Item | Value |
---|---|
geneid | 51512 |
ensemblid | ENSG00000075218.19 |
hgncid | 13698 |
symbol | GTSE1 |
name | G2 and S-phase expressed 1 |
refseq_nuc | NM_016426.7 |
refseq_prot | NP_057510.5 |
ensembl_nuc | ENST00000454366.2 |
ensembl_prot | ENSP00000415430.1 |
mane_status | MANE Select |
chr | chr22 |
start | 46296870 |
end | 46330810 |
strand | + |
ver | v1.2 |
region | chr22:46296870-46330810 |
region5000 | chr22:46291870-46335810 |
regionname0 | GTSE1_chr22_46296870_46330810 |
regionname5000 | GTSE1_chr22_46291870_46335810 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 739 | 118 | 30 | 31 | 38 | 1 | 17 | 24 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0002 | 0/0 | 739 | 28 | 21 | 3 | 0 | 2 | 2 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0003 | 0/0 | 739 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0004 | 0/0 | 739 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0005 | 0/0 | 739 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0006 | 0/0 | 739 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0007 | 1/0 | 739 | 5 | 1 | 2 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0008 | 0/0 | 739 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0009 | 0/0 | 739 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0010 | 0/0 | 739 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0011 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0012 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0013 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0014 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0015 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0016 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0017 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0018 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0019 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2220 | 107 | 22 | 29 | 37 | 1 | 17 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0002 | 0/0 | 2220 | 16 | 16 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0003 | 0/0 | 2220 | 13 | 12 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0004 | 0/0 | 2220 | 8 | 1 | 3 | 0 | 2 | 2 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0005 | 0/0 | 2220 | 7 | 6 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0006 | 0/0 | 2220 | 6 | 4 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0007 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0008 | 1/0 | 2220 | 5 | 1 | 2 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0009 | 0/0 | 2220 | 5 | 5 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0010 | 0/0 | 2220 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0011 | 0/0 | 2220 | 3 | 1 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0012 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0013 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0014 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0015 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0016 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0017 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0018 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0019 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0020 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0021 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0022 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0023 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0024 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0025 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0026 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0027 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
c0028 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 764 | 198 | 90 | 39 | 41 | 4 | 22 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
t0002 | 0/0 | 764 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
t0003 | 0/0 | 764 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 20 | 3 | 7 | 5 | 0 | 5 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0010 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2220 | 107 | 22 | 29 | 37 | 1 | 17 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0001c0009 | 0/0 | 2220 | 5 | 5 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0001c0011 | 0/0 | 2220 | 3 | 1 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0001c0017 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0001c0020 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0001c0025 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0002c0002 | 0/0 | 2220 | 16 | 16 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0002c0004 | 0/0 | 2220 | 8 | 1 | 3 | 0 | 2 | 2 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0002c0014 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0002c0026 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0002c0028 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0003c0003 | 0/0 | 2220 | 13 | 12 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0004c0005 | 0/0 | 2220 | 7 | 6 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0005c0007 | 0/0 | 2220 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0006c0006 | 0/0 | 2220 | 6 | 4 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0007c0008 | 1/0 | 2220 | 5 | 1 | 2 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0008c0010 | 0/0 | 2220 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0009c0012 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0010c0013 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0011c0016 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0012c0027 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0013c0024 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0014c0023 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0015c0018 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0016c0021 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0017c0019 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0018c0022 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 | |
a0019c0015 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2983 | 105 | 22 | 28 | 36 | 1 | 17 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0001t0002 | 0/0 | 2983 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0001t0003 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0009t0001 | 0/0 | 2983 | 5 | 5 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0011t0001 | 0/0 | 2983 | 3 | 1 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0017t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0020t0001 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0001c0025t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0002c0002t0001 | 0/0 | 2983 | 16 | 16 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0002c0004t0001 | 0/0 | 2983 | 8 | 1 | 3 | 0 | 2 | 2 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0002c0014t0001 | 0/0 | 2983 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0002c0026t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0002c0028t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0003c0003t0001 | 0/0 | 2983 | 13 | 12 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0004c0005t0001 | 0/0 | 2983 | 7 | 6 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0005c0007t0001 | 0/0 | 2983 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0006c0006t0001 | 0/0 | 2983 | 6 | 4 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0007c0008t0001 | 1/0 | 2983 | 5 | 1 | 2 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0008c0010t0001 | 0/0 | 2983 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0009c0012t0001 | 0/0 | 2983 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0010c0013t0001 | 0/0 | 2983 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0011c0016t0001 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0012c0027t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0013c0024t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0014c0023t0001 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0015c0018t0001 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0016c0021t0001 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0017c0019t0001 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0018c0022t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
a0019c0015t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | copy fasta | chr22 | 46291870 | 46335810 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 19 | 3 | 7 | 4 | 0 | 5 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0010 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0009t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0009t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0011t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0011t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0017t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0020t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0001c0025t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0014t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0014t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0026t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0002c0028t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0004c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0004c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0004c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0004c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0004c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0004c0005t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0005c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0005c0007t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0005c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0005c0007t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0005c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0005c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0006c0006t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0006c0006t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0006c0006t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0006c0006t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0006c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0007c0008t0001g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0007c0008t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0007c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0007c0008t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0007c0008t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0008c0010t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0008c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0009c0012t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0009c0012t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0010c0013t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0010c0013t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0011c0016t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0012c0027t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0013c0024t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0014c0023t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0015c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0016c0021t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0017c0019t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0018c0022t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
a0019c0015t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00639 | hp2 | a0001 | c0011 | t0001 | g0005 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00738 | hp2 | a0007 | c0008 | t0001 | g0126 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00741 | hp1 | a0007 | c0008 | t0001 | g0125 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01070 | hp1 | a0002 | c0004 | t0001 | g0041 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01106 | hp2 | a0002 | c0004 | t0001 | g0042 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01167 | hp1 | a0006 | c0006 | t0001 | g0148 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01169 | hp1 | a0006 | c0006 | t0001 | g0147 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01358 | hp1 | a0002 | c0004 | t0001 | g0043 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01433 | hp1 | a0004 | c0005 | t0001 | g0120 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01433 | hp2 | a0001 | c0011 | t0001 | g0005 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02145 | hp2 | a0006 | c0006 | t0001 | g0018 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02257 | hp1 | a0001 | c0009 | t0001 | g0055 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02257 | hp2 | a0007 | c0008 | t0001 | g0123 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02258 | hp1 | a0012 | c0027 | t0001 | g0028 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02258 | hp2 | a0001 | c0011 | t0001 | g0029 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02572 | hp1 | a0001 | c0009 | t0001 | g0054 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02622 | hp2 | a0002 | c0028 | t0001 | g0036 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02647 | hp2 | a0008 | c0010 | t0001 | g0006 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02683 | hp1 | a0002 | c0004 | t0001 | g0040 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02723 | hp1 | a0004 | c0005 | t0001 | g0011 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02723 | hp2 | a0001 | c0009 | t0001 | g0053 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02738 | hp1 | a0011 | c0016 | t0001 | g0020 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02809 | hp1 | a0002 | c0014 | t0001 | g0132 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02809 | hp2 | a0005 | c0007 | t0001 | g0023 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02818 | hp1 | a0005 | c0007 | t0001 | g0027 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0145 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02895 | hp1 | a0005 | c0007 | t0001 | g0026 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02896 | hp1 | a0001 | c0017 | t0001 | g0100 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02922 | hp2 | a0010 | c0013 | t0001 | g0113 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02965 | hp1 | a0006 | c0006 | t0001 | g0018 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02965 | hp2 | a0019 | c0015 | t0001 | g0119 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03098 | hp1 | a0004 | c0005 | t0001 | g0011 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03098 | hp2 | a0008 | c0010 | t0001 | g0006 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03130 | hp1 | a0008 | c0010 | t0001 | g0037 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03130 | hp2 | a0005 | c0007 | t0001 | g0025 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03139 | hp1 | a0004 | c0005 | t0001 | g0128 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03139 | hp2 | a0010 | c0013 | t0001 | g0112 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03209 | hp1 | a0006 | c0006 | t0001 | g0149 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03225 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03453 | hp2 | a0008 | c0010 | t0001 | g0006 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03486 | hp1 | a0004 | c0005 | t0001 | g0121 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03516 | hp2 | a0003 | c0003 | t0001 | g0144 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03540 | hp1 | a0004 | c0005 | t0001 | g0143 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03540 | hp2 | a0002 | c0014 | t0001 | g0115 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0146 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG04184 | hp2 | a0014 | c0023 | t0001 | g0067 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG04204 | hp2 | a0016 | c0021 | t0001 | g0005 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18522 | hp1 | a0001 | c0025 | t0001 | g0106 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18906 | hp1 | a0006 | c0006 | t0001 | g0150 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18952 | hp2 | a0001 | c0020 | t0001 | g0137 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18968 | hp2 | a0009 | c0012 | t0001 | g0134 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA18998 | hp2 | a0015 | c0018 | t0001 | g0001 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19002 | hp1 | a0009 | c0012 | t0001 | g0135 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19012 | hp2 | a0017 | c0019 | t0001 | g0062 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19030 | hp1 | a0002 | c0026 | t0001 | g0033 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19030 | hp2 | a0018 | c0022 | t0001 | g0002 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19043 | hp1 | a0005 | c0007 | t0001 | g0021 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20752 | hp2 | a0002 | c0004 | t0001 | g0045 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20805 | hp1 | a0002 | c0004 | t0001 | g0047 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20805 | hp2 | a0007 | c0008 | t0001 | g0122 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20905 | hp2 | a0002 | c0004 | t0001 | g0046 | SAS | GIH | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02486 | hp2 | a0005 | c0007 | t0001 | g0024 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02559 | hp1 | a0004 | c0005 | t0001 | g0129 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG02559 | hp2 | a0001 | c0009 | t0001 | g0009 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
HG06807 | hp2 | a0002 | c0004 | t0001 | g0044 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA20300 | hp2 | a0001 | c0009 | t0001 | g0009 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
NA21309 | hp2 | a0013 | c0024 | t0001 | g0059 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0010 | REF | REF | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
homoSapiens_grch38 | hp1 | a0007 | c0008 | t0001 | g0068 | REF | REF | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46308680 | T | G | 1 | a0011 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.499T>G | p.Tyr167Asp | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 582/2983 | 499/2220 | 167/739 | chr22 | 46308680 | ||
chr22:46308713 | G | T | 1 | a0005 | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
missense_variant | MODERATE | c.532G>T | p.Val178Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 615/2983 | 532/2220 | 178/739 | chr22 | 46308713 | ||
chr22:46308779 | A | G | 6 | a0002a0005a0006others(3): Show | 46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
missense_variant | MODERATE | c.598A>G | p.Thr200Ala | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 681/2983 | 598/2220 | 200/739 | chr22 | 46308779 | ||
chr22:46308837 | C | T | 2 | a0004a0019 | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.656C>T | p.Ala219Val | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 739/2983 | 656/2220 | 219/739 | chr22 | 46308837 | ||
chr22:46312255 | G | A | 2 | a0004a0019 | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.877G>A | p.Ala293Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/12 | 960/2983 | 877/2220 | 293/739 | chr22 | 46312255 | ||
chr22:46313984 | G | A | 4 | a0002a0006a0008others(1): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
missense_variant | MODERATE | c.1022G>A | p.Ser341Asn | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/12 | 1105/2983 | 1022/2220 | 341/739 | chr22 | 46313984 | ||
chr22:46316251 | C | T | 1 | a0014 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1271C>T | p.Pro424Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1354/2983 | 1271/2220 | 424/739 | chr22 | 46316251 | ||
chr22:46316331 | C | T | 1 | a0012 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1351C>T | p.Arg451Trp | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1434/2983 | 1351/2220 | 451/739 | chr22 | 46316331 | ||
chr22:46316332 | G | A | 1 | a0015 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.1352G>A | p.Arg451Gln | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1435/2983 | 1352/2220 | 451/739 | chr22 | 46316332 | ||
chr22:46323203 | C | G | 5 | a0002a0010a0012others(2): Show | 33 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(30): Show |
missense_variant | MODERATE | c.1446C>G | p.Asp482Glu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/12 | 1529/2983 | 1446/2220 | 482/739 | chr22 | 46323203 | ||
chr22:46323244 | C | T | 1 | a0016 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1487C>T | p.Ser496Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/12 | 1570/2983 | 1487/2220 | 496/739 | chr22 | 46323244 | ||
chr22:46326500 | G | A | 2 | a0005a0006 | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.1570G>A | p.Ala524Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1653/2983 | 1570/2220 | 524/739 | chr22 | 46326500 | ||
chr22:46326503 | T | C | 18 | a0001a0002a0003others(15): Show | 195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
missense_variant | MODERATE | c.1573T>C | p.Trp525Arg | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1656/2983 | 1573/2220 | 525/739 | chr22 | 46326503 | ||
chr22:46326504 | G | A | 1 | a0009 | 2 | NA18968.hp2 NA19002.hp1 |
stop_gained | HIGH | c.1574G>A | p.Trp525* | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1657/2983 | 1574/2220 | 525/739 | chr22 | 46326504 | ||
chr22:46328753 | G | C | 1 | a0017 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1790G>C | p.Arg597Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/12 | 1873/2983 | 1790/2220 | 597/739 | chr22 | 46328753 | ||
chr22:46329391 | G | A | 3 | a0003a0013a0018 | 15 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
missense_variant | MODERATE | c.1960G>A | p.Ala654Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/12 | 2043/2983 | 1960/2220 | 654/739 | chr22 | 46329391 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46308166 | C | T | 1 | a0002c0028 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.96C>T | p.Ala32Ala | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 3/12 | 179/2983 | 96/2220 | 32/739 | chr22 | 46308166 | ||
chr22:46308346 | C | T | 9 | a0002c0002a0002c0004a0002c0014others(6): Show | 45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
synonymous_variant | LOW | c.165C>T | p.Phe55Phe | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 248/2983 | 165/2220 | 55/739 | chr22 | 46308346 | ||
chr22:46308493 | A | G | 1 | a0001c0025 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.312A>G | p.Glu104Glu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 395/2983 | 312/2220 | 104/739 | chr22 | 46308493 | ||
chr22:46308658 | G | A | 2 | a0004c0005a0019c0015 | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.477G>A | p.Thr159Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 560/2983 | 477/2220 | 159/739 | chr22 | 46308658 | ||
chr22:46308683 | C | T | 1 | a0001c0009 | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
synonymous_variant | LOW | c.502C>T | p.Leu168Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 585/2983 | 502/2220 | 168/739 | chr22 | 46308683 | ||
chr22:46308790 | G | A | 1 | a0002c0026 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.609G>A | p.Pro203Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 692/2983 | 609/2220 | 203/739 | chr22 | 46308790 | ||
chr22:46308793 | G | A | 1 | a0001c0017 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.612G>A | p.Gly204Gly | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 695/2983 | 612/2220 | 204/739 | chr22 | 46308793 | ||
chr22:46308874 | C | T | 1 | a0011c0016 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.693C>T | p.Pro231Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 776/2983 | 693/2220 | 231/739 | chr22 | 46308874 | ||
chr22:46316180 | C | T | 1 | a0002c0004 | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
synonymous_variant | LOW | c.1200C>T | p.Val400Val | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1283/2983 | 1200/2220 | 400/739 | chr22 | 46316180 | ||
chr22:46326529 | C | T | 4 | a0001c0009a0003c0003a0013c0024others(1): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
synonymous_variant | LOW | c.1599C>T | p.Pro533Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1682/2983 | 1599/2220 | 533/739 | chr22 | 46326529 | ||
chr22:46326634 | C | T | 3 | a0002c0004a0002c0014a0010c0013 | 12 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(9): Show |
synonymous_variant | LOW | c.1704C>T | p.Pro568Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1787/2983 | 1704/2220 | 568/739 | chr22 | 46326634 | ||
chr22:46328865 | G | C | 1 | a0001c0020 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.1902G>C | p.Pro634Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/12 | 1985/2983 | 1902/2220 | 634/739 | chr22 | 46328865 | ||
chr22:46329453 | T | C | 2 | a0001c0011a0016c0021 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
synonymous_variant | LOW | c.2022T>C | p.Asp674Asp | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/12 | 2105/2983 | 2022/2220 | 674/739 | chr22 | 46329453 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46330255 | C | T | 1 | a0001c0001t0003 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 12/12 | 125 | chr22 | 46330255 | |||||
chr22:46330324 | A | G | 1 | a0001c0001t0002 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 12/12 | 194 | chr22 | 46330324 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:46296988 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-22+57G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46296988 | ||||||
chr22:46297008 | G | A | 25 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(22): Show | 31 | HG00639.hp2 HG01433.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.-22+77G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297008 | ||||||
chr22:46297105 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-22+174C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297105 | ||||||
chr22:46297137 | C | G | 1 | a0001c0001t0002g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-22+206C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297137 | ||||||
chr22:46297163 | A | T | 25 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(22): Show | 33 | HG00639.hp2 HG01433.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.-21-217A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297163 | ||||||
chr22:46297181 | CG | C | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-196delG | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 46297181 | |||||
chr22:46297195 | G | A | 1 | a0002c0004t0001g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-21-185G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297195 | ||||||
chr22:46297260 | C | T | 12 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0031others(9): Show | 16 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-21-120C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297260 | ||||||
chr22:46297581 | T | G | 8 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(5): Show | 9 | HG02486.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+102T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297581 | ||||||
chr22:46297611 | T | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG00408.hp2 HG00423.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.79+132T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297611 | ||||||
chr22:46297669 | C | G | 6 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(3): Show | 9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+190C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297669 | ||||||
chr22:46297764 | G | A | 1 | a0005c0007t0001g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+285G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297764 | ||||||
chr22:46297854 | A | C | 4 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0030others(1): Show | 5 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+375A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297854 | ||||||
chr22:46297936 | C | T | 1 | a0012c0027t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+457C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297936 | ||||||
chr22:46297956 | T | TTTTATTT others(1): Show |
3 | a0003c0003t0001g0144a0003c0003t0001g0145a0003c0003t0001g0146 | 3 | HG02818.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79+496_79+503dupTA others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46297956 | |||||
chr22:46298128 | C | A | 8 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(5): Show | 9 | HG02486.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+649C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298128 | ||||||
chr22:46298153 | G | A | 4 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0030others(1): Show | 5 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+674G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298153 | ||||||
chr22:46298226 | G | T | 9 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(6): Show | 10 | HG02258.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+747G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298226 | ||||||
chr22:46298411 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.79+932G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298411 | ||||||
chr22:46298470 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.79+991G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298470 | ||||||
chr22:46298519 | G | T | 1 | a0004c0005t0001g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.79+1040G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298519 | ||||||
chr22:46298520 | C | A | 1 | a0004c0005t0001g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.79+1041C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298520 | ||||||
chr22:46298600 | G | A | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1121G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298600 | ||||||
chr22:46298892 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.79+1413C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298892 | ||||||
chr22:46298970 | T | G | 1 | a0001c0001t0001g0056 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.79+1491T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298970 | ||||||
chr22:46299129 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.79+1650A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299129 | ||||||
chr22:46299193 | T | C | 1 | a0012c0027t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+1714T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299193 | ||||||
chr22:46299271 | G | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 7 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1792G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299271 | ||||||
chr22:46299272 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.79+1793C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299272 | ||||||
chr22:46299287 | C | T | 2 | a0009c0012t0001g0134a0009c0012t0001g0135 | 2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.79+1808C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299287 | ||||||
chr22:46299288 | G | A | 2 | a0003c0003t0001g0144a0003c0003t0001g0145 | 2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.79+1809G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299288 | ||||||
chr22:46299353 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.79+1874C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299353 | ||||||
chr22:46299357 | C | T | 1 | a0002c0014t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+1878C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299357 | ||||||
chr22:46299392 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+1913C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299392 | ||||||
chr22:46299469 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.79+1990T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299469 | ||||||
chr22:46299556 | G | A | 3 | a0001c0011t0001g0029a0002c0002t0001g0007a0002c0002t0001g0022 | 4 | HG02258.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+2077G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299556 | ||||||
chr22:46299652 | G | A | 11 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0031others(8): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+2173G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299652 | ||||||
chr22:46299706 | C | T | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+2227C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299706 | ||||||
chr22:46299740 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.79+2261C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299740 | ||||||
chr22:46299786 | T | A | 1 | a0012c0027t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+2307T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299786 | ||||||
chr22:46299792 | T | G | 1 | a0001c0001t0001g0010 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+2313T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299792 | ||||||
chr22:46299862 | G | C | 2 | a0004c0005t0001g0011a0004c0005t0001g0143 | 3 | HG02723.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+2383G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299862 | ||||||
chr22:46299878 | C | T | 1 | a0004c0005t0001g0011 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+2399C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299878 | ||||||
chr22:46299941 | C | T | 6 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(3): Show | 9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+2462C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299941 | ||||||
chr22:46299942 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.79+2463G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299942 | ||||||
chr22:46299959 | A | AT | 33 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0127others(30): Show | 36 | HG00609.hp2 HG00735.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+2505dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46299959 | |||||
chr22:46299959 | AT | A | 15 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(12): Show | 17 | HG01257.hp2 HG02155.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+2505delT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46299959 | |||||
chr22:46300021 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.79+2542T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300021 | ||||||
chr22:46300427 | T | G | 1 | a0002c0014t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+2948T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300427 | ||||||
chr22:46300488 | C | G | 1 | a0006c0006t0001g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+3009C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300488 | ||||||
chr22:46300548 | C | T | 1 | a0008c0010t0001g0006 | 3 | HG02647.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79+3069C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300548 | ||||||
chr22:46300565 | T | A | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+3086T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300565 | ||||||
chr22:46300635 | T | C | 1 | a0014c0023t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.79+3156T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300635 | ||||||
chr22:46300733 | G | A | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+3254G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300733 | ||||||
chr22:46301005 | A | T | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+3526A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301005 | ||||||
chr22:46301073 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.79+3594C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301073 | ||||||
chr22:46301466 | A | C | 2 | a0004c0005t0001g0128a0004c0005t0001g0129 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79+3987A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301466 | ||||||
chr22:46301484 | A | AT | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(145): Show | 192 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.79+4006dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46301484 | |||||
chr22:46301486 | A | T | 6 | a0001c0001t0001g0069a0001c0011t0001g0029a0002c0002t0001g0007others(3): Show | 7 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4007A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301486 | ||||||
chr22:46301487 | C | A | 6 | a0001c0001t0001g0069a0001c0011t0001g0029a0002c0002t0001g0007others(3): Show | 7 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4008C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301487 | ||||||
chr22:46301487 | CTT | C | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+4024_79+4025del others(2): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46301487 | |||||
chr22:46301488 | T | C | 6 | a0001c0001t0001g0069a0001c0011t0001g0029a0002c0002t0001g0007others(3): Show | 7 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4009T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301488 | ||||||
chr22:46301557 | G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0070others(3): Show | 7 | HG00741.hp2 HG01257.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4078G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301557 | ||||||
chr22:46301576 | C | G | 5 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(2): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+4097C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301576 | ||||||
chr22:46301644 | G | C | 11 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+4165G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301644 | ||||||
chr22:46301847 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.79+4368G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301847 | ||||||
chr22:46301919 | G | A | 1 | a0005c0007t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79+4440G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301919 | ||||||
chr22:46301927 | C | G | 15 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(12): Show | 19 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+4448C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301927 | ||||||
chr22:46302001 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79+4522A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302001 | ||||||
chr22:46302006 | T | C | 10 | a0001c0011t0001g0005a0001c0011t0001g0029a0004c0005t0001g0011others(7): Show | 12 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+4527T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302006 | ||||||
chr22:46302026 | A | G | 28 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(25): Show | 35 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.79+4547A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302026 | ||||||
chr22:46302064 | G | T | 1 | a0003c0003t0001g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79+4585G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302064 | ||||||
chr22:46302121 | G | A | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4642G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302121 | ||||||
chr22:46302341 | A | AC | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4862_79+4863ins others(1): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302341 | ||||||
chr22:46302399 | T | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4920T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302399 | ||||||
chr22:46302428 | G | A | 10 | a0001c0011t0001g0005a0001c0011t0001g0029a0004c0005t0001g0011others(7): Show | 12 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+4949G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302428 | ||||||
chr22:46302493 | G | GCCT | 25 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0030others(22): Show | 29 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+5017_79+5019dup others(3): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46302493 | |||||
chr22:46302522 | T | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+5043T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302522 | ||||||
chr22:46302562 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.79+5083A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302562 | ||||||
chr22:46302664 | C | T | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+5185C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302664 | ||||||
chr22:46302765 | T | G | 2 | a0002c0004t0001g0040a0002c0004t0001g0041 | 2 | HG01070.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.79+5286T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302765 | ||||||
chr22:46302783 | C | T | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+5304C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302783 | ||||||
chr22:46302837 | T | C | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-5313T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302837 | ||||||
chr22:46302895 | C | CT | 31 | a0001c0001t0001g0065a0001c0001t0001g0140a0001c0011t0001g0005others(28): Show | 36 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-5237dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46302895 | |||||
chr22:46302911 | T | TC | 3 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024 | 3 | HG02486.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.80-5239_80-5238ins others(1): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302911 | ||||||
chr22:46302961 | G | A | 1 | a0017c0019t0001g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.80-5189G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302961 | ||||||
chr22:46302962 | T | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-5188T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302962 | ||||||
chr22:46303000 | T | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-5150T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303000 | ||||||
chr22:46303048 | T | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-5102T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303048 | ||||||
chr22:46303066 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.80-5084A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303066 | ||||||
chr22:46303067 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.80-5083T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303067 | ||||||
chr22:46303192 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.80-4958G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303192 | ||||||
chr22:46303195 | C | T | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-4955C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303195 | ||||||
chr22:46303240 | C | A | 2 | a0001c0011t0001g0005a0016c0021t0001g0005 | 3 | HG00639.hp2 HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.80-4910C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303240 | ||||||
chr22:46303291 | G | A | 1 | a0002c0004t0001g0041 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.80-4859G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303291 | ||||||
chr22:46303322 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-4828C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303322 | ||||||
chr22:46303364 | G | A | 1 | a0007c0008t0001g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.80-4786G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303364 | ||||||
chr22:46303422 | C | G | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-4728C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303422 | ||||||
chr22:46303596 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-4554C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303596 | ||||||
chr22:46303684 | T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA19063.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.80-4466T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303684 | ||||||
chr22:46303886 | G | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-4264G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303886 | ||||||
chr22:46303939 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.80-4211G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303939 | ||||||
chr22:46303960 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.80-4190C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303960 | ||||||
chr22:46304038 | T | C | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-4112T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304038 | ||||||
chr22:46304090 | C | T | 8 | a0002c0002t0001g0007a0002c0002t0001g0022a0006c0006t0001g0018others(5): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-4060C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304090 | ||||||
chr22:46304180 | C | A | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-3970C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304180 | ||||||
chr22:46304251 | T | A | 14 | a0002c0002t0001g0007a0002c0002t0001g0022a0005c0007t0001g0021others(11): Show | 18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-3899T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304251 | ||||||
chr22:46304312 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.80-3838G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304312 | ||||||
chr22:46304504 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-3646C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304504 | ||||||
chr22:46304845 | T | G | 55 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(52): Show | 67 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.80-3305T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304845 | ||||||
chr22:46304849 | C | T | 6 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(3): Show | 7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-3301C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304849 | ||||||
chr22:46305012 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-3138G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305012 | ||||||
chr22:46305040 | A | G | 1 | a0002c0014t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.80-3110A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305040 | ||||||
chr22:46305405 | C | G | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-2745C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305405 | ||||||
chr22:46305505 | A | G | 2 | a0002c0002t0001g0007a0002c0002t0001g0022 | 3 | HG02717.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-2645A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305505 | ||||||
chr22:46305644 | C | T | 5 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2506C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305644 | ||||||
chr22:46305694 | G | A | 5 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(2): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2456G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305694 | ||||||
chr22:46305780 | G | A | 10 | a0001c0011t0001g0005a0001c0011t0001g0029a0004c0005t0001g0011others(7): Show | 12 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-2370G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305780 | ||||||
chr22:46305899 | T | G | 1 | a0002c0002t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-2251T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305899 | ||||||
chr22:46306040 | C | T | 3 | a0001c0001t0001g0016a0010c0013t0001g0112a0010c0013t0001g0113 | 4 | HG02109.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-2110C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306040 | ||||||
chr22:46306040 | CT | C | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-2106delT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46306040 | |||||
chr22:46306094 | A | G | 37 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(34): Show | 45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-2056A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306094 | ||||||
chr22:46306323 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-1827A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306323 | ||||||
chr22:46306442 | A | T | 14 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0030others(11): Show | 20 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-1708A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306442 | ||||||
chr22:46306460 | C | T | 2 | a0005c0007t0001g0025a0005c0007t0001g0026 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.80-1690C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306460 | ||||||
chr22:46306552 | T | C | 38 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(35): Show | 46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.80-1598T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306552 | ||||||
chr22:46306629 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.80-1521C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306629 | ||||||
chr22:46306637 | C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02132.hp1 HG02145.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.80-1513C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306637 | ||||||
chr22:46306641 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.80-1509C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306641 | ||||||
chr22:46306657 | T | G | 3 | a0001c0001t0001g0010a0001c0011t0001g0005a0016c0021t0001g0005 | 5 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-1493T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306657 | ||||||
chr22:46306689 | C | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.80-1461C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306689 | ||||||
chr22:46307193 | C | T | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-957C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307193 | ||||||
chr22:46307314 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.80-836A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307314 | ||||||
chr22:46307480 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-670C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307480 | ||||||
chr22:46307511 | C | CT | 22 | a0002c0002t0001g0007a0002c0004t0001g0040a0002c0004t0001g0041others(19): Show | 24 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-629dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307511 | |||||
chr22:46307511 | C | CTT | 14 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0022others(11): Show | 20 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-630_80-629dupTT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307511 | |||||
chr22:46307606 | C | T | 1 | a0001c0025t0001g0106 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80-544C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307606 | ||||||
chr22:46307607 | G | A | 4 | a0001c0001t0001g0010a0001c0011t0001g0005a0001c0011t0001g0029others(1): Show | 6 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-543G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307607 | ||||||
chr22:46307608 | A | T | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-542A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307608 | ||||||
chr22:46307699 | C | T | 5 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-451C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307699 | ||||||
chr22:46307767 | T | C | 37 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(34): Show | 45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-383T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307767 | ||||||
chr22:46307792 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80-358C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307792 | ||||||
chr22:46307813 | TA | T | 14 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(11): Show | 15 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.80-323delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307813 | |||||
chr22:46307813 | TAA | T | 29 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(26): Show | 37 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(34): Show |
intron_variant | MODIFIER | c.80-324_80-323delAA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307813 | |||||
chr22:46307850 | G | A | 1 | a0002c0002t0001g0007 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-300G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307850 | ||||||
chr22:46307879 | C | T | 37 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(34): Show | 45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-271C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307879 | ||||||
chr22:46307963 | A | T | 38 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(35): Show | 46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.80-187A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307963 | ||||||
chr22:46308007 | A | C | 38 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(35): Show | 46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.80-143A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46308007 | ||||||
chr22:46308116 | G | A | 3 | a0003c0003t0001g0144a0003c0003t0001g0145a0003c0003t0001g0146 | 3 | HG02818.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80-34G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46308116 | ||||||
chr22:46308142 | C | T | 1 | a0002c0002t0001g0007 | 2 | HG02717.hp2 HG02886.hp2 |
splice_region_variant&intron_variant | LOW | c.80-8C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46308142 | ||||||
chr22:46308977 | C | G | 1 | a0002c0014t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.762+34C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46308977 | ||||||
chr22:46309019 | C | G | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.762+76C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309019 | ||||||
chr22:46309110 | G | T | 2 | a0001c0009t0001g0009a0001c0009t0001g0055 | 3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.762+167G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309110 | ||||||
chr22:46309127 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.762+184G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309127 | ||||||
chr22:46309237 | A | G | 2 | a0005c0007t0001g0025a0005c0007t0001g0026 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.762+294A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309237 | ||||||
chr22:46309253 | C | G | 1 | a0002c0014t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.762+310C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309253 | ||||||
chr22:46309254 | C | G | 1 | a0012c0027t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.762+311C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309254 | ||||||
chr22:46309429 | C | G | 29 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(26): Show | 37 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.762+486C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309429 | ||||||
chr22:46309506 | G | A | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.762+563G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309506 | ||||||
chr22:46309510 | C | T | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.762+567C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309510 | ||||||
chr22:46309523 | C | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.762+580C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309523 | ||||||
chr22:46309543 | G | A | 7 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.762+600G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309543 | ||||||
chr22:46309590 | C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG00408.hp2 HG00423.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.762+647C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309590 | ||||||
chr22:46309596 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.762+653G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309596 | ||||||
chr22:46309687 | A | G | 30 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(27): Show | 38 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.762+744A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309687 | ||||||
chr22:46309766 | G | A | 1 | a0002c0004t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.762+823G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309766 | ||||||
chr22:46309774 | C | T | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.762+831C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309774 | ||||||
chr22:46309848 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.762+905C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309848 | ||||||
chr22:46309897 | A | G | 12 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0031others(9): Show | 18 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.762+954A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309897 | ||||||
chr22:46309932 | G | A | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.762+989G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309932 | ||||||
chr22:46309934 | G | A | 1 | a0014c0023t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.762+991G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309934 | ||||||
chr22:46310092 | T | G | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1149T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310092 | ||||||
chr22:46310341 | C | G | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.762+1398C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310341 | ||||||
chr22:46310352 | C | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.762+1409C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310352 | ||||||
chr22:46310384 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.762+1441C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310384 | ||||||
chr22:46310412 | CA | C | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1476delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | 46310412 | |||||
chr22:46310700 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.763-1441G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310700 | ||||||
chr22:46310799 | G | A | 1 | a0009c0012t0001g0134 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.763-1342G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310799 | ||||||
chr22:46311062 | GT | G | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-1068delT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | 46311062 | |||||
chr22:46311069 | T | G | 2 | a0004c0005t0001g0128a0004c0005t0001g0129 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.763-1072T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311069 | ||||||
chr22:46311202 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.763-939C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311202 | ||||||
chr22:46311213 | G | A | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.763-928G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311213 | ||||||
chr22:46311222 | C | T | 6 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.763-919C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311222 | ||||||
chr22:46311276 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.763-865T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311276 | ||||||
chr22:46311290 | C | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-851C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311290 | ||||||
chr22:46311329 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.763-812C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311329 | ||||||
chr22:46311378 | G | A | 1 | a0002c0002t0001g0007 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.763-763G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311378 | ||||||
chr22:46311482 | A | G | 1 | a0002c0002t0001g0007 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.763-659A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311482 | ||||||
chr22:46311672 | C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 5 | HG00609.hp2 NA18964.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-469C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311672 | ||||||
chr22:46311942 | C | G | 1 | a0002c0002t0001g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.763-199C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311942 | ||||||
chr22:46312010 | G | A | 60 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(57): Show | 77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.763-131G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312010 | ||||||
chr22:46312027 | G | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-114G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312027 | ||||||
chr22:46312031 | G | A | 25 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(22): Show | 30 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.763-110G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312031 | ||||||
chr22:46312057 | A | G | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-84A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312057 | ||||||
chr22:46312410 | T | C | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+105T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46312410 | ||||||
chr22:46312638 | C | CA | 6 | a0001c0001t0001g0080a0002c0002t0001g0022a0002c0002t0001g0034others(3): Show | 6 | HG00639.hp1 HG01358.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+351dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46312638 | |||||
chr22:46312638 | C | CAA | 5 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(2): Show | 8 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+350_927+351dup others(2): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46312638 | |||||
chr22:46312638 | CA | C | 16 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0103others(13): Show | 23 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.927+351delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46312638 | |||||
chr22:46313166 | TA | T | 11 | a0001c0001t0001g0071a0001c0001t0001g0101a0002c0004t0001g0047others(8): Show | 17 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-704delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46313166 | |||||
chr22:46313258 | G | A | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-632G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313258 | ||||||
chr22:46313266 | C | A | 6 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(3): Show | 9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-624C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313266 | ||||||
chr22:46313373 | C | T | 6 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-517C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313373 | ||||||
chr22:46313404 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.928-486G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313404 | ||||||
chr22:46313504 | C | G | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-386C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313504 | ||||||
chr22:46313622 | C | T | 7 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(4): Show | 10 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-268C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313622 | ||||||
chr22:46313752 | C | T | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-138C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313752 | ||||||
chr22:46314025 | G | A | 1 | a0003c0003t0001g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1051+12G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314025 | ||||||
chr22:46314127 | G | A | 24 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(21): Show | 29 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.1051+114G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314127 | ||||||
chr22:46314144 | C | T | 2 | a0009c0012t0001g0134a0009c0012t0001g0135 | 2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1051+131C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314144 | ||||||
chr22:46314236 | C | T | 1 | a0008c0010t0001g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1051+223C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314236 | ||||||
chr22:46314237 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1051+224G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314237 | ||||||
chr22:46314257 | G | A | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1051+244G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314257 | ||||||
chr22:46314259 | A | G | 37 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(34): Show | 45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1051+246A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314259 | ||||||
chr22:46314535 | C | T | 1 | a0019c0015t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1051+522C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314535 | ||||||
chr22:46314613 | C | T | 3 | a0006c0006t0001g0147a0006c0006t0001g0148a0006c0006t0001g0150 | 3 | HG01167.hp1 HG01169.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1051+600C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314613 | ||||||
chr22:46314732 | C | T | 1 | a0001c0017t0001g0100 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1051+719C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314732 | ||||||
chr22:46314784 | G | A | 12 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0030others(9): Show | 16 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+771G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314784 | ||||||
chr22:46314796 | A | C | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1051+783A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314796 | ||||||
chr22:46314801 | G | A | 7 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1051+788G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314801 | ||||||
chr22:46314806 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1051+793G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314806 | ||||||
chr22:46314818 | A | G | 5 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0031others(2): Show | 9 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1051+805A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314818 | ||||||
chr22:46314825 | G | A | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1051+812G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314825 | ||||||
chr22:46314850 | C | CA | 17 | a0001c0001t0001g0019a0001c0009t0001g0053a0002c0002t0001g0004others(14): Show | 21 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1051+854dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46314850 | |||||
chr22:46314850 | C | CAA | 3 | a0006c0006t0001g0018a0008c0010t0001g0006a0012c0027t0001g0028 | 6 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+853_1051+854d others(4): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46314850 | |||||
chr22:46314850 | CA | C | 15 | a0001c0001t0001g0076a0001c0001t0001g0099a0001c0011t0001g0005others(12): Show | 22 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051+854delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46314850 | |||||
chr22:46314940 | G | C | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1051+927G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314940 | ||||||
chr22:46315065 | G | GT | 35 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0070others(32): Show | 43 | HG00408.hp1 HG00408.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1052-955dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46315065 | |||||
chr22:46315127 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1052-905T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315127 | ||||||
chr22:46315168 | C | T | 11 | a0002c0002t0001g0007a0002c0002t0001g0022a0002c0004t0001g0040others(8): Show | 12 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1052-864C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315168 | ||||||
chr22:46315279 | G | A | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052-753G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315279 | ||||||
chr22:46315299 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1052-733C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315299 | ||||||
chr22:46315426 | C | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(28): Show | 39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1052-606C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315426 | ||||||
chr22:46315439 | T | C | 47 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(44): Show | 57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.1052-593T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315439 | ||||||
chr22:46315472 | G | A | 16 | a0001c0011t0001g0005a0001c0011t0001g0029a0004c0005t0001g0011others(13): Show | 18 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1052-560G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315472 | ||||||
chr22:46315492 | G | GC | 51 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(48): Show | 62 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.1052-539dupC | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46315492 | |||||
chr22:46315532 | C | T | 6 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1052-500C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315532 | ||||||
chr22:46315550 | T | C | 7 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1052-482T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315550 | ||||||
chr22:46315826 | G | A | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052-206G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315826 | ||||||
chr22:46315894 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1052-138T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315894 | ||||||
chr22:46316023 | A | AC | 47 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(44): Show | 57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.1052-7dupC | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46316023 | |||||
chr22:46316435 | T | C | 1 | a0002c0014t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1432+23T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316435 | ||||||
chr22:46316538 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1432+126G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316538 | ||||||
chr22:46316562 | G | A | 4 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432+150G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316562 | ||||||
chr22:46316743 | T | G | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432+331T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316743 | ||||||
chr22:46316947 | T | C | 1 | a0002c0002t0001g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1432+535T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316947 | ||||||
chr22:46316963 | T | A | 1 | a0002c0002t0001g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1432+551T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316963 | ||||||
chr22:46317122 | C | T | 47 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(44): Show | 57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.1432+710C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317122 | ||||||
chr22:46317129 | T | A | 1 | a0001c0017t0001g0100 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1432+717T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317129 | ||||||
chr22:46317175 | C | A | 1 | a0004c0005t0001g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1432+763C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317175 | ||||||
chr22:46317218 | C | T | 2 | a0005c0007t0001g0025a0005c0007t0001g0026 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1432+806C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317218 | ||||||
chr22:46317459 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1432+1047A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317459 | ||||||
chr22:46317504 | C | T | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1432+1092C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317504 | ||||||
chr22:46317646 | G | T | 1 | a0001c0025t0001g0106 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1432+1234G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317646 | ||||||
chr22:46317734 | C | T | 41 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(38): Show | 48 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1432+1322C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317734 | ||||||
chr22:46317754 | A | G | 7 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432+1342A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317754 | ||||||
chr22:46317881 | C | T | 9 | a0001c0011t0001g0005a0001c0011t0001g0029a0005c0007t0001g0021others(6): Show | 10 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1432+1469C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317881 | ||||||
chr22:46318020 | G | A | 47 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0002t0001g0004others(44): Show | 57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.1432+1608G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318020 | ||||||
chr22:46318431 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1432+2019C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318431 | ||||||
chr22:46318432 | C | G | 5 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0031others(2): Show | 9 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1432+2020C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318432 | ||||||
chr22:46318516 | G | C | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1432+2104G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318516 | ||||||
chr22:46318625 | C | A | 6 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(3): Show | 7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432+2213C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318625 | ||||||
chr22:46318717 | G | A | 9 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(6): Show | 15 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1432+2305G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318717 | ||||||
chr22:46318767 | C | T | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432+2355C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318767 | ||||||
chr22:46318838 | A | G | 26 | a0002c0002t0001g0004a0002c0002t0001g0007a0002c0002t0001g0008others(23): Show | 33 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1432+2426A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318838 | ||||||
chr22:46318851 | C | T | 28 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(25): Show | 37 | HG00639.hp2 HG01243.hp1 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.1432+2439C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318851 | ||||||
chr22:46318855 | C | G | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1432+2443C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318855 | ||||||
chr22:46318919 | G | T | 5 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(2): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2507G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318919 | ||||||
chr22:46318920 | G | T | 5 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(2): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2508G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318920 | ||||||
chr22:46318921 | C | CTTCT | 5 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(2): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2509_1432+251 others(8): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318921 | ||||||
chr22:46318923 | G | GGT | 5 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(2): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2512_1432+251 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46318923 | |||||
chr22:46319002 | T | C | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1432+2590T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319002 | ||||||
chr22:46319016 | G | T | 29 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(26): Show | 38 | HG00639.hp2 HG01243.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.1432+2604G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319016 | ||||||
chr22:46319049 | C | T | 1 | a0012c0027t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1432+2637C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319049 | ||||||
chr22:46319172 | G | A | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432+2760G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319172 | ||||||
chr22:46319201 | C | T | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432+2789C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319201 | ||||||
chr22:46319207 | G | A | 1 | a0010c0013t0001g0112 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1432+2795G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319207 | ||||||
chr22:46319256 | G | C | 1 | a0002c0014t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1432+2844G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319256 | ||||||
chr22:46319310 | G | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG00408.hp2 HG00423.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1432+2898G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319310 | ||||||
chr22:46319408 | C | T | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432+2996C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319408 | ||||||
chr22:46319525 | G | A | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1432+3113G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319525 | ||||||
chr22:46319539 | C | T | 2 | a0009c0012t0001g0134a0009c0012t0001g0135 | 2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1432+3127C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319539 | ||||||
chr22:46319581 | GAGGCCAC others(2): Show |
G | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432+3174_1432+318 others(13): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46319581 | |||||
chr22:46319628 | G | C | 9 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0116others(6): Show | 15 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1432+3216G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319628 | ||||||
chr22:46319803 | T | C | 1 | a0002c0004t0001g0047 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1433-3387T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319803 | ||||||
chr22:46319971 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1433-3219C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319971 | ||||||
chr22:46319982 | C | CA | 9 | a0001c0001t0001g0052a0001c0001t0001g0114a0001c0011t0001g0005others(6): Show | 11 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1433-3194dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46319982 | |||||
chr22:46319982 | C | CAA | 12 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(9): Show | 19 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1433-3195_1433-319 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46319982 | |||||
chr22:46320057 | C | T | 3 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024 | 3 | HG02486.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1433-3133C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320057 | ||||||
chr22:46320139 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1433-3051A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320139 | ||||||
chr22:46320308 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1433-2882G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320308 | ||||||
chr22:46320372 | ATTCATCA others(34): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1433-2817_1433-277 others(45): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320372 | ||||||
chr22:46320425 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1433-2765C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320425 | ||||||
chr22:46320430 | G | A | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1433-2760G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320430 | ||||||
chr22:46320578 | C | T | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-2612C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320578 | ||||||
chr22:46320706 | T | C | 60 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(57): Show | 77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1433-2484T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320706 | ||||||
chr22:46320790 | G | A | 1 | a0002c0002t0001g0008 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1433-2400G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320790 | ||||||
chr22:46320800 | G | C | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-2390G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320800 | ||||||
chr22:46320963 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1433-2227G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320963 | ||||||
chr22:46321023 | A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0094 | 4 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-2167A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321023 | ||||||
chr22:46321093 | G | T | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1433-2097G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321093 | ||||||
chr22:46321306 | A | G | 1 | a0002c0004t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1433-1884A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321306 | ||||||
chr22:46321419 | G | C | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-1771G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321419 | ||||||
chr22:46321657 | C | T | 6 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-1533C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321657 | ||||||
chr22:46321658 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1433-1532G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321658 | ||||||
chr22:46321668 | T | G | 60 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(57): Show | 77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1433-1522T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321668 | ||||||
chr22:46321774 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1433-1416A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321774 | ||||||
chr22:46321848 | G | A | 1 | a0017c0019t0001g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1433-1342G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321848 | ||||||
chr22:46321909 | A | G | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-1281A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321909 | ||||||
chr22:46321928 | T | G | 54 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(51): Show | 69 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.1433-1262T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321928 | ||||||
chr22:46322052 | C | T | 1 | a0002c0026t0001g0033 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1433-1138C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322052 | ||||||
chr22:46322068 | TGTCTCAA others(1): Show |
T | 12 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(9): Show | 19 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1433-1121_1433-111 others(12): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322068 | ||||||
chr22:46322073 | C | CA | 31 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0051others(28): Show | 39 | HG00423.hp1 HG00735.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1433-1092dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | |||||
chr22:46322073 | C | CAA | 6 | a0001c0001t0001g0048a0001c0001t0001g0050a0002c0028t0001g0036others(3): Show | 6 | HG00408.hp2 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-1093_1433-109 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | |||||
chr22:46322073 | CA | C | 14 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0092others(11): Show | 15 | HG00639.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1433-1092delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | |||||
chr22:46322073 | CAA | C | 6 | a0002c0014t0001g0132a0005c0007t0001g0021a0005c0007t0001g0023others(3): Show | 6 | HG02486.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-1093_1433-109 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | |||||
chr22:46322073 | CAAA | C | 6 | a0001c0011t0001g0005a0001c0011t0001g0029a0002c0014t0001g0115others(3): Show | 7 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-1094_1433-109 others(7): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | |||||
chr22:46322076 | A | C | 1 | a0003c0003t0001g0116 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1433-1114A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322076 | ||||||
chr22:46322077 | A | C | 12 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(9): Show | 19 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1433-1113A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322077 | ||||||
chr22:46322276 | G | T | 1 | a0002c0002t0001g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1433-914G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322276 | ||||||
chr22:46322437 | C | T | 1 | a0002c0014t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1433-753C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322437 | ||||||
chr22:46322477 | T | C | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1433-713T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322477 | ||||||
chr22:46322520 | A | T | 60 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(57): Show | 77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1433-670A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322520 | ||||||
chr22:46322876 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1433-314C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322876 | ||||||
chr22:46322933 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1433-257C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322933 | ||||||
chr22:46322991 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1433-199C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322991 | ||||||
chr22:46323116 | C | T | 11 | a0001c0009t0001g0053a0001c0009t0001g0054a0001c0009t0001g0055others(8): Show | 11 | HG02257.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1433-74C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46323116 | ||||||
chr22:46323157 | T | C | 20 | a0001c0001t0001g0010a0001c0009t0001g0053a0001c0009t0001g0054others(17): Show | 25 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1433-33T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46323157 | ||||||
chr22:46323274 | T | C | 7 | a0002c0002t0001g0007a0004c0005t0001g0011a0004c0005t0001g0120others(4): Show | 9 | HG01433.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1505+12T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323274 | ||||||
chr22:46323280 | G | A | 6 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(3): Show | 7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1505+18G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323280 | ||||||
chr22:46323288 | T | C | 1 | a0019c0015t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1505+26T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323288 | ||||||
chr22:46323344 | T | G | 1 | a0011c0016t0001g0020 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1505+82T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323344 | ||||||
chr22:46323396 | G | A | 4 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1505+134G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323396 | ||||||
chr22:46323460 | C | T | 19 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(16): Show | 29 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1505+198C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323460 | ||||||
chr22:46323503 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1505+241C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323503 | ||||||
chr22:46323627 | T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA19063.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1505+365T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323627 | ||||||
chr22:46323648 | G | A | 16 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0022others(13): Show | 26 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1505+386G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323648 | ||||||
chr22:46323700 | C | A | 4 | a0001c0001t0001g0010a0001c0011t0001g0005a0001c0011t0001g0029others(1): Show | 6 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+438C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323700 | ||||||
chr22:46323780 | C | T | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1505+518C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323780 | ||||||
chr22:46323807 | C | T | 11 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1505+545C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323807 | ||||||
chr22:46323865 | A | AT | 6 | a0001c0001t0001g0010a0001c0011t0001g0005a0001c0011t0001g0029others(3): Show | 9 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1505+611dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr22 | 46323865 | |||||
chr22:46323893 | C | T | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1505+631C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323893 | ||||||
chr22:46324051 | C | T | 1 | a0002c0014t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1505+789C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324051 | ||||||
chr22:46324361 | TTTTTC | T | 3 | a0002c0002t0001g0007a0002c0002t0001g0030a0012c0027t0001g0028 | 4 | HG02258.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+1114_1505+111 others(9): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr22 | 46324361 | |||||
chr22:46324381 | T | C | 8 | a0002c0028t0001g0036a0005c0007t0001g0021a0005c0007t0001g0023others(5): Show | 8 | HG02486.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+1119T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324381 | ||||||
chr22:46324396 | C | T | 3 | a0002c0014t0001g0132a0010c0013t0001g0112a0010c0013t0001g0113 | 3 | HG02809.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1505+1134C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324396 | ||||||
chr22:46324456 | C | T | 1 | a0001c0009t0001g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1505+1194C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324456 | ||||||
chr22:46324513 | G | A | 6 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(3): Show | 7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1505+1251G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324513 | ||||||
chr22:46324524 | C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0152 | 2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1505+1262C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324524 | ||||||
chr22:46324525 | G | A | 1 | a0002c0014t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1505+1263G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324525 | ||||||
chr22:46324598 | G | A | 1 | a0002c0014t0001g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1505+1336G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324598 | ||||||
chr22:46324625 | G | T | 2 | a0010c0013t0001g0112a0010c0013t0001g0113 | 2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1505+1363G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324625 | ||||||
chr22:46324824 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1505+1562G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324824 | ||||||
chr22:46324889 | A | C | 7 | a0004c0005t0001g0011a0004c0005t0001g0120a0004c0005t0001g0121others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-1547A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324889 | ||||||
chr22:46324957 | C | A | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-1479C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324957 | ||||||
chr22:46325015 | C | T | 11 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1506-1421C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325015 | ||||||
chr22:46325024 | G | A | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-1412G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325024 | ||||||
chr22:46325191 | C | T | 62 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(59): Show | 79 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.1506-1245C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325191 | ||||||
chr22:46325326 | G | A | 63 | a0001c0001t0001g0133a0001c0009t0001g0009a0001c0009t0001g0053others(60): Show | 80 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.1506-1110G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325326 | ||||||
chr22:46325770 | G | A | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-666G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325770 | ||||||
chr22:46325997 | G | A | 3 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024 | 3 | HG02486.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1506-439G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325997 | ||||||
chr22:46326028 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1506-408C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326028 | ||||||
chr22:46326031 | A | G | 1 | a0019c0015t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1506-405A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326031 | ||||||
chr22:46326044 | C | T | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-392C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326044 | ||||||
chr22:46326178 | T | C | 3 | a0002c0004t0001g0042a0002c0004t0001g0044a0002c0004t0001g0047 | 3 | HG01106.hp2 HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1506-258T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326178 | ||||||
chr22:46326190 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1506-246T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326190 | ||||||
chr22:46326297 | G | A | 8 | a0002c0004t0001g0040a0002c0004t0001g0041a0002c0004t0001g0042others(5): Show | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-139G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326297 | ||||||
chr22:46326359 | A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0014others(83): Show | 110 | HG00408.hp2 HG00423.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1506-77A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326359 | ||||||
chr22:46326384 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1506-52C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326384 | ||||||
chr22:46326663 | C | T | 59 | a0001c0001t0001g0093a0001c0009t0001g0009a0001c0009t0001g0053others(56): Show | 75 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(72): Show |
intron_variant | MODIFIER | c.1724+9C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46326663 | ||||||
chr22:46326772 | AGTTT | A | 11 | a0005c0007t0001g0021a0005c0007t0001g0023a0005c0007t0001g0024others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1724+127_1724+130d others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 46326772 | |||||
chr22:46326861 | G | C | 60 | a0001c0001t0001g0010a0001c0001t0001g0093a0001c0009t0001g0009others(57): Show | 77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1724+207G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46326861 | ||||||
chr22:46327020 | T | C | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1724+366T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327020 | ||||||
chr22:46327096 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1724+442G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327096 | ||||||
chr22:46327126 | C | T | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1724+472C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327126 | ||||||
chr22:46327183 | C | T | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1724+529C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327183 | ||||||
chr22:46327277 | C | G | 1 | a0013c0024t0001g0059 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1724+623C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327277 | ||||||
chr22:46327373 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1724+719G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327373 | ||||||
chr22:46327476 | A | G | 64 | a0001c0001t0001g0010a0001c0001t0001g0093a0001c0009t0001g0009others(61): Show | 82 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(79): Show |
intron_variant | MODIFIER | c.1724+822A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327476 | ||||||
chr22:46327547 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1724+893C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327547 | ||||||
chr22:46327800 | G | C | 1 | a0019c0015t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1725-888G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327800 | ||||||
chr22:46328104 | G | A | 3 | a0001c0011t0001g0005a0001c0011t0001g0029a0016c0021t0001g0005 | 4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725-584G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328104 | ||||||
chr22:46328168 | C | T | 1 | a0007c0008t0001g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1725-520C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328168 | ||||||
chr22:46328263 | G | T | 13 | a0001c0001t0001g0093a0002c0002t0001g0004a0002c0002t0001g0008others(10): Show | 19 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1725-425G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328263 | ||||||
chr22:46328363 | A | G | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1725-325A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328363 | ||||||
chr22:46328661 | T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(147): Show | 195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1725-27T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328661 | ||||||
chr22:46328904 | C | T | 3 | a0003c0003t0001g0144a0003c0003t0001g0145a0003c0003t0001g0146 | 3 | HG02818.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1926+15C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46328904 | ||||||
chr22:46328941 | G | A | 13 | a0001c0009t0001g0009a0001c0009t0001g0053a0001c0009t0001g0054others(10): Show | 20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1926+52G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46328941 | ||||||
chr22:46328986 | C | T | 1 | a0005c0007t0001g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1926+97C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46328986 | ||||||
chr22:46329010 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1926+121G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329010 | ||||||
chr22:46329120 | C | T | 2 | a0004c0005t0001g0128a0004c0005t0001g0129 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1926+231C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329120 | ||||||
chr22:46329190 | G | A | 3 | a0002c0002t0001g0007a0002c0002t0001g0022a0002c0002t0001g0030 | 4 | HG02717.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1927-168G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329190 | ||||||
chr22:46329211 | A | G | 5 | a0006c0006t0001g0018a0006c0006t0001g0147a0006c0006t0001g0148others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927-147A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329211 | ||||||
chr22:46329766 | C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG01081.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2136+199C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/11 | chr22 | 46329766 | ||||||
chr22:46329793 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2136+226C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/11 | chr22 | 46329793 |