geneid | 5834 |
---|---|
ensemblid | ENSG00000100994.12 |
hgncid | 9723 |
symbol | PYGB |
name | glycogen phosphorylase B |
refseq_nuc | NM_002862.4 |
refseq_prot | NP_002853.2 |
ensembl_nuc | ENST00000216962.9 |
ensembl_prot | ENSP00000216962.3 |
mane_status | MANE Select |
chr | chr20 |
start | 25248085 |
end | 25298012 |
strand | + |
ver | v1.2 |
region | chr20:25248085-25298012 |
region5000 | chr20:25243085-25303012 |
regionname0 | PYGB_chr20_25248085_25298012 |
regionname5000 | PYGB_chr20_25243085_25303012 |
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 | 843 | 296 | 91 | 68 | 81 | 12 | 42 | 58 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0002 | 0/0 | 843 | 57 | 1 | 5 | 47 | 2 | 2 | 34 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0003 | 0/0 | 843 | 7 | 0 | 1 | 6 | 0 | 0 | 3 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0004 | 0/0 | 843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0005 | 0/0 | 843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0006 | 0/0 | 843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0007 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0008 | 0/0 | 843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0009 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0010 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0011 | 0/0 | 843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0012 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0013 | 0/0 | 843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
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 | 0/1 | 2532 | 131 | 37 | 21 | 53 | 2 | 17 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0002 | 1/0 | 2532 | 90 | 18 | 39 | 2 | 9 | 21 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0003 | 0/0 | 2532 | 57 | 1 | 5 | 47 | 2 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0004 | 0/0 | 2532 | 51 | 29 | 4 | 18 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0005 | 0/0 | 2532 | 7 | 0 | 1 | 6 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0006 | 0/0 | 2532 | 7 | 0 | 0 | 7 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0007 | 0/0 | 2532 | 6 | 3 | 3 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0008 | 0/0 | 2532 | 3 | 1 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0009 | 0/0 | 2532 | 3 | 1 | 1 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0010 | 0/0 | 2532 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0011 | 0/0 | 2532 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0012 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0013 | 0/0 | 2532 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0014 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0015 | 0/0 | 2532 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0016 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0017 | 0/0 | 2532 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0018 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0019 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0020 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0021 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0022 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0023 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
c0024 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
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 | 0/1 | 1590 | 186 | 24 | 27 | 112 | 4 | 18 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0002 | 1/0 | 1585 | 144 | 44 | 45 | 22 | 9 | 23 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0003 | 0/0 | 1585 | 19 | 14 | 2 | 0 | 0 | 3 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0004 | 0/0 | 1585 | 4 | 4 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0005 | 0/0 | 1585 | 3 | 1 | 1 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0006 | 0/0 | 1585 | 2 | 0 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0007 | 0/0 | 1575 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0008 | 0/0 | 1585 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0009 | 0/0 | 1585 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0010 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0011 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0012 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0013 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0014 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0015 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0016 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
t0017 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
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 | 9 | 0 | 1 | 6 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0002 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0005 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0006 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
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 | 0/1 | 2532 | 131 | 37 | 21 | 53 | 2 | 17 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0002 | 1/0 | 2532 | 90 | 18 | 39 | 2 | 9 | 21 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0004 | 0/0 | 2532 | 51 | 29 | 4 | 18 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0006 | 0/0 | 2532 | 7 | 0 | 0 | 7 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0007 | 0/0 | 2532 | 6 | 3 | 3 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0008 | 0/0 | 2532 | 3 | 1 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0009 | 0/0 | 2532 | 3 | 1 | 1 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0012 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0015 | 0/0 | 2532 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0018 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0021 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0024 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0002c0003 | 0/0 | 2532 | 57 | 1 | 5 | 47 | 2 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0003c0005 | 0/0 | 2532 | 7 | 0 | 1 | 6 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0004c0010 | 0/0 | 2532 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0005c0011 | 0/0 | 2532 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0006c0023 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0007c0013 | 0/0 | 2532 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0008c0014 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0009c0022 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0010c0020 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0011c0019 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0012c0017 | 0/0 | 2532 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0013c0016 | 0/0 | 2532 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4121 | 111 | 23 | 18 | 53 | 2 | 14 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0001t0003 | 0/0 | 4116 | 19 | 14 | 2 | 0 | 0 | 3 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0001t0016 | 0/0 | 4121 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0002t0002 | 1/0 | 4116 | 86 | 16 | 39 | 2 | 9 | 19 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0002t0006 | 0/0 | 4116 | 2 | 0 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0002t0009 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0004t0002 | 0/0 | 4116 | 48 | 26 | 4 | 18 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0004t0007 | 0/0 | 4106 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0004t0011 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0006t0001 | 0/0 | 4121 | 7 | 0 | 0 | 7 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0007t0001 | 0/0 | 4121 | 3 | 0 | 3 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0007t0004 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0008t0002 | 0/0 | 4116 | 2 | 0 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0008t0010 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0009t0005 | 0/0 | 4116 | 3 | 1 | 1 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0012t0002 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0015t0001 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0018t0004 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0021t0002 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0001c0024t0001 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0002c0003t0001 | 0/0 | 4121 | 55 | 1 | 5 | 45 | 2 | 2 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0002c0003t0014 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0002c0003t0015 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0003c0005t0001 | 0/0 | 4121 | 6 | 0 | 1 | 5 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0003c0005t0017 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0004c0010t0008 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0005c0011t0002 | 0/0 | 4116 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0006c0023t0002 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0007c0013t0013 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0008c0014t0002 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0009c0022t0012 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0010c0020t0002 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0011c0019t0002 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0012c0017t0001 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
a0013c0016t0001 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | copy fasta | chr20 | 25243085 | 25303012 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0001t0016g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0002 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0006g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0002t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0004t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0006t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0007t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0007t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0007t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0007t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0007t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0007t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0008t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0008t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0008t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0009t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0009t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0009t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0012t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0015t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0018t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0021t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0001c0024t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0014g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0002c0003t0015g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0003c0005t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0003c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0003c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0003c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0003c0005t0017g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0004c0010t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0004c0010t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0005c0011t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0005c0011t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0006c0023t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0007c0013t0013g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0008c0014t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0009c0022t0012g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0010c0020t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0011c0019t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0012c0017t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
a0013c0016t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0118 | EUR | GBR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0239 | EUR | GBR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0023 | EUR | GBR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0097 | EUR | FIN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00544 | hp2 | a0001 | c0004 | t0002 | g0064 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0224 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00609 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0214 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00741 | hp1 | a0011 | c0019 | t0002 | g0281 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01069 | hp1 | a0001 | c0007 | t0001 | g0179 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01109 | hp1 | a0001 | c0004 | t0002 | g0274 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01192 | hp1 | a0001 | c0001 | t0016 | g0172 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01255 | hp1 | a0001 | c0004 | t0002 | g0026 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0110 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01261 | hp2 | a0006 | c0023 | t0002 | g0103 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0229 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01496 | hp1 | a0001 | c0004 | t0002 | g0026 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01496 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | IBS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01515 | hp2 | a0001 | c0009 | t0005 | g0266 | EUR | IBS | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01884 | hp1 | a0001 | c0004 | t0002 | g0074 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01884 | hp2 | a0001 | c0004 | t0007 | g0269 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01891 | hp1 | a0001 | c0004 | t0002 | g0076 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01934 | hp2 | a0001 | c0007 | t0001 | g0178 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01943 | hp2 | a0002 | c0003 | t0001 | g0192 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01975 | hp2 | a0001 | c0009 | t0005 | g0271 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01981 | hp1 | a0001 | c0004 | t0002 | g0070 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02004 | hp1 | a0003 | c0005 | t0001 | g0014 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02027 | hp1 | a0001 | c0004 | t0002 | g0069 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02027 | hp2 | a0001 | c0006 | t0001 | g0141 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02055 | hp1 | a0001 | c0004 | t0002 | g0282 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02056 | hp2 | a0003 | c0005 | t0001 | g0130 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0213 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02080 | hp2 | a0003 | c0005 | t0001 | g0176 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02083 | hp1 | a0007 | c0013 | t0013 | g0005 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0219 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02129 | hp2 | a0002 | c0003 | t0001 | g0217 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02145 | hp2 | a0001 | c0007 | t0004 | g0255 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02155 | hp2 | a0002 | c0003 | t0001 | g0196 | EAS | CDX | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0223 | EAS | CDX | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02257 | hp1 | a0001 | c0008 | t0010 | g0006 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02258 | hp1 | a0001 | c0004 | t0002 | g0275 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02280 | hp1 | a0001 | c0002 | t0009 | g0107 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02300 | hp1 | a0001 | c0007 | t0001 | g0122 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02300 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | PEL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02523 | hp1 | a0003 | c0005 | t0017 | g0175 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02523 | hp2 | a0001 | c0004 | t0002 | g0067 | EAS | KHV | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02572 | hp1 | a0010 | c0020 | t0002 | g0028 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02602 | hp2 | a0001 | c0024 | t0001 | g0149 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0101 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02723 | hp2 | a0001 | c0004 | t0002 | g0073 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0197 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02809 | hp1 | a0001 | c0007 | t0004 | g0256 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02818 | hp2 | a0001 | c0004 | t0002 | g0270 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0251 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02895 | hp1 | a0001 | c0004 | t0002 | g0040 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02897 | hp2 | a0001 | c0004 | t0002 | g0040 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02922 | hp2 | a0001 | c0009 | t0005 | g0272 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02976 | hp2 | a0001 | c0004 | t0011 | g0264 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0104 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0041 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03098 | hp1 | a0004 | c0010 | t0008 | g0252 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03098 | hp2 | a0001 | c0004 | t0002 | g0278 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03130 | hp1 | a0001 | c0004 | t0002 | g0265 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03139 | hp2 | a0001 | c0004 | t0002 | g0257 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03195 | hp1 | a0001 | c0004 | t0002 | g0072 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0277 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0075 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03225 | hp2 | a0001 | c0004 | t0002 | g0041 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03239 | hp2 | a0008 | c0014 | t0002 | g0059 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03453 | hp1 | a0001 | c0004 | t0007 | g0268 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03453 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03486 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03490 | hp1 | a0001 | c0002 | t0006 | g0029 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03491 | hp1 | a0001 | c0008 | t0002 | g0005 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0259 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03492 | hp2 | a0001 | c0002 | t0006 | g0029 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03516 | hp1 | a0001 | c0002 | t0009 | g0051 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03516 | hp2 | a0001 | c0004 | t0002 | g0021 | AFR | ESN | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03540 | hp2 | a0001 | c0021 | t0002 | g0279 | AFR | GWD | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03579 | hp1 | a0001 | c0004 | t0002 | g0280 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03654 | hp2 | a0001 | c0008 | t0002 | g0047 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0058 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0081 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03834 | hp1 | a0013 | c0016 | t0001 | g0246 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03927 | hp2 | a0001 | c0012 | t0002 | g0060 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0261 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0024 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | BEB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0079 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | STU | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | YRI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | CHB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0248 | AFR | YRI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0027 | AFR | YRI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18939 | hp1 | a0001 | c0006 | t0001 | g0157 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0066 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18942 | hp1 | a0001 | c0004 | t0002 | g0025 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18942 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0225 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18945 | hp1 | a0002 | c0003 | t0001 | g0218 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18945 | hp2 | a0002 | c0003 | t0001 | g0228 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18946 | hp1 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18949 | hp2 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18956 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0234 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18960 | hp2 | a0001 | c0006 | t0001 | g0013 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0233 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18966 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18966 | hp2 | a0001 | c0015 | t0001 | g0133 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18967 | hp2 | a0001 | c0006 | t0001 | g0013 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18968 | hp1 | a0001 | c0004 | t0002 | g0062 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18969 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18970 | hp1 | a0001 | c0004 | t0002 | g0065 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0236 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18974 | hp1 | a0002 | c0003 | t0001 | g0227 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18979 | hp1 | a0003 | c0005 | t0001 | g0014 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18980 | hp1 | a0001 | c0004 | t0002 | g0009 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18980 | hp2 | a0002 | c0003 | t0015 | g0198 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18982 | hp2 | a0003 | c0005 | t0001 | g0174 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18984 | hp2 | a0002 | c0003 | t0014 | g0015 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18985 | hp2 | a0001 | c0004 | t0002 | g0063 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0216 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18993 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18997 | hp1 | a0002 | c0003 | t0001 | g0222 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18998 | hp2 | a0005 | c0011 | t0002 | g0003 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19005 | hp2 | a0012 | c0017 | t0001 | g0232 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19010 | hp1 | a0002 | c0003 | t0001 | g0243 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19010 | hp2 | a0001 | c0006 | t0001 | g0162 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19011 | hp2 | a0001 | c0006 | t0001 | g0139 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | LWK | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19043 | hp1 | a0001 | c0004 | t0002 | g0273 | AFR | LWK | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19043 | hp2 | a0001 | c0007 | t0004 | g0254 | AFR | LWK | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19057 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19063 | hp2 | a0001 | c0004 | t0002 | g0025 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19066 | hp1 | a0001 | c0004 | t0002 | g0009 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19067 | hp1 | a0001 | c0006 | t0001 | g0013 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19067 | hp2 | a0002 | c0003 | t0001 | g0235 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19068 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19072 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19079 | hp1 | a0001 | c0004 | t0002 | g0068 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19079 | hp2 | a0003 | c0005 | t0001 | g0014 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19080 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19082 | hp2 | a0005 | c0011 | t0002 | g0009 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19091 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19240 | hp1 | a0004 | c0010 | t0008 | g0253 | AFR | YRI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA19240 | hp2 | a0001 | c0004 | t0002 | g0071 | AFR | YRI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ASW | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0045 | EUR | TSI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0096 | EUR | TSI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0215 | EUR | TSI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0106 | EUR | TSI | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | GIH | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0086 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0231 | AMR | CLM | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02109 | hp1 | a0001 | c0004 | t0002 | g0276 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02486 | hp1 | a0009 | c0022 | t0012 | g0267 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG02559 | hp2 | a0001 | c0018 | t0004 | g0258 | AFR | ACB | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0220 | AFR | USA | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18955 | hp1 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA18955 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | USA | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA20300 | hp2 | a0001 | c0004 | t0002 | g0027 | AFR | USA | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | LWK | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0099 | REF | REF | PYGB_chr20_25243085_25303012 | PYGB | chr20 | 25243085 | 25303012 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:25269140
|
C | G | 1 | a0005 | 2 | NA18998.hp2 NA19082.hp2 |
missense_variant | MODERATE | c.357C>G | p.Asp119Glu | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/20 | 451/4116 | 357/2532 | 119/843 | chr20 | 25269140 | ||
chr20:25271391
|
C | T | 1 | a0006 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.433C>T | p.Leu145Phe | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/20 | 527/4116 | 433/2532 | 145/843 | chr20 | 25271391 | ||
chr20:25274679
|
C | T | 1 | a0004 | 2 | HG03098.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.616C>T | p.Arg206Cys | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/20 | 710/4116 | 616/2532 | 206/843 | chr20 | 25274679 | ||
chr20:25278370
|
G | T | 3 | a0002a0012a0013 | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
missense_variant | MODERATE | c.907G>T | p.Ala303Ser | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/20 | 1001/4116 | 907/2532 | 303/843 | chr20 | 25278370 | ||
chr20:25279126
|
G | A | 1 | a0007 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1069G>A | p.Val357Met | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/20 | 1163/4116 | 1069/2532 | 357/843 | chr20 | 25279126 | ||
chr20:25281009
|
G | A | 1 | a0011 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1300G>A | p.Glu434Lys | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/20 | 1394/4116 | 1300/2532 | 434/843 | chr20 | 25281009 | ||
chr20:25282097
|
C | A | 1 | a0010 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1468C>A | p.Arg490Ser | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/20 | 1562/4116 | 1468/2532 | 490/843 | chr20 | 25282097 | ||
chr20:25282133
|
G | A | 2 | a0002a0013 | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
missense_variant | MODERATE | c.1504G>A | p.Asp502Asn | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/20 | 1598/4116 | 1504/2532 | 502/843 | chr20 | 25282133 | ||
chr20:25283198
|
C | G | 1 | a0003 | 7 | HG02004.hp1 HG02056.hp2 HG02080.hp2 others(4): Show |
missense_variant | MODERATE | c.1541C>G | p.Thr514Ser | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/20 | 1635/4116 | 1541/2532 | 514/843 | chr20 | 25283198 | ||
chr20:25283228
|
C | T | 1 | a0008 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1571C>T | p.Pro524Leu | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/20 | 1665/4116 | 1571/2532 | 524/843 | chr20 | 25283228 | ||
chr20:25295668
|
C | T | 1 | a0013 | 1 | HG03834.hp1 | missense_variant&splice_region_variant | MODERATE | c.2377C>T | p.Arg793Trp | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/20 | 2471/4116 | 2377/2532 | 793/843 | chr20 | 25295668 | ||
chr20:25296497
|
C | T | 1 | a0009 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2507C>T | p.Pro836Leu | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 2601/4116 | 2507/2532 | 836/843 | chr20 | 25296497 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:25248196
|
G | C | 1 | a0001c0012 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.18G>C | p.Thr6Thr | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/20 | 112/4116 | 18/2532 | 6/843 | chr20 | 25248196 | ||
chr20:25259279
|
C | T | 1 | a0001c0024 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.286C>T | p.Leu96Leu | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/20 | 380/4116 | 286/2532 | 96/843 | chr20 | 25259279 | ||
chr20:25274702
|
C | T | 7 | a0001c0004a0001c0009a0001c0021others(4): Show | 60 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(57): Show |
synonymous_variant | LOW | c.639C>T | p.Gly213Gly | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/20 | 733/4116 | 639/2532 | 213/843 | chr20 | 25274702 | ||
chr20:25276687
|
C | T | 1 | a0001c0018 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.702C>T | p.Tyr234Tyr | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 6/20 | 796/4116 | 702/2532 | 234/843 | chr20 | 25276687 | ||
chr20:25280295
|
A | G | 11 | a0001c0001a0001c0006a0001c0007others(8): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
synonymous_variant | LOW | c.1122A>G | p.Ala374Ala | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/20 | 1216/4116 | 1122/2532 | 374/843 | chr20 | 25280295 | ||
chr20:25280340
|
C | G | 1 | a0001c0006 | 7 | HG02027.hp2 NA18939.hp1 NA18960.hp2 others(4): Show |
synonymous_variant | LOW | c.1167C>G | p.Pro389Pro | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/20 | 1261/4116 | 1167/2532 | 389/843 | chr20 | 25280340 | ||
chr20:25280954
|
G | A | 1 | a0004c0010 | 2 | HG03098.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1245G>A | p.Val415Val | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/20 | 1339/4116 | 1245/2532 | 415/843 | chr20 | 25280954 | ||
chr20:25280969
|
C | T | 1 | a0001c0009 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.1260C>T | p.Pro420Pro | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/20 | 1354/4116 | 1260/2532 | 420/843 | chr20 | 25280969 | ||
chr20:25283259
|
C | T | 1 | a0001c0008 | 3 | HG02257.hp1 HG03491.hp1 HG03654.hp2 |
synonymous_variant | LOW | c.1602C>T | p.Asp534Asp | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/20 | 1696/4116 | 1602/2532 | 534/843 | chr20 | 25283259 | ||
chr20:25284178
|
T | C | 11 | a0001c0001a0001c0006a0001c0007others(8): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
synonymous_variant | LOW | c.1695T>C | p.Asp565Asp | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/20 | 1789/4116 | 1695/2532 | 565/843 | chr20 | 25284178 | ||
chr20:25292413
|
G | A | 1 | a0001c0021 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1977G>A | p.Pro659Pro | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/20 | 2071/4116 | 1977/2532 | 659/843 | chr20 | 25292413 | ||
chr20:25294179
|
C | T | 1 | a0001c0015 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.2199C>T | p.Tyr733Tyr | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/20 | 2293/4116 | 2199/2532 | 733/843 | chr20 | 25294179 | ||
chr20:25295661
|
G | A | 8 | a0001c0001a0001c0006a0001c0015others(5): Show | 206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
synonymous_variant | LOW | c.2370G>A | p.Gln790Gln | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/20 | 2464/4116 | 2370/2532 | 790/843 | chr20 | 25295661 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:25296595
|
C | T | 1 | a0001c0009t0005 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*73C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 73 | chr20 | 25296595 | |||||
chr20:25296608
|
A | G | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(16): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*86A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 86 | chr20 | 25296608 | |||||
chr20:25296693
|
GGAATGTG others(3): Show |
G | 1 | a0001c0004t0007 | 2 | HG01884.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*175_*184delTGTGCT others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 175 | INFO_REALIGN_3_PRIME | chr20 | 25296693 | ||||
chr20:25296729
|
G | A | 1 | a0004c0010t0008 | 2 | HG03098.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*207G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 207 | chr20 | 25296729 | |||||
chr20:25297359
|
G | C | 1 | a0001c0008t0010 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 837 | chr20 | 25297359 | |||||
chr20:25297515
|
G | A | 1 | a0002c0003t0014 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 993 | chr20 | 25297515 | |||||
chr20:25297578
|
G | A | 1 | a0002c0003t0015 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1056G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1056 | chr20 | 25297578 | |||||
chr20:25297625
|
A | G | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(11): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*1103A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1103 | chr20 | 25297625 | |||||
chr20:25297642
|
C | T | 13 | a0001c0001t0001a0001c0001t0016a0001c0006t0001others(10): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1120C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1120 | chr20 | 25297642 | |||||
chr20:25297700
|
G | A | 1 | a0001c0004t0011 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1178G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1178 | chr20 | 25297700 | |||||
chr20:25297719
|
A | G | 1 | a0001c0002t0006 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1197 | chr20 | 25297719 | |||||
chr20:25297786
|
C | T | 1 | a0007c0013t0013 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1264 | chr20 | 25297786 | |||||
chr20:25297790
|
C | T | 1 | a0003c0005t0017 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1268 | chr20 | 25297790 | |||||
chr20:25297828
|
A | AGTGGG | 13 | a0001c0001t0001a0001c0001t0016a0001c0006t0001others(10): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1308_*1312dupTGGG others(1): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1313 | INFO_REALIGN_3_PRIME | chr20 | 25297828 | ||||
chr20:25297883
|
G | C | 1 | a0009c0022t0012 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1361G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1361 | chr20 | 25297883 | |||||
chr20:25297936
|
G | C | 2 | a0001c0007t0004a0001c0018t0004 | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1414G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1414 | chr20 | 25297936 | |||||
chr20:25297964
|
G | A | 13 | a0001c0001t0001a0001c0001t0003a0001c0006t0001others(10): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*1442G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 20/20 | 1442 | chr20 | 25297964 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:25248486
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.243+65C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248486 | ||||||
chr20:25248531
|
C | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG00438.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.243+110C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248531 | ||||||
chr20:25248560
|
A | AT | 5 | a0001c0001t0003g0022a0001c0001t0003g0292a0001c0001t0003g0293others(2): Show | 7 | HG02145.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+139_243+140ins others(1): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248560 | ||||||
chr20:25248577
|
A | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.243+156A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248577 | ||||||
chr20:25248594
|
G | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+173G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248594 | ||||||
chr20:25248595
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(198): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.243+174C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248595 | ||||||
chr20:25248618
|
C | T | 2 | a0001c0002t0002g0118a0001c0002t0002g0119 | 2 | HG00099.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.243+197C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248618 | ||||||
chr20:25248651
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.243+230G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248651 | ||||||
chr20:25248686
|
T | TGAGCCCG others(14): Show |
22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+267_243+287dup others(21): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25248686 | |||||
chr20:25248693
|
G | T | 5 | a0001c0001t0003g0020a0001c0001t0003g0259a0001c0001t0003g0260others(2): Show | 7 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+272G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248693 | ||||||
chr20:25248894
|
C | CT | 7 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+481dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25248894 | |||||
chr20:25248894
|
C | CTT | 20 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(17): Show | 24 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.243+480_243+481dup others(2): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25248894 | |||||
chr20:25248901
|
T | G | 10 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0259others(7): Show | 14 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+480T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248901 | ||||||
chr20:25248908
|
C | T | 10 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0259others(7): Show | 14 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+487C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248908 | ||||||
chr20:25248928
|
C | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.243+507C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248928 | ||||||
chr20:25248953
|
A | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+532A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248953 | ||||||
chr20:25248986
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.243+565C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25248986 | ||||||
chr20:25249010
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+589G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249010 | ||||||
chr20:25249059
|
A | G | 2 | a0001c0002t0002g0247a0001c0002t0002g0248 | 2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.243+638A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249059 | ||||||
chr20:25249109
|
A | G | 1 | a0001c0004t0002g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.243+688A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249109 | ||||||
chr20:25249231
|
T | TA | 29 | a0001c0001t0001g0061a0001c0002t0002g0002a0001c0002t0002g0005others(26): Show | 40 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.243+811dupA | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25249231 | |||||
chr20:25249342
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(76): Show | 94 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.243+921G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249342 | ||||||
chr20:25249388
|
T | G | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.243+967T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249388 | ||||||
chr20:25249406
|
C | T | 1 | a0001c0004t0002g0265 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.243+985C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249406 | ||||||
chr20:25249542
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.243+1121A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249542 | ||||||
chr20:25249850
|
A | AT | 172 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(169): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.243+1445dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25249850 | |||||
chr20:25249890
|
G | A | 1 | a0002c0003t0015g0198 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.243+1469G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25249890 | ||||||
chr20:25250091
|
C | T | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.243+1670C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250091 | ||||||
chr20:25250141
|
A | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0262 | 4 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1720A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250141 | ||||||
chr20:25250149
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG01346.hp2 HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.243+1728C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250149 | ||||||
chr20:25250205
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+1784A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250205 | ||||||
chr20:25250261
|
G | A | 1 | a0009c0022t0012g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.243+1840G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250261 | ||||||
chr20:25250288
|
C | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+1867C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250288 | ||||||
chr20:25250393
|
T | C | 2 | a0001c0004t0007g0268a0001c0004t0007g0269 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.243+1972T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250393 | ||||||
chr20:25250450
|
CTGTAAGT others(32): Show |
C | 1 | a0001c0004t0002g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.243+2035_243+2073d others(41): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25250450 | |||||
chr20:25250458
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.243+2037C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250458 | ||||||
chr20:25250489
|
G | C | 21 | a0001c0004t0002g0021a0001c0004t0002g0041a0001c0004t0002g0265others(18): Show | 24 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.243+2068G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250489 | ||||||
chr20:25250711
|
C | T | 1 | a0001c0012t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.243+2290C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250711 | ||||||
chr20:25250725
|
C | T | 2 | a0001c0004t0002g0074a0001c0004t0002g0075 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.243+2304C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250725 | ||||||
chr20:25250727
|
G | T | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+2306G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250727 | ||||||
chr20:25250850
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+2429T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25250850 | ||||||
chr20:25251156
|
G | T | 1 | a0001c0004t0007g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.243+2735G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251156 | ||||||
chr20:25251222
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.243+2801G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251222 | ||||||
chr20:25251263
|
A | G | 1 | a0001c0002t0002g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.243+2842A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251263 | ||||||
chr20:25251346
|
G | A | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.243+2925G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251346 | ||||||
chr20:25251393
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+2972G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251393 | ||||||
chr20:25251461
|
A | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.243+3040A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251461 | ||||||
chr20:25251494
|
A | G | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.243+3073A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251494 | ||||||
chr20:25251509
|
A | T | 1 | a0013c0016t0001g0246 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.243+3088A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251509 | ||||||
chr20:25251664
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.243+3243A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251664 | ||||||
chr20:25251691
|
G | T | 1 | a0001c0002t0002g0112 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.243+3270G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251691 | ||||||
chr20:25251717
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+3296T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251717 | ||||||
chr20:25251770
|
A | G | 53 | a0001c0002t0002g0250a0001c0002t0002g0251a0002c0003t0001g0015others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.243+3349A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251770 | ||||||
chr20:25251858
|
T | G | 16 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(13): Show | 23 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.243+3437T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251858 | ||||||
chr20:25251938
|
G | GA | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+3519dupA | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25251938 | |||||
chr20:25251968
|
C | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 121 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.243+3547C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251968 | ||||||
chr20:25251975
|
C | T | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.243+3554C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25251975 | ||||||
chr20:25252025
|
C | T | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+3604C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252025 | ||||||
chr20:25252114
|
C | T | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+3693C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252114 | ||||||
chr20:25252346
|
A | G | 1 | a0008c0014t0002g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.243+3925A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252346 | ||||||
chr20:25252347
|
C | T | 1 | a0001c0004t0002g0280 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243+3926C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252347 | ||||||
chr20:25252363
|
G | T | 1 | a0002c0003t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.243+3942G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252363 | ||||||
chr20:25252428
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.243+4007C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252428 | ||||||
chr20:25252438
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+4017A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252438 | ||||||
chr20:25252516
|
G | A | 2 | a0001c0004t0007g0268a0001c0004t0007g0269 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.243+4095G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252516 | ||||||
chr20:25252605
|
C | T | 1 | a0001c0002t0002g0024 | 2 | HG01175.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.243+4184C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252605 | ||||||
chr20:25252710
|
G | A | 1 | a0001c0004t0007g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.243+4289G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252710 | ||||||
chr20:25252723
|
A | G | 1 | a0002c0003t0001g0245 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.243+4302A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25252723 | ||||||
chr20:25252911
|
T | TAC | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.243+4491_243+4492i others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25252911 | |||||
chr20:25253023
|
C | T | 1 | a0001c0002t0002g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.243+4602C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253023 | ||||||
chr20:25253064
|
C | G | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+4643C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253064 | ||||||
chr20:25253153
|
C | T | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.243+4732C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253153 | ||||||
chr20:25253349
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.243+4928C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253349 | ||||||
chr20:25253530
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(201): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.243+5109C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253530 | ||||||
chr20:25253623
|
T | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+5202T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253623 | ||||||
chr20:25253623
|
T | TAAATA | 28 | a0001c0001t0001g0123a0001c0001t0001g0180a0001c0001t0001g0181others(25): Show | 30 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.243+5234_243+5238d others(7): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25253623 | |||||
chr20:25253623
|
T | TAAATAAA others(3): Show |
90 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 113 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.243+5229_243+5238d others(12): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25253623 | |||||
chr20:25253623
|
T | TAAATAAA others(8): Show |
18 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(15): Show | 18 | HG01081.hp2 HG01943.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.243+5224_243+5238d others(17): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25253623 | |||||
chr20:25253623
|
TAAATA | T | 16 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(13): Show | 20 | HG01167.hp1 HG01361.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.243+5234_243+5238d others(7): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25253623 | |||||
chr20:25253623
|
TAAATAAA others(3): Show |
T | 53 | a0001c0002t0002g0250a0001c0002t0002g0251a0002c0003t0001g0015others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.243+5229_243+5238d others(12): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25253623 | |||||
chr20:25253660
|
G | A | 3 | a0001c0007t0001g0122a0001c0007t0001g0178a0001c0007t0001g0179 | 3 | HG01069.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.243+5239G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253660 | ||||||
chr20:25253773
|
C | T | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.243+5352C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253773 | ||||||
chr20:25253853
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-5384C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253853 | ||||||
chr20:25253854
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.244-5383G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253854 | ||||||
chr20:25253876
|
A | G | 3 | a0001c0007t0001g0122a0001c0007t0001g0178a0001c0007t0001g0179 | 3 | HG01069.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.244-5361A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25253876 | ||||||
chr20:25253899
|
CCTT | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-5334_244-5332d others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25253899 | |||||
chr20:25254046
|
T | C | 1 | a0002c0003t0001g0211 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.244-5191T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254046 | ||||||
chr20:25254071
|
CA | C | 90 | a0001c0001t0001g0042a0001c0001t0001g0124a0001c0001t0001g0132others(87): Show | 101 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.244-5149delA | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25254071 | |||||
chr20:25254071
|
CAA | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(131): Show | 168 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.244-5150_244-5149d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25254071 | |||||
chr20:25254096
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-5141A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254096 | ||||||
chr20:25254141
|
C | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-5096C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254141 | ||||||
chr20:25254176
|
T | A | 53 | a0001c0002t0002g0250a0001c0002t0002g0251a0002c0003t0001g0015others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.244-5061T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254176 | ||||||
chr20:25254205
|
C | T | 7 | a0001c0001t0001g0061a0001c0002t0002g0023a0001c0002t0002g0024others(4): Show | 9 | HG00140.hp2 HG00741.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-5032C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254205 | ||||||
chr20:25254230
|
C | A | 1 | a0001c0006t0001g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.244-5007C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254230 | ||||||
chr20:25254493
|
G | A | 53 | a0001c0002t0002g0250a0001c0002t0002g0251a0002c0003t0001g0015others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.244-4744G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254493 | ||||||
chr20:25254599
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-4638A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254599 | ||||||
chr20:25254604
|
T | G | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.244-4633T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254604 | ||||||
chr20:25254640
|
A | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-4597A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254640 | ||||||
chr20:25254685
|
G | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-4552G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254685 | ||||||
chr20:25254722
|
G | T | 1 | a0002c0003t0001g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.244-4515G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254722 | ||||||
chr20:25254827
|
C | G | 1 | a0001c0009t0005g0272 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244-4410C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254827 | ||||||
chr20:25254886
|
C | G | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.244-4351C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25254886 | ||||||
chr20:25255100
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.244-4137A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255100 | ||||||
chr20:25255150
|
C | T | 1 | a0001c0002t0002g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.244-4087C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255150 | ||||||
chr20:25255367
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.244-3870G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255367 | ||||||
chr20:25255413
|
G | GC | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.244-3819dupC | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25255413 | |||||
chr20:25255536
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.244-3701G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255536 | ||||||
chr20:25255599
|
G | C | 1 | a0001c0002t0002g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.244-3638G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255599 | ||||||
chr20:25255612
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.244-3625C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255612 | ||||||
chr20:25255632
|
A | G | 1 | a0001c0021t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.244-3605A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255632 | ||||||
chr20:25255656
|
G | T | 1 | a0002c0003t0001g0244 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.244-3581G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255656 | ||||||
chr20:25255663
|
G | C | 1 | a0002c0003t0001g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.244-3574G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255663 | ||||||
chr20:25255664
|
AGG | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-3570_244-3569d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25255664 | |||||
chr20:25255736
|
C | CT | 14 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(11): Show | 15 | HG01109.hp2 HG01928.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-3487dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25255736 | |||||
chr20:25255736
|
CT | C | 36 | a0001c0001t0001g0078a0001c0001t0001g0202a0001c0001t0003g0113others(33): Show | 44 | HG00544.hp2 HG01255.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.244-3487delT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25255736 | |||||
chr20:25255736
|
CTT | C | 20 | a0001c0002t0002g0083a0001c0004t0002g0021a0001c0004t0002g0040others(17): Show | 24 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.244-3488_244-3487d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25255736 | |||||
chr20:25255741
|
T | C | 3 | a0002c0003t0001g0216a0002c0003t0001g0217a0002c0003t0001g0218 | 3 | HG02129.hp2 NA18945.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.244-3496T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255741 | ||||||
chr20:25255763
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(254): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.244-3474T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255763 | ||||||
chr20:25255808
|
A | G | 2 | a0001c0002t0002g0106a0001c0002t0009g0107 | 2 | HG02280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.244-3429A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255808 | ||||||
chr20:25255865
|
G | C | 21 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(18): Show | 25 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.244-3372G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255865 | ||||||
chr20:25255891
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02015.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.244-3346G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255891 | ||||||
chr20:25255895
|
A | G | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.244-3342A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25255895 | ||||||
chr20:25256009
|
A | C | 1 | a0002c0003t0001g0245 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.244-3228A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256009 | ||||||
chr20:25256149
|
A | G | 53 | a0001c0002t0002g0250a0001c0002t0002g0251a0002c0003t0001g0015others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.244-3088A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256149 | ||||||
chr20:25256176
|
A | G | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.244-3061A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256176 | ||||||
chr20:25256379
|
ACT | A | 3 | a0003c0005t0001g0130a0003c0005t0001g0176a0003c0005t0017g0175 | 3 | HG02056.hp2 HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.244-2855_244-2854d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25256379 | |||||
chr20:25256400
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-2837T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256400 | ||||||
chr20:25256507
|
A | C | 3 | a0001c0007t0001g0122a0001c0007t0001g0178a0001c0007t0001g0179 | 3 | HG01069.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.244-2730A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256507 | ||||||
chr20:25256508
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(198): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.244-2729A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256508 | ||||||
chr20:25256508
|
AC | A | 3 | a0001c0007t0001g0122a0001c0007t0001g0178a0001c0007t0001g0179 | 3 | HG01069.hp1 HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.244-2728delC | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256508 | ||||||
chr20:25256509
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(225): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.244-2728C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256509 | ||||||
chr20:25256509
|
C | CA | 27 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0004t0002g0021others(24): Show | 31 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.244-2723dupA | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr20 | 25256509 | |||||
chr20:25256684
|
G | T | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.244-2553G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256684 | ||||||
chr20:25256702
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(255): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.244-2535A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256702 | ||||||
chr20:25256743
|
A | G | 1 | a0002c0003t0001g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.244-2494A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256743 | ||||||
chr20:25256754
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.244-2483A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256754 | ||||||
chr20:25256843
|
T | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-2394T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256843 | ||||||
chr20:25256895
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-2342A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256895 | ||||||
chr20:25256923
|
A | G | 19 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(16): Show | 23 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.244-2314A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256923 | ||||||
chr20:25256979
|
C | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-2258C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25256979 | ||||||
chr20:25257024
|
C | T | 2 | a0001c0002t0002g0002a0001c0002t0002g0008 | 8 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-2213C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257024 | ||||||
chr20:25257037
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.244-2200G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257037 | ||||||
chr20:25257060
|
A | G | 4 | a0002c0003t0001g0240a0002c0003t0001g0241a0002c0003t0001g0242others(1): Show | 4 | NA18956.hp2 NA18971.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-2177A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257060 | ||||||
chr20:25257069
|
C | T | 1 | a0003c0005t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.244-2168C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257069 | ||||||
chr20:25257131
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-2106T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257131 | ||||||
chr20:25257193
|
A | C | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-2044A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257193 | ||||||
chr20:25257214
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.244-2023C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257214 | ||||||
chr20:25257381
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.244-1856G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257381 | ||||||
chr20:25257402
|
C | T | 1 | a0001c0002t0002g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.244-1835C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257402 | ||||||
chr20:25257403
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.244-1834G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257403 | ||||||
chr20:25257486
|
C | G | 2 | a0001c0001t0003g0259a0001c0001t0003g0260 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.244-1751C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257486 | ||||||
chr20:25257537
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.244-1700T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257537 | ||||||
chr20:25257599
|
C | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-1638C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257599 | ||||||
chr20:25257673
|
A | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(174): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.244-1564A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257673 | ||||||
chr20:25257680
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(77): Show | 95 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.244-1557A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257680 | ||||||
chr20:25257870
|
G | A | 1 | a0001c0002t0002g0096 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.244-1367G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25257870 | ||||||
chr20:25258083
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.244-1154T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258083 | ||||||
chr20:25258204
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.244-1033A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258204 | ||||||
chr20:25258226
|
C | T | 1 | a0003c0005t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.244-1011C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258226 | ||||||
chr20:25258346
|
C | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-891C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258346 | ||||||
chr20:25258506
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.244-731C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258506 | ||||||
chr20:25258594
|
C | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.244-643C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258594 | ||||||
chr20:25258597
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.244-640G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258597 | ||||||
chr20:25258629
|
C | T | 2 | a0001c0009t0005g0266a0001c0009t0005g0271 | 2 | HG01515.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.244-608C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258629 | ||||||
chr20:25258630
|
G | A | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-607G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258630 | ||||||
chr20:25258633
|
C | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.244-604C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258633 | ||||||
chr20:25258777
|
G | A | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.244-460G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258777 | ||||||
chr20:25258886
|
G | T | 1 | a0001c0001t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.244-351G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258886 | ||||||
chr20:25258915
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0189others(6): Show | 13 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.244-322G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258915 | ||||||
chr20:25258949
|
C | G | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-288C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25258949 | ||||||
chr20:25259031
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.244-206G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25259031 | ||||||
chr20:25259144
|
T | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-93T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25259144 | ||||||
chr20:25259145
|
G | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.244-92G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25259145 | ||||||
chr20:25259165
|
C | T | 6 | a0001c0002t0002g0002a0001c0002t0002g0007a0001c0002t0002g0008others(3): Show | 14 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-72C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 1/19 | chr20 | 25259165 | ||||||
chr20:25259453
|
G | A | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.345+115G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259453 | ||||||
chr20:25259464
|
G | A | 1 | a0001c0021t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.345+126G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259464 | ||||||
chr20:25259525
|
G | C | 1 | a0003c0005t0017g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.345+187G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259525 | ||||||
chr20:25259552
|
C | T | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.345+214C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259552 | ||||||
chr20:25259553
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 121 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.345+215G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259553 | ||||||
chr20:25259808
|
A | G | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.345+470A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259808 | ||||||
chr20:25259897
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.345+559G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25259897 | ||||||
chr20:25260079
|
G | A | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+741G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260079 | ||||||
chr20:25260102
|
G | A | 1 | a0001c0004t0002g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.345+764G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260102 | ||||||
chr20:25260142
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.345+804C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260142 | ||||||
chr20:25260174
|
C | T | 1 | a0001c0002t0002g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.345+836C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260174 | ||||||
chr20:25260358
|
C | T | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1020C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260358 | ||||||
chr20:25260447
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(290): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.345+1109A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260447 | ||||||
chr20:25260519
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.345+1181T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260519 | ||||||
chr20:25260626
|
G | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+1288G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260626 | ||||||
chr20:25260630
|
T | C | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1292T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260630 | ||||||
chr20:25260659
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.345+1321A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260659 | ||||||
chr20:25260709
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.345+1371C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260709 | ||||||
chr20:25260819
|
C | T | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1481C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260819 | ||||||
chr20:25260835
|
C | T | 27 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(24): Show | 35 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.345+1497C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260835 | ||||||
chr20:25260836
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.345+1498G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260836 | ||||||
chr20:25260847
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+1509A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260847 | ||||||
chr20:25260865
|
G | A | 7 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG02015.hp1 HG02129.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.345+1527G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260865 | ||||||
chr20:25260889
|
A | G | 2 | a0001c0002t0002g0050a0001c0002t0009g0051 | 2 | HG01099.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.345+1551A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260889 | ||||||
chr20:25260913
|
C | T | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.345+1575C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260913 | ||||||
chr20:25260937
|
G | A | 1 | a0001c0009t0005g0272 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.345+1599G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260937 | ||||||
chr20:25260959
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.345+1621G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25260959 | ||||||
chr20:25261033
|
G | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(159): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.345+1695G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261033 | ||||||
chr20:25261075
|
C | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+1737C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261075 | ||||||
chr20:25261113
|
T | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+1775T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261113 | ||||||
chr20:25261169
|
G | A | 1 | a0001c0002t0002g0045 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.345+1831G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261169 | ||||||
chr20:25261260
|
C | T | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.345+1922C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261260 | ||||||
chr20:25261363
|
C | G | 1 | a0002c0003t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.345+2025C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261363 | ||||||
chr20:25261399
|
G | A | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345+2061G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261399 | ||||||
chr20:25261410
|
G | A | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345+2072G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261410 | ||||||
chr20:25261415
|
A | G | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345+2077A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261415 | ||||||
chr20:25261474
|
G | A | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345+2136G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261474 | ||||||
chr20:25261477
|
T | G | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345+2139T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261477 | ||||||
chr20:25261482
|
G | A | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345+2144G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261482 | ||||||
chr20:25261612
|
A | G | 24 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(21): Show | 28 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.345+2274A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261612 | ||||||
chr20:25261621
|
C | G | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2283C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261621 | ||||||
chr20:25261627
|
G | A | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2289G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261627 | ||||||
chr20:25261631
|
G | A | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2293G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261631 | ||||||
chr20:25261642
|
T | C | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2304T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261642 | ||||||
chr20:25261653
|
G | A | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2315G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261653 | ||||||
chr20:25261667
|
C | T | 1 | a0001c0002t0002g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.345+2329C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261667 | ||||||
chr20:25261677
|
T | G | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2339T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261677 | ||||||
chr20:25261680
|
C | T | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2342C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261680 | ||||||
chr20:25261697
|
G | A | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2359G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261697 | ||||||
chr20:25261698
|
A | T | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2360A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261698 | ||||||
chr20:25261700
|
C | T | 19 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(16): Show | 23 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.345+2362C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261700 | ||||||
chr20:25261710
|
A | G | 2 | a0002c0003t0001g0237a0002c0003t0001g0238 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.345+2372A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261710 | ||||||
chr20:25261855
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.345+2517C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261855 | ||||||
chr20:25261976
|
T | C | 1 | a0001c0002t0002g0031 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.345+2638T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25261976 | ||||||
chr20:25262020
|
G | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0002t0002g0138 | 3 | HG02129.hp1 NA19011.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.345+2682G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262020 | ||||||
chr20:25262031
|
T | C | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.345+2693T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262031 | ||||||
chr20:25262082
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.345+2744C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262082 | ||||||
chr20:25262168
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.345+2830T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262168 | ||||||
chr20:25262188
|
A | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0292a0001c0001t0003g0293others(2): Show | 7 | HG02145.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.345+2850A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262188 | ||||||
chr20:25262202
|
G | A | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+2864G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262202 | ||||||
chr20:25262274
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.345+2936G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262274 | ||||||
chr20:25262449
|
G | A | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+3111G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262449 | ||||||
chr20:25262501
|
C | T | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.345+3163C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262501 | ||||||
chr20:25262589
|
C | T | 2 | a0001c0002t0002g0090a0001c0002t0002g0091 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345+3251C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262589 | ||||||
chr20:25262658
|
C | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+3320C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262658 | ||||||
chr20:25262663
|
T | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+3325T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262663 | ||||||
chr20:25262665
|
T | TAAAAGAC others(2): Show |
22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+3327_345+3328i others(11): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262665 | ||||||
chr20:25262666
|
T | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+3328T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262666 | ||||||
chr20:25262669
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.345+3331C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262669 | ||||||
chr20:25262670
|
T | TGGC | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+3332_345+3333i others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262670 | ||||||
chr20:25262671
|
T | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+3333T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262671 | ||||||
chr20:25262674
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.345+3336C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262674 | ||||||
chr20:25262732
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345+3394G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262732 | ||||||
chr20:25262736
|
A | G | 3 | a0003c0005t0001g0130a0003c0005t0001g0176a0003c0005t0017g0175 | 3 | HG02056.hp2 HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.345+3398A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25262736 | ||||||
chr20:25263057
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.345+3719C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263057 | ||||||
chr20:25263121
|
A | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.345+3783A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263121 | ||||||
chr20:25263464
|
A | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+4126A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263464 | ||||||
chr20:25263465
|
C | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.345+4127C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263465 | ||||||
chr20:25263470
|
A | T | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.345+4132A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263470 | ||||||
chr20:25263484
|
C | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(226): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.345+4146C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263484 | ||||||
chr20:25263535
|
A | T | 1 | a0001c0002t0002g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.345+4197A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263535 | ||||||
chr20:25263607
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+4269T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263607 | ||||||
chr20:25263750
|
A | G | 5 | a0001c0004t0002g0270a0001c0004t0002g0277a0001c0004t0002g0280others(2): Show | 5 | HG00741.hp1 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.345+4412A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263750 | ||||||
chr20:25263770
|
G | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.345+4432G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263770 | ||||||
chr20:25263818
|
C | T | 3 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0261 | 3 | HG03491.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.345+4480C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263818 | ||||||
chr20:25263877
|
T | G | 1 | a0002c0003t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.345+4539T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263877 | ||||||
chr20:25263908
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(228): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.345+4570A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25263908 | ||||||
chr20:25264027
|
T | TC | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.345+4689_345+4690i others(3): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264027 | ||||||
chr20:25264191
|
A | G | 2 | a0001c0009t0005g0266a0001c0009t0005g0271 | 2 | HG01515.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.345+4853A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264191 | ||||||
chr20:25264208
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 120 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.345+4870C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264208 | ||||||
chr20:25264497
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-4632T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264497 | ||||||
chr20:25264814
|
A | G | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.346-4315A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264814 | ||||||
chr20:25264924
|
T | G | 6 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-4205T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264924 | ||||||
chr20:25264958
|
C | T | 1 | a0001c0002t0002g0049 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.346-4171C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264958 | ||||||
chr20:25264964
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.346-4165G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25264964 | ||||||
chr20:25265148
|
A | G | 1 | a0001c0001t0016g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.346-3981A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265148 | ||||||
chr20:25265285
|
AT | A | 23 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(20): Show | 27 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.346-3834delT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25265285 | |||||
chr20:25265289
|
T | C | 1 | a0001c0002t0002g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.346-3840T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265289 | ||||||
chr20:25265314
|
G | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(226): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.346-3815G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265314 | ||||||
chr20:25265352
|
G | C | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.346-3777G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265352 | ||||||
chr20:25265392
|
T | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.346-3737T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265392 | ||||||
chr20:25265517
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.346-3612A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265517 | ||||||
chr20:25265518
|
T | G | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.346-3611T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265518 | ||||||
chr20:25265592
|
A | AT | 18 | a0001c0004t0002g0041a0001c0004t0002g0265a0001c0004t0002g0270others(15): Show | 19 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.346-3517dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25265592 | |||||
chr20:25265592
|
A | ATT | 6 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0275others(3): Show | 9 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.346-3518_346-3517d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25265592 | |||||
chr20:25265592
|
AT | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(188): Show | 232 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.346-3517delT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25265592 | |||||
chr20:25265592
|
ATT | A | 9 | a0001c0001t0001g0125a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00280.hp1 HG01934.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.346-3518_346-3517d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25265592 | |||||
chr20:25265619
|
G | T | 1 | a0012c0017t0001g0232 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.346-3510G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265619 | ||||||
chr20:25265838
|
AC | A | 31 | a0001c0001t0001g0061a0001c0002t0002g0002a0001c0002t0002g0005others(28): Show | 42 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.346-3288delC | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25265838 | |||||
chr20:25265874
|
C | T | 1 | a0001c0002t0002g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.346-3255C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265874 | ||||||
chr20:25265926
|
A | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 25 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.346-3203A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265926 | ||||||
chr20:25265947
|
C | T | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.346-3182C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265947 | ||||||
chr20:25265958
|
T | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.346-3171T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25265958 | ||||||
chr20:25266003
|
C | T | 1 | a0001c0001t0003g0295 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.346-3126C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266003 | ||||||
chr20:25266016
|
A | T | 19 | a0002c0003t0001g0196a0002c0003t0001g0197a0002c0003t0001g0211others(16): Show | 19 | HG00099.hp2 HG00621.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.346-3113A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266016 | ||||||
chr20:25266097
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(226): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.346-3032T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266097 | ||||||
chr20:25266098
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.346-3031G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266098 | ||||||
chr20:25266130
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0189others(6): Show | 13 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.346-2999C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266130 | ||||||
chr20:25266252
|
AT | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(202): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.346-2864delT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25266252 | |||||
chr20:25266252
|
ATT | A | 7 | a0001c0001t0001g0210a0001c0001t0001g0289a0001c0001t0001g0291others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.346-2865_346-2864d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25266252 | |||||
chr20:25266617
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-2512T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266617 | ||||||
chr20:25266618
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.346-2511A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266618 | ||||||
chr20:25266733
|
A | G | 1 | a0001c0018t0004g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.346-2396A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266733 | ||||||
chr20:25266752
|
A | G | 1 | a0001c0002t0002g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.346-2377A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266752 | ||||||
chr20:25266809
|
C | T | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.346-2320C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266809 | ||||||
chr20:25266813
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.346-2316G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266813 | ||||||
chr20:25266827
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-2302A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266827 | ||||||
chr20:25266921
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-2208A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266921 | ||||||
chr20:25266985
|
G | A | 2 | a0001c0004t0002g0265a0001c0004t0011g0264 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.346-2144G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25266985 | ||||||
chr20:25267059
|
A | G | 1 | a0002c0003t0001g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.346-2070A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267059 | ||||||
chr20:25267065
|
G | A | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.346-2064G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267065 | ||||||
chr20:25267320
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0291 | 2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.346-1809C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267320 | ||||||
chr20:25267449
|
G | A | 1 | a0001c0006t0001g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.346-1680G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267449 | ||||||
chr20:25267534
|
ATTG | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.346-1582_346-1580d others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25267534 | |||||
chr20:25267593
|
C | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-1536C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267593 | ||||||
chr20:25267829
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.346-1300C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267829 | ||||||
chr20:25267956
|
C | T | 1 | a0001c0002t0002g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.346-1173C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267956 | ||||||
chr20:25267981
|
T | C | 1 | a0001c0004t0002g0063 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.346-1148T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25267981 | ||||||
chr20:25268012
|
G | A | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.346-1117G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268012 | ||||||
chr20:25268089
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.346-1040C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268089 | ||||||
chr20:25268108
|
C | G | 27 | a0001c0002t0002g0250a0001c0002t0002g0251a0001c0004t0002g0003others(24): Show | 35 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.346-1021C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268108 | ||||||
chr20:25268123
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.346-1006T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268123 | ||||||
chr20:25268157
|
A | ACCCGCC | 24 | a0001c0001t0001g0033a0001c0001t0001g0120a0001c0001t0001g0121others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.346-968_346-963dup others(6): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268157 | |||||
chr20:25268161
|
G | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-968G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268161 | ||||||
chr20:25268161
|
G | GC | 33 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0005others(30): Show | 46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.346-958dupC | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268161
|
G | GCC | 57 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0001g0080others(54): Show | 67 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.346-959_346-958dup others(2): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268161
|
G | GCCC | 32 | a0001c0001t0001g0042a0001c0001t0001g0284a0001c0001t0001g0285others(29): Show | 36 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.346-960_346-958dup others(3): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268161
|
G | GCCCC | 16 | a0001c0001t0003g0020a0001c0001t0003g0113a0001c0001t0003g0114others(13): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.346-961_346-958dup others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268161
|
G | GCCCCCCC others(3): Show |
1 | a0001c0001t0001g0199 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346-967_346-958dup others(10): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268161
|
G | GCCCCCCC others(4): Show |
1 | a0001c0001t0001g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.346-958_346-957ins others(11): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268161
|
G | GCCCCCGC | 43 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(40): Show | 57 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.346-963_346-962ins others(7): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268161 | |||||
chr20:25268165
|
C | CG | 8 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(5): Show | 12 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.346-964_346-963ins others(1): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268165 | ||||||
chr20:25268167
|
C | CCCCCCCT | 15 | a0001c0002t0002g0250a0001c0002t0002g0251a0001c0004t0002g0009others(12): Show | 20 | HG01255.hp1 HG01496.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.346-958_346-957ins others(7): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268167 | |||||
chr20:25268197
|
GTAC | G | 1 | a0001c0001t0001g0016 | 3 | HG00140.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.346-931_346-929del others(3): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268197 | ||||||
chr20:25268218
|
C | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(290): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.346-911C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268218 | ||||||
chr20:25268281
|
A | C | 1 | a0001c0004t0002g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.346-848A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268281 | ||||||
chr20:25268302
|
G | A | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.346-827G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268302 | ||||||
chr20:25268346
|
T | C | 19 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(16): Show | 23 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.346-783T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268346 | ||||||
chr20:25268389
|
C | CT | 37 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0114others(34): Show | 45 | HG00741.hp1 HG01109.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.346-729dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268389 | |||||
chr20:25268389
|
CT | C | 15 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0002t0002g0030others(12): Show | 17 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.346-729delT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr20 | 25268389 | |||||
chr20:25268675
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.346-454T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268675 | ||||||
chr20:25268717
|
C | T | 2 | a0001c0002t0002g0032a0001c0002t0002g0104 | 3 | HG02486.hp2 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.346-412C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268717 | ||||||
chr20:25268982
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.346-147T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25268982 | ||||||
chr20:25269098
|
A | G | 27 | a0001c0002t0002g0250a0001c0002t0002g0251a0001c0004t0002g0003others(24): Show | 35 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.346-31A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25269098 | ||||||
chr20:25269111
|
C | G | 5 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.346-18C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 2/19 | chr20 | 25269111 | ||||||
chr20:25269405
|
G | A | 2 | a0001c0004t0002g0064a0001c0004t0002g0068 | 2 | HG00544.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.424+198G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269405 | ||||||
chr20:25269451
|
T | C | 1 | a0001c0015t0001g0133 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.424+244T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269451 | ||||||
chr20:25269470
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+263C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269470 | ||||||
chr20:25269527
|
G | A | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.424+320G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269527 | ||||||
chr20:25269706
|
T | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+499T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269706 | ||||||
chr20:25269757
|
C | A | 1 | a0001c0004t0002g0257 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.424+550C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269757 | ||||||
chr20:25269801
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+594T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269801 | ||||||
chr20:25269910
|
T | A | 25 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(22): Show | 33 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+703T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269910 | ||||||
chr20:25269941
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.424+734T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25269941 | ||||||
chr20:25270187
|
G | GGT | 4 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0256others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+980_424+981ins others(2): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270187 | ||||||
chr20:25270188
|
T | G | 1 | a0001c0007t0004g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.424+981T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270188 | ||||||
chr20:25270193
|
TTTGTTTT others(1): Show |
T | 18 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(15): Show | 22 | HG01109.hp1 HG01515.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+989_424+996del others(8): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr20 | 25270193 | |||||
chr20:25270196
|
G | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(264): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.424+989G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270196 | ||||||
chr20:25270197
|
T | TTG | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+991_424+992ins others(2): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr20 | 25270197 | |||||
chr20:25270198
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.424+991T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270198 | ||||||
chr20:25270200
|
T | G | 4 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0256others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+993T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270200 | ||||||
chr20:25270201
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(195): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.424+994G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270201 | ||||||
chr20:25270202
|
T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(191): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.424+995T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270202 | ||||||
chr20:25270204
|
T | G | 4 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0256others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+997T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270204 | ||||||
chr20:25270205
|
T | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0160a0001c0001t0001g0283others(8): Show | 12 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+998T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270205 | ||||||
chr20:25270206
|
G | T | 37 | a0001c0001t0001g0042a0001c0001t0001g0160a0001c0001t0001g0283others(34): Show | 42 | HG00741.hp1 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.424+999G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270206 | ||||||
chr20:25270208
|
T | G | 4 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0256others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1001T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270208 | ||||||
chr20:25270210
|
T | G | 16 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0022others(13): Show | 20 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+1003T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270210 | ||||||
chr20:25270259
|
G | A | 1 | a0001c0021t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.424+1052G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270259 | ||||||
chr20:25270282
|
A | G | 1 | a0001c0004t0002g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.424+1075A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270282 | ||||||
chr20:25270352
|
G | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-1031G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270352 | ||||||
chr20:25270404
|
G | A | 1 | a0001c0007t0004g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.425-979G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270404 | ||||||
chr20:25270554
|
C | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-829C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270554 | ||||||
chr20:25270568
|
G | A | 2 | a0001c0004t0002g0257a0001c0018t0004g0258 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.425-815G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270568 | ||||||
chr20:25270573
|
C | CT | 3 | a0001c0004t0002g0026a0001c0004t0002g0067a0001c0004t0002g0070 | 4 | HG01255.hp1 HG01496.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-809dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr20 | 25270573 | |||||
chr20:25270601
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(75): Show | 93 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.425-782A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270601 | ||||||
chr20:25270917
|
T | C | 7 | a0001c0004t0002g0027a0001c0004t0002g0028a0001c0004t0002g0071others(4): Show | 8 | HG01891.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-466T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270917 | ||||||
chr20:25270932
|
T | C | 1 | a0001c0009t0005g0266 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.425-451T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270932 | ||||||
chr20:25270944
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-439A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25270944 | ||||||
chr20:25271099
|
T | TG | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-278dupG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr20 | 25271099 | |||||
chr20:25271109
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0262 | 4 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-274C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271109 | ||||||
chr20:25271136
|
C | T | 6 | a0002c0003t0001g0039a0002c0003t0001g0146a0002c0003t0001g0193others(3): Show | 7 | HG00597.hp2 HG02132.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-247C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271136 | ||||||
chr20:25271160
|
C | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-223C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271160 | ||||||
chr20:25271164
|
C | A | 1 | a0002c0003t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.425-219C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271164 | ||||||
chr20:25271179
|
C | T | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-204C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271179 | ||||||
chr20:25271195
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-188C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271195 | ||||||
chr20:25271219
|
C | A | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-164C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271219 | ||||||
chr20:25271271
|
G | A | 1 | a0003c0005t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.425-112G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271271 | ||||||
chr20:25271333
|
C | A | 1 | a0001c0024t0001g0149 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.425-50C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271333 | ||||||
chr20:25271364
|
T | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-19T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 3/19 | chr20 | 25271364 | ||||||
chr20:25271525
|
C | T | 52 | a0002c0003t0001g0015a0002c0003t0001g0019a0002c0003t0001g0036others(49): Show | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.528+39C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25271525 | ||||||
chr20:25271591
|
G | C | 1 | a0002c0003t0001g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.528+105G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25271591 | ||||||
chr20:25271621
|
A | G | 26 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(23): Show | 34 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.528+135A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25271621 | ||||||
chr20:25271905
|
G | C | 1 | a0002c0003t0001g0230 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.528+419G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25271905 | ||||||
chr20:25271938
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.528+452T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25271938 | ||||||
chr20:25272263
|
A | G | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+777A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25272263 | ||||||
chr20:25272460
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0169 | 2 | NA18990.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.528+974C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25272460 | ||||||
chr20:25272536
|
C | T | 1 | a0001c0004t0002g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.528+1050C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25272536 | ||||||
chr20:25272602
|
C | T | 23 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(20): Show | 31 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.528+1116C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25272602 | ||||||
chr20:25272617
|
G | A | 5 | a0001c0004t0002g0257a0001c0007t0004g0254a0001c0007t0004g0255others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1131G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25272617 | ||||||
chr20:25272836
|
G | A | 14 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0025others(11): Show | 19 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.528+1350G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25272836 | ||||||
chr20:25273142
|
G | A | 1 | a0003c0005t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.529-1450G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273142 | ||||||
chr20:25273305
|
G | T | 2 | a0001c0004t0002g0277a0001c0004t0002g0280 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.529-1287G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273305 | ||||||
chr20:25273348
|
TGCCTGCT others(10): Show |
T | 5 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-1222_529-1206d others(19): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr20 | 25273348 | |||||
chr20:25273360
|
G | A | 21 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(18): Show | 25 | HG01109.hp1 HG01515.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.529-1232G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273360 | ||||||
chr20:25273459
|
C | T | 24 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(21): Show | 28 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.529-1133C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273459 | ||||||
chr20:25273498
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.529-1094G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273498 | ||||||
chr20:25273549
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0262 | 4 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1043G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273549 | ||||||
chr20:25273567
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.529-1025G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273567 | ||||||
chr20:25273739
|
G | A | 7 | a0001c0004t0002g0265a0001c0004t0002g0270a0001c0004t0002g0277others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-853G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273739 | ||||||
chr20:25273766
|
CA | C | 22 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(19): Show | 26 | HG00741.hp1 HG01109.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.529-825delA | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273766 | ||||||
chr20:25273785
|
G | C | 2 | a0001c0009t0005g0266a0001c0009t0005g0271 | 2 | HG01515.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.529-807G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273785 | ||||||
chr20:25273916
|
T | C | 1 | a0001c0001t0003g0292 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.529-676T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25273916 | ||||||
chr20:25274052
|
A | G | 48 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(45): Show | 60 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.529-540A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274052 | ||||||
chr20:25274110
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.529-482C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274110 | ||||||
chr20:25274203
|
G | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.529-389G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274203 | ||||||
chr20:25274204
|
C | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.529-388C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274204 | ||||||
chr20:25274300
|
A | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(8): Show | 12 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-292A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274300 | ||||||
chr20:25274393
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0015t0001g0133 | 3 | HG02015.hp1 NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.529-199G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274393 | ||||||
chr20:25274569
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0202others(2): Show | 9 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-23C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 4/19 | chr20 | 25274569 | ||||||
chr20:25274779
|
C | T | 45 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(42): Show | 57 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.660+56C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25274779 | ||||||
chr20:25274906
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.660+183C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25274906 | ||||||
chr20:25274915
|
C | G | 48 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(45): Show | 60 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.660+192C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25274915 | ||||||
chr20:25274939
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.660+216C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25274939 | ||||||
chr20:25274976
|
G | T | 1 | a0001c0004t0007g0268 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.660+253G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25274976 | ||||||
chr20:25275004
|
C | CGT | 48 | a0001c0004t0002g0003a0001c0004t0002g0009a0001c0004t0002g0010others(45): Show | 60 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.660+282_660+283dup others(2): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr20 | 25275004 | |||||
chr20:25275100
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.660+377C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275100 | ||||||
chr20:25275262
|
C | T | 1 | a0002c0003t0001g0220 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660+539C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275262 | ||||||
chr20:25275377
|
C | T | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.660+654C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275377 | ||||||
chr20:25275395
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.660+672G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275395 | ||||||
chr20:25275470
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.660+747C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275470 | ||||||
chr20:25275473
|
G | T | 2 | a0001c0001t0003g0259a0001c0001t0003g0260 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.660+750G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275473 | ||||||
chr20:25275557
|
A | C | 2 | a0001c0004t0002g0027a0001c0004t0002g0073 | 3 | HG02723.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.660+834A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275557 | ||||||
chr20:25275630
|
G | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(169): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.660+907G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275630 | ||||||
chr20:25275787
|
C | T | 2 | a0001c0004t0002g0027a0001c0004t0002g0073 | 3 | HG02723.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.661-859C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275787 | ||||||
chr20:25275900
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.661-746C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275900 | ||||||
chr20:25275922
|
C | T | 1 | a0002c0003t0001g0234 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.661-724C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275922 | ||||||
chr20:25275962
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(136): Show | 172 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.661-684A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25275962 | ||||||
chr20:25276069
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.661-577G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276069 | ||||||
chr20:25276097
|
G | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(25): Show | 33 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.661-549G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276097 | ||||||
chr20:25276195
|
C | T | 1 | a0001c0004t0007g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661-451C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276195 | ||||||
chr20:25276365
|
A | G | 57 | a0001c0001t0001g0018a0001c0001t0001g0166a0001c0001t0001g0167others(54): Show | 73 | HG00544.hp2 HG00738.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.661-281A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276365 | ||||||
chr20:25276384
|
C | G | 18 | a0001c0001t0001g0018a0001c0001t0001g0210a0001c0001t0001g0287others(15): Show | 23 | HG00741.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-262C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276384 | ||||||
chr20:25276391
|
G | A | 13 | a0001c0002t0002g0030a0001c0002t0002g0077a0001c0002t0002g0079others(10): Show | 15 | HG01175.hp2 HG01943.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.661-255G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276391 | ||||||
chr20:25276424
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.661-222C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276424 | ||||||
chr20:25276425
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0150 | 3 | HG01071.hp2 HG01256.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.661-221G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276425 | ||||||
chr20:25276433
|
C | T | 1 | a0001c0007t0004g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.661-213C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276433 | ||||||
chr20:25276523
|
A | AG | 17 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(14): Show | 21 | HG01167.hp1 HG01361.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.661-118dupG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr20 | 25276523 | |||||
chr20:25276551
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(77): Show | 95 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.661-95C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276551 | ||||||
chr20:25276566
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(78): Show | 96 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.661-80A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276566 | ||||||
chr20:25276579
|
G | A | 56 | a0001c0001t0001g0163a0001c0002t0002g0085a0001c0006t0001g0162others(53): Show | 62 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.661-67G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276579 | ||||||
chr20:25276624
|
G | C | 53 | a0001c0002t0002g0085a0001c0006t0001g0162a0002c0003t0001g0015others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.661-22G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 5/19 | chr20 | 25276624 | ||||||
chr20:25276775
|
TG | T | 5 | a0001c0001t0003g0020a0001c0001t0003g0259a0001c0001t0003g0260others(2): Show | 7 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.772+20delG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr20 | 25276775 | |||||
chr20:25276826
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(156): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.772+69G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 6/19 | chr20 | 25276826 | ||||||
chr20:25276867
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.772+110C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 6/19 | chr20 | 25276867 | ||||||
chr20:25277093
|
C | G | 3 | a0001c0021t0002g0279a0004c0010t0008g0252a0004c0010t0008g0253 | 3 | HG03098.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.773-151C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 6/19 | chr20 | 25277093 | ||||||
chr20:25277399
|
G | A | 1 | a0001c0004t0002g0277 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.855+73G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277399 | ||||||
chr20:25277408
|
A | C | 7 | a0001c0001t0001g0206a0001c0001t0016g0172a0001c0002t0002g0032others(4): Show | 8 | HG00639.hp2 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.855+82A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277408 | ||||||
chr20:25277413
|
G | C | 1 | a0001c0002t0002g0112 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.855+87G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277413 | ||||||
chr20:25277506
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0207a0001c0001t0001g0210 | 5 | HG02257.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+180T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277506 | ||||||
chr20:25277509
|
A | G | 1 | a0012c0017t0001g0232 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.855+183A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277509 | ||||||
chr20:25277551
|
T | C | 1 | a0001c0004t0007g0268 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.855+225T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277551 | ||||||
chr20:25277558
|
C | G | 1 | a0001c0004t0007g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.855+232C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277558 | ||||||
chr20:25277675
|
C | T | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.855+349C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277675 | ||||||
chr20:25277689
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.855+363C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25277689 | ||||||
chr20:25278103
|
T | TCTC | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.856-214_856-213ins others(3): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr20 | 25278103 | |||||
chr20:25278201
|
C | T | 1 | a0003c0005t0001g0014 | 3 | HG02004.hp1 NA18979.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.856-118C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25278201 | ||||||
chr20:25278223
|
T | C | 1 | a0001c0002t0002g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.856-96T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | chr20 | 25278223 | ||||||
chr20:25278280
|
G | GCCCTGGG others(22): Show |
232 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(229): Show | 277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.856-36_856-35insTG others(27): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr20 | 25278280 | |||||
chr20:25278472
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.999+10G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278472 | ||||||
chr20:25278564
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.999+102T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278564 | ||||||
chr20:25278666
|
C | G | 2 | a0001c0004t0002g0265a0001c0004t0011g0264 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.999+204C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278666 | ||||||
chr20:25278820
|
G | A | 1 | a0001c0002t0002g0057 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1000-237G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278820 | ||||||
chr20:25278867
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1000-190G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278867 | ||||||
chr20:25278890
|
C | T | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1000-167C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278890 | ||||||
chr20:25278996
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1000-61A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25278996 | ||||||
chr20:25279001
|
C | T | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-56C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 8/19 | chr20 | 25279001 | ||||||
chr20:25279171
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(171): Show | 207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1092+22G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279171 | ||||||
chr20:25279196
|
G | A | 9 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(6): Show | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1092+47G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279196 | ||||||
chr20:25279218
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1092+69G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279218 | ||||||
chr20:25279233
|
C | G | 1 | a0002c0003t0001g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1092+84C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279233 | ||||||
chr20:25279274
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1092+125A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279274 | ||||||
chr20:25279283
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1092+134G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279283 | ||||||
chr20:25279397
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1092+248C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279397 | ||||||
chr20:25279546
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1092+397C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279546 | ||||||
chr20:25279547
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1092+398G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279547 | ||||||
chr20:25279649
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1092+500C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279649 | ||||||
chr20:25279675
|
T | C | 1 | a0001c0002t0002g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1092+526T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279675 | ||||||
chr20:25279705
|
C | G | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1092+556C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279705 | ||||||
chr20:25279919
|
T | C | 2 | a0001c0004t0007g0268a0001c0004t0007g0269 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1093-347T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25279919 | ||||||
chr20:25280005
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1093-261T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25280005 | ||||||
chr20:25280016
|
TTGTG | T | 1 | a0001c0001t0001g0018 | 3 | HG02257.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1093-242_1093-239d others(6): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr20 | 25280016 | |||||
chr20:25280031
|
G | A | 1 | a0001c0002t0002g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1093-235G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25280031 | ||||||
chr20:25280046
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0181 | 2 | NA18950.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1093-220G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 9/19 | chr20 | 25280046 | ||||||
chr20:25280435
|
G | A | 5 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(2): Show | 5 | HG02145.hp2 HG02155.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+23G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280435 | ||||||
chr20:25280446
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0078a0001c0001t0001g0080others(5): Show | 9 | HG00544.hp1 HG01978.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1239+34C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280446 | ||||||
chr20:25280464
|
C | T | 4 | a0002c0003t0001g0242a0002c0003t0001g0244a0004c0010t0008g0252others(1): Show | 4 | HG03098.hp1 NA19005.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+52C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280464 | ||||||
chr20:25280509
|
C | T | 1 | a0002c0003t0001g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1239+97C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280509 | ||||||
chr20:25280670
|
G | A | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239+258G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280670 | ||||||
chr20:25280854
|
A | G | 4 | a0002c0003t0001g0197a0002c0003t0001g0215a0002c0003t0001g0229others(1): Show | 4 | HG01123.hp2 HG01358.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-95A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280854 | ||||||
chr20:25280854
|
A | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240-95A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 10/19 | chr20 | 25280854 | ||||||
chr20:25281135
|
C | T | 14 | a0002c0003t0001g0019a0002c0003t0001g0039a0002c0003t0001g0146others(11): Show | 17 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1403+23C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281135 | ||||||
chr20:25281148
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(173): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1403+36G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281148 | ||||||
chr20:25281302
|
A | G | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1403+190A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281302 | ||||||
chr20:25281655
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1404-378G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281655 | ||||||
chr20:25281672
|
A | G | 1 | a0002c0003t0001g0245 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1404-361A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281672 | ||||||
chr20:25281692
|
G | A | 1 | a0001c0009t0005g0272 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1404-341G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281692 | ||||||
chr20:25281694
|
G | A | 1 | a0001c0012t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1404-339G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281694 | ||||||
chr20:25281759
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1404-274G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281759 | ||||||
chr20:25281760
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1404-273G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281760 | ||||||
chr20:25281767
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1404-266C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281767 | ||||||
chr20:25281816
|
C | G | 1 | a0011c0019t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1404-217C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281816 | ||||||
chr20:25281873
|
AGCCTGCA others(16): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1404-159_1404-137d others(25): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281873 | ||||||
chr20:25281874
|
G | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0292a0001c0001t0003g0293others(2): Show | 7 | HG02145.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1404-159G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281874 | ||||||
chr20:25281900
|
TCTC | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(148): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1404-130_1404-128d others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr20 | 25281900 | |||||
chr20:25281966
|
A | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0292a0001c0001t0003g0293others(2): Show | 7 | HG02145.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1404-67A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 11/19 | chr20 | 25281966 | ||||||
chr20:25282153
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
splice_region_variant&intron_variant | LOW | c.1518+6T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282153 | ||||||
chr20:25282198
|
G | A | 3 | a0001c0002t0002g0077a0001c0002t0002g0088a0001c0002t0002g0089 | 3 | HG01943.hp1 HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1518+51G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282198 | ||||||
chr20:25282200
|
G | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1518+53G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282200 | ||||||
chr20:25282426
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1518+279T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282426 | ||||||
chr20:25282500
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(181): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1518+353T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282500 | ||||||
chr20:25282570
|
G | A | 1 | a0001c0002t0002g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1518+423G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282570 | ||||||
chr20:25282640
|
G | A | 3 | a0002c0003t0001g0240a0002c0003t0001g0242a0002c0003t0001g0244 | 3 | NA18956.hp2 NA19005.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1518+493G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282640 | ||||||
chr20:25282641
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1518+494T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282641 | ||||||
chr20:25282765
|
C | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0004t0007g0268 | 4 | HG01071.hp2 HG01256.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1519-411C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282765 | ||||||
chr20:25282821
|
T | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(229): Show | 277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1519-355T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282821 | ||||||
chr20:25282876
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1519-300T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282876 | ||||||
chr20:25282915
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1519-261G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282915 | ||||||
chr20:25282917
|
G | A | 1 | a0001c0018t0004g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1519-259G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282917 | ||||||
chr20:25282974
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1519-202C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25282974 | ||||||
chr20:25283012
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1519-164G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25283012 | ||||||
chr20:25283041
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1519-135T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25283041 | ||||||
chr20:25283120
|
G | A | 47 | a0001c0002t0002g0085a0001c0002t0002g0138a0001c0004t0002g0003others(44): Show | 59 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.1519-56G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 12/19 | chr20 | 25283120 | ||||||
chr20:25283304
|
G | C | 3 | a0001c0002t0002g0077a0001c0002t0002g0088a0001c0002t0002g0089 | 3 | HG01943.hp1 HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1620+27G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25283304 | ||||||
chr20:25283432
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1620+155A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25283432 | ||||||
chr20:25283539
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1620+262C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25283539 | ||||||
chr20:25283560
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(175): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1620+283A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25283560 | ||||||
chr20:25283585
|
A | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0189others(5): Show | 12 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1620+308A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25283585 | ||||||
chr20:25283827
|
C | T | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1621-277C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25283827 | ||||||
chr20:25284024
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1621-80C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25284024 | ||||||
chr20:25284028
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1621-76T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 13/19 | chr20 | 25284028 | ||||||
chr20:25284272
|
C | T | 1 | a0001c0001t0003g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1768+21C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284272 | ||||||
chr20:25284274
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+23T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284274 | ||||||
chr20:25284281
|
G | A | 1 | a0001c0002t0002g0056 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1768+30G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284281 | ||||||
chr20:25284373
|
A | G | 1 | a0002c0003t0001g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1768+122A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284373 | ||||||
chr20:25284523
|
T | G | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1768+272T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284523 | ||||||
chr20:25284679
|
G | C | 1 | a0001c0009t0005g0271 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1768+428G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284679 | ||||||
chr20:25284862
|
A | C | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1768+611A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284862 | ||||||
chr20:25284899
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1768+648C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284899 | ||||||
chr20:25284918
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+667A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25284918 | ||||||
chr20:25285039
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1768+788C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285039 | ||||||
chr20:25285123
|
C | T | 1 | a0001c0021t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1768+872C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285123 | ||||||
chr20:25285176
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1768+925G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285176 | ||||||
chr20:25285216
|
C | T | 1 | a0001c0002t0002g0105 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1768+965C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285216 | ||||||
chr20:25285236
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+985C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285236 | ||||||
chr20:25285324
|
G | A | 1 | a0001c0001t0003g0022 | 3 | HG02630.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1768+1073G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285324 | ||||||
chr20:25285348
|
G | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+1097G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285348 | ||||||
chr20:25285474
|
C | G | 2 | a0003c0005t0001g0176a0003c0005t0017g0175 | 2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1768+1223C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285474 | ||||||
chr20:25285478
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1768+1227C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285478 | ||||||
chr20:25285496
|
C | G | 1 | a0001c0001t0001g0038 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1768+1245C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285496 | ||||||
chr20:25285636
|
C | T | 3 | a0002c0003t0001g0221a0002c0003t0001g0233a0002c0003t0001g0236 | 3 | NA18962.hp1 NA18971.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1768+1385C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285636 | ||||||
chr20:25285719
|
TGTG | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+1473_1768+147 others(7): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr20 | 25285719 | |||||
chr20:25285784
|
C | T | 2 | a0002c0003t0001g0222a0002c0003t0001g0223 | 2 | HG02165.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1768+1533C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285784 | ||||||
chr20:25285814
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+1563G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285814 | ||||||
chr20:25285840
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1768+1589C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285840 | ||||||
chr20:25285877
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(180): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1768+1626A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285877 | ||||||
chr20:25285968
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1768+1717G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285968 | ||||||
chr20:25285997
|
C | T | 24 | a0001c0002t0002g0011a0001c0002t0002g0030a0001c0002t0002g0031others(21): Show | 29 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1768+1746C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25285997 | ||||||
chr20:25286087
|
C | T | 31 | a0001c0002t0002g0085a0001c0002t0002g0138a0001c0004t0002g0003others(28): Show | 39 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1768+1836C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286087 | ||||||
chr20:25286116
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1768+1865C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286116 | ||||||
chr20:25286260
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1768+2009G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286260 | ||||||
chr20:25286361
|
G | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1769-2064G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286361 | ||||||
chr20:25286610
|
T | TGCTGGGC others(18): Show |
1 | a0001c0002t0002g0102 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1769-1812_1769-178 others(29): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr20 | 25286610 | |||||
chr20:25286665
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1769-1760G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286665 | ||||||
chr20:25286737
|
G | A | 1 | a0001c0002t0002g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1769-1688G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286737 | ||||||
chr20:25286776
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1769-1649G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286776 | ||||||
chr20:25286813
|
C | T | 1 | a0001c0007t0004g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1769-1612C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286813 | ||||||
chr20:25286986
|
C | T | 53 | a0002c0003t0001g0015a0002c0003t0001g0019a0002c0003t0001g0036others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1769-1439C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25286986 | ||||||
chr20:25287257
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(180): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1769-1168A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287257 | ||||||
chr20:25287272
|
G | A | 1 | a0003c0005t0001g0014 | 3 | HG02004.hp1 NA18979.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1769-1153G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287272 | ||||||
chr20:25287431
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1769-994T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287431 | ||||||
chr20:25287447
|
C | A | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1769-978C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287447 | ||||||
chr20:25287449
|
G | A | 1 | a0001c0002t0002g0057 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1769-976G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287449 | ||||||
chr20:25287673
|
C | T | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1769-752C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287673 | ||||||
chr20:25287681
|
A | C | 6 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0275others(3): Show | 9 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1769-744A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287681 | ||||||
chr20:25287754
|
A | AG | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769-668dupG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr20 | 25287754 | |||||
chr20:25287959
|
C | T | 1 | a0001c0006t0001g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1769-466C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287959 | ||||||
chr20:25287981
|
A | G | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 22 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769-444A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25287981 | ||||||
chr20:25288025
|
C | T | 66 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0147others(63): Show | 74 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1769-400C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288025 | ||||||
chr20:25288131
|
G | C | 1 | a0001c0018t0004g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1769-294G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288131 | ||||||
chr20:25288176
|
C | T | 2 | a0001c0002t0002g0086a0001c0004t0002g0063 | 2 | HG01123.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1769-249C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288176 | ||||||
chr20:25288284
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1769-141T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288284 | ||||||
chr20:25288285
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1769-140C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288285 | ||||||
chr20:25288317
|
G | A | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1769-108G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288317 | ||||||
chr20:25288378
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1769-47G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 14/19 | chr20 | 25288378 | ||||||
chr20:25288507
|
T | C | 1 | a0001c0002t0002g0050 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1827+24T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288507 | ||||||
chr20:25288551
|
C | T | 1 | a0001c0006t0001g0162 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1827+68C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288551 | ||||||
chr20:25288571
|
C | T | 1 | a0001c0001t0003g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1827+88C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288571 | ||||||
chr20:25288577
|
TACTCGGG others(19): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1827+97_1827+122de others(27): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr20 | 25288577 | |||||
chr20:25288764
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1827+281C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288764 | ||||||
chr20:25288803
|
C | T | 2 | a0001c0002t0002g0002a0001c0002t0002g0008 | 8 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1827+320C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288803 | ||||||
chr20:25288848
|
T | A | 1 | a0002c0003t0001g0222 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1827+365T>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288848 | ||||||
chr20:25288888
|
GTCA | G | 3 | a0002c0003t0001g0192a0004c0010t0008g0252a0004c0010t0008g0253 | 3 | HG01943.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1827+408_1827+410d others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr20 | 25288888 | |||||
chr20:25288951
|
C | T | 1 | a0002c0003t0001g0231 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1827+468C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288951 | ||||||
chr20:25288967
|
G | T | 1 | a0002c0003t0001g0237 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1827+484G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288967 | ||||||
chr20:25288994
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1827+511A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25288994 | ||||||
chr20:25289084
|
C | A | 1 | a0001c0002t0002g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1827+601C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289084 | ||||||
chr20:25289107
|
G | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1827+624G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289107 | ||||||
chr20:25289257
|
G | A | 1 | a0001c0002t0002g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1827+774G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289257 | ||||||
chr20:25289349
|
A | G | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1827+866A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289349 | ||||||
chr20:25289367
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1827+884T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289367 | ||||||
chr20:25289488
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(229): Show | 277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1828-993G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289488 | ||||||
chr20:25289655
|
G | GAA | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1828-817_1828-816d others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr20 | 25289655 | |||||
chr20:25289703
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1828-778T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289703 | ||||||
chr20:25289928
|
C | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1828-553C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25289928 | ||||||
chr20:25290098
|
C | T | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1828-383C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25290098 | ||||||
chr20:25290231
|
TAAC | T | 3 | a0001c0002t0002g0024a0001c0002t0002g0055a0001c0002t0002g0056 | 4 | HG01175.hp1 HG01361.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1828-243_1828-241d others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr20 | 25290231 | |||||
chr20:25290267
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1828-214G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25290267 | ||||||
chr20:25290363
|
C | T | 20 | a0002c0003t0001g0058a0002c0003t0001g0196a0002c0003t0001g0197others(17): Show | 20 | HG00099.hp2 HG00621.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1828-118C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25290363 | ||||||
chr20:25290367
|
G | A | 5 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1828-114G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25290367 | ||||||
chr20:25290397
|
C | G | 53 | a0002c0003t0001g0015a0002c0003t0001g0019a0002c0003t0001g0036others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1828-84C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25290397 | ||||||
chr20:25290450
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1828-31T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 15/19 | chr20 | 25290450 | ||||||
chr20:25290650
|
A | G | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 22 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1969+28A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25290650 | ||||||
chr20:25290690
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1969+68C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25290690 | ||||||
chr20:25290746
|
C | T | 1 | a0002c0003t0001g0222 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1969+124C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25290746 | ||||||
chr20:25290940
|
C | CCTTCTGC others(86): Show |
15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1969+350_1969+442d others(95): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr20 | 25290940 | |||||
chr20:25291029
|
C | T | 1 | a0001c0006t0001g0162 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1969+407C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291029 | ||||||
chr20:25291406
|
G | A | 2 | a0001c0004t0007g0268a0001c0004t0007g0269 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1969+784G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291406 | ||||||
chr20:25291476
|
G | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02015.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1969+854G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291476 | ||||||
chr20:25291599
|
G | A | 9 | a0001c0001t0001g0042a0001c0001t0001g0151a0001c0001t0001g0155others(6): Show | 10 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1970-807G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291599 | ||||||
chr20:25291662
|
C | T | 1 | a0001c0001t0016g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1970-744C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291662 | ||||||
chr20:25291687
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1970-719C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291687 | ||||||
chr20:25291747
|
G | C | 1 | a0002c0003t0015g0198 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1970-659G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291747 | ||||||
chr20:25291768
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1970-638G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291768 | ||||||
chr20:25291854
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1970-552G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291854 | ||||||
chr20:25291895
|
T | G | 40 | a0001c0002t0002g0085a0001c0002t0002g0138a0001c0004t0002g0003others(37): Show | 52 | HG00544.hp2 HG01109.hp1 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.1970-511T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291895 | ||||||
chr20:25291911
|
AGAAAGCG others(4): Show |
A | 53 | a0002c0003t0001g0015a0002c0003t0001g0019a0002c0003t0001g0036others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1970-493_1970-483d others(13): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr20 | 25291911 | |||||
chr20:25291946
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1970-460G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291946 | ||||||
chr20:25291997
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1970-409T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25291997 | ||||||
chr20:25292110
|
G | C | 1 | a0001c0004t0002g0041 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1970-296G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292110 | ||||||
chr20:25292117
|
G | A | 10 | a0002c0003t0001g0015a0002c0003t0001g0036a0002c0003t0001g0037others(7): Show | 13 | HG01496.hp2 HG01943.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1970-289G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292117 | ||||||
chr20:25292203
|
C | T | 2 | a0001c0007t0004g0254a0001c0007t0004g0255 | 2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1970-203C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292203 | ||||||
chr20:25292210
|
G | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 22 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1970-196G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292210 | ||||||
chr20:25292242
|
C | T | 21 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 28 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1970-164C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292242 | ||||||
chr20:25292259
|
C | CA | 19 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 26 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1970-147_1970-146i others(3): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292259 | ||||||
chr20:25292259
|
C | CGGGAGCG others(12): Show |
1 | a0013c0016t0001g0246 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1970-142_1970-141i others(21): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr20 | 25292259 | |||||
chr20:25292259
|
C | CGGGAGTG others(6): Show |
162 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0034others(159): Show | 188 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.1970-138_1970-137i others(15): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr20 | 25292259 | |||||
chr20:25292277
|
C | T | 3 | a0001c0002t0002g0007a0001c0002t0002g0053a0001c0002t0002g0054 | 5 | HG01106.hp1 HG01255.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1970-129C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292277 | ||||||
chr20:25292289
|
A | G | 1 | a0006c0023t0002g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1970-117A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292289 | ||||||
chr20:25292295
|
C | T | 2 | a0001c0004t0002g0010a0001c0004t0002g0066 | 4 | NA18939.hp2 NA18966.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1970-111C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292295 | ||||||
chr20:25292314
|
G | A | 9 | a0001c0004t0002g0021a0001c0004t0002g0040a0001c0004t0002g0041others(6): Show | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1970-92G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292314 | ||||||
chr20:25292389
|
C | T | 2 | a0001c0007t0004g0256a0001c0018t0004g0258 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1970-17C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 16/19 | chr20 | 25292389 | ||||||
chr20:25292645
|
C | T | 1 | a0001c0004t0011g0264 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2177+32C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292645 | ||||||
chr20:25292726
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 120 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2177+113G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292726 | ||||||
chr20:25292760
|
A | AG | 17 | a0001c0002t0002g0138a0001c0004t0002g0003a0001c0004t0002g0009others(14): Show | 24 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2177+151dupG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr20 | 25292760 | |||||
chr20:25292799
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2177+186C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292799 | ||||||
chr20:25292802
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2177+189G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292802 | ||||||
chr20:25292918
|
G | A | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177+305G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292918 | ||||||
chr20:25292989
|
A | C | 1 | a0001c0018t0004g0258 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2177+376A>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292989 | ||||||
chr20:25292997
|
G | C | 1 | a0001c0002t0002g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2177+384G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25292997 | ||||||
chr20:25293070
|
T | C | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 24 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2177+457T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293070 | ||||||
chr20:25293088
|
A | G | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2177+475A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293088 | ||||||
chr20:25293089
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2177+476T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293089 | ||||||
chr20:25293127
|
CG | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(282): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.2177+522delG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr20 | 25293127 | |||||
chr20:25293144
|
TG | T | 52 | a0001c0009t0005g0266a0002c0003t0001g0015a0002c0003t0001g0019others(49): Show | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2177+538delG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr20 | 25293144 | |||||
chr20:25293151
|
G | A | 2 | a0002c0003t0001g0197a0002c0003t0001g0240 | 2 | HG02738.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2177+538G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293151 | ||||||
chr20:25293152
|
A | T | 2 | a0002c0003t0001g0197a0002c0003t0001g0240 | 2 | HG02738.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2177+539A>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293152 | ||||||
chr20:25293153
|
T | G | 2 | a0002c0003t0001g0197a0002c0003t0001g0240 | 2 | HG02738.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2177+540T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293153 | ||||||
chr20:25293162
|
TG | T | 9 | a0002c0003t0001g0015a0002c0003t0001g0036a0002c0003t0001g0037others(6): Show | 12 | HG01496.hp2 HG01943.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.2177+555delG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr20 | 25293162 | |||||
chr20:25293292
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2177+679C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293292 | ||||||
chr20:25293293
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(181): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2177+680A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293293 | ||||||
chr20:25293434
|
G | GT | 304 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(301): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.2178-723dupT | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr20 | 25293434 | |||||
chr20:25293471
|
T | C | 3 | a0001c0009t0005g0266a0001c0009t0005g0271a0001c0009t0005g0272 | 3 | HG01515.hp2 HG01975.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2178-687T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293471 | ||||||
chr20:25293485
|
A | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0292a0001c0001t0003g0293others(2): Show | 7 | HG02145.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2178-673A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293485 | ||||||
chr20:25293636
|
C | T | 1 | a0001c0021t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2178-522C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293636 | ||||||
chr20:25293638
|
T | G | 1 | a0001c0004t0002g0069 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2178-520T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293638 | ||||||
chr20:25293647
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2178-511C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293647 | ||||||
chr20:25293682
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(181): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.2178-476C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293682 | ||||||
chr20:25293796
|
G | A | 1 | a0001c0006t0001g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2178-362G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293796 | ||||||
chr20:25293814
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2178-344C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293814 | ||||||
chr20:25293875
|
C | T | 2 | a0001c0002t0002g0090a0001c0002t0002g0091 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2178-283C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293875 | ||||||
chr20:25293896
|
TCTG | T | 26 | a0001c0002t0002g0085a0001c0002t0002g0138a0001c0004t0002g0003others(23): Show | 34 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.2178-259_2178-257d others(5): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr20 | 25293896 | |||||
chr20:25293973
|
G | C | 2 | a0001c0002t0002g0109a0001c0002t0002g0110 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2178-185G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 17/19 | chr20 | 25293973 | ||||||
chr20:25294315
|
G | A | 30 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0006others(27): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2312+23G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294315 | ||||||
chr20:25294317
|
T | G | 30 | a0001c0002t0002g0002a0001c0002t0002g0005a0001c0002t0002g0006others(27): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2312+25T>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294317 | ||||||
chr20:25294321
|
T | TGGGA | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.2312+49_2312+52dup others(4): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr20 | 25294321 | |||||
chr20:25294420
|
G | C | 31 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(28): Show | 36 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.2312+128G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294420 | ||||||
chr20:25294435
|
C | G | 5 | a0001c0004t0002g0028a0001c0004t0002g0071a0001c0004t0002g0072others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2312+143C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294435 | ||||||
chr20:25294469
|
C | T | 4 | a0001c0007t0004g0254a0001c0007t0004g0255a0001c0007t0004g0256others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2312+177C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294469 | ||||||
chr20:25294594
|
G | A | 16 | a0001c0001t0001g0034a0001c0001t0003g0020a0001c0001t0003g0022others(13): Show | 21 | HG00597.hp1 HG01167.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.2312+302G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294594 | ||||||
chr20:25294600
|
C | G | 16 | a0001c0001t0001g0034a0001c0001t0003g0020a0001c0001t0003g0022others(13): Show | 21 | HG00597.hp1 HG01167.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.2312+308C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294600 | ||||||
chr20:25294630
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG01081.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2312+338T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294630 | ||||||
chr20:25294664
|
G | A | 1 | a0001c0002t0002g0138 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2312+372G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294664 | ||||||
chr20:25294739
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2312+447G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294739 | ||||||
chr20:25294831
|
G | T | 1 | a0001c0021t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2312+539G>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294831 | ||||||
chr20:25294869
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2312+577C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294869 | ||||||
chr20:25294874
|
AG | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0262 | 4 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.2312+585delG | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr20 | 25294874 | |||||
chr20:25294917
|
GTTAGTT | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(197): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2312+634_2312+639d others(8): Show |
PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr20 | 25294917 | |||||
chr20:25294981
|
G | A | 15 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0113others(12): Show | 19 | HG01167.hp1 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.2313-623G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294981 | ||||||
chr20:25294985
|
T | C | 28 | a0001c0002t0002g0085a0001c0002t0002g0138a0001c0004t0002g0003others(25): Show | 36 | HG00544.hp2 HG01255.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.2313-619T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25294985 | ||||||
chr20:25295159
|
C | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2313-445C>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295159 | ||||||
chr20:25295207
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(148): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2313-397C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295207 | ||||||
chr20:25295234
|
A | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(290): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.2313-370A>G | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295234 | ||||||
chr20:25295254
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2313-350C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295254 | ||||||
chr20:25295282
|
C | T | 1 | a0002c0003t0001g0230 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2313-322C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295282 | ||||||
chr20:25295367
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2313-237G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295367 | ||||||
chr20:25295472
|
G | A | 53 | a0002c0003t0001g0015a0002c0003t0001g0019a0002c0003t0001g0036others(50): Show | 59 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2313-132G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295472 | ||||||
chr20:25295512
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2313-92G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 18/19 | chr20 | 25295512 | ||||||
chr20:25295707
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(176): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2379+37G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25295707 | ||||||
chr20:25295907
|
G | A | 2 | a0004c0010t0008g0252a0004c0010t0008g0253 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2379+237G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25295907 | ||||||
chr20:25296044
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(179): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2380-326G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25296044 | ||||||
chr20:25296094
|
C | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02015.hp1 NA18747.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.2380-276C>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25296094 | ||||||
chr20:25296128
|
G | A | 2 | a0001c0001t0003g0259a0001c0001t0003g0260 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2380-242G>A | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25296128 | ||||||
chr20:25296169
|
C | T | 5 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2380-201C>T | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25296169 | ||||||
chr20:25296201
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2380-169G>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25296201 | ||||||
chr20:25296312
|
T | C | 1 | a0001c0004t0007g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2380-58T>C | PYGB | ENSG00000100994.12 | transcript | ENST00000216962.9 | protein_coding | 19/19 | chr20 | 25296312 |