geneid | 652991 |
---|---|
ensemblid | ENSG00000215474.8 |
hgncid | 32695 |
symbol | SKOR2 |
name | SKI family transcriptional corepressor 2 |
refseq_nuc | NM_001278063.4 |
refseq_prot | NP_001264992.1 |
ensembl_nuc | ENST00000425639.3 |
ensembl_prot | ENSP00000414750.3 |
mane_status | MANE Select |
chr | chr18 |
start | 47206169 |
end | 47251660 |
strand | - |
ver | v1.2 |
region | chr18:47206169-47251660 |
region5000 | chr18:47201169-47256660 |
regionname0 | SKOR2_chr18_47206169_47251660 |
regionname5000 | SKOR2_chr18_47201169_47256660 |
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 | 1/0 | 1015 | 188 | 54 | 26 | 81 | 7 | 19 | 53 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002 | 0/1 | 1015 | 130 | 25 | 26 | 65 | 7 | 6 | 51 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0003 | 0/0 | 1015 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0004 | 0/0 | 1016 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0005 | 0/0 | 1016 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0006 | 0/0 | 1016 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0007 | 0/0 | 1015 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0008 | 0/0 | 1015 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0009 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0010 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0011 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0012 | 0/0 | 1015 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0013 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0014 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0015 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0016 | 0/0 | 1015 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3048 | 175 | 47 | 24 | 79 | 6 | 18 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0002 | 0/1 | 3048 | 127 | 25 | 26 | 64 | 7 | 4 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0003 | 0/0 | 3048 | 7 | 7 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0004 | 0/0 | 3048 | 5 | 0 | 0 | 0 | 0 | 5 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0005 | 0/0 | 3051 | 4 | 4 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0006 | 0/0 | 3048 | 3 | 0 | 1 | 0 | 1 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0007 | 0/0 | 3051 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0008 | 0/0 | 3048 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0009 | 0/0 | 3048 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0010 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0011 | 0/0 | 3048 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0012 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0013 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0014 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0015 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0016 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0017 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0018 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0019 | 0/0 | 3048 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0020 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0021 | 0/0 | 3048 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0022 | 0/0 | 3048 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
c0023 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1062 | 150 | 45 | 25 | 55 | 8 | 15 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0002 | 0/0 | 1062 | 135 | 34 | 20 | 64 | 3 | 14 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0003 | 0/0 | 1062 | 50 | 7 | 8 | 31 | 3 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0004 | 0/0 | 1062 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0005 | 0/0 | 1062 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0006 | 0/0 | 1062 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0007 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0008 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
t0009 | 0/0 | 1062 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
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 | 1 | 5 | 2 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0002 | 1/0 | 8 | 0 | 3 | 1 | 0 | 3 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0003 | 0/0 | 8 | 0 | 1 | 6 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0020 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3048 | 175 | 47 | 24 | 79 | 6 | 18 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0003 | 0/0 | 3048 | 7 | 7 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0006 | 0/0 | 3048 | 3 | 0 | 1 | 0 | 1 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0014 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0020 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0021 | 0/0 | 3048 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0002 | 0/1 | 3048 | 127 | 25 | 26 | 64 | 7 | 4 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0008 | 0/0 | 3048 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0012 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0003c0004 | 0/0 | 3048 | 5 | 0 | 0 | 0 | 0 | 5 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0004c0005 | 0/0 | 3051 | 4 | 4 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0005c0007 | 0/0 | 3051 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0006c0010 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0007c0011 | 0/0 | 3048 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0008c0009 | 0/0 | 3048 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0009c0013 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0010c0019 | 0/0 | 3048 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0011c0018 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0012c0017 | 0/0 | 3048 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0013c0015 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0014c0016 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0015c0022 | 0/0 | 3048 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0016c0023 | 0/0 | 3048 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4109 | 124 | 32 | 19 | 52 | 5 | 15 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0001t0002 | 0/0 | 4109 | 39 | 8 | 2 | 26 | 0 | 3 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0001t0003 | 0/0 | 4109 | 6 | 3 | 2 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0001t0004 | 0/0 | 4109 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0001t0006 | 0/0 | 4109 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0001t0007 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0001t0009 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0003t0001 | 0/0 | 4109 | 7 | 7 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0006t0003 | 0/0 | 4109 | 3 | 0 | 1 | 0 | 1 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0014t0001 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0020t0001 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0001c0021t0001 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0002t0001 | 0/1 | 4109 | 9 | 1 | 4 | 0 | 3 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0002t0002 | 0/0 | 4109 | 78 | 21 | 17 | 33 | 3 | 4 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0002t0003 | 0/0 | 4109 | 39 | 3 | 5 | 30 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0002t0008 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0008t0002 | 0/0 | 4109 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0002c0012t0003 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0003c0004t0002 | 0/0 | 4109 | 5 | 0 | 0 | 0 | 0 | 5 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0004c0005t0001 | 0/0 | 4112 | 4 | 4 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0005c0007t0002 | 0/0 | 4112 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0006c0010t0005 | 0/0 | 4112 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0007c0011t0002 | 0/0 | 4109 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0008c0009t0002 | 0/0 | 4109 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0009c0013t0003 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0010c0019t0002 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0011c0018t0001 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0012c0017t0001 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0013c0015t0002 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0014c0016t0002 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0015c0022t0001 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
a0016c0023t0002 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | copy fasta | chr18 | 47201169 | 47256660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 1/0 | 8 | 0 | 3 | 1 | 0 | 3 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 1 | 6 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0003g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0001t0009g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0003t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0006t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0006t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0006t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0014t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0020t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0001c0021t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0020 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0001 | 0/0 | 9 | 1 | 5 | 2 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0002t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0008t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0008t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0002c0012t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0003c0004t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0003c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0003c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0003c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0004c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0004c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0004c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0004c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0005c0007t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0005c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0005c0007t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0006c0010t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0006c0010t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0007c0011t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0008c0009t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0008c0009t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0009c0013t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0010c0019t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0011c0018t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0012c0017t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0013c0015t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0014c0016t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0015c0022t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
a0016c0023t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0115 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0233 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00140 | hp2 | a0002 | c0002 | t0003 | g0026 | EUR | GBR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00438 | hp1 | a0001 | c0020 | t0001 | g0111 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00544 | hp1 | a0005 | c0007 | t0002 | g0159 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00597 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0220 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0197 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0208 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0210 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0278 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01257 | hp2 | a0010 | c0019 | t0002 | g0262 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01361 | hp1 | a0001 | c0006 | t0003 | g0155 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01515 | hp1 | a0001 | c0006 | t0003 | g0156 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01884 | hp2 | a0009 | c0013 | t0003 | g0141 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01891 | hp1 | a0014 | c0016 | t0002 | g0212 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01934 | hp1 | a0001 | c0021 | t0001 | g0112 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01952 | hp1 | a0002 | c0002 | t0003 | g0170 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0191 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0216 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01993 | hp1 | a0002 | c0002 | t0003 | g0026 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02015 | hp1 | a0002 | c0002 | t0008 | g0186 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02040 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02071 | hp1 | a0002 | c0002 | t0003 | g0194 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CDX | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | CDX | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0164 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02293 | hp1 | a0015 | c0022 | t0001 | g0113 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02293 | hp2 | a0002 | c0002 | t0003 | g0171 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0165 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02572 | hp2 | a0011 | c0018 | t0001 | g0106 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0203 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0223 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02630 | hp1 | a0004 | c0005 | t0001 | g0038 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0204 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02698 | hp2 | a0002 | c0008 | t0002 | g0148 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02717 | hp2 | a0013 | c0015 | t0002 | g0218 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02896 | hp2 | a0002 | c0002 | t0002 | g0230 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02965 | hp1 | a0007 | c0011 | t0002 | g0030 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02970 | hp1 | a0016 | c0023 | t0002 | g0263 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02976 | hp2 | a0004 | c0005 | t0001 | g0039 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03041 | hp1 | a0002 | c0002 | t0003 | g0162 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0276 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0143 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0163 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03139 | hp2 | a0006 | c0010 | t0005 | g0268 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0227 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03490 | hp2 | a0003 | c0004 | t0002 | g0154 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03492 | hp1 | a0003 | c0004 | t0002 | g0024 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03516 | hp2 | a0006 | c0010 | t0005 | g0267 | AFR | ESN | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03540 | hp2 | a0004 | c0005 | t0001 | g0037 | AFR | GWD | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0229 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0173 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03704 | hp2 | a0001 | c0006 | t0003 | g0157 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0211 | SAS | PJL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03942 | hp1 | a0003 | c0004 | t0002 | g0153 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG04204 | hp1 | a0003 | c0004 | t0002 | g0024 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18522 | hp2 | a0007 | c0011 | t0002 | g0030 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18612 | hp2 | a0002 | c0002 | t0003 | g0269 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18747 | hp1 | a0005 | c0007 | t0002 | g0158 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18939 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18940 | hp2 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18947 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0275 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18950 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18957 | hp1 | a0001 | c0014 | t0001 | g0052 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18962 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18968 | hp2 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18969 | hp2 | a0002 | c0002 | t0003 | g0181 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18972 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18974 | hp1 | a0012 | c0017 | t0001 | g0053 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18974 | hp2 | a0008 | c0009 | t0002 | g0151 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18975 | hp2 | a0002 | c0002 | t0003 | g0167 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18980 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18980 | hp2 | a0002 | c0002 | t0003 | g0274 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18988 | hp1 | a0005 | c0007 | t0002 | g0160 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19007 | hp2 | a0002 | c0002 | t0003 | g0174 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19011 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19012 | hp1 | a0002 | c0002 | t0003 | g0271 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0224 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0226 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19055 | hp1 | a0002 | c0002 | t0003 | g0270 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0201 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19062 | hp1 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0273 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19064 | hp2 | a0002 | c0012 | t0003 | g0139 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19070 | hp2 | a0002 | c0002 | t0003 | g0272 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19082 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19085 | hp2 | a0008 | c0009 | t0002 | g0150 | EAS | JPT | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | YRI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0028 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0118 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0221 | EUR | TSI | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20905 | hp1 | a0003 | c0004 | t0002 | g0152 | SAS | GIH | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20905 | hp2 | a0002 | c0008 | t0002 | g0149 | SAS | GIH | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG02559 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | ACB | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | MSL | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0217 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0172 | AFR | USA | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0189 | AFR | LWK | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0020 | REF | REF | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | SKOR2_chr18_47201169_47256660 | SKOR2 | chr18 | 47201169 | 47256660 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:47230518
|
C | T | 1 | a0013 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2858G>A | p.Arg953Gln | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/9 | 3192/4109 | 2858/3048 | 953/1015 | chr18 | 47230518 | ||
chr18:47230536
|
A | C | 2 | a0004a0011 | 5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.2840T>G | p.Phe947Cys | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/9 | 3174/4109 | 2840/3048 | 947/1015 | chr18 | 47230536 | ||
chr18:47230973
|
G | A | 3 | a0005a0013a0014 | 5 | HG00544.hp1 HG01891.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.2780C>T | p.Pro927Leu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/9 | 3114/4109 | 2780/3048 | 927/1015 | chr18 | 47230973 | ||
chr18:47244924
|
A | C | 2 | a0007a0016 | 3 | HG02965.hp1 HG02970.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.2736T>G | p.Phe912Leu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/9 | 3070/4109 | 2736/3048 | 912/1015 | chr18 | 47244924 | ||
chr18:47246702
|
C | G | 1 | a0012 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.2482G>C | p.Asp828His | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2816/4109 | 2482/3048 | 828/1015 | chr18 | 47246702 | ||
chr18:47247011
|
A | T | 7 | a0002a0003a0005others(4): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
missense_variant | MODERATE | c.2173T>A | p.Cys725Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2507/4109 | 2173/3048 | 725/1015 | chr18 | 47247011 | ||
chr18:47247103
|
G | T | 1 | a0016 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2081C>A | p.Ala694Asp | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2415/4109 | 2081/3048 | 694/1015 | chr18 | 47247103 | ||
chr18:47247178
|
G | GGGT | 3 | a0004a0005a0006 | 9 | HG00544.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
conservative_inframe_insertion | MODERATE | c.2003_2005dupACC | p.His668dup | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2339/4109 | 2005/3048 | 669/1015 | chr18 | 47247178 | ||
chr18:47247638
|
G | C | 1 | a0010 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.1546C>G | p.Pro516Ala | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1880/4109 | 1546/3048 | 516/1015 | chr18 | 47247638 | ||
chr18:47247834
|
C | G | 1 | a0003 | 5 | HG03490.hp2 HG03492.hp1 HG03942.hp1 others(2): Show |
missense_variant | MODERATE | c.1350G>C | p.Leu450Phe | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1684/4109 | 1350/3048 | 450/1015 | chr18 | 47247834 | ||
chr18:47247961
|
G | T | 1 | a0009 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1223C>A | p.Pro408His | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1557/4109 | 1223/3048 | 408/1015 | chr18 | 47247961 | ||
chr18:47247980
|
C | T | 1 | a0008 | 2 | NA18974.hp2 NA19085.hp2 |
missense_variant | MODERATE | c.1204G>A | p.Gly402Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1538/4109 | 1204/3048 | 402/1015 | chr18 | 47247980 | ||
chr18:47248802
|
T | G | 1 | a0015 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.382A>C | p.Lys128Gln | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 716/4109 | 382/3048 | 128/1015 | chr18 | 47248802 | ||
chr18:47249152
|
T | C | 1 | a0016 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.32A>G | p.Asp11Gly | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 366/4109 | 32/3048 | 11/1015 | chr18 | 47249152 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:47246703
|
C | T | 1 | a0012c0017 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.2481G>A | p.Gly827Gly | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2815/4109 | 2481/3048 | 827/1015 | chr18 | 47246703 | ||
chr18:47246838
|
G | C | 1 | a0001c0003 | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
synonymous_variant | LOW | c.2346C>G | p.Val782Val | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 2680/4109 | 2346/3048 | 782/1015 | chr18 | 47246838 | ||
chr18:47247558
|
G | C | 1 | a0006c0010 | 2 | HG03139.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1626C>G | p.Ser542Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1960/4109 | 1626/3048 | 542/1015 | chr18 | 47247558 | ||
chr18:47247705
|
C | T | 1 | a0001c0006 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.1479G>A | p.Ser493Ser | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1813/4109 | 1479/3048 | 493/1015 | chr18 | 47247705 | ||
chr18:47247759
|
G | T | 1 | a0001c0014 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1425C>A | p.Thr475Thr | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1759/4109 | 1425/3048 | 475/1015 | chr18 | 47247759 | ||
chr18:47247909
|
C | T | 1 | a0006c0010 | 2 | HG03139.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1275G>A | p.Glu425Glu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1609/4109 | 1275/3048 | 425/1015 | chr18 | 47247909 | ||
chr18:47248089
|
G | A | 1 | a0001c0020 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1095C>T | p.Gly365Gly | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1429/4109 | 1095/3048 | 365/1015 | chr18 | 47248089 | ||
chr18:47248317
|
C | T | 1 | a0002c0008 | 2 | HG02698.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.867G>A | p.Pro289Pro | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1201/4109 | 867/3048 | 289/1015 | chr18 | 47248317 | ||
chr18:47248344
|
G | A | 1 | a0001c0021 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.840C>T | p.His280His | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 1174/4109 | 840/3048 | 280/1015 | chr18 | 47248344 | ||
chr18:47248812
|
C | T | 1 | a0002c0012 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.372G>A | p.Glu124Glu | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 706/4109 | 372/3048 | 124/1015 | chr18 | 47248812 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:47206316
|
T | C | 6 | a0001c0001t0003a0001c0001t0004a0001c0006t0003others(3): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 9/9 | 5773 | chr18 | 47206316 | |||||
chr18:47206428
|
G | A | 1 | a0002c0002t0008 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 9/9 | 5661 | chr18 | 47206428 | |||||
chr18:47206696
|
C | T | 1 | a0001c0001t0007 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 9/9 | 5393 | chr18 | 47206696 | |||||
chr18:47249200
|
C | G | 1 | a0006c0010t0005 | 2 | HG03139.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-17G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/9 | 17 | chr18 | 47249200 | |||||
chr18:47251385
|
T | C | 1 | a0001c0001t0006 | 2 | HG03098.hp2 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/9 | 2202 | chr18 | 47251385 | |||||
chr18:47251510
|
G | C | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(16): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
5_prime_UTR_variant | MODIFIER | c.-184C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/9 | 2327 | chr18 | 47251510 | |||||
chr18:47251603
|
G | C | 1 | a0001c0001t0009 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-277C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/9 | 2420 | chr18 | 47251603 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:47206904
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*4-12G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47206904 | ||||||
chr18:47207153
|
C | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-261G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207153 | ||||||
chr18:47207243
|
T | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0131a0001c0001t0001g0134others(2): Show | 5 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.*4-351A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207243 | ||||||
chr18:47207244
|
G | A | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-352C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207244 | ||||||
chr18:47207351
|
G | A | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | HG03225.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*4-459C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207351 | ||||||
chr18:47207397
|
A | G | 3 | a0001c0001t0003g0236a0001c0001t0004g0123a0001c0001t0004g0124 | 3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.*4-505T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207397 | ||||||
chr18:47207569
|
G | A | 1 | a0002c0002t0002g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*4-677C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207569 | ||||||
chr18:47207632
|
C | G | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-740G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207632 | ||||||
chr18:47207769
|
G | A | 2 | a0002c0008t0002g0148a0002c0008t0002g0149 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.*4-877C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207769 | ||||||
chr18:47207875
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0072others(3): Show | 6 | HG00673.hp1 HG02027.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-983C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207875 | ||||||
chr18:47207931
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0002g0146a0001c0001t0002g0147 | 3 | HG02109.hp1 HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.*4-1039G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47207931 | ||||||
chr18:47208093
|
AGAGT | A | 4 | a0001c0001t0002g0031a0001c0001t0002g0242a0001c0001t0002g0260others(1): Show | 5 | HG02056.hp2 HG02129.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.*4-1205_*4-1202del others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208093 | ||||||
chr18:47208165
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*4-1273T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208165 | ||||||
chr18:47208194
|
A | G | 39 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(36): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*4-1302T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208194 | ||||||
chr18:47208329
|
G | T | 1 | a0002c0002t0002g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.*4-1437C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208329 | ||||||
chr18:47208554
|
A | C | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.*4-1662T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208554 | ||||||
chr18:47208566
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0094others(1): Show | 6 | HG00408.hp1 HG00438.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-1674T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208566 | ||||||
chr18:47208946
|
A | C | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-2054T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47208946 | ||||||
chr18:47209008
|
G | C | 5 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(2): Show | 6 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-2116C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209008 | ||||||
chr18:47209151
|
C | CAA | 28 | a0002c0002t0003g0004a0002c0002t0003g0010a0002c0002t0003g0012others(25): Show | 40 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.*4-2261_*4-2260dup others(2): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209151 | ||||||
chr18:47209180
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.*4-2288C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209180 | ||||||
chr18:47209243
|
A | C | 1 | a0002c0008t0002g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*4-2351T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209243 | ||||||
chr18:47209409
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*4-2517G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209409 | ||||||
chr18:47209874
|
T | G | 2 | a0002c0002t0002g0229a0002c0002t0002g0230 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*3+2212A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209874 | ||||||
chr18:47209934
|
A | G | 39 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(36): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+2152T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209934 | ||||||
chr18:47209965
|
C | T | 96 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0042others(93): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.*3+2121G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47209965 | ||||||
chr18:47210070
|
C | A | 3 | a0005c0007t0002g0158a0005c0007t0002g0159a0005c0007t0002g0160 | 3 | HG00544.hp1 NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.*3+2016G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210070 | ||||||
chr18:47210221
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*3+1865C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210221 | ||||||
chr18:47210395
|
C | T | 39 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(36): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+1691G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210395 | ||||||
chr18:47210396
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*3+1690C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210396 | ||||||
chr18:47210447
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0084 | 2 | NA18969.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.*3+1639C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210447 | ||||||
chr18:47210606
|
A | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*3+1480T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210606 | ||||||
chr18:47210708
|
G | T | 1 | a0001c0001t0002g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.*3+1378C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210708 | ||||||
chr18:47210713
|
G | C | 1 | a0001c0006t0003g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.*3+1373C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210713 | ||||||
chr18:47210726
|
G | A | 39 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(36): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+1360C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210726 | ||||||
chr18:47210859
|
A | G | 143 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0042others(140): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.*3+1227T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210859 | ||||||
chr18:47210938
|
C | T | 2 | a0004c0005t0001g0037a0011c0018t0001g0106 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.*3+1148G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47210938 | ||||||
chr18:47211019
|
AATT | A | 11 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(8): Show | 12 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.*3+1064_*3+1066del others(3): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211019 | ||||||
chr18:47211089
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.*3+997T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211089 | ||||||
chr18:47211209
|
G | A | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*3+877C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211209 | ||||||
chr18:47211242
|
C | T | 28 | a0002c0002t0003g0004a0002c0002t0003g0010a0002c0002t0003g0012others(25): Show | 40 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.*3+844G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211242 | ||||||
chr18:47211649
|
G | A | 1 | a0001c0021t0001g0112 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.*3+437C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211649 | ||||||
chr18:47211789
|
T | A | 1 | a0002c0002t0001g0021 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.*3+297A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47211789 | ||||||
chr18:47212041
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*3+45T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 8/8 | chr18 | 47212041 | ||||||
chr18:47212455
|
A | T | 3 | a0001c0001t0001g0122a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2986-304T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212455 | ||||||
chr18:47212749
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2986-598C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212749 | ||||||
chr18:47212902
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0009g0278 | 3 | HG01243.hp2 HG01255.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2986-751C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212902 | ||||||
chr18:47212998
|
T | C | 1 | a0002c0002t0002g0209 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2986-847A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47212998 | ||||||
chr18:47213278
|
C | G | 1 | a0002c0002t0002g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2986-1127G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213278 | ||||||
chr18:47213382
|
T | TATATTTA others(30): Show |
2 | a0002c0008t0002g0148a0002c0008t0002g0149 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2986-1268_2986-123 others(41): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213382 | ||||||
chr18:47213457
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0121 | 3 | HG03041.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2986-1306G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213457 | ||||||
chr18:47213519
|
C | T | 1 | a0002c0002t0003g0162 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2986-1368G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213519 | ||||||
chr18:47213606
|
A | C | 11 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(8): Show | 12 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2986-1455T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213606 | ||||||
chr18:47213632
|
G | A | 192 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(189): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2986-1481C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213632 | ||||||
chr18:47213923
|
C | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2986-1772G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47213923 | ||||||
chr18:47214577
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2986-2426G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214577 | ||||||
chr18:47214583
|
T | A | 1 | a0002c0002t0008g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2986-2432A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214583 | ||||||
chr18:47214592
|
A | G | 8 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(5): Show | 9 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2986-2441T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214592 | ||||||
chr18:47214692
|
A | G | 28 | a0002c0002t0003g0004a0002c0002t0003g0010a0002c0002t0003g0012others(25): Show | 40 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2986-2541T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214692 | ||||||
chr18:47214789
|
A | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2986-2638T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214789 | ||||||
chr18:47214844
|
C | A | 2 | a0001c0001t0001g0102a0002c0002t0002g0193 | 2 | HG00558.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.2986-2693G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214844 | ||||||
chr18:47214958
|
C | T | 1 | a0002c0002t0003g0164 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2986-2807G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214958 | ||||||
chr18:47214991
|
G | GT | 38 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(35): Show | 51 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2986-2841dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214991 | ||||||
chr18:47214994
|
T | TA | 105 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0042others(102): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2986-2844dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214994 | ||||||
chr18:47214995
|
A | T | 35 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(32): Show | 48 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2986-2844T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47214995 | ||||||
chr18:47215177
|
C | A | 1 | a0002c0002t0002g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2986-3026G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215177 | ||||||
chr18:47215211
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2986-3060T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215211 | ||||||
chr18:47215255
|
A | G | 2 | a0004c0005t0001g0037a0011c0018t0001g0106 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2986-3104T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215255 | ||||||
chr18:47215367
|
T | A | 2 | a0001c0001t0002g0243a0010c0019t0002g0262 | 2 | HG01257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.2986-3216A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215367 | ||||||
chr18:47215368
|
A | T | 9 | a0001c0001t0001g0049a0001c0001t0001g0086a0001c0001t0001g0131others(6): Show | 9 | HG01361.hp1 HG01515.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2986-3217T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215368 | ||||||
chr18:47215684
|
G | C | 3 | a0005c0007t0002g0158a0005c0007t0002g0159a0005c0007t0002g0160 | 3 | HG00544.hp1 NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2986-3533C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215684 | ||||||
chr18:47215695
|
C | A | 79 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0069others(76): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2986-3544G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215695 | ||||||
chr18:47215718
|
A | C | 39 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(36): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2986-3567T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47215718 | ||||||
chr18:47216037
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0231others(1): Show | 4 | HG02976.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2986-3886A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216037 | ||||||
chr18:47216128
|
T | G | 1 | a0002c0002t0002g0222 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2985+3815A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216128 | ||||||
chr18:47216226
|
A | T | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2985+3717T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216226 | ||||||
chr18:47216497
|
A | C | 101 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(98): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.2985+3446T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216497 | ||||||
chr18:47216544
|
C | T | 2 | a0001c0001t0003g0029a0009c0013t0003g0141 | 3 | HG01243.hp1 HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2985+3399G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216544 | ||||||
chr18:47216559
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2985+3384T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216559 | ||||||
chr18:47216815
|
C | A | 2 | a0001c0001t0002g0231a0002c0002t0002g0163 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2985+3128G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216815 | ||||||
chr18:47216855
|
A | G | 5 | a0001c0003t0001g0007a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2985+3088T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47216855 | ||||||
chr18:47217344
|
G | A | 13 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(10): Show | 16 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2985+2599C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217344 | ||||||
chr18:47217357
|
G | A | 5 | a0001c0003t0001g0007a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2985+2586C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217357 | ||||||
chr18:47217399
|
C | A | 2 | a0004c0005t0001g0038a0004c0005t0001g0039 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2985+2544G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217399 | ||||||
chr18:47217926
|
G | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0002g0140 | 3 | HG02922.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2985+2017C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47217926 | ||||||
chr18:47218019
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2985+1924G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218019 | ||||||
chr18:47218051
|
G | A | 20 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0002g0140others(17): Show | 24 | HG00140.hp2 HG00639.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.2985+1892C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218051 | ||||||
chr18:47218183
|
C | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2985+1760G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218183 | ||||||
chr18:47218589
|
C | CA | 44 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0043others(41): Show | 52 | HG00673.hp2 HG01243.hp2 HG02056.hp1 others(49): Show |
intron_variant | MODIFIER | c.2985+1353dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218589
|
C | CAA | 12 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(9): Show | 13 | HG00544.hp1 HG01361.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.2985+1352_2985+135 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218589
|
C | CAAA | 80 | a0001c0001t0001g0017a0001c0001t0001g0047a0001c0001t0001g0048others(77): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2985+1351_2985+135 others(7): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218589
|
C | CAAAA | 12 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0004g0124others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2985+1350_2985+135 others(8): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218589
|
C | CAAAAA | 19 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0002g0140others(16): Show | 20 | HG00140.hp2 HG00639.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.2985+1349_2985+135 others(9): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218589
|
C | CAAAAAA | 13 | a0001c0001t0003g0029a0001c0001t0003g0232a0001c0001t0003g0233others(10): Show | 17 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2985+1348_2985+135 others(10): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218589
|
CA | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0060others(5): Show | 8 | HG00558.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2985+1353delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218589 | ||||||
chr18:47218685
|
A | G | 137 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(134): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2985+1258T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218685 | ||||||
chr18:47218814
|
A | C | 137 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(134): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2985+1129T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218814 | ||||||
chr18:47218907
|
C | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2985+1036G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47218907 | ||||||
chr18:47219175
|
T | C | 17 | a0002c0002t0002g0172a0002c0002t0003g0010a0002c0002t0003g0025others(14): Show | 21 | HG00140.hp2 HG00639.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.2985+768A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219175 | ||||||
chr18:47219350
|
C | G | 106 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(103): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2985+593G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219350 | ||||||
chr18:47219372
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2985+571A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219372 | ||||||
chr18:47219398
|
GT | G | 137 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(134): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2985+544delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219398 | ||||||
chr18:47219533
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2985+410G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219533 | ||||||
chr18:47219545
|
G | A | 2 | a0002c0002t0003g0162a0002c0002t0003g0164 | 2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2985+398C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219545 | ||||||
chr18:47219662
|
G | T | 3 | a0001c0001t0003g0236a0001c0001t0004g0123a0001c0001t0004g0124 | 3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2985+281C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219662 | ||||||
chr18:47219663
|
C | T | 3 | a0001c0001t0003g0236a0001c0001t0004g0123a0001c0001t0004g0124 | 3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2985+280G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219663 | ||||||
chr18:47219691
|
G | T | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2985+252C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 7/8 | chr18 | 47219691 | ||||||
chr18:47220089
|
A | T | 96 | a0001c0001t0001g0017a0001c0001t0001g0069a0001c0001t0001g0081others(93): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2918-79T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220089 | ||||||
chr18:47220306
|
G | C | 2 | a0002c0002t0003g0162a0002c0002t0003g0164 | 2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2918-296C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220306 | ||||||
chr18:47220368
|
C | G | 137 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(134): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.2918-358G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220368 | ||||||
chr18:47220416
|
C | T | 4 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | NA18968.hp1 NA18981.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2918-406G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220416 | ||||||
chr18:47220576
|
G | C | 121 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0046others(118): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.2918-566C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220576 | ||||||
chr18:47220626
|
G | A | 91 | a0001c0001t0001g0017a0001c0001t0002g0257a0001c0021t0001g0112others(88): Show | 120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2918-616C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220626 | ||||||
chr18:47220726
|
G | C | 1 | a0001c0001t0002g0266 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2918-716C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220726 | ||||||
chr18:47220767
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2918-757C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220767 | ||||||
chr18:47220778
|
T | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(34): Show | 42 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.2918-768A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220778 | ||||||
chr18:47220822
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2918-812C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220822 | ||||||
chr18:47220928
|
A | G | 25 | a0001c0001t0001g0058a0001c0001t0001g0125a0001c0001t0002g0013others(22): Show | 28 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.2918-918T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47220928 | ||||||
chr18:47221012
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2918-1002C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221012 | ||||||
chr18:47221084
|
A | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2918-1074T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221084 | ||||||
chr18:47221314
|
A | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-1304T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221314 | ||||||
chr18:47221374
|
T | C | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-1364A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221374 | ||||||
chr18:47221395
|
G | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2918-1385C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221395 | ||||||
chr18:47221552
|
C | A | 1 | a0001c0001t0002g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2918-1542G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221552 | ||||||
chr18:47221675
|
A | AT | 47 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0077others(44): Show | 52 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.2918-1666dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221675 | ||||||
chr18:47221693
|
C | G | 6 | a0002c0002t0003g0025a0002c0002t0003g0166a0002c0002t0003g0167others(3): Show | 7 | NA18940.hp2 NA18968.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.2918-1683G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221693 | ||||||
chr18:47221708
|
T | G | 141 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(138): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.2918-1698A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221708 | ||||||
chr18:47221821
|
A | T | 2 | a0001c0001t0001g0069a0002c0002t0003g0026 | 3 | HG00140.hp1 HG00140.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2918-1811T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47221821 | ||||||
chr18:47222096
|
A | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(144): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2918-2086T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222096 | ||||||
chr18:47222174
|
T | G | 186 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(183): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2918-2164A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222174 | ||||||
chr18:47222183
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2918-2173T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222183 | ||||||
chr18:47222238
|
C | T | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2918-2228G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222238 | ||||||
chr18:47222249
|
G | A | 2 | a0001c0001t0002g0235a0002c0002t0002g0163 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2918-2239C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222249 | ||||||
chr18:47222289
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2918-2279G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222289 | ||||||
chr18:47222312
|
C | T | 192 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(189): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2918-2302G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222312 | ||||||
chr18:47222315
|
CA | C | 41 | a0001c0001t0001g0058a0001c0001t0001g0077a0001c0001t0001g0122others(38): Show | 44 | HG00673.hp2 HG01243.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2918-2306delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222315 | ||||||
chr18:47222521
|
G | A | 1 | a0002c0002t0008g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2918-2511C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222521 | ||||||
chr18:47222538
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 8 | HG02486.hp1 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2918-2528G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222538 | ||||||
chr18:47222775
|
G | C | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-2765C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47222775 | ||||||
chr18:47223014
|
A | G | 1 | a0002c0002t0003g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2918-3004T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223014 | ||||||
chr18:47223216
|
C | T | 1 | a0002c0008t0002g0149 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2918-3206G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223216 | ||||||
chr18:47223374
|
G | A | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2918-3364C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223374 | ||||||
chr18:47223513
|
A | C | 80 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(77): Show | 107 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.2918-3503T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223513 | ||||||
chr18:47223903
|
CT | C | 184 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(181): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2918-3894delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223903 | ||||||
chr18:47223917
|
TA | T | 5 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0095others(2): Show | 5 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2918-3908delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223917 | ||||||
chr18:47223919
|
A | T | 5 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0095others(2): Show | 5 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2918-3909T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223919 | ||||||
chr18:47223932
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | HG02257.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2918-3922C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223932 | ||||||
chr18:47223945
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2918-3935C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223945 | ||||||
chr18:47223994
|
C | T | 170 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0042others(167): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2918-3984G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47223994 | ||||||
chr18:47224072
|
C | CT | 5 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2918-4063dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224072 | ||||||
chr18:47224120
|
G | C | 1 | a0016c0023t0002g0263 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2918-4110C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224120 | ||||||
chr18:47224434
|
T | C | 1 | a0001c0001t0003g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2918-4424A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224434 | ||||||
chr18:47224620
|
C | CT | 185 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(182): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2918-4611dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224620 | ||||||
chr18:47224706
|
C | T | 2 | a0001c0003t0001g0007a0001c0003t0001g0033 | 4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2918-4696G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224706 | ||||||
chr18:47224962
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2918-4952T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47224962 | ||||||
chr18:47225003
|
A | G | 192 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(189): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2918-4993T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225003 | ||||||
chr18:47225050
|
A | G | 1 | a0002c0002t0002g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2918-5040T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225050 | ||||||
chr18:47225053
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2918-5043T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225053 | ||||||
chr18:47225485
|
A | G | 192 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(189): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2917+4974T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225485 | ||||||
chr18:47225499
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2917+4960G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225499 | ||||||
chr18:47225589
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2917+4870G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225589 | ||||||
chr18:47225633
|
A | C | 1 | a0001c0001t0001g0078 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2917+4826T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225633 | ||||||
chr18:47225670
|
A | G | 192 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(189): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2917+4789T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225670 | ||||||
chr18:47225754
|
G | A | 189 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(186): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2917+4705C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225754 | ||||||
chr18:47225754
|
G | C | 3 | a0001c0001t0002g0231a0002c0002t0002g0138a0002c0002t0002g0163 | 3 | HG02486.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2917+4705C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225754 | ||||||
chr18:47225867
|
G | C | 186 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(183): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.2917+4592C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47225867 | ||||||
chr18:47226139
|
C | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0004g0123 | 3 | HG01891.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2917+4320G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226139 | ||||||
chr18:47226522
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2917+3937G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226522 | ||||||
chr18:47226870
|
A | C | 3 | a0001c0001t0002g0231a0002c0002t0002g0138a0002c0002t0002g0163 | 3 | HG02486.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2917+3589T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226870 | ||||||
chr18:47226871
|
A | G | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2917+3588T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226871 | ||||||
chr18:47226968
|
G | A | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2917+3491C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47226968 | ||||||
chr18:47227203
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2917+3256G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227203 | ||||||
chr18:47227206
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2917+3253G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227206 | ||||||
chr18:47227326
|
A | AT | 58 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0055others(55): Show | 64 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2917+3132dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227326
|
A | ATT | 10 | a0001c0001t0001g0040a0001c0001t0006g0276a0001c0001t0006g0277others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2917+3131_2917+313 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227326
|
AT | A | 27 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(24): Show | 29 | HG01515.hp2 HG01517.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.2917+3132delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227326
|
ATT | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2917+3131_2917+313 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227326
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2917+3121_2917+313 others(16): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227326
|
ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2917+3119_2917+313 others(18): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227326
|
ATTTTTTT others(8): Show |
A | 2 | a0002c0002t0002g0198a0002c0002t0002g0224 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2917+3118_2917+313 others(19): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227326 | ||||||
chr18:47227360
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2917+3099G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227360 | ||||||
chr18:47227374
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0004g0123 | 3 | HG01891.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2917+3085C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227374 | ||||||
chr18:47227430
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2917+3029G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227430 | ||||||
chr18:47227447
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2917+3012G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227447 | ||||||
chr18:47227658
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2917+2801T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227658 | ||||||
chr18:47227732
|
T | C | 170 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0122others(167): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.2917+2727A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227732 | ||||||
chr18:47227793
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2917+2666T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227793 | ||||||
chr18:47227804
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2917+2655G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227804 | ||||||
chr18:47227891
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2917+2568C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47227891 | ||||||
chr18:47228008
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2917+2451A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228008 | ||||||
chr18:47228280
|
G | A | 78 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2917+2179C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228280 | ||||||
chr18:47228502
|
A | G | 5 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0038others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2917+1957T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228502 | ||||||
chr18:47228645
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2917+1814T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228645 | ||||||
chr18:47228678
|
A | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2917+1781T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228678 | ||||||
chr18:47228984
|
C | T | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2917+1475G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47228984 | ||||||
chr18:47230050
|
A | C | 91 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(88): Show | 116 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.2917+409T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47230050 | ||||||
chr18:47230140
|
A | G | 1 | a0002c0002t0003g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2917+319T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47230140 | ||||||
chr18:47230350
|
CTG | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2917+107_2917+108d others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 6/8 | chr18 | 47230350 | ||||||
chr18:47230562
|
TA | T | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.2819-6delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230562 | ||||||
chr18:47230667
|
A | C | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2819-110T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230667 | ||||||
chr18:47230765
|
T | C | 30 | a0001c0001t0001g0125a0001c0001t0002g0013a0001c0001t0002g0031others(27): Show | 33 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2818+170A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230765 | ||||||
chr18:47230766
|
T | G | 3 | a0005c0007t0002g0158a0005c0007t0002g0159a0005c0007t0002g0160 | 3 | HG00544.hp1 NA18747.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.2818+169A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230766 | ||||||
chr18:47230855
|
G | T | 80 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(77): Show | 103 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2818+80C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 5/8 | chr18 | 47230855 | ||||||
chr18:47231184
|
T | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-184A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231184 | ||||||
chr18:47231370
|
G | T | 1 | a0001c0001t0002g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2753-370C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231370 | ||||||
chr18:47231371
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2753-371G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231371 | ||||||
chr18:47231407
|
G | A | 1 | a0001c0001t0003g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2753-407C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231407 | ||||||
chr18:47231447
|
A | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-447T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231447 | ||||||
chr18:47231546
|
T | A | 17 | a0001c0001t0001g0105a0002c0002t0002g0006a0002c0002t0002g0027others(14): Show | 21 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.2753-546A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231546 | ||||||
chr18:47231547
|
A | T | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-547T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231547 | ||||||
chr18:47231565
|
C | T | 1 | a0004c0005t0001g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2753-565G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231565 | ||||||
chr18:47231570
|
G | A | 5 | a0001c0001t0001g0122a0001c0001t0002g0231a0001c0006t0003g0155others(2): Show | 5 | HG01361.hp1 HG01515.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2753-570C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231570 | ||||||
chr18:47231689
|
C | G | 2 | a0002c0002t0002g0138a0002c0002t0002g0163 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2753-689G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231689 | ||||||
chr18:47231843
|
C | CA | 8 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2753-844dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | ||||||
chr18:47231843
|
C | CAA | 32 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0161others(29): Show | 40 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.2753-845_2753-844d others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | ||||||
chr18:47231843
|
C | CAAAA | 5 | a0001c0003t0001g0007a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2753-847_2753-844d others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | ||||||
chr18:47231843
|
CA | C | 112 | a0001c0001t0001g0065a0001c0001t0001g0099a0001c0001t0001g0125others(109): Show | 139 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2753-844delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231843 | ||||||
chr18:47231911
|
C | T | 1 | a0002c0002t0003g0274 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2753-911G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231911 | ||||||
chr18:47231948
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2753-948G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47231948 | ||||||
chr18:47232153
|
TA | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-1154delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232153 | ||||||
chr18:47232225
|
C | T | 1 | a0004c0005t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2753-1225G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232225 | ||||||
chr18:47232242
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2753-1242T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232242 | ||||||
chr18:47232294
|
G | T | 78 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2753-1294C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232294 | ||||||
chr18:47232301
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2753-1301G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232301 | ||||||
chr18:47232643
|
G | A | 1 | a0002c0002t0002g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2753-1643C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232643 | ||||||
chr18:47232704
|
T | C | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-1704A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232704 | ||||||
chr18:47232779
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2753-1779C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232779 | ||||||
chr18:47232832
|
C | G | 36 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(33): Show | 44 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.2753-1832G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232832 | ||||||
chr18:47232850
|
G | A | 1 | a0002c0002t0003g0274 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2753-1850C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47232850 | ||||||
chr18:47233276
|
A | C | 1 | a0002c0002t0002g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2753-2276T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233276 | ||||||
chr18:47233347
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2753-2347G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233347 | ||||||
chr18:47233452
|
G | A | 3 | a0001c0001t0002g0235a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG02922.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2753-2452C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233452 | ||||||
chr18:47233842
|
G | A | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-2842C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47233842 | ||||||
chr18:47234110
|
C | T | 1 | a0002c0002t0002g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2753-3110G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234110 | ||||||
chr18:47234113
|
T | C | 1 | a0002c0002t0002g0179 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2753-3113A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234113 | ||||||
chr18:47234149
|
C | T | 2 | a0002c0002t0002g0138a0002c0002t0002g0163 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2753-3149G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234149 | ||||||
chr18:47234165
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0231 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2753-3165C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234165 | ||||||
chr18:47234256
|
TA | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 10 | HG01884.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2753-3257delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234256 | ||||||
chr18:47234292
|
C | T | 39 | a0001c0001t0002g0235a0001c0001t0006g0276a0001c0001t0006g0277others(36): Show | 47 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.2753-3292G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234292 | ||||||
chr18:47234355
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2753-3355T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234355 | ||||||
chr18:47234530
|
G | A | 78 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2753-3530C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234530 | ||||||
chr18:47234541
|
G | C | 1 | a0004c0005t0001g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2753-3541C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234541 | ||||||
chr18:47234864
|
G | GAAAAAAA others(2): Show |
10 | a0001c0001t0001g0055a0001c0001t0002g0240a0001c0001t0002g0246others(7): Show | 12 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2753-3873_2753-386 others(13): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | ||||||
chr18:47234864
|
G | GAAAAAAA others(3): Show |
100 | a0001c0001t0001g0125a0001c0001t0002g0013a0001c0001t0002g0031others(97): Show | 126 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.2753-3874_2753-386 others(14): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | ||||||
chr18:47234864
|
G | GAAAAAAA others(4): Show |
17 | a0001c0001t0001g0122a0001c0001t0002g0140a0001c0001t0002g0147others(14): Show | 17 | HG00735.hp2 HG01361.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.2753-3875_2753-386 others(15): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | ||||||
chr18:47234864
|
G | GAAAAAAA others(5): Show |
1 | a0011c0018t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2753-3865_2753-386 others(16): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234864 | ||||||
chr18:47234879
|
A | G | 2 | a0001c0001t0003g0029a0009c0013t0003g0141 | 3 | HG01243.hp1 HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2753-3879T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47234879 | ||||||
chr18:47235298
|
A | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-4298T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235298 | ||||||
chr18:47235447
|
T | A | 1 | a0001c0001t0004g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2753-4447A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235447 | ||||||
chr18:47235487
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2753-4487C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235487 | ||||||
chr18:47235780
|
C | CA | 50 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0046others(47): Show | 56 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2753-4781dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | ||||||
chr18:47235780
|
C | CAA | 19 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(16): Show | 21 | HG01884.hp1 HG02486.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2753-4782_2753-478 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | ||||||
chr18:47235780
|
CA | C | 13 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(10): Show | 13 | HG00673.hp1 HG00733.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2753-4781delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | ||||||
chr18:47235780
|
CAA | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG01975.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2753-4782_2753-478 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235780 | ||||||
chr18:47235793
|
A | AC | 8 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(5): Show | 9 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.2753-4794_2753-479 others(5): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235793 | ||||||
chr18:47235793
|
A | C | 1 | a0001c0001t0003g0233 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2753-4793T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235793 | ||||||
chr18:47235801
|
AC | A | 8 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(5): Show | 8 | HG01361.hp1 HG01515.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2753-4802delG | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235801 | ||||||
chr18:47235802
|
C | A | 71 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(68): Show | 94 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2753-4802G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235802 | ||||||
chr18:47235805
|
C | G | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2753-4805G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235805 | ||||||
chr18:47235936
|
C | T | 81 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(78): Show | 104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2753-4936G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235936 | ||||||
chr18:47235964
|
T | C | 5 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0038others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2753-4964A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47235964 | ||||||
chr18:47236016
|
G | A | 35 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(32): Show | 43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2753-5016C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236016 | ||||||
chr18:47236037
|
C | T | 81 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(78): Show | 104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2753-5037G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236037 | ||||||
chr18:47236038
|
G | A | 16 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0161others(13): Show | 20 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2753-5038C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236038 | ||||||
chr18:47236071
|
A | G | 1 | a0002c0002t0002g0182 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2753-5071T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236071 | ||||||
chr18:47236161
|
G | C | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-5161C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236161 | ||||||
chr18:47236179
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2753-5179G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236179 | ||||||
chr18:47236205
|
G | A | 1 | a0004c0005t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2753-5205C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236205 | ||||||
chr18:47236221
|
G | T | 35 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(32): Show | 43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2753-5221C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236221 | ||||||
chr18:47236269
|
G | A | 9 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(6): Show | 10 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2753-5269C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236269 | ||||||
chr18:47236377
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2753-5377G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236377 | ||||||
chr18:47236581
|
C | A | 1 | a0002c0002t0002g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2753-5581G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236581 | ||||||
chr18:47236674
|
C | T | 1 | a0002c0002t0002g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2753-5674G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236674 | ||||||
chr18:47236922
|
T | C | 1 | a0001c0003t0001g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2753-5922A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47236922 | ||||||
chr18:47237223
|
A | T | 3 | a0001c0001t0002g0235a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG02922.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2753-6223T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237223 | ||||||
chr18:47237428
|
A | G | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2753-6428T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237428 | ||||||
chr18:47237519
|
C | T | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-6519G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237519 | ||||||
chr18:47237623
|
T | G | 81 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(78): Show | 104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2753-6623A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237623 | ||||||
chr18:47237624
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2753-6624G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237624 | ||||||
chr18:47237699
|
C | CT | 33 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0100others(30): Show | 38 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.2753-6700dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237699 | ||||||
chr18:47237699
|
CT | C | 91 | a0001c0001t0001g0065a0001c0001t0001g0098a0001c0001t0001g0099others(88): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2753-6700delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237699 | ||||||
chr18:47237704
|
T | C | 2 | a0001c0006t0003g0155a0001c0006t0003g0157 | 2 | HG01361.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2753-6704A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237704 | ||||||
chr18:47237785
|
C | T | 2 | a0002c0002t0002g0198a0002c0002t0002g0224 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2753-6785G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237785 | ||||||
chr18:47237967
|
T | C | 1 | a0013c0015t0002g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2752+6941A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47237967 | ||||||
chr18:47238000
|
C | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | HG02257.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2752+6908G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238000 | ||||||
chr18:47238018
|
G | C | 2 | a0002c0002t0002g0138a0002c0002t0002g0163 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2752+6890C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238018 | ||||||
chr18:47238191
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2752+6717A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238191 | ||||||
chr18:47238196
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2752+6712T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238196 | ||||||
chr18:47238311
|
T | G | 1 | a0002c0002t0002g0188 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2752+6597A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238311 | ||||||
chr18:47238320
|
CT | C | 65 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(62): Show | 72 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.2752+6587delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238320 | ||||||
chr18:47238320
|
CTT | C | 69 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(66): Show | 92 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2752+6586_2752+658 others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238320 | ||||||
chr18:47238325
|
T | C | 30 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0161others(27): Show | 38 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2752+6583A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238325 | ||||||
chr18:47238326
|
T | C | 1 | a0002c0002t0003g0181 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2752+6582A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238326 | ||||||
chr18:47238447
|
C | T | 1 | a0001c0001t0003g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2752+6461G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238447 | ||||||
chr18:47238448
|
G | A | 1 | a0013c0015t0002g0218 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2752+6460C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238448 | ||||||
chr18:47238614
|
C | T | 35 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(32): Show | 43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+6294G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238614 | ||||||
chr18:47238669
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2752+6239C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47238669 | ||||||
chr18:47239098
|
G | A | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2752+5810C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239098 | ||||||
chr18:47239306
|
CT | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0102others(2): Show | 9 | HG00597.hp2 HG01070.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.2752+5601delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239306 | ||||||
chr18:47239530
|
G | A | 30 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0161others(27): Show | 38 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2752+5378C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239530 | ||||||
chr18:47239572
|
G | A | 81 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(78): Show | 104 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2752+5336C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239572 | ||||||
chr18:47239600
|
G | A | 35 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(32): Show | 43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+5308C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239600 | ||||||
chr18:47239712
|
A | G | 35 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(32): Show | 43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+5196T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239712 | ||||||
chr18:47239807
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2752+5101G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239807 | ||||||
chr18:47239982
|
T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0132 | 2 | HG02970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2752+4926A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239982 | ||||||
chr18:47239982
|
T | TA | 76 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(73): Show | 99 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2752+4925dupT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47239982 | ||||||
chr18:47240162
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2752+4746T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240162 | ||||||
chr18:47240521
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2752+4387C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240521 | ||||||
chr18:47240539
|
C | G | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2752+4369G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240539 | ||||||
chr18:47240584
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2752+4324G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240584 | ||||||
chr18:47240838
|
C | T | 5 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0038others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2752+4070G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47240838 | ||||||
chr18:47241187
|
C | T | 3 | a0002c0002t0003g0165a0002c0002t0003g0170a0002c0002t0003g0171 | 3 | HG01952.hp1 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2752+3721G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241187 | ||||||
chr18:47241231
|
A | G | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2752+3677T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241231 | ||||||
chr18:47241395
|
G | T | 3 | a0001c0001t0002g0238a0001c0001t0002g0239a0001c0001t0002g0244 | 3 | HG00609.hp2 NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2752+3513C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241395 | ||||||
chr18:47241414
|
A | G | 35 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0138others(32): Show | 43 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2752+3494T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241414 | ||||||
chr18:47241450
|
T | G | 2 | a0002c0002t0002g0197a0002c0002t0002g0219 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.2752+3458A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241450 | ||||||
chr18:47241638
|
CA | C | 78 | a0001c0001t0002g0140a0002c0002t0001g0020a0002c0002t0001g0021others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2752+3269delT | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241638 | ||||||
chr18:47241642
|
A | C | 36 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157others(33): Show | 44 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.2752+3266T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241642 | ||||||
chr18:47241653
|
T | C | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2752+3255A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241653 | ||||||
chr18:47241746
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2752+3162T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241746 | ||||||
chr18:47241924
|
T | C | 31 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0161others(28): Show | 39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2752+2984A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241924 | ||||||
chr18:47241970
|
C | A | 7 | a0002c0002t0002g0221a0002c0002t0002g0222a0002c0002t0003g0220others(4): Show | 8 | HG00639.hp2 HG02280.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.2752+2938G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47241970 | ||||||
chr18:47242030
|
C | T | 1 | a0003c0004t0002g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2752+2878G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242030 | ||||||
chr18:47242122
|
A | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(188): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2752+2786T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242122 | ||||||
chr18:47242212
|
A | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2752+2696T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242212 | ||||||
chr18:47242368
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2752+2540C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242368 | ||||||
chr18:47242718
|
T | C | 1 | a0002c0002t0002g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2752+2190A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242718 | ||||||
chr18:47242771
|
G | C | 1 | a0001c0001t0001g0019 | 2 | HG01070.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2752+2137C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47242771 | ||||||
chr18:47243026
|
A | G | 1 | a0002c0002t0002g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2752+1882T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243026 | ||||||
chr18:47243060
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2752+1848T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243060 | ||||||
chr18:47243163
|
T | A | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2752+1745A>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243163 | ||||||
chr18:47243449
|
C | T | 191 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(188): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2752+1459G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243449 | ||||||
chr18:47243886
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2752+1022A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243886 | ||||||
chr18:47243946
|
C | A | 261 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(258): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.2752+962G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47243946 | ||||||
chr18:47244079
|
A | G | 1 | a0001c0001t0003g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2752+829T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244079 | ||||||
chr18:47244228
|
A | G | 3 | a0002c0002t0002g0226a0002c0002t0002g0227a0002c0002t0002g0228 | 3 | HG03195.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2752+680T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244228 | ||||||
chr18:47244250
|
T | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(188): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2752+658A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244250 | ||||||
chr18:47244369
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2752+539T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244369 | ||||||
chr18:47244375
|
T | C | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2752+533A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244375 | ||||||
chr18:47244590
|
A | G | 1 | a0002c0002t0003g0170 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2752+318T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244590 | ||||||
chr18:47244593
|
A | G | 2 | a0002c0002t0002g0199a0002c0002t0002g0225 | 2 | NA18959.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2752+315T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244593 | ||||||
chr18:47244594
|
G | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 5 | HG02922.hp1 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+314C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244594 | ||||||
chr18:47244788
|
T | C | 11 | a0001c0001t0001g0122a0001c0001t0002g0231a0001c0001t0002g0264others(8): Show | 12 | HG00099.hp2 HG01123.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2752+120A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 4/8 | chr18 | 47244788 | ||||||
chr18:47245048
|
A | AT | 8 | a0001c0003t0001g0007a0001c0003t0001g0032a0001c0003t0001g0033others(5): Show | 10 | HG00099.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2678-67dupA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245048 | ||||||
chr18:47245110
|
C | T | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2678-128G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245110 | ||||||
chr18:47245208
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2678-226T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245208 | ||||||
chr18:47245478
|
A | ATT | 6 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 8 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2677+18_2677+19dup others(2): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(1): Show |
13 | a0002c0002t0001g0021a0002c0002t0002g0023a0002c0002t0002g0142others(10): Show | 15 | HG01070.hp2 HG01071.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.2677+12_2677+19dup others(8): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(2): Show |
55 | a0001c0001t0003g0236a0002c0002t0001g0020a0002c0002t0001g0115others(52): Show | 76 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2677+11_2677+19dup others(9): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(3): Show |
14 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(11): Show | 14 | HG00558.hp1 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.2677+10_2677+19dup others(10): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(4): Show |
20 | a0001c0001t0002g0013a0001c0001t0002g0031a0001c0001t0002g0147others(17): Show | 23 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.2677+9_2677+19dupA others(10): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(5): Show |
7 | a0001c0001t0001g0125a0001c0001t0002g0146a0001c0001t0002g0238others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2677+8_2677+19dupA others(11): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(6): Show |
13 | a0002c0002t0002g0006a0002c0002t0002g0027a0002c0002t0002g0161others(10): Show | 20 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2677+7_2677+19dupA others(12): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(7): Show |
15 | a0001c0001t0001g0135a0001c0006t0003g0157a0002c0002t0002g0172others(12): Show | 16 | HG01952.hp1 HG02080.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2677+6_2677+19dupA others(13): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(8): Show |
11 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0003t0001g0035others(8): Show | 12 | HG00408.hp2 HG01515.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2677+5_2677+19dupA others(14): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(9): Show |
6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0235others(3): Show | 8 | HG01361.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2677+4_2677+19dupA others(15): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(10): Show |
5 | a0001c0001t0001g0130a0001c0001t0006g0277a0001c0003t0001g0033others(2): Show | 5 | HG03041.hp1 HG03471.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2677+3_2677+19dupA others(16): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0049a0001c0003t0001g0032 | 2 | HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(18): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0006g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2677+19_2677+20ins others(19): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(14): Show |
2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(21): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(15): Show |
2 | a0001c0001t0004g0123a0002c0002t0002g0138 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(22): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(17): Show |
3 | a0001c0001t0003g0029a0001c0001t0003g0232a0009c0013t0003g0141 | 4 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(24): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(22): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0002g0266 | 3 | HG02896.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(29): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(23): Show |
2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(30): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(24): Show |
1 | a0001c0001t0002g0231 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2677+19_2677+20ins others(31): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
A | ATTTTTTT others(25): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0122 | 2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2677+19_2677+20ins others(32): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245478
|
AT | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0050others(5): Show | 12 | HG00673.hp1 HG01070.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2677+19delA | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 3/8 | chr18 | 47245478 | ||||||
chr18:47245598
|
C | G | 3 | a0001c0006t0003g0155a0001c0006t0003g0156a0001c0006t0003g0157 | 3 | HG01361.hp1 HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2614-37G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245598 | ||||||
chr18:47245883
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2614-322G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245883 | ||||||
chr18:47245956
|
C | T | 2 | a0008c0009t0002g0150a0008c0009t0002g0151 | 2 | NA18974.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2614-395G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245956 | ||||||
chr18:47245997
|
T | TGGAG | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2614-437_2614-436i others(6): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47245997 | ||||||
chr18:47246000
|
T | TGA | 78 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0114others(75): Show | 101 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.2614-440_2614-439i others(4): Show |
SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246000 | ||||||
chr18:47246236
|
A | C | 1 | a0002c0002t0002g0161 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2613+335T>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246236 | ||||||
chr18:47246238
|
T | C | 30 | a0001c0001t0001g0125a0001c0001t0002g0013a0001c0001t0002g0031others(27): Show | 33 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.2613+333A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246238 | ||||||
chr18:47246253
|
G | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02451.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2613+318C>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246253 | ||||||
chr18:47246284
|
C | G | 2 | a0001c0001t0001g0054a0001c0001t0002g0145 | 2 | NA18959.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2613+287G>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246284 | ||||||
chr18:47246449
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 5 | HG02922.hp1 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2613+122T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 2/8 | chr18 | 47246449 | ||||||
chr18:47249319
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG00673.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-47-89T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249319 | ||||||
chr18:47249526
|
G | A | 197 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0040others(194): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-47-296C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249526 | ||||||
chr18:47249666
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47-436C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249666 | ||||||
chr18:47249700
|
C | A | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-470G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249700 | ||||||
chr18:47249743
|
T | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-513A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249743 | ||||||
chr18:47249818
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 17 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-588T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249818 | ||||||
chr18:47249963
|
T | G | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-47-733A>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47249963 | ||||||
chr18:47250182
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 17 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47-952T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250182 | ||||||
chr18:47250511
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+863T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250511 | ||||||
chr18:47250705
|
G | A | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | HG03225.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-48+669C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250705 | ||||||
chr18:47250794
|
G | A | 2 | a0006c0010t0005g0267a0006c0010t0005g0268 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-48+580C>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250794 | ||||||
chr18:47250811
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-48+563A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250811 | ||||||
chr18:47250863
|
C | T | 5 | a0002c0002t0002g0023a0002c0002t0002g0142a0002c0002t0002g0143others(2): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+511G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250863 | ||||||
chr18:47250913
|
C | A | 8 | a0002c0002t0003g0004a0002c0002t0003g0269a0002c0002t0003g0270others(5): Show | 14 | HG00597.hp1 NA18612.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+461G>T | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250913 | ||||||
chr18:47250934
|
A | G | 4 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0038others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+440T>C | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250934 | ||||||
chr18:47250984
|
G | T | 5 | a0001c0003t0001g0007a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG02451.hp1 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+390C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47250984 | ||||||
chr18:47251109
|
G | T | 1 | a0001c0001t0002g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-48+265C>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251109 | ||||||
chr18:47251161
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-48+213A>G | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251161 | ||||||
chr18:47251186
|
A | T | 1 | a0002c0012t0003g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-48+188T>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251186 | ||||||
chr18:47251241
|
C | T | 1 | a0002c0002t0002g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-48+133G>A | SKOR2 | ENSG00000215474.8 | transcript | ENST00000425639.3 | protein_coding | 1/8 | chr18 | 47251241 |