1906+5545G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086215 | ||||||
chr11:101086307
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1906+5453C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086307 | ||||||
chr11:101086318
|
TG | T | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+5441delC | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086318 | ||||||
chr11:101086470
|
T | C | 200 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1906+5290A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086470 | ||||||
chr11:101086568
|
C | T | 38 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1906+5192G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086568 | ||||||
chr11:101086806
|
C | T | 38 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1906+4954G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086806 | ||||||
chr11:101086905
|
ACTACAT | A | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1906+4849_1906+485 others(10): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086905 | ||||||
chr11:101086914
|
C | G | 54 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(51): Show | 54 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1906+4846G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086914 | ||||||
chr11:101086938
|
A | G | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+4822T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086938 | ||||||
chr11:101086939
|
C | A | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+4821G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101086939 | ||||||
chr11:101087340
|
C | T | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1906+4420G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087340 | ||||||
chr11:101087628
|
C | G | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1906+4132G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087628 | ||||||
chr11:101087728
|
T | C | 2 | a0002c0004t0005g0031a0002c0004t0043g0032 | 2 | HG01106.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1906+4032A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087728 | ||||||
chr11:101087737
|
C | CA | 99 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(96): Show | 100 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1906+4022dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087737 | ||||||
chr11:101087750
|
T | A | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1906+4010A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087750 | ||||||
chr11:101087755
|
C | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+4005G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087755 | ||||||
chr11:101087786
|
A | G | 16 | a0001c0001t0002g0001a0001c0001t0004g0221a0001c0001t0007g0045others(13): Show | 17 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1906+3974T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087786 | ||||||
chr11:101087935
|
G | A | 2 | a0002c0004t0005g0027a0008c0021t0005g0205 | 2 | HG01175.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1906+3825C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101087935 | ||||||
chr11:101088002
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1906+3758C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088002 | ||||||
chr11:101088027
|
CA | C | 66 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(63): Show | 67 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.1906+3732delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088027 | ||||||
chr11:101088063
|
T | C | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1906+3697A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088063 | ||||||
chr11:101088197
|
CAAAAA | C | 5 | a0001c0001t0003g0056a0001c0001t0003g0070a0001c0001t0003g0071others(2): Show | 5 | HG01192.hp1 HG02040.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1906+3558_1906+356 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088197 | ||||||
chr11:101088234
|
T | C | 1 | a0001c0001t0003g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1906+3526A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088234 | ||||||
chr11:101088371
|
G | A | 46 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(43): Show | 46 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1906+3389C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088371 | ||||||
chr11:101088463
|
G | A | 1 | a0001c0002t0026g0042 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1906+3297C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088463 | ||||||
chr11:101088464
|
T | C | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906+3296A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088464 | ||||||
chr11:101088582
|
T | C | 1 | a0011c0009t0047g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1906+3178A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088582 | ||||||
chr11:101088598
|
C | G | 1 | a0001c0001t0033g0003 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1906+3162G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088598 | ||||||
chr11:101088603
|
A | T | 1 | a0001c0001t0033g0003 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1906+3157T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088603 | ||||||
chr11:101088624
|
T | G | 67 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(64): Show | 68 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.1906+3136A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088624 | ||||||
chr11:101088641
|
C | T | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+3119G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088641 | ||||||
chr11:101088717
|
G | A | 65 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(62): Show | 66 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1906+3043C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088717 | ||||||
chr11:101088723
|
C | T | 64 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(61): Show | 65 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1906+3037G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088723 | ||||||
chr11:101088893
|
G | A | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906+2867C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088893 | ||||||
chr11:101088963
|
A | G | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1906+2797T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088963 | ||||||
chr11:101088980
|
A | T | 1 | a0001c0007t0003g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1906+2780T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088980 | ||||||
chr11:101088982
|
T | G | 1 | a0001c0007t0003g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1906+2778A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101088982 | ||||||
chr11:101089020
|
C | T | 6 | a0001c0001t0027g0151a0004c0006t0011g0012a0004c0006t0011g0014others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1906+2740G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089020 | ||||||
chr11:101089196
|
A | G | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1906+2564T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089196 | ||||||
chr11:101089205
|
C | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1906+2555G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089205 | ||||||
chr11:101089227
|
T | C | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+2533A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089227 | ||||||
chr11:101089591
|
C | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1906+2169G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089591 | ||||||
chr11:101089635
|
T | C | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1906+2125A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089635 | ||||||
chr11:101089676
|
C | T | 1 | a0001c0002t0046g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1906+2084G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089676 | ||||||
chr11:101089731
|
C | T | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1906+2029G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089731 | ||||||
chr11:101089844
|
A | G | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1906+1916T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089844 | ||||||
chr11:101089920
|
C | T | 1 | a0001c0002t0048g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1906+1840G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089920 | ||||||
chr11:101089921
|
G | A | 1 | a0007c0023t0005g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1906+1839C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089921 | ||||||
chr11:101089965
|
G | A | 15 | a0001c0002t0048g0079a0001c0002t0049g0080a0003c0005t0006g0157others(12): Show | 16 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1906+1795C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089965 | ||||||
chr11:101089976
|
A | G | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1906+1784T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101089976 | ||||||
chr11:101090032
|
C | T | 1 | a0001c0001t0034g0005 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1906+1728G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090032 | ||||||
chr11:101090199
|
A | AAAAT | 69 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(66): Show | 70 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.1906+1557_1906+156 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090199 | ||||||
chr11:101090220
|
A | G | 1 | a0001c0001t0090g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1906+1540T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090220 | ||||||
chr11:101090251
|
G | C | 8 | a0003c0005t0006g0161a0003c0005t0006g0162a0003c0005t0006g0163others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1906+1509C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090251 | ||||||
chr11:101090258
|
T | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1906+1502A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090258 | ||||||
chr11:101090450
|
C | T | 1 | a0001c0002t0022g0055 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1906+1310G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090450 | ||||||
chr11:101090451
|
G | A | 51 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(48): Show | 51 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1906+1309C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090451 | ||||||
chr11:101090526
|
T | C | 1 | a0001c0001t0007g0052 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1906+1234A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090526 | ||||||
chr11:101090749
|
A | G | 4 | a0003c0005t0006g0157a0003c0005t0006g0161a0003c0005t0006g0162others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+1011T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101090749 | ||||||
chr11:101091096
|
C | G | 200 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1906+664G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101091096 | ||||||
chr11:101091097
|
G | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906+663C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101091097 | ||||||
chr11:101091469
|
C | A | 65 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(62): Show | 66 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1906+291G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 3/7 | chr11 | 101091469 | ||||||
chr11:101092005
|
G | C | 1 | a0004c0006t0038g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1790-129C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092005 | ||||||
chr11:101092126
|
A | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-250T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092126 | ||||||
chr11:101092142
|
T | A | 56 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(53): Show | 56 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1790-266A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092142 | ||||||
chr11:101092394
|
A | G | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-518T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092394 | ||||||
chr11:101092408
|
A | G | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1790-532T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092408 | ||||||
chr11:101092478
|
A | G | 1 | a0001c0003t0003g0203 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1790-602T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092478 | ||||||
chr11:101092684
|
C | T | 3 | a0001c0001t0004g0219a0001c0001t0027g0151a0001c0001t0082g0107 | 3 | HG01884.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1790-808G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092684 | ||||||
chr11:101092778
|
T | C | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1790-902A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092778 | ||||||
chr11:101092849
|
G | T | 249 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1790-973C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092849 | ||||||
chr11:101092889
|
T | C | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1790-1013A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092889 | ||||||
chr11:101092989
|
G | A | 1 | a0001c0001t0086g0226 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1790-1113C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092989 | ||||||
chr11:101092990
|
C | G | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1790-1114G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101092990 | ||||||
chr11:101093012
|
C | T | 65 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(62): Show | 66 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1790-1136G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093012 | ||||||
chr11:101093233
|
G | C | 1 | a0001c0019t0075g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1790-1357C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093233 | ||||||
chr11:101093291
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1790-1415G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093291 | ||||||
chr11:101093312
|
A | AT | 47 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(44): Show | 48 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1790-1437dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093312 | ||||||
chr11:101093312
|
A | ATTT | 7 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1790-1439_1790-143 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093312 | ||||||
chr11:101093312
|
AT | A | 7 | a0001c0001t0004g0241a0001c0001t0008g0081a0001c0001t0029g0062others(4): Show | 7 | HG01109.hp2 HG01346.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1790-1437delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093312 | ||||||
chr11:101093451
|
T | C | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1790-1575A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093451 | ||||||
chr11:101093529
|
C | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-1653G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093529 | ||||||
chr11:101093529
|
C | T | 40 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1790-1653G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093529 | ||||||
chr11:101093802
|
G | A | 65 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(62): Show | 66 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1790-1926C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093802 | ||||||
chr11:101093818
|
G | A | 1 | a0001c0002t0026g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1790-1942C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093818 | ||||||
chr11:101093859
|
C | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-1983G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093859 | ||||||
chr11:101093860
|
G | A | 2 | a0001c0003t0002g0178a0001c0003t0002g0195 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1790-1984C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093860 | ||||||
chr11:101093934
|
C | T | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1790-2058G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093934 | ||||||
chr11:101093938
|
C | T | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1790-2062G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101093938 | ||||||
chr11:101094025
|
C | A | 1 | a0001c0019t0075g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1790-2149G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094025 | ||||||
chr11:101094245
|
C | A | 1 | a0010c0013t0015g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1790-2369G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094245 | ||||||
chr11:101094390
|
C | T | 1 | a0005c0008t0031g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1790-2514G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094390 | ||||||
chr11:101094508
|
G | T | 143 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0036g0007others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1790-2632C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094508 | ||||||
chr11:101094626
|
T | C | 1 | a0001c0002t0051g0135 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1790-2750A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094626 | ||||||
chr11:101094699
|
C | T | 10 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1790-2823G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094699 | ||||||
chr11:101094731
|
A | G | 5 | a0001c0002t0001g0116a0001c0002t0001g0123a0001c0002t0001g0144others(2): Show | 5 | HG00621.hp1 HG02015.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-2855T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094731 | ||||||
chr11:101094736
|
G | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1790-2860C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094736 | ||||||
chr11:101094770
|
T | C | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-2894A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094770 | ||||||
chr11:101094935
|
T | C | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1790-3059A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101094935 | ||||||
chr11:101095271
|
C | T | 7 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1790-3395G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095271 | ||||||
chr11:101095319
|
C | T | 2 | a0001c0002t0050g0141a0001c0002t0056g0142 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1790-3443G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095319 | ||||||
chr11:101095475
|
T | C | 10 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1790-3599A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095475 | ||||||
chr11:101095516
|
T | G | 1 | a0001c0001t0063g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1790-3640A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095516 | ||||||
chr11:101095667
|
T | G | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1790-3791A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095667 | ||||||
chr11:101095693
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1790-3817A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095693 | ||||||
chr11:101095907
|
T | A | 156 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1790-4031A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095907 | ||||||
chr11:101095976
|
C | T | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1790-4100G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101095976 | ||||||
chr11:101096102
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1790-4226G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096102 | ||||||
chr11:101096200
|
G | A | 1 | a0001c0003t0002g0197 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1790-4324C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096200 | ||||||
chr11:101096324
|
A | G | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-4448T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096324 | ||||||
chr11:101096333
|
T | C | 3 | a0001c0002t0016g0120a0001c0002t0016g0138a0001c0002t0016g0140 | 3 | NA18946.hp1 NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1790-4457A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096333 | ||||||
chr11:101096402
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1790-4526A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096402 | ||||||
chr11:101096450
|
G | A | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1790-4574C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096450 | ||||||
chr11:101096581
|
A | G | 1 | a0001c0001t0007g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1790-4705T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096581 | ||||||
chr11:101096780
|
C | T | 13 | a0003c0005t0006g0157a0003c0005t0006g0161a0003c0005t0006g0162others(10): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1790-4904G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096780 | ||||||
chr11:101096821
|
A | G | 213 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1790-4945T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096821 | ||||||
chr11:101096841
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-4965A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096841 | ||||||
chr11:101096998
|
TA | T | 76 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(73): Show | 78 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1790-5123delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101096998 | ||||||
chr11:101097071
|
C | A | 2 | a0001c0002t0050g0141a0001c0002t0056g0142 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1790-5195G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097071 | ||||||
chr11:101097136
|
T | C | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1790-5260A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097136 | ||||||
chr11:101097389
|
A | C | 2 | a0001c0001t0036g0007a0001c0001t0037g0006 | 2 | HG01256.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1790-5513T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097389 | ||||||
chr11:101097392
|
T | C | 76 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(73): Show | 78 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1790-5516A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097392 | ||||||
chr11:101097405
|
C | T | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1790-5529G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097405 | ||||||
chr11:101097448
|
A | C | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1790-5572T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097448 | ||||||
chr11:101097539
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-5663C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097539 | ||||||
chr11:101097557
|
C | A | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1790-5681G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097557 | ||||||
chr11:101097558
|
C | T | 1 | a0001c0002t0023g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1790-5682G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097558 | ||||||
chr11:101097560
|
A | G | 1 | a0001c0003t0014g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1790-5684T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097560 | ||||||
chr11:101097672
|
A | G | 1 | a0001c0003t0002g0207 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1790-5796T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097672 | ||||||
chr11:101097724
|
G | T | 1 | a0003c0005t0053g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1790-5848C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097724 | ||||||
chr11:101097733
|
C | T | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1790-5857G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097733 | ||||||
chr11:101097778
|
C | CT | 5 | a0001c0003t0002g0200a0001c0003t0003g0203a0001c0003t0003g0204others(2): Show | 5 | HG00323.hp2 HG01167.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-5903dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097778 | ||||||
chr11:101097778
|
CT | C | 131 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(128): Show | 133 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1790-5903delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097778 | ||||||
chr11:101097799
|
C | T | 29 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1790-5923G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097799 | ||||||
chr11:101097813
|
G | A | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1790-5937C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097813 | ||||||
chr11:101097902
|
G | A | 43 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1790-6026C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097902 | ||||||
chr11:101097933
|
C | T | 2 | a0001c0001t0030g0099a0001c0001t0030g0100 | 2 | HG00423.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1790-6057G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097933 | ||||||
chr11:101097960
|
T | A | 42 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1790-6084A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101097960 | ||||||
chr11:101098055
|
C | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1790-6179G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098055 | ||||||
chr11:101098151
|
G | C | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1790-6275C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098151 | ||||||
chr11:101098154
|
T | C | 7 | a0001c0002t0009g0227a0001c0002t0009g0228a0001c0002t0009g0229others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1790-6278A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098154 | ||||||
chr11:101098239
|
G | T | 81 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(78): Show | 83 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1790-6363C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098239 | ||||||
chr11:101098261
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1790-6385C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098261 | ||||||
chr11:101098416
|
G | A | 156 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1790-6540C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098416 | ||||||
chr11:101098502
|
G | A | 3 | a0001c0001t0004g0234a0001c0001t0089g0235a0001c0001t0090g0233 | 3 | HG02280.hp1 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1790-6626C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098502 | ||||||
chr11:101098599
|
T | C | 1 | a0001c0003t0081g0192 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1790-6723A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098599 | ||||||
chr11:101098629
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-6753A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098629 | ||||||
chr11:101098775
|
G | C | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-6899C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098775 | ||||||
chr11:101098776
|
G | A | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1790-6900C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098776 | ||||||
chr11:101098814
|
A | G | 106 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1790-6938T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098814 | ||||||
chr11:101098839
|
T | A | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1790-6963A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098839 | ||||||
chr11:101098923
|
C | T | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1790-7047G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098923 | ||||||
chr11:101098998
|
C | A | 1 | a0001c0002t0016g0120 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1790-7122G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101098998 | ||||||
chr11:101099130
|
G | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-7254C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101099130 | ||||||
chr11:101099549
|
T | C | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1790-7673A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101099549 | ||||||
chr11:101099555
|
TC | T | 7 | a0003c0005t0006g0161a0003c0005t0006g0162a0003c0005t0006g0163others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1790-7680delG | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101099555 | ||||||
chr11:101099793
|
AC | A | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-7918delG | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101099793 | ||||||
chr11:101100109
|
T | C | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1790-8233A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100109 | ||||||
chr11:101100187
|
C | T | 1 | a0001c0001t0013g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1790-8311G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100187 | ||||||
chr11:101100381
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8505A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100381 | ||||||
chr11:101100389
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8513A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100389 | ||||||
chr11:101100397
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8521A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100397 | ||||||
chr11:101100398
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8522A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100398 | ||||||
chr11:101100411
|
T | C | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8535A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100411 | ||||||
chr11:101100420
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8544A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100420 | ||||||
chr11:101100427
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8551A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100427 | ||||||
chr11:101100428
|
C | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8552G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100428 | ||||||
chr11:101100429
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8553A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100429 | ||||||
chr11:101100430
|
T | C | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8554A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100430 | ||||||
chr11:101100433
|
G | T | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8557C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100433 | ||||||
chr11:101100434
|
T | A | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8558A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100434 | ||||||
chr11:101100436
|
T | C | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8560A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100436 | ||||||
chr11:101100452
|
T | G | 1 | a0001c0001t0008g0092 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1790-8576A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100452 | ||||||
chr11:101100605
|
C | CCA | 34 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0004g0242others(31): Show | 34 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1790-8731_1790-873 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100605 | ||||||
chr11:101100605
|
C | CCACA | 32 | a0001c0001t0003g0093a0001c0001t0007g0049a0001c0001t0014g0047others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1790-8733_1790-873 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100605 | ||||||
chr11:101100605
|
C | CCACACA | 4 | a0001c0003t0002g0178a0001c0003t0002g0193a0001c0003t0002g0195others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-8735_1790-873 others(10): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100605 | ||||||
chr11:101100605
|
CCA | C | 25 | a0001c0001t0008g0092a0001c0001t0027g0059a0001c0001t0027g0151others(22): Show | 26 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1790-8731_1790-873 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100605 | ||||||
chr11:101100605
|
CCACA | C | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1790-8733_1790-873 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100605 | ||||||
chr11:101100640
|
A | G | 1 | a0001c0002t0023g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1790-8764T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100640 | ||||||
chr11:101100648
|
A | G | 1 | a0001c0001t0003g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1790-8772T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100648 | ||||||
chr11:101100765
|
T | C | 1 | a0002c0004t0005g0033 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1790-8889A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100765 | ||||||
chr11:101100775
|
T | C | 1 | a0001c0001t0003g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1790-8899A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100775 | ||||||
chr11:101100845
|
T | C | 4 | a0002c0004t0015g0021a0002c0004t0015g0022a0002c0004t0045g0035others(1): Show | 4 | HG00099.hp1 HG00735.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1790-8969A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100845 | ||||||
chr11:101100869
|
C | T | 1 | a0002c0004t0005g0026 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1790-8993G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100869 | ||||||
chr11:101100884
|
G | C | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-9008C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101100884 | ||||||
chr11:101101037
|
C | T | 3 | a0001c0001t0003g0091a0001c0002t0001g0121a0006c0011t0009g0212 | 3 | HG01255.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1790-9161G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101037 | ||||||
chr11:101101038
|
G | A | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1790-9162C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101038 | ||||||
chr11:101101209
|
A | C | 80 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(77): Show | 82 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1790-9333T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101209 | ||||||
chr11:101101257
|
T | A | 156 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1790-9381A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101257 | ||||||
chr11:101101304
|
G | C | 2 | a0003c0005t0006g0157a0003c0005t0019g0002 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1790-9428C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101304 | ||||||
chr11:101101335
|
A | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1790-9459T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101335 | ||||||
chr11:101101396
|
A | G | 80 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(77): Show | 82 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1790-9520T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101396 | ||||||
chr11:101101466
|
T | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1790-9590A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101466 | ||||||
chr11:101101605
|
T | G | 41 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1790-9729A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101605 | ||||||
chr11:101101961
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1790-10085C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101961 | ||||||
chr11:101101967
|
C | T | 69 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(66): Show | 70 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.1790-10091G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101101967 | ||||||
chr11:101102158
|
A | T | 1 | a0001c0001t0003g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1790-10282T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102158 | ||||||
chr11:101102181
|
G | T | 40 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1790-10305C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102181 | ||||||
chr11:101102350
|
T | G | 1 | a0001c0007t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1790-10474A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102350 | ||||||
chr11:101102600
|
G | C | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1790-10724C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102600 | ||||||
chr11:101102703
|
C | A | 1 | a0001c0002t0024g0137 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1790-10827G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102703 | ||||||
chr11:101102797
|
T | C | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1790-10921A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102797 | ||||||
chr11:101102805
|
G | A | 1 | a0003c0005t0019g0002 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1790-10929C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102805 | ||||||
chr11:101102867
|
G | A | 1 | a0001c0002t0016g0138 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1790-10991C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102867 | ||||||
chr11:101102934
|
A | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1790-11058T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102934 | ||||||
chr11:101102955
|
T | A | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1790-11079A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101102955 | ||||||
chr11:101103016
|
C | T | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-11140G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103016 | ||||||
chr11:101103228
|
C | T | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1790-11352G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103228 | ||||||
chr11:101103302
|
G | A | 155 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1790-11426C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103302 | ||||||
chr11:101103422
|
C | A | 1 | a0001c0001t0063g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1790-11546G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103422 | ||||||
chr11:101103460
|
C | T | 9 | a0003c0005t0006g0161a0003c0005t0006g0162a0003c0005t0006g0163others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1790-11584G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103460 | ||||||
chr11:101103547
|
A | G | 116 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1790-11671T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103547 | ||||||
chr11:101103735
|
T | C | 2 | a0001c0001t0029g0062a0001c0001t0029g0104 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1790-11859A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103735 | ||||||
chr11:101103888
|
G | A | 1 | a0003c0005t0006g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1790-12012C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103888 | ||||||
chr11:101103949
|
A | G | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1790-12073T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101103949 | ||||||
chr11:101104156
|
A | G | 64 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(61): Show | 65 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1790-12280T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104156 | ||||||
chr11:101104283
|
G | C | 1 | a0001c0002t0026g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1790-12407C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104283 | ||||||
chr11:101104390
|
T | A | 1 | a0002c0004t0005g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1790-12514A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104390 | ||||||
chr11:101104440
|
T | C | 1 | a0001c0001t0087g0240 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1790-12564A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104440 | ||||||
chr11:101104722
|
G | T | 3 | a0001c0003t0002g0199a0001c0003t0002g0202a0001c0003t0070g0201 | 3 | HG01993.hp1 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1790-12846C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104722 | ||||||
chr11:101104769
|
T | C | 3 | a0001c0002t0016g0120a0001c0002t0016g0138a0001c0002t0016g0140 | 3 | NA18946.hp1 NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1790-12893A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104769 | ||||||
chr11:101104800
|
C | T | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1790-12924G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104800 | ||||||
chr11:101104830
|
A | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1790-12954T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101104830 | ||||||
chr11:101105015
|
G | T | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1790-13139C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105015 | ||||||
chr11:101105128
|
A | G | 1 | a0001c0001t0003g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1790-13252T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105128 | ||||||
chr11:101105165
|
AG | A | 10 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1790-13290delC | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105165 | ||||||
chr11:101105180
|
A | G | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1790-13304T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105180 | ||||||
chr11:101105243
|
C | G | 111 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(108): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1790-13367G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105243 | ||||||
chr11:101105254
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1790-13378A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105254 | ||||||
chr11:101105460
|
A | G | 41 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1790-13584T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105460 | ||||||
chr11:101105467
|
T | TTAAAGAA others(674): Show |
1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1790-13592_1790-13 others(687): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105467 | ||||||
chr11:101105495
|
C | CT | 28 | a0001c0001t0008g0063a0001c0001t0029g0062a0001c0003t0002g0173others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1790-13620dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105495 | ||||||
chr11:101105495
|
C | CTT | 14 | a0001c0003t0002g0170a0001c0003t0002g0184a0001c0003t0002g0198others(11): Show | 14 | HG00323.hp2 HG00738.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1790-13621_1790-13 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105495 | ||||||
chr11:101105495
|
CT | C | 98 | a0001c0001t0002g0001a0001c0001t0004g0230a0001c0001t0007g0045others(95): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1790-13620delA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105495 | ||||||
chr11:101105495
|
CTT | C | 7 | a0001c0001t0007g0052a0001c0001t0027g0059a0001c0001t0062g0058others(4): Show | 7 | HG00323.hp1 HG01515.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1790-13621_1790-13 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105495 | ||||||
chr11:101105527
|
T | C | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1790-13651A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105527 | ||||||
chr11:101105632
|
A | C | 245 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1790-13756T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105632 | ||||||
chr11:101105740
|
A | G | 58 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(55): Show | 59 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1790-13864T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101105740 | ||||||
chr11:101106000
|
G | A | 1 | a0006c0010t0004g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1790-14124C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106000 | ||||||
chr11:101106075
|
C | G | 1 | a0001c0001t0017g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1790-14199G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106075 | ||||||
chr11:101106386
|
A | T | 1 | a0001c0001t0073g0086 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1790-14510T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106386 | ||||||
chr11:101106414
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1790-14538C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106414 | ||||||
chr11:101106448
|
C | T | 13 | a0003c0005t0006g0157a0003c0005t0006g0161a0003c0005t0006g0162others(10): Show | 14 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1790-14572G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106448 | ||||||
chr11:101106571
|
G | A | 41 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1790-14695C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106571 | ||||||
chr11:101106627
|
T | C | 1 | a0011c0009t0047g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1790-14751A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106627 | ||||||
chr11:101106720
|
A | T | 213 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1790-14844T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106720 | ||||||
chr11:101106867
|
A | G | 7 | a0001c0001t0003g0057a0001c0001t0003g0087a0001c0001t0003g0095others(4): Show | 7 | HG01109.hp2 HG01346.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1790-14991T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106867 | ||||||
chr11:101106868
|
T | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1790-14992A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106868 | ||||||
chr11:101106875
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1790-14999G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106875 | ||||||
chr11:101106982
|
T | C | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1790-15106A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101106982 | ||||||
chr11:101107045
|
C | T | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1790-15169G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107045 | ||||||
chr11:101107073
|
G | C | 1 | a0001c0003t0002g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1790-15197C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107073 | ||||||
chr11:101107125
|
C | T | 4 | a0001c0001t0082g0107a0005c0008t0031g0154a0005c0008t0031g0155others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1790-15249G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107125 | ||||||
chr11:101107748
|
G | A | 251 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1790-15872C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107748 | ||||||
chr11:101107865
|
T | TA | 10 | a0001c0001t0003g0057a0001c0001t0003g0065a0001c0001t0003g0087others(7): Show | 10 | HG01109.hp2 HG01346.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.1790-15990dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0062g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1790-15999_1790-15 others(16): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(4): Show |
5 | a0001c0001t0027g0059a0001c0001t0078g0046a0001c0002t0023g0146others(2): Show | 5 | HG01346.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1790-16000_1790-15 others(17): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(5): Show |
50 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(47): Show | 52 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1790-16001_1790-15 others(18): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(6): Show |
10 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0027g0151others(7): Show | 10 | HG00323.hp1 HG01074.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1790-16002_1790-15 others(19): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(7): Show |
2 | a0001c0002t0001g0144a0001c0002t0001g0145 | 2 | NA18982.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1790-16003_1790-15 others(20): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(8): Show |
5 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(2): Show | 5 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-16004_1790-15 others(21): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(9): Show |
4 | a0003c0005t0006g0161a0003c0005t0006g0162a0003c0005t0006g0163others(1): Show | 4 | HG01243.hp1 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-15990_1790-15 others(22): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(10): Show |
2 | a0003c0005t0006g0165a0003c0005t0052g0169 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1790-15990_1790-15 others(23): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(11): Show |
1 | a0003c0005t0053g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1790-15990_1790-15 others(24): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1790-15990_1790-15 others(27): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107865
|
TA | T | 52 | a0001c0001t0003g0066a0001c0003t0002g0170a0001c0003t0002g0173others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1790-15990delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107865 | ||||||
chr11:101107877
|
A | G | 1 | a0002c0004t0005g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1790-16001T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107877 | ||||||
chr11:101107881
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1790-16005C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107881 | ||||||
chr11:101107885
|
GAA | G | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1790-16011_1790-16 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107885 | ||||||
chr11:101107891
|
G | T | 1 | a0001c0003t0002g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1790-16015C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107891 | ||||||
chr11:101107945
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(74): Show | 79 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1790-16069C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101107945 | ||||||
chr11:101108109
|
G | C | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1790-16233C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108109 | ||||||
chr11:101108248
|
T | TA | 12 | a0001c0001t0007g0045a0001c0001t0013g0089a0001c0001t0013g0090others(9): Show | 13 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1790-16373dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108248 | ||||||
chr11:101108248
|
T | TAA | 63 | a0001c0001t0002g0001a0001c0001t0007g0048a0001c0001t0007g0049others(60): Show | 64 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1790-16374_1790-16 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108248 | ||||||
chr11:101108248
|
T | TAAA | 13 | a0001c0001t0014g0053a0001c0001t0027g0059a0001c0001t0062g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1790-16375_1790-16 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108248 | ||||||
chr11:101108248
|
TA | T | 6 | a0001c0001t0003g0065a0001c0001t0076g0064a0001c0001t0087g0240others(3): Show | 6 | HG00642.hp2 HG01081.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1790-16373delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108248 | ||||||
chr11:101108327
|
G | A | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-16451C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108327 | ||||||
chr11:101108414
|
C | T | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1790-16538G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108414 | ||||||
chr11:101108501
|
A | T | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1790-16625T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108501 | ||||||
chr11:101108540
|
C | T | 1 | a0001c0001t0007g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1790-16664G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108540 | ||||||
chr11:101108744
|
T | C | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1790-16868A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108744 | ||||||
chr11:101108996
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1789+17011C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101108996 | ||||||
chr11:101109245
|
G | A | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1789+16762C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109245 | ||||||
chr11:101109281
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1789+16726C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109281 | ||||||
chr11:101109378
|
G | A | 1 | a0002c0004t0021g0037 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1789+16629C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109378 | ||||||
chr11:101109465
|
C | T | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1789+16542G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109465 | ||||||
chr11:101109487
|
A | G | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1789+16520T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109487 | ||||||
chr11:101109491
|
C | G | 41 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1789+16516G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109491 | ||||||
chr11:101109492
|
G | A | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1789+16515C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109492 | ||||||
chr11:101109975
|
T | C | 245 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1789+16032A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101109975 | ||||||
chr11:101110118
|
G | T | 1 | a0001c0001t0010g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1789+15889C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110118 | ||||||
chr11:101110245
|
A | G | 245 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1789+15762T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110245 | ||||||
chr11:101110295
|
G | A | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1789+15712C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110295 | ||||||
chr11:101110312
|
T | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1789+15695A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110312 | ||||||
chr11:101110337
|
G | A | 1 | a0001c0001t0003g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1789+15670C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110337 | ||||||
chr11:101110600
|
C | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1789+15407G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110600 | ||||||
chr11:101110832
|
C | G | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1789+15175G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101110832 | ||||||
chr11:101111039
|
A | G | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1789+14968T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111039 | ||||||
chr11:101111130
|
C | A | 1 | a0001c0001t0087g0240 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1789+14877G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111130 | ||||||
chr11:101111164
|
A | T | 1 | a0001c0001t0008g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1789+14843T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111164 | ||||||
chr11:101111247
|
T | G | 3 | a0001c0001t0003g0093a0001c0001t0008g0092a0001c0007t0003g0152 | 3 | NA18955.hp2 NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1789+14760A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111247 | ||||||
chr11:101111452
|
T | C | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1789+14555A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111452 | ||||||
chr11:101111644
|
C | G | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1789+14363G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111644 | ||||||
chr11:101111713
|
T | A | 69 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(66): Show | 70 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.1789+14294A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111713 | ||||||
chr11:101111841
|
G | T | 69 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(66): Show | 70 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.1789+14166C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101111841 | ||||||
chr11:101112096
|
A | G | 1 | a0001c0001t0012g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1789+13911T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112096 | ||||||
chr11:101112124
|
C | A | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1789+13883G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112124 | ||||||
chr11:101112263
|
A | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1789+13744T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112263 | ||||||
chr11:101112304
|
G | C | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1789+13703C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112304 | ||||||
chr11:101112367
|
G | A | 68 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(65): Show | 69 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1789+13640C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112367 | ||||||
chr11:101112609
|
G | A | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1789+13398C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112609 | ||||||
chr11:101112857
|
C | G | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1789+13150G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112857 | ||||||
chr11:101112898
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1789+13109A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112898 | ||||||
chr11:101112993
|
G | C | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1789+13014C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101112993 | ||||||
chr11:101113109
|
CA | C | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1789+12897delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113109 | ||||||
chr11:101113282
|
C | T | 144 | a0001c0001t0027g0059a0001c0001t0027g0151a0001c0001t0036g0007others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1789+12725G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113282 | ||||||
chr11:101113369
|
C | G | 46 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(43): Show | 46 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1789+12638G>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113369 | ||||||
chr11:101113401
|
A | G | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1789+12606T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113401 | ||||||
chr11:101113422
|
T | C | 79 | a0001c0001t0027g0059a0001c0001t0036g0007a0001c0001t0037g0006others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1789+12585A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113422 | ||||||
chr11:101113427
|
A | AT | 133 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0065others(130): Show | 134 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.1789+12579dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113427 | ||||||
chr11:101113427
|
A | ATT | 60 | a0001c0001t0029g0062a0001c0001t0029g0104a0001c0003t0002g0170others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.1789+12578_1789+12 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113427 | ||||||
chr11:101113427
|
A | ATTT | 6 | a0001c0001t0027g0151a0001c0003t0061g0171a0004c0018t0042g0039others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789+12577_1789+12 others(9): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113427 | ||||||
chr11:101113529
|
C | A | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1789+12478G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113529 | ||||||
chr11:101113549
|
C | T | 44 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(41): Show | 44 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1789+12458G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113549 | ||||||
chr11:101113564
|
C | T | 2 | a0001c0001t0027g0059a0001c0001t0063g0060 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1789+12443G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113564 | ||||||
chr11:101113605
|
T | G | 1 | a0001c0002t0001g0148 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1789+12402A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113605 | ||||||
chr11:101113666
|
C | T | 1 | a0001c0001t0072g0061 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1789+12341G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113666 | ||||||
chr11:101113682
|
A | G | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1789+12325T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113682 | ||||||
chr11:101113686
|
G | T | 20 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1789+12321C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113686 | ||||||
chr11:101113834
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1789+12173A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113834 | ||||||
chr11:101113950
|
G | GC | 17 | a0001c0001t0004g0234a0001c0001t0004g0249a0001c0001t0010g0251others(14): Show | 17 | HG01109.hp2 HG01167.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1789+12056dupG | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113950 | ||||||
chr11:101113965
|
G | A | 1 | a0001c0002t0001g0143 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1789+12042C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101113965 | ||||||
chr11:101114113
|
G | A | 140 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1789+11894C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101114113 | ||||||
chr11:101114283
|
C | T | 141 | a0001c0001t0027g0151a0001c0001t0036g0007a0001c0001t0037g0006others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1789+11724G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101114283 | ||||||
chr11:101114350
|
G | T | 9 | a0003c0020t0064g0168a0004c0006t0011g0012a0004c0006t0011g0014others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1789+11657C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101114350 | ||||||
chr11:101114523
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1789+11484G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101114523 | ||||||
chr11:101114818
|
C | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789+11189G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101114818 | ||||||
chr11:101114943
|
G | A | 3 | a0001c0002t0001g0116a0001c0002t0001g0144a0001c0002t0001g0145 | 3 | NA18959.hp2 NA18982.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1789+11064C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101114943 | ||||||
chr11:101115046
|
A | G | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+10961T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115046 | ||||||
chr11:101115051
|
G | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1789+10956C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115051 | ||||||
chr11:101115204
|
T | C | 2 | a0001c0002t0023g0146a0001c0002t0023g0147 | 2 | HG01346.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1789+10803A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115204 | ||||||
chr11:101115262
|
C | A | 1 | a0004c0006t0038g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1789+10745G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115262 | ||||||
chr11:101115365
|
A | G | 3 | a0001c0001t0027g0059a0001c0001t0062g0058a0001c0001t0063g0060 | 3 | HG02559.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1789+10642T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115365 | ||||||
chr11:101115439
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1789+10568G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115439 | ||||||
chr11:101115686
|
G | A | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+10321C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115686 | ||||||
chr11:101115747
|
C | T | 82 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(79): Show | 84 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1789+10260G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115747 | ||||||
chr11:101115769
|
C | CAA | 91 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(88): Show | 93 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1789+10236_1789+10 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115769 | ||||||
chr11:101115866
|
T | C | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1789+10141A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101115866 | ||||||
chr11:101116086
|
G | A | 2 | a0001c0001t0003g0097a0004c0006t0011g0016 | 2 | HG02258.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1789+9921C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116086 | ||||||
chr11:101116096
|
G | C | 1 | a0004c0006t0011g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1789+9911C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116096 | ||||||
chr11:101116195
|
T | C | 1 | a0005c0012t0058g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1789+9812A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116195 | ||||||
chr11:101116292
|
C | T | 8 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1789+9715G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116292 | ||||||
chr11:101116377
|
C | A | 1 | a0001c0003t0002g0197 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1789+9630G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116377 | ||||||
chr11:101116739
|
C | CA | 7 | a0001c0003t0002g0198a0001c0003t0002g0199a0001c0003t0002g0202others(4): Show | 7 | HG00323.hp2 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1789+9267dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116739 | ||||||
chr11:101116739
|
CA | C | 102 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(99): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.1789+9267delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116739 | ||||||
chr11:101116739
|
CAA | C | 9 | a0001c0001t0037g0006a0001c0001t0062g0058a0001c0002t0001g0109others(6): Show | 9 | HG01069.hp2 HG01070.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1789+9266_1789+926 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116739 | ||||||
chr11:101116899
|
C | T | 2 | a0005c0008t0031g0154a0005c0008t0031g0155 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1789+9108G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116899 | ||||||
chr11:101116941
|
G | A | 5 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1789+9066C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101116941 | ||||||
chr11:101117160
|
C | A | 3 | a0004c0006t0038g0017a0004c0006t0039g0011a0004c0006t0040g0010 | 3 | HG02055.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1789+8847G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117160 | ||||||
chr11:101117303
|
C | T | 152 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1789+8704G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117303 | ||||||
chr11:101117611
|
C | T | 1 | a0001c0001t0003g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1789+8396G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117611 | ||||||
chr11:101117614
|
A | T | 1 | a0004c0006t0039g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1789+8393T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117614 | ||||||
chr11:101117673
|
G | A | 1 | a0001c0019t0075g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1789+8334C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117673 | ||||||
chr11:101117693
|
TA | T | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+8313delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117693 | ||||||
chr11:101117797
|
GAC | G | 4 | a0001c0003t0002g0174a0001c0003t0002g0175a0001c0003t0002g0176others(1): Show | 4 | HG01099.hp2 HG01261.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789+8208_1789+820 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117797 | ||||||
chr11:101117852
|
C | T | 4 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(1): Show | 4 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1789+8155G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101117852 | ||||||
chr11:101118064
|
G | C | 1 | a0001c0003t0014g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1789+7943C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101118064 | ||||||
chr11:101118661
|
A | G | 1 | a0001c0002t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1789+7346T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101118661 | ||||||
chr11:101118682
|
T | C | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1789+7325A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101118682 | ||||||
chr11:101118717
|
T | C | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+7290A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101118717 | ||||||
chr11:101119058
|
C | T | 1 | a0001c0001t0004g0219 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1789+6949G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119058 | ||||||
chr11:101119365
|
T | TAAAAGAT others(107): Show |
1 | a0001c0001t0003g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1789+6641_1789+664 others(118): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119365 | ||||||
chr11:101119365
|
T | TAAAAGAT others(115): Show |
1 | a0001c0001t0030g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1789+6641_1789+664 others(126): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119365 | ||||||
chr11:101119365
|
T | TAAAAGAT others(129): Show |
4 | a0001c0001t0003g0105a0001c0001t0030g0100a0001c0001t0074g0102others(1): Show | 4 | NA18971.hp2 NA18984.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789+6641_1789+664 others(140): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119365 | ||||||
chr11:101119365
|
T | TAAAAGAT others(130): Show |
1 | a0001c0001t0003g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1789+6641_1789+664 others(141): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119365 | ||||||
chr11:101119511
|
G | A | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1789+6496C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119511 | ||||||
chr11:101119541
|
C | T | 1 | a0010c0013t0015g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1789+6466G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119541 | ||||||
chr11:101119575
|
G | A | 2 | a0001c0001t0036g0007a0001c0001t0037g0006 | 2 | HG01256.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1789+6432C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119575 | ||||||
chr11:101119716
|
A | G | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+6291T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119716 | ||||||
chr11:101119733
|
A | T | 5 | a0001c0002t0022g0043a0001c0002t0022g0055a0001c0002t0026g0042others(2): Show | 5 | HG00733.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1789+6274T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119733 | ||||||
chr11:101119959
|
A | G | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1789+6048T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101119959 | ||||||
chr11:101120031
|
C | T | 1 | a0011c0009t0047g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1789+5976G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120031 | ||||||
chr11:101120057
|
A | G | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1789+5950T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120057 | ||||||
chr11:101120268
|
A | T | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1789+5739T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120268 | ||||||
chr11:101120314
|
T | G | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+5693A>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120314 | ||||||
chr11:101120405
|
C | T | 1 | a0001c0002t0001g0112 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1789+5602G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120405 | ||||||
chr11:101120431
|
A | C | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1789+5576T>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120431 | ||||||
chr11:101120522
|
T | C | 1 | a0001c0001t0003g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1789+5485A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120522 | ||||||
chr11:101120954
|
T | C | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1789+5053A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101120954 | ||||||
chr11:101121047
|
C | A | 140 | a0001c0001t0027g0151a0001c0001t0036g0007a0001c0001t0037g0006others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1789+4960G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121047 | ||||||
chr11:101121048
|
T | C | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+4959A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121048 | ||||||
chr11:101121071
|
C | A | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1789+4936G>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121071 | ||||||
chr11:101121403
|
T | C | 5 | a0001c0001t0004g0218a0001c0001t0004g0236a0001c0001t0004g0237others(2): Show | 5 | HG02615.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1789+4604A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121403 | ||||||
chr11:101121445
|
A | T | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789+4562T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121445 | ||||||
chr11:101121731
|
G | A | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1789+4276C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121731 | ||||||
chr11:101121818
|
C | T | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1789+4189G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121818 | ||||||
chr11:101121888
|
C | T | 1 | a0003c0005t0055g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1789+4119G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121888 | ||||||
chr11:101121889
|
A | G | 152 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1789+4118T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121889 | ||||||
chr11:101121932
|
C | T | 41 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(38): Show | 41 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1789+4075G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121932 | ||||||
chr11:101121933
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1789+4074C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101121933 | ||||||
chr11:101122080
|
G | A | 1 | a0002c0015t0054g0023 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1789+3927C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122080 | ||||||
chr11:101122124
|
C | T | 1 | a0003c0005t0059g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1789+3883G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122124 | ||||||
chr11:101122136
|
C | CAG | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+3869_1789+387 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122136 | ||||||
chr11:101122152
|
C | CA | 25 | a0001c0001t0029g0104a0001c0002t0001g0109a0001c0002t0001g0111others(22): Show | 26 | HG00733.hp1 HG01069.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1789+3854dupT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122152 | ||||||
chr11:101122152
|
C | CAA | 56 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(53): Show | 57 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1789+3853_1789+385 others(6): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122152 | ||||||
chr11:101122152
|
C | CAAA | 6 | a0001c0001t0027g0151a0001c0002t0001g0148a0001c0002t0001g0149others(3): Show | 6 | HG01516.hp1 HG01517.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789+3852_1789+385 others(7): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122152 | ||||||
chr11:101122152
|
C | CAAAA | 38 | a0001c0003t0002g0170a0001c0003t0002g0174a0001c0003t0002g0175others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1789+3851_1789+385 others(8): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122152 | ||||||
chr11:101122152
|
CA | C | 5 | a0001c0001t0003g0056a0001c0001t0004g0218a0001c0001t0087g0240others(2): Show | 5 | HG01168.hp2 HG01256.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1789+3854delT | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122152 | ||||||
chr11:101122182
|
A | AT | 251 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1789+3824dupA | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122182 | ||||||
chr11:101122341
|
G | A | 154 | a0001c0001t0002g0001a0001c0001t0003g0105a0001c0001t0003g0106others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1789+3666C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122341 | ||||||
chr11:101122427
|
G | A | 1 | a0001c0001t0014g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1789+3580C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122427 | ||||||
chr11:101122959
|
G | A | 18 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(15): Show | 18 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1789+3048C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122959 | ||||||
chr11:101122982
|
T | C | 2 | a0003c0005t0006g0157a0003c0005t0019g0002 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1789+3025A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101122982 | ||||||
chr11:101123115
|
C | T | 140 | a0001c0001t0027g0151a0001c0001t0036g0007a0001c0001t0037g0006others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1789+2892G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123115 | ||||||
chr11:101123339
|
T | C | 2 | a0003c0005t0025g0159a0003c0005t0025g0160 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1789+2668A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123339 | ||||||
chr11:101123381
|
C | T | 6 | a0003c0005t0006g0161a0003c0005t0006g0162a0003c0005t0006g0163others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1789+2626G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123381 | ||||||
chr11:101123407
|
G | A | 2 | a0001c0002t0001g0149a0001c0002t0001g0150 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1789+2600C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123407 | ||||||
chr11:101123420
|
G | A | 1 | a0001c0001t0007g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1789+2587C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123420 | ||||||
chr11:101123463
|
T | C | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1789+2544A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123463 | ||||||
chr11:101123559
|
T | C | 1 | a0001c0003t0061g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1789+2448A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123559 | ||||||
chr11:101123631
|
C | T | 2 | a0001c0002t0001g0109a0001c0002t0001g0110 | 2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1789+2376G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123631 | ||||||
chr11:101123638
|
A | G | 2 | a0001c0001t0004g0241a0001c0001t0004g0242 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1789+2369T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123638 | ||||||
chr11:101123944
|
G | A | 40 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1789+2063C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101123944 | ||||||
chr11:101124108
|
G | A | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1789+1899C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124108 | ||||||
chr11:101124114
|
T | C | 8 | a0001c0003t0002g0199a0001c0003t0002g0200a0001c0003t0002g0202others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1789+1893A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124114 | ||||||
chr11:101124118
|
T | C | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789+1889A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124118 | ||||||
chr11:101124135
|
T | C | 211 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1789+1872A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124135 | ||||||
chr11:101124151
|
C | T | 242 | a0001c0001t0002g0001a0001c0001t0003g0056a0001c0001t0003g0057others(239): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1789+1856G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124151 | ||||||
chr11:101124192
|
A | G | 1 | a0004c0006t0040g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1789+1815T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124192 | ||||||
chr11:101124209
|
C | T | 1 | a0004c0018t0042g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1789+1798G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124209 | ||||||
chr11:101124288
|
C | T | 1 | a0001c0007t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1789+1719G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124288 | ||||||
chr11:101124290
|
A | G | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+1717T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124290 | ||||||
chr11:101124410
|
G | T | 1 | a0001c0001t0004g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1789+1597C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124410 | ||||||
chr11:101124539
|
C | T | 3 | a0001c0002t0032g0214a0001c0002t0032g0215a0001c0002t0084g0216 | 3 | HG01433.hp1 HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1789+1468G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124539 | ||||||
chr11:101124568
|
G | T | 2 | a0003c0005t0006g0157a0003c0005t0019g0002 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1789+1439C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124568 | ||||||
chr11:101124607
|
T | C | 1 | a0001c0002t0022g0055 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1789+1400A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124607 | ||||||
chr11:101124696
|
T | C | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+1311A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124696 | ||||||
chr11:101124935
|
A | G | 2 | a0002c0004t0015g0021a0002c0004t0015g0022 | 2 | HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1789+1072T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124935 | ||||||
chr11:101124954
|
G | A | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789+1053C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124954 | ||||||
chr11:101124978
|
C | T | 42 | a0001c0001t0027g0151a0001c0003t0002g0170a0001c0003t0002g0173others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1789+1029G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101124978 | ||||||
chr11:101125133
|
A | G | 1 | a0001c0001t0065g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1789+874T>C | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125133 | ||||||
chr11:101125238
|
G | T | 1 | a0001c0001t0082g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1789+769C>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125238 | ||||||
chr11:101125276
|
A | AAC | 152 | a0001c0001t0002g0001a0001c0001t0007g0045a0001c0001t0007g0048others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1789+729_1789+730d others(4): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125276 | ||||||
chr11:101125574
|
C | T | 1 | a0001c0001t0008g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1789+433G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125574 | ||||||
chr11:101125575
|
G | A | 64 | a0001c0001t0036g0007a0001c0001t0037g0006a0001c0001t0065g0108others(61): Show | 64 | HG00597.hp1 HG00621.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1789+432C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125575 | ||||||
chr11:101125602
|
C | T | 1 | a0001c0003t0002g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1789+405G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125602 | ||||||
chr11:101125695
|
T | C | 1 | a0001c0001t0027g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789+312A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125695 | ||||||
chr11:101125697
|
T | C | 1 | a0003c0005t0052g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1789+310A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125697 | ||||||
chr11:101125785
|
G | C | 3 | a0005c0008t0031g0154a0005c0008t0031g0155a0005c0012t0058g0019 | 3 | HG02451.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1789+222C>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125785 | ||||||
chr11:101125834
|
T | C | 1 | a0001c0007t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1789+173A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125834 | ||||||
chr11:101125913
|
A | T | 1 | a0001c0001t0079g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1789+94T>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125913 | ||||||
chr11:101125999
|
G | A | 1 | a0001c0001t0036g0007 | 1 | HG03927.hp1 | splice_region_variant&intron_variant | LOW | c.1789+8C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 2/7 | chr11 | 101125999 | ||||||
chr11:101126435
|
G | A | 10 | a0003c0005t0006g0161a0003c0005t0006g0162a0003c0005t0006g0163others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1638-277C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101126435 | ||||||
chr11:101126862
|
T | C | 2 | a0001c0001t0010g0250a0001c0001t0010g0251 | 2 | HG01123.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1637+572A>G | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101126862 | ||||||
chr11:101127244
|
C | CAA | 8 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+188_1637+189d others(4): Show |
PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101127244 | ||||||
chr11:101127283
|
G | A | 1 | a0001c0001t0012g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637+151C>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101127283 | ||||||
chr11:101127345
|
T | A | 19 | a0002c0004t0005g0025a0002c0004t0005g0026a0002c0004t0005g0027others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1637+89A>T | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101127345 | ||||||
chr11:101127371
|
C | T | 8 | a0004c0006t0011g0012a0004c0006t0011g0014a0004c0006t0011g0015others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1637+63G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101127371 | ||||||
chr11:101127374
|
C | T | 39 | a0001c0003t0002g0170a0001c0003t0002g0173a0001c0003t0002g0174others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1637+60G>A | PGR | ENSG00000082175.16 | transcript | ENST00000325455.10 | protein_coding | 1/7 | chr11 | 101127374 |