geneid | 222659 |
---|---|
ensemblid | ENSG00000179165.12 |
hgncid | 18312 |
symbol | PXT1 |
name | peroxisomal testis enriched protein 1 |
refseq_nuc | NM_152990.4 |
refseq_prot | NP_694535.2 |
ensembl_nuc | ENST00000454782.3 |
ensembl_prot | ENSP00000419944.1 |
mane_status | MANE Select |
chr | chr6 |
start | 36390551 |
end | 36442854 |
strand | - |
ver | v1.2 |
region | chr6:36390551-36442854 |
region5000 | chr6:36385551-36447854 |
regionname0 | PXT1_chr6_36390551_36442854 |
regionname5000 | PXT1_chr6_36385551_36447854 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 134 | 223 | 66 | 41 | 92 | 6 | 18 | 69 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0002 | 1/1 | 134 | 166 | 24 | 30 | 82 | 6 | 22 | 63 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0003 | 0/0 | 134 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 405 | 216 | 66 | 38 | 88 | 6 | 18 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
c0002 | 1/1 | 405 | 166 | 24 | 30 | 82 | 6 | 22 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
c0003 | 0/0 | 405 | 7 | 0 | 3 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
c0004 | 0/0 | 405 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1669 | 369 | 71 | 71 | 173 | 12 | 40 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0002 | 0/0 | 1669 | 6 | 6 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0003 | 0/0 | 1669 | 5 | 5 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0004 | 0/0 | 1669 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0005 | 0/0 | 1669 | 2 | 1 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0006 | 0/0 | 1669 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0007 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0008 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0009 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0010 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
t0011 | 0/0 | 1669 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 405 | 216 | 66 | 38 | 88 | 6 | 18 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0003 | 0/0 | 405 | 7 | 0 | 3 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0002c0002 | 1/1 | 405 | 166 | 24 | 30 | 82 | 6 | 22 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0003c0004 | 0/0 | 405 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2073 | 197 | 49 | 37 | 87 | 6 | 18 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0002 | 0/0 | 2073 | 4 | 4 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0003 | 0/0 | 2073 | 5 | 5 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0004 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0005 | 0/0 | 2073 | 2 | 1 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0006 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0007 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0008 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0009 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0010 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0001t0011 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0001c0003t0001 | 0/0 | 2073 | 7 | 0 | 3 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0002c0002t0001 | 1/1 | 2073 | 164 | 22 | 30 | 82 | 6 | 22 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0002c0002t0002 | 0/0 | 2073 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
a0003c0004t0001 | 0/0 | 2073 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | copy fasta | chr6 | 36385551 | 36447854 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0008g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0009g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0010g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0001t0011g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0002c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
a0003c0004t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0001 | g0289 | EUR | GBR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0238 | EUR | GBR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0232 | EUR | FIN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0229 | EUR | FIN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0292 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0303 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0306 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0307 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0281 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01261 | hp1 | a0003 | c0004 | t0001 | g0334 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0160 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0011 | EUR | IBS | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0282 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | CDX | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CDX | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | CDX | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0360 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0219 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0271 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0362 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0291 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0352 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0226 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0294 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0349 | AFR | ESN | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0364 | AFR | GWD | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0365 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0277 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0280 | SAS | STU | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0288 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0310 | SAS | STU | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0268 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0302 | SAS | STU | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0285 | SAS | STU | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | YRI | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | CHB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0304 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | LWK | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | LWK | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | LWK | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | ASW | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ASW | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0223 | EUR | TSI | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0218 | SAS | GIH | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ACB | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0363 | AFR | MSL | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | USA | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | USA | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | LWK | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0252 | REF | REF | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0154 | REF | REF | PXT1_chr6_36385551_36447854 | PXT1 | chr6 | 36385551 | 36447854 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36425944
|
G | C | 1 | a0003 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.139C>G | p.Gln47Glu | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/5 | 588/2073 | 139/405 | 47/134 | chr6 | 36425944 | ||
chr6:36426039
|
A | G | 2 | a0001a0003 | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
missense_variant | MODERATE | c.44T>C | p.Val15Ala | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/5 | 493/2073 | 44/405 | 15/134 | chr6 | 36426039 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36400499
|
C | T | 1 | a0001c0003 | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
synonymous_variant | LOW | c.255G>A | p.Gln85Gln | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/5 | 704/2073 | 255/405 | 85/134 | chr6 | 36400499 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36390728
|
G | A | 1 | a0001c0001t0005 | 2 | HG01361.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1042C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 5/5 | 1042 | chr6 | 36390728 | |||||
chr6:36390994
|
C | T | 1 | a0001c0001t0005 | 2 | HG01361.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*776G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 5/5 | 776 | chr6 | 36390994 | |||||
chr6:36391208
|
T | C | 1 | a0001c0001t0011 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*562A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 5/5 | 562 | chr6 | 36391208 | |||||
chr6:36391348
|
A | G | 1 | a0001c0001t0004 | 2 | HG03225.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*422T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 5/5 | 422 | chr6 | 36391348 | |||||
chr6:36391550
|
T | C | 3 | a0001c0001t0002a0001c0001t0009a0002c0002t0002 | 7 | HG02257.hp1 HG02486.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 5/5 | 220 | chr6 | 36391550 | |||||
chr6:36391615
|
C | T | 1 | a0001c0001t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 5/5 | 155 | chr6 | 36391615 | |||||
chr6:36438836
|
C | G | 2 | a0001c0001t0008a0001c0001t0009 | 2 | HG02886.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/5 | 12754 | chr6 | 36438836 | |||||
chr6:36442609
|
T | C | 2 | a0001c0001t0008a0001c0001t0009 | 2 | HG02886.hp1 HG03471.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-204A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/5 | chr6 | 36442609 | ||||||
chr6:36442695
|
G | A | 2 | a0001c0001t0010a0001c0001t0011 | 2 | HG03540.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-290C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/5 | 16613 | chr6 | 36442695 | |||||
chr6:36442748
|
C | T | 1 | a0001c0001t0003 | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-343G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/5 | 16666 | chr6 | 36442748 | |||||
chr6:36442766
|
C | T | 1 | a0001c0001t0006 | 1 | NA18947.hp1 | 5_prime_UTR_variant | MODIFIER | c.-361G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/5 | 16684 | chr6 | 36442766 | |||||
chr6:36442771
|
T | A | 4 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(1): Show | 4 | HG02886.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-366A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/5 | chr6 | 36442771 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36391905
|
GT | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-32delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36391905 | ||||||
chr6:36391905
|
GTT | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(53): Show | 64 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.301-33_301-32delAA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36391905 | ||||||
chr6:36391918
|
TTTA | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(114): Show | 124 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.301-47_301-45delTA others(1): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36391918 | ||||||
chr6:36391919
|
TTA | T | 124 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0050others(121): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.301-47_301-46delTA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36391919 | ||||||
chr6:36391920
|
TA | T | 17 | a0001c0001t0001g0264a0001c0001t0002g0266a0001c0001t0002g0267others(14): Show | 18 | HG00738.hp2 HG01169.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.301-47delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36391920 | ||||||
chr6:36391931
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0125 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.301-57C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36391931 | ||||||
chr6:36392065
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-191G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392065 | ||||||
chr6:36392066
|
G | A | 1 | a0001c0001t0001g0004 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.301-192C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392066 | ||||||
chr6:36392102
|
C | T | 118 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(115): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.301-228G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392102 | ||||||
chr6:36392104
|
C | T | 142 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(139): Show | 150 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.301-230G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392104 | ||||||
chr6:36392144
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.301-270G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392144 | ||||||
chr6:36392348
|
G | A | 11 | a0001c0001t0001g0264a0001c0001t0005g0160a0001c0001t0008g0362others(8): Show | 11 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-474C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392348 | ||||||
chr6:36392431
|
G | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-557C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392431 | ||||||
chr6:36392452
|
T | G | 2 | a0002c0002t0001g0282a0002c0002t0001g0289 | 2 | HG00140.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.301-578A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392452 | ||||||
chr6:36392516
|
C | G | 5 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(2): Show | 5 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-642G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392516 | ||||||
chr6:36392543
|
C | T | 1 | a0002c0002t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.301-669G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392543 | ||||||
chr6:36392664
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.301-790T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392664 | ||||||
chr6:36392898
|
C | T | 1 | a0001c0001t0001g0361 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.301-1024G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392898 | ||||||
chr6:36392940
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.301-1066T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392940 | ||||||
chr6:36392962
|
C | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-1088G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36392962 | ||||||
chr6:36393103
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-1229G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393103 | ||||||
chr6:36393210
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(251): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.301-1336T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393210 | ||||||
chr6:36393234
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.301-1360C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393234 | ||||||
chr6:36393286
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.301-1412G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393286 | ||||||
chr6:36393341
|
C | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.301-1467G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393341 | ||||||
chr6:36393399
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0001g0077others(24): Show | 28 | HG00438.hp2 HG00609.hp2 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.301-1525G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393399 | ||||||
chr6:36393503
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.301-1629C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393503 | ||||||
chr6:36393621
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0035 | 2 | NA18964.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.301-1747G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393621 | ||||||
chr6:36393632
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-1758C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393632 | ||||||
chr6:36393663
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.301-1789C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393663 | ||||||
chr6:36393711
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.301-1837C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393711 | ||||||
chr6:36393725
|
C | CA | 126 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.301-1852dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393725 | ||||||
chr6:36393905
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-2031C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393905 | ||||||
chr6:36393905
|
G | C | 1 | a0002c0002t0001g0272 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.301-2031C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36393905 | ||||||
chr6:36394071
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301-2197C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394071 | ||||||
chr6:36394186
|
C | T | 1 | a0002c0002t0001g0222 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.301-2312G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394186 | ||||||
chr6:36394350
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0125 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.301-2476G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394350 | ||||||
chr6:36394502
|
C | T | 1 | a0001c0001t0011g0364 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.301-2628G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394502 | ||||||
chr6:36394551
|
G | A | 10 | a0002c0002t0001g0008a0002c0002t0001g0012a0002c0002t0001g0013others(7): Show | 13 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.301-2677C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394551 | ||||||
chr6:36394563
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.301-2689C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394563 | ||||||
chr6:36394585
|
G | A | 2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.301-2711C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394585 | ||||||
chr6:36394664
|
A | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-2790T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394664 | ||||||
chr6:36394710
|
C | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(251): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.301-2836G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394710 | ||||||
chr6:36394725
|
T | TA | 252 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(249): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.301-2852dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394725 | ||||||
chr6:36394801
|
A | AT | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-2928dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36394801 | ||||||
chr6:36395493
|
A | AT | 27 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0034others(24): Show | 28 | HG00738.hp2 HG01071.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.301-3620dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395493 | ||||||
chr6:36395493
|
A | ATT | 55 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0005g0160others(52): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.301-3621_301-3620d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395493 | ||||||
chr6:36395493
|
A | ATTT | 54 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0083others(51): Show | 54 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.301-3622_301-3620d others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395493 | ||||||
chr6:36395493
|
A | ATTTT | 17 | a0001c0001t0011g0364a0002c0002t0001g0165a0002c0002t0001g0169others(14): Show | 17 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(14): Show |
intron_variant | MODIFIER | c.301-3623_301-3620d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395493 | ||||||
chr6:36395493
|
AT | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.301-3620delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395493 | ||||||
chr6:36395493
|
ATT | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0063others(13): Show | 16 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.301-3621_301-3620d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395493 | ||||||
chr6:36395551
|
G | A | 10 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-3677C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395551 | ||||||
chr6:36395710
|
G | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-3836C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395710 | ||||||
chr6:36395737
|
C | T | 129 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(126): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.301-3863G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395737 | ||||||
chr6:36395752
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-3878G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395752 | ||||||
chr6:36395779
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-3905A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395779 | ||||||
chr6:36395779
|
T | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.301-3905A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395779 | ||||||
chr6:36395865
|
T | A | 1 | a0002c0002t0001g0360 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.301-3991A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395865 | ||||||
chr6:36395880
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.301-4006C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36395880 | ||||||
chr6:36396042
|
C | T | 141 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(138): Show | 149 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.301-4168G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396042 | ||||||
chr6:36396146
|
A | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(102): Show | 112 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.301-4272T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396146 | ||||||
chr6:36396181
|
C | T | 1 | a0001c0001t0002g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.300+4273G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396181 | ||||||
chr6:36396231
|
C | T | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+4223G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396231 | ||||||
chr6:36396388
|
C | T | 10 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+4066G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396388 | ||||||
chr6:36396526
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.300+3928C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396526 | ||||||
chr6:36396671
|
G | A | 129 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(126): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.300+3783C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396671 | ||||||
chr6:36396708
|
CTGAGGTC others(11): Show |
C | 1 | a0001c0001t0001g0330 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.300+3728_300+3745d others(20): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396708 | ||||||
chr6:36396718
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | HG02257.hp2 HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.300+3736A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396718 | ||||||
chr6:36396845
|
A | G | 1 | a0002c0002t0001g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.300+3609T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396845 | ||||||
chr6:36396930
|
G | A | 12 | a0002c0002t0001g0008a0002c0002t0001g0012a0002c0002t0001g0013others(9): Show | 15 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.300+3524C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396930 | ||||||
chr6:36396948
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+3506C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396948 | ||||||
chr6:36396988
|
C | T | 126 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+3466G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396988 | ||||||
chr6:36396990
|
C | G | 126 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+3464G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396990 | ||||||
chr6:36396991
|
C | CTG | 126 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+3462_300+3463i others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36396991 | ||||||
chr6:36397413
|
G | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.300+3041C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36397413 | ||||||
chr6:36397450
|
G | C | 1 | a0002c0002t0001g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.300+3004C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36397450 | ||||||
chr6:36397581
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2873C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36397581 | ||||||
chr6:36397790
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.300+2664T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36397790 | ||||||
chr6:36397959
|
G | A | 126 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+2495C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36397959 | ||||||
chr6:36398014
|
C | CA | 12 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0159others(9): Show | 12 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+2439dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398014 | ||||||
chr6:36398068
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(251): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.300+2386T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398068 | ||||||
chr6:36398129
|
G | A | 12 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(9): Show | 12 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+2325C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398129 | ||||||
chr6:36398346
|
T | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.300+2108A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398346 | ||||||
chr6:36398432
|
A | G | 2 | a0002c0002t0001g0271a0002c0002t0001g0295 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.300+2022T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398432 | ||||||
chr6:36398547
|
A | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+1907T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398547 | ||||||
chr6:36398572
|
A | T | 1 | a0001c0003t0001g0303 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.300+1882T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398572 | ||||||
chr6:36398777
|
A | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+1677T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36398777 | ||||||
chr6:36399113
|
C | CTTTAT | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 133 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.300+1336_300+1340d others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399113 | ||||||
chr6:36399113
|
C | CTTTATTT others(3): Show |
1 | a0001c0001t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300+1331_300+1340d others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399113 | ||||||
chr6:36399131
|
T | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.300+1323A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399131 | ||||||
chr6:36399131
|
T | TATTTC | 10 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+1318_300+1322d others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399131 | ||||||
chr6:36399131
|
TATTTCAT others(3): Show |
T | 35 | a0001c0001t0001g0096a0002c0002t0001g0011a0002c0002t0001g0151others(32): Show | 36 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.300+1313_300+1322d others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399131 | ||||||
chr6:36399146
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.300+1308G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399146 | ||||||
chr6:36399367
|
G | A | 1 | a0002c0002t0001g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.300+1087C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399367 | ||||||
chr6:36399443
|
G | C | 1 | a0001c0001t0001g0343 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.300+1011C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399443 | ||||||
chr6:36399739
|
G | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.300+715C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399739 | ||||||
chr6:36399806
|
C | T | 1 | a0002c0002t0002g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.300+648G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36399806 | ||||||
chr6:36400002
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0035 | 2 | NA18964.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.300+452T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400002 | ||||||
chr6:36400055
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.300+399G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400055 | ||||||
chr6:36400100
|
T | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+354A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400100 | ||||||
chr6:36400180
|
T | A | 1 | a0002c0002t0001g0314 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.300+274A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400180 | ||||||
chr6:36400252
|
C | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+202G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400252 | ||||||
chr6:36400358
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+96C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400358 | ||||||
chr6:36400392
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.300+62C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 4/4 | chr6 | 36400392 | ||||||
chr6:36400591
|
T | G | 2 | a0001c0001t0001g0353a0001c0001t0004g0352 | 2 | HG02886.hp2 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.170-7A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36400591 | ||||||
chr6:36400683
|
G | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-99C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36400683 | ||||||
chr6:36400735
|
G | A | 119 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(116): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.170-151C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36400735 | ||||||
chr6:36400769
|
A | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.170-185T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36400769 | ||||||
chr6:36400838
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-254G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36400838 | ||||||
chr6:36401292
|
C | T | 3 | a0002c0002t0001g0183a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | NA18967.hp2 NA18973.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.170-708G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401292 | ||||||
chr6:36401342
|
C | T | 2 | a0001c0001t0001g0353a0001c0001t0004g0352 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-758G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401342 | ||||||
chr6:36401397
|
G | T | 3 | a0001c0003t0001g0304a0001c0003t0001g0308a0001c0003t0001g0309 | 3 | NA18942.hp1 NA18957.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.170-813C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401397 | ||||||
chr6:36401413
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.170-829G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401413 | ||||||
chr6:36401473
|
A | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.170-889T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401473 | ||||||
chr6:36401483
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-899G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401483 | ||||||
chr6:36401560
|
G | A | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-976C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401560 | ||||||
chr6:36401615
|
CAA | C | 120 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(117): Show | 128 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.170-1033_170-1032d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401615 | ||||||
chr6:36401693
|
A | G | 12 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(9): Show | 12 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-1109T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401693 | ||||||
chr6:36401734
|
A | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-1150T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401734 | ||||||
chr6:36401894
|
G | GTA | 3 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0080 | 3 | NA18940.hp1 NA18963.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.170-1312_170-1311d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401894 | ||||||
chr6:36401895
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.170-1311A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401895 | ||||||
chr6:36401957
|
C | CAT | 12 | a0001c0001t0001g0063a0001c0001t0001g0316a0001c0001t0008g0362others(9): Show | 13 | HG02155.hp1 HG02451.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-1375_170-1374d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401957 | ||||||
chr6:36401957
|
CAT | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-1375_170-1374d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401957 | ||||||
chr6:36401998
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-1414T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36401998 | ||||||
chr6:36402009
|
G | C | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.170-1425C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402009 | ||||||
chr6:36402163
|
T | C | 1 | a0002c0002t0001g0242 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.170-1579A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402163 | ||||||
chr6:36402183
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-1599A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402183 | ||||||
chr6:36402477
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(241): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.170-1893A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402477 | ||||||
chr6:36402617
|
A | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-2033T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402617 | ||||||
chr6:36402851
|
C | T | 2 | a0001c0003t0001g0304a0001c0003t0001g0308 | 2 | NA18942.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.170-2267G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402851 | ||||||
chr6:36402891
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-2307G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402891 | ||||||
chr6:36402951
|
CT | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 132 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-2368delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402951 | ||||||
chr6:36402951
|
CTT | C | 114 | a0001c0001t0001g0082a0002c0002t0001g0002a0002c0002t0001g0008others(111): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-2369_170-2368d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402951 | ||||||
chr6:36402955
|
T | C | 10 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.170-2371A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36402955 | ||||||
chr6:36403069
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0138a0001c0001t0005g0160 | 3 | HG01361.hp2 NA18965.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.170-2485C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403069 | ||||||
chr6:36403419
|
T | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-2835A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403419 | ||||||
chr6:36403539
|
C | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-2955G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403539 | ||||||
chr6:36403652
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0071 | 2 | HG00423.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.170-3068A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403652 | ||||||
chr6:36403714
|
A | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-3130T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403714 | ||||||
chr6:36403883
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.170-3299T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403883 | ||||||
chr6:36403924
|
A | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-3340T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36403924 | ||||||
chr6:36404161
|
A | G | 5 | a0002c0002t0001g0193a0002c0002t0001g0220a0002c0002t0001g0225others(2): Show | 5 | NA18939.hp2 NA18951.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-3577T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404161 | ||||||
chr6:36404240
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.170-3656T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404240 | ||||||
chr6:36404283
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-3699G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404283 | ||||||
chr6:36404302
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.170-3718A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404302 | ||||||
chr6:36404424
|
T | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-3840A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404424 | ||||||
chr6:36404559
|
C | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | NA18956.hp2 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.170-3975G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404559 | ||||||
chr6:36404597
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-4013G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404597 | ||||||
chr6:36404603
|
T | A | 1 | a0002c0002t0001g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.170-4019A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404603 | ||||||
chr6:36404707
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0197a0001c0001t0002g0266others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-4123G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404707 | ||||||
chr6:36404748
|
A | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-4164T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404748 | ||||||
chr6:36404815
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.170-4231C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404815 | ||||||
chr6:36404830
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-4246G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404830 | ||||||
chr6:36404888
|
G | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-4304C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404888 | ||||||
chr6:36404927
|
A | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-4343T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404927 | ||||||
chr6:36404964
|
A | T | 2 | a0002c0002t0001g0173a0002c0002t0001g0312 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.170-4380T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404964 | ||||||
chr6:36404966
|
G | T | 1 | a0002c0002t0001g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.170-4382C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36404966 | ||||||
chr6:36405031
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.170-4447A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405031 | ||||||
chr6:36405377
|
G | GT | 10 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0152others(7): Show | 12 | HG00673.hp1 HG00741.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.170-4794dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405377 | ||||||
chr6:36405377
|
GT | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-4794delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405377 | ||||||
chr6:36405379
|
T | A | 1 | a0002c0002t0001g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.170-4795A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405379 | ||||||
chr6:36405390
|
T | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-4806A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405390 | ||||||
chr6:36405439
|
C | T | 2 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.170-4855G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405439 | ||||||
chr6:36405519
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.170-4935G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405519 | ||||||
chr6:36405621
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-5037A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405621 | ||||||
chr6:36405674
|
T | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-5090A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405674 | ||||||
chr6:36405770
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.170-5186A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405770 | ||||||
chr6:36405898
|
C | T | 54 | a0002c0002t0001g0150a0002c0002t0001g0162a0002c0002t0001g0163others(51): Show | 54 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.170-5314G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405898 | ||||||
chr6:36405909
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG01243.hp2 HG01258.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.170-5325C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405909 | ||||||
chr6:36405914
|
G | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-5330C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36405914 | ||||||
chr6:36406017
|
C | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-5433G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406017 | ||||||
chr6:36406145
|
A | T | 1 | a0002c0002t0001g0298 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.170-5561T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406145 | ||||||
chr6:36406320
|
C | G | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-5736G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406320 | ||||||
chr6:36406431
|
A | G | 2 | a0001c0001t0010g0365a0001c0001t0011g0364 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.170-5847T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406431 | ||||||
chr6:36406439
|
T | C | 4 | a0002c0002t0001g0011a0002c0002t0001g0206a0002c0002t0001g0223others(1): Show | 5 | HG00280.hp2 HG01192.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-5855A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406439 | ||||||
chr6:36406527
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-5943T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406527 | ||||||
chr6:36406639
|
C | G | 1 | a0002c0002t0001g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.170-6055G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406639 | ||||||
chr6:36406748
|
T | G | 122 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(119): Show | 130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.170-6164A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406748 | ||||||
chr6:36406756
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.170-6172C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406756 | ||||||
chr6:36406756
|
G | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-6172C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406756 | ||||||
chr6:36406807
|
T | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-6223A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406807 | ||||||
chr6:36406810
|
CA | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(226): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.170-6227delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406810 | ||||||
chr6:36406810
|
CAA | C | 6 | a0001c0001t0001g0139a0002c0002t0001g0226a0002c0002t0001g0227others(3): Show | 6 | HG01943.hp2 HG02451.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-6228_170-6227d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406810 | ||||||
chr6:36406845
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-6261G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36406845 | ||||||
chr6:36407004
|
T | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-6420A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407004 | ||||||
chr6:36407048
|
T | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0110others(5): Show | 8 | HG00438.hp2 HG02083.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-6464A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407048 | ||||||
chr6:36407176
|
T | C | 3 | a0002c0002t0001g0183a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | NA18967.hp2 NA18973.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.170-6592A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407176 | ||||||
chr6:36407316
|
A | G | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-6732T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407316 | ||||||
chr6:36407527
|
G | A | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.170-6943C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407527 | ||||||
chr6:36407552
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.170-6968C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407552 | ||||||
chr6:36407578
|
CT | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0152others(22): Show | 28 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.170-6995delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407578 | ||||||
chr6:36407578
|
CTT | C | 116 | a0002c0002t0001g0002a0002c0002t0001g0011a0002c0002t0001g0012others(113): Show | 123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.170-6996_170-6995d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407578 | ||||||
chr6:36407631
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.170-7047A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407631 | ||||||
chr6:36407661
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-7077C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407661 | ||||||
chr6:36407708
|
C | T | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022 | 3 | HG02622.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.170-7124G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407708 | ||||||
chr6:36407916
|
C | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-7332G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407916 | ||||||
chr6:36407957
|
C | CT | 21 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0034others(18): Show | 24 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.170-7374dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407957 | ||||||
chr6:36407957
|
CT | C | 129 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0050others(126): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.170-7374delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36407957 | ||||||
chr6:36408026
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | NA18956.hp2 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.170-7442T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408026 | ||||||
chr6:36408038
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-7454G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408038 | ||||||
chr6:36408136
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.170-7552T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408136 | ||||||
chr6:36408142
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.170-7558T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408142 | ||||||
chr6:36408146
|
G | T | 6 | a0002c0002t0001g0166a0002c0002t0001g0175a0002c0002t0001g0187others(3): Show | 6 | HG00673.hp1 NA18979.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-7562C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408146 | ||||||
chr6:36408209
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0095a0001c0001t0001g0113 | 3 | HG00741.hp2 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.170-7625C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408209 | ||||||
chr6:36408244
|
GA | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.170-7661delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408244 | ||||||
chr6:36408261
|
C | CT | 13 | a0001c0001t0001g0069a0001c0001t0001g0125a0001c0001t0001g0131others(10): Show | 14 | HG01257.hp1 HG01258.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-7678dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408261 | ||||||
chr6:36408261
|
CT | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0102others(10): Show | 13 | HG00438.hp2 HG01981.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-7678delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408261 | ||||||
chr6:36408343
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0070 | 2 | NA18946.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.170-7759T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408343 | ||||||
chr6:36408591
|
A | AT | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.170-8008dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408591 | ||||||
chr6:36408591
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0264 | 2 | NA19057.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.170-8007T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408591 | ||||||
chr6:36408592
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(52): Show | 61 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.170-8008A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408592 | ||||||
chr6:36408593
|
T | A | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | NA18946.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.170-8009A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408593 | ||||||
chr6:36408703
|
CAA | C | 22 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 22 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.170-8121_170-8120d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408703 | ||||||
chr6:36408703
|
CAAA | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 179 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.170-8122_170-8120d others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408703 | ||||||
chr6:36408703
|
CAAAA | C | 112 | a0001c0001t0001g0091a0001c0001t0001g0097a0001c0001t0001g0106others(109): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.170-8123_170-8120d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408703 | ||||||
chr6:36408703
|
CAAAAA | C | 8 | a0002c0002t0001g0193a0002c0002t0001g0220a0002c0002t0001g0225others(5): Show | 8 | HG00423.hp1 HG02155.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-8124_170-8120d others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408703 | ||||||
chr6:36408703
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0264a0001c0001t0008g0362a0001c0001t0009g0363 | 3 | HG02886.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.170-8129_170-8120d others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408703 | ||||||
chr6:36408752
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-8168C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408752 | ||||||
chr6:36408876
|
C | CA | 8 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 10 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-8293dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408876 | ||||||
chr6:36408876
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.170-8292G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36408876 | ||||||
chr6:36409111
|
G | A | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8527C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409111 | ||||||
chr6:36409112
|
A | G | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8528T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409112 | ||||||
chr6:36409113
|
T | A | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8529A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409113 | ||||||
chr6:36409114
|
T | C | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8530A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409114 | ||||||
chr6:36409115
|
T | C | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8531A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409115 | ||||||
chr6:36409116
|
T | C | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8532A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409116 | ||||||
chr6:36409117
|
G | C | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8533C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409117 | ||||||
chr6:36409119
|
T | A | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8535A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409119 | ||||||
chr6:36409120
|
C | G | 1 | a0002c0002t0001g0270 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.170-8536G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409120 | ||||||
chr6:36409215
|
T | A | 1 | a0002c0002t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.170-8631A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409215 | ||||||
chr6:36409365
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.170-8781G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409365 | ||||||
chr6:36409489
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-8905G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409489 | ||||||
chr6:36409655
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.170-9071C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409655 | ||||||
chr6:36409789
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-9205C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409789 | ||||||
chr6:36409824
|
T | TGGAA | 123 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(120): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.170-9244_170-9241d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409824 | ||||||
chr6:36409824
|
T | TGGAAGGA others(1): Show |
60 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0047others(57): Show | 61 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.170-9248_170-9241d others(10): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409824 | ||||||
chr6:36409824
|
T | TGGAAGGA others(5): Show |
68 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(65): Show | 72 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.170-9252_170-9241d others(14): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409824 | ||||||
chr6:36409824
|
T | TGGAAGGA others(9): Show |
40 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(37): Show | 43 | HG00140.hp1 HG00735.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.170-9256_170-9241d others(18): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409824 | ||||||
chr6:36409824
|
T | TGGAAGGA others(13): Show |
10 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0117others(7): Show | 10 | HG01952.hp1 HG02004.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-9260_170-9241d others(22): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409824 | ||||||
chr6:36409824
|
TGGAA | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0034a0001c0001t0004g0352 | 5 | HG02615.hp1 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-9244_170-9241d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409824 | ||||||
chr6:36409862
|
G | GAAGGAAG others(9): Show |
1 | a0001c0001t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.170-9279_170-9278i others(18): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409862 | ||||||
chr6:36409863
|
A | AAGGAAGG others(3): Show |
1 | a0001c0001t0001g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.170-9280_170-9279i others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409863 | ||||||
chr6:36409867
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0128 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.170-9283T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409867 | ||||||
chr6:36409881
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0128 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.170-9297C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409881 | ||||||
chr6:36409909
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-9325C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409909 | ||||||
chr6:36409915
|
G | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.170-9331C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409915 | ||||||
chr6:36409932
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-9348G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409932 | ||||||
chr6:36409939
|
A | AAGAAAGA others(3): Show |
135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 144 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.170-9365_170-9356d others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409939 | ||||||
chr6:36409965
|
G | GA | 300 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.170-9382dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409965 | ||||||
chr6:36409968
|
A | AAAAAG | 6 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0070others(3): Show | 6 | HG00544.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-9385_170-9384i others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409968 | ||||||
chr6:36409969
|
AAAG | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0111a0001c0001t0001g0152others(5): Show | 10 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.170-9388_170-9386d others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36409969 | ||||||
chr6:36410043
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.170-9459C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410043 | ||||||
chr6:36410144
|
G | GGA | 18 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0048others(15): Show | 18 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.170-9562_170-9561d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410144 | ||||||
chr6:36410144
|
G | GGAGAGA | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.170-9566_170-9561d others(8): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410144 | ||||||
chr6:36410253
|
C | T | 7 | a0001c0003t0001g0303a0001c0003t0001g0304a0001c0003t0001g0305others(4): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-9669G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410253 | ||||||
chr6:36410710
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(97): Show | 106 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.170-10126T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410710 | ||||||
chr6:36410820
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.170-10236G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410820 | ||||||
chr6:36410825
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0195a0002c0002t0001g0205 | 3 | HG02809.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.170-10241C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36410825 | ||||||
chr6:36411224
|
T | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-10640A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411224 | ||||||
chr6:36411280
|
G | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 120 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.170-10696C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411280 | ||||||
chr6:36411393
|
A | G | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.170-10809T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411393 | ||||||
chr6:36411493
|
G | A | 2 | a0001c0001t0001g0353a0001c0001t0004g0352 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-10909C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411493 | ||||||
chr6:36411809
|
C | T | 1 | a0002c0002t0001g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.170-11225G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411809 | ||||||
chr6:36411844
|
A | C | 1 | a0002c0002t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.170-11260T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411844 | ||||||
chr6:36411851
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 111 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.170-11267C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411851 | ||||||
chr6:36411911
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.170-11327C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411911 | ||||||
chr6:36411926
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.170-11342A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411926 | ||||||
chr6:36411929
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.170-11345A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36411929 | ||||||
chr6:36412074
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(241): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.170-11490T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412074 | ||||||
chr6:36412078
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(48): Show | 57 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.170-11494C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412078 | ||||||
chr6:36412147
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0121 | 2 | NA18971.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.170-11563A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412147 | ||||||
chr6:36412221
|
G | A | 2 | a0002c0002t0001g0235a0002c0002t0001g0236 | 2 | HG00423.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.170-11637C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412221 | ||||||
chr6:36412245
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.170-11661C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412245 | ||||||
chr6:36412448
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.170-11864A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412448 | ||||||
chr6:36412550
|
C | T | 1 | a0002c0002t0001g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-11966G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412550 | ||||||
chr6:36412592
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-12008C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412592 | ||||||
chr6:36412654
|
G | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(117): Show | 127 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.170-12070C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412654 | ||||||
chr6:36412658
|
C | CA | 152 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0046others(149): Show | 162 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.170-12075dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412658 | ||||||
chr6:36412658
|
C | CAA | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 113 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.170-12076_170-1207 others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412658 | ||||||
chr6:36412698
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.170-12114G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412698 | ||||||
chr6:36412719
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.170-12135G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412719 | ||||||
chr6:36412765
|
C | T | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-12181G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412765 | ||||||
chr6:36412771
|
G | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-12187C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412771 | ||||||
chr6:36412831
|
C | T | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-12247G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412831 | ||||||
chr6:36412867
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.170-12283G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412867 | ||||||
chr6:36412931
|
T | A | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.170-12347A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36412931 | ||||||
chr6:36413184
|
C | T | 117 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(114): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.170-12600G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413184 | ||||||
chr6:36413194
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.170-12610C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413194 | ||||||
chr6:36413404
|
G | A | 1 | a0002c0002t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.169+12510C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413404 | ||||||
chr6:36413424
|
ATAAG | A | 119 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(116): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.169+12486_169+1248 others(8): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413424 | ||||||
chr6:36413425
|
T | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 212 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.169+12489A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413425 | ||||||
chr6:36413491
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169+12423A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413491 | ||||||
chr6:36413647
|
T | G | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+12267A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413647 | ||||||
chr6:36413763
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | NA18940.hp1 NA18954.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+12151C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413763 | ||||||
chr6:36413928
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.169+11986G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413928 | ||||||
chr6:36413928
|
C | G | 243 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(240): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.169+11986G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413928 | ||||||
chr6:36413990
|
T | A | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169+11924A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36413990 | ||||||
chr6:36414014
|
A | T | 1 | a0002c0002t0001g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.169+11900T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414014 | ||||||
chr6:36414020
|
T | G | 7 | a0001c0003t0001g0303a0001c0003t0001g0304a0001c0003t0001g0305others(4): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+11894A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414020 | ||||||
chr6:36414030
|
G | A | 3 | a0002c0002t0001g0279a0002c0002t0001g0281a0002c0002t0001g0286 | 3 | HG01257.hp1 HG01258.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.169+11884C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414030 | ||||||
chr6:36414035
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+11879C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414035 | ||||||
chr6:36414088
|
C | T | 125 | a0001c0001t0001g0080a0001c0001t0008g0362a0001c0001t0009g0363others(122): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.169+11826G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414088 | ||||||
chr6:36414159
|
G | GA | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(241): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.169+11754dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414159 | ||||||
chr6:36414169
|
C | A | 1 | a0001c0001t0001g0004 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.169+11745G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414169 | ||||||
chr6:36414257
|
T | C | 2 | a0002c0002t0001g0015a0002c0002t0001g0275 | 3 | NA18983.hp1 NA19004.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.169+11657A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414257 | ||||||
chr6:36414267
|
A | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.169+11647T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414267 | ||||||
chr6:36414275
|
T | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+11639A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414275 | ||||||
chr6:36414609
|
A | G | 14 | a0001c0001t0001g0161a0001c0001t0001g0177a0001c0001t0001g0197others(11): Show | 14 | HG00642.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+11305T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414609 | ||||||
chr6:36414708
|
G | GA | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+11205dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414708 | ||||||
chr6:36414807
|
T | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+11107A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36414807 | ||||||
chr6:36415038
|
C | T | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+10876G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415038 | ||||||
chr6:36415046
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+10868C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415046 | ||||||
chr6:36415064
|
G | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169+10850C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415064 | ||||||
chr6:36415091
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.169+10823G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415091 | ||||||
chr6:36415280
|
T | C | 3 | a0002c0002t0001g0183a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | NA18967.hp2 NA18973.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.169+10634A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415280 | ||||||
chr6:36415300
|
A | C | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.169+10614T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415300 | ||||||
chr6:36415311
|
C | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169+10603G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415311 | ||||||
chr6:36415311
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169+10603G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415311 | ||||||
chr6:36415313
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.169+10601G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415313 | ||||||
chr6:36415415
|
G | C | 1 | a0002c0002t0001g0165 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.169+10499C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415415 | ||||||
chr6:36415432
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169+10482T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415432 | ||||||
chr6:36415470
|
A | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169+10444T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415470 | ||||||
chr6:36415551
|
A | T | 1 | a0002c0002t0001g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.169+10363T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415551 | ||||||
chr6:36415645
|
A | T | 1 | a0002c0002t0001g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.169+10269T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415645 | ||||||
chr6:36415947
|
T | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+9967A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36415947 | ||||||
chr6:36416051
|
G | T | 1 | a0002c0002t0001g0183 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.169+9863C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416051 | ||||||
chr6:36416085
|
A | G | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+9829T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416085 | ||||||
chr6:36416174
|
C | CA | 17 | a0002c0002t0001g0023a0002c0002t0001g0150a0002c0002t0001g0162others(14): Show | 17 | HG00408.hp2 HG02165.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.169+9739dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416174 | ||||||
chr6:36416180
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(333): Show |
intron_variant | MODIFIER | c.169+9734C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416180 | ||||||
chr6:36416185
|
G | A | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+9729C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416185 | ||||||
chr6:36416647
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.169+9267T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416647 | ||||||
chr6:36416696
|
C | T | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+9218G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416696 | ||||||
chr6:36416805
|
G | C | 1 | a0001c0001t0003g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+9109C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416805 | ||||||
chr6:36416813
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0264 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.169+9101A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416813 | ||||||
chr6:36416935
|
A | T | 1 | a0002c0002t0001g0151 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169+8979T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36416935 | ||||||
chr6:36417083
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.169+8831G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417083 | ||||||
chr6:36417093
|
C | A | 2 | a0002c0002t0001g0181a0002c0002t0001g0215 | 2 | HG00408.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.169+8821G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417093 | ||||||
chr6:36417095
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0112a0001c0001t0001g0136others(1): Show | 5 | HG02922.hp1 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+8819G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417095 | ||||||
chr6:36417215
|
C | T | 1 | a0002c0002t0001g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.169+8699G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417215 | ||||||
chr6:36417240
|
A | G | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+8674T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417240 | ||||||
chr6:36417304
|
G | A | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+8610C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417304 | ||||||
chr6:36417342
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+8572C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417342 | ||||||
chr6:36417348
|
AAAT | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+8563_169+8565d others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417348 | ||||||
chr6:36417447
|
G | A | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+8467C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417447 | ||||||
chr6:36417561
|
T | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+8353A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417561 | ||||||
chr6:36417591
|
C | CAA | 11 | a0001c0001t0001g0053a0001c0001t0008g0362a0001c0001t0009g0363others(8): Show | 12 | HG02451.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+8321_169+8322d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417591 | ||||||
chr6:36417591
|
C | CAAA | 104 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(101): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.169+8320_169+8322d others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417591 | ||||||
chr6:36417591
|
C | CAAAA | 10 | a0002c0002t0001g0086a0002c0002t0001g0172a0002c0002t0001g0173others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+8319_169+8322d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417591 | ||||||
chr6:36417591
|
CA | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 190 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.169+8322delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417591 | ||||||
chr6:36417640
|
C | T | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+8274G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417640 | ||||||
chr6:36417644
|
T | A | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+8270A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417644 | ||||||
chr6:36417662
|
G | A | 1 | a0002c0002t0001g0188 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.169+8252C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417662 | ||||||
chr6:36417767
|
C | CA | 22 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(19): Show | 22 | HG00140.hp2 HG01123.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.169+8146dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417767 | ||||||
chr6:36417767
|
CA | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0122a0001c0001t0001g0264others(8): Show | 11 | HG02723.hp2 HG02735.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+8146delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417767 | ||||||
chr6:36417943
|
T | A | 1 | a0002c0002t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+7971A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417943 | ||||||
chr6:36417967
|
C | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.169+7947G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417967 | ||||||
chr6:36417972
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.169+7942C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36417972 | ||||||
chr6:36418065
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+7849C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418065 | ||||||
chr6:36418158
|
T | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+7756A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418158 | ||||||
chr6:36418195
|
C | CA | 56 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0055others(53): Show | 62 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.169+7718dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418195 | ||||||
chr6:36418251
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.169+7663A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418251 | ||||||
chr6:36418287
|
C | G | 2 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | HG02647.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.169+7627G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418287 | ||||||
chr6:36418293
|
T | C | 6 | a0002c0002t0001g0192a0002c0002t0001g0240a0002c0002t0001g0271others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+7621A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418293 | ||||||
chr6:36418687
|
A | G | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+7227T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418687 | ||||||
chr6:36418715
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0337 | 2 | HG00673.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.169+7199G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418715 | ||||||
chr6:36418762
|
T | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0112a0001c0001t0002g0137 | 4 | HG02922.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+7152A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418762 | ||||||
chr6:36418764
|
G | T | 2 | a0002c0002t0001g0249a0002c0002t0001g0250 | 2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.169+7150C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418764 | ||||||
chr6:36418773
|
G | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+7141C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418773 | ||||||
chr6:36418851
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.169+7063A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418851 | ||||||
chr6:36418985
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.169+6929G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36418985 | ||||||
chr6:36419102
|
C | T | 1 | a0002c0002t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.169+6812G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419102 | ||||||
chr6:36419104
|
C | G | 1 | a0001c0001t0001g0342 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.169+6810G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419104 | ||||||
chr6:36419207
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.169+6707G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419207 | ||||||
chr6:36419480
|
G | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+6434C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419480 | ||||||
chr6:36419546
|
A | T | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0346others(1): Show | 4 | HG01257.hp2 HG01346.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+6368T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419546 | ||||||
chr6:36419803
|
T | C | 124 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.169+6111A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419803 | ||||||
chr6:36419832
|
C | A | 2 | a0002c0002t0001g0287a0002c0002t0001g0294 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.169+6082G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419832 | ||||||
chr6:36419916
|
A | G | 4 | a0001c0001t0001g0323a0001c0001t0001g0337a0001c0001t0001g0338others(1): Show | 4 | HG00673.hp2 NA18998.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5998T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36419916 | ||||||
chr6:36420228
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169+5686A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420228 | ||||||
chr6:36420242
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169+5672A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420242 | ||||||
chr6:36420322
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+5592G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420322 | ||||||
chr6:36420395
|
A | G | 4 | a0001c0001t0001g0348a0001c0001t0001g0358a0001c0001t0001g0359others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5519T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420395 | ||||||
chr6:36420454
|
A | C | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+5460T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420454 | ||||||
chr6:36420461
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.169+5453C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420461 | ||||||
chr6:36420564
|
G | C | 1 | a0002c0002t0001g0296 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.169+5350C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420564 | ||||||
chr6:36420577
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.169+5337C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420577 | ||||||
chr6:36420599
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.169+5315T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420599 | ||||||
chr6:36420659
|
T | TA | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169+5254_169+5255i others(3): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420659 | ||||||
chr6:36420685
|
C | A | 116 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(113): Show | 123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.169+5229G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420685 | ||||||
chr6:36420788
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.169+5126G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420788 | ||||||
chr6:36420820
|
A | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+5094T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420820 | ||||||
chr6:36420909
|
G | A | 114 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(111): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.169+5005C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420909 | ||||||
chr6:36420960
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.169+4954G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420960 | ||||||
chr6:36420988
|
G | A | 2 | a0001c0001t0001g0353a0001c0001t0004g0352 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.169+4926C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36420988 | ||||||
chr6:36421054
|
C | CAAA | 11 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(8): Show | 11 | HG00609.hp2 NA18942.hp2 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+4857_169+4859d others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421054 | ||||||
chr6:36421054
|
CA | C | 17 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0001g0319others(14): Show | 17 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+4859delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421054 | ||||||
chr6:36421169
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.169+4745T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421169 | ||||||
chr6:36421190
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.169+4724G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421190 | ||||||
chr6:36421294
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.169+4620A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421294 | ||||||
chr6:36421374
|
C | T | 116 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(113): Show | 123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.169+4540G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421374 | ||||||
chr6:36421423
|
T | A | 1 | a0001c0001t0001g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169+4491A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421423 | ||||||
chr6:36421424
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169+4490C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421424 | ||||||
chr6:36421425
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169+4489G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421425 | ||||||
chr6:36421448
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0095a0001c0001t0001g0113 | 3 | HG00741.hp2 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.169+4466T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421448 | ||||||
chr6:36421468
|
G | C | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169+4446C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421468 | ||||||
chr6:36421518
|
A | G | 1 | a0002c0002t0001g0255 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.169+4396T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421518 | ||||||
chr6:36421571
|
T | C | 14 | a0001c0001t0001g0161a0001c0001t0001g0177a0001c0001t0001g0197others(11): Show | 14 | HG00642.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+4343A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421571 | ||||||
chr6:36421600
|
T | C | 116 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(113): Show | 123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.169+4314A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421600 | ||||||
chr6:36421641
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169+4273A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421641 | ||||||
chr6:36421820
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+4094G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421820 | ||||||
chr6:36421860
|
C | T | 121 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0002others(118): Show | 129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.169+4054G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421860 | ||||||
chr6:36421975
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169+3939A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36421975 | ||||||
chr6:36422051
|
C | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+3863G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422051 | ||||||
chr6:36422069
|
G | A | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+3845C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422069 | ||||||
chr6:36422559
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.169+3355A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422559 | ||||||
chr6:36422592
|
T | C | 1 | a0001c0003t0001g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.169+3322A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422592 | ||||||
chr6:36422643
|
T | A | 1 | a0002c0002t0001g0246 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.169+3271A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422643 | ||||||
chr6:36422657
|
A | C | 119 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(116): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.169+3257T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422657 | ||||||
chr6:36422749
|
G | A | 1 | a0002c0002t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+3165C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422749 | ||||||
chr6:36422813
|
T | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+3101A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422813 | ||||||
chr6:36422912
|
T | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+3002A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36422912 | ||||||
chr6:36423027
|
C | CAG | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(95): Show | 104 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.169+2886_169+2887i others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423027 | ||||||
chr6:36423027
|
C | T | 2 | a0002c0002t0001g0282a0002c0002t0001g0289 | 2 | HG00140.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.169+2887G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423027 | ||||||
chr6:36423358
|
G | A | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+2556C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423358 | ||||||
chr6:36423459
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169+2455A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423459 | ||||||
chr6:36423483
|
G | A | 1 | a0002c0002t0001g0165 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.169+2431C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423483 | ||||||
chr6:36423551
|
C | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169+2363G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423551 | ||||||
chr6:36423551
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+2363G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423551 | ||||||
chr6:36423738
|
A | G | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169+2176T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423738 | ||||||
chr6:36423828
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.169+2086C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36423828 | ||||||
chr6:36424062
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.169+1852G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424062 | ||||||
chr6:36424113
|
A | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.169+1801T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424113 | ||||||
chr6:36424124
|
A | G | 10 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.169+1790T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424124 | ||||||
chr6:36424490
|
A | T | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+1424T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424490 | ||||||
chr6:36424556
|
C | A | 1 | a0001c0001t0010g0365 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169+1358G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424556 | ||||||
chr6:36424626
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(51): Show | 60 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.169+1288C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424626 | ||||||
chr6:36424979
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169+935G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36424979 | ||||||
chr6:36425389
|
G | A | 7 | a0002c0002t0001g0168a0002c0002t0001g0172a0002c0002t0001g0178others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+525C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425389 | ||||||
chr6:36425479
|
T | C | 3 | a0002c0002t0001g0183a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | NA18967.hp2 NA18973.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.169+435A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425479 | ||||||
chr6:36425632
|
T | A | 1 | a0001c0001t0001g0079 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.169+282A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425632 | ||||||
chr6:36425633
|
A | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.169+281T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425633 | ||||||
chr6:36425661
|
G | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169+253C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425661 | ||||||
chr6:36425774
|
C | T | 1 | a0001c0001t0007g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169+140G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425774 | ||||||
chr6:36425796
|
A | AAAACAAA others(3): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(48): Show | 57 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.169+117_169+118ins others(10): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425796 | ||||||
chr6:36425796
|
A | AAAACAAA others(11): Show |
1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.169+117_169+118ins others(18): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425796 | ||||||
chr6:36425796
|
A | AAAACAAA others(9): Show |
3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052 | 3 | HG01891.hp1 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.169+117_169+118ins others(16): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425796 | ||||||
chr6:36425800
|
C | CAAAAACA others(8): Show |
1 | a0001c0001t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.169+113_169+114ins others(15): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAAACA others(9): Show |
1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+113_169+114ins others(16): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAAACA others(11): Show |
1 | a0001c0001t0001g0005 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169+113_169+114ins others(18): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAAACA others(12): Show |
1 | a0001c0001t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169+113_169+114ins others(19): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAAACA others(13): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0155 | 2 | HG00741.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.169+113_169+114ins others(20): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAAACA others(12): Show |
1 | a0001c0001t0001g0156 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+113_169+114ins others(19): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAAACA others(13): Show |
1 | a0001c0001t0001g0157 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.169+113_169+114ins others(20): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAAACAA others(16): Show |
1 | a0001c0001t0008g0362 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.169+113_169+114ins others(23): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAACAAA others(6): Show |
1 | a0001c0001t0010g0365 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169+113_169+114ins others(13): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425800
|
C | CAAACAAA others(7): Show |
1 | a0001c0001t0011g0364 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+113_169+114ins others(14): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425800 | ||||||
chr6:36425802
|
A | AAAACAAA others(5): Show |
1 | a0001c0001t0001g0028 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.169+111_169+112ins others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425802 | ||||||
chr6:36425802
|
A | AACAAACA others(7): Show |
1 | a0001c0001t0001g0051 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.169+111_169+112ins others(14): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425802 | ||||||
chr6:36425803
|
A | AAACAAAC others(4): Show |
7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0032others(4): Show | 7 | HG01261.hp2 HG01516.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+110_169+111ins others(11): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425803 | ||||||
chr6:36425803
|
A | AACAAACA others(15): Show |
1 | a0001c0001t0009g0363 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.169+110_169+111ins others(22): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425803 | ||||||
chr6:36425804
|
A | AACAAACA others(3): Show |
13 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0029others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.169+109_169+110ins others(10): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425804 | ||||||
chr6:36425805
|
A | AAT | 9 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0217others(6): Show | 9 | HG00140.hp1 HG02148.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+107_169+108dup others(2): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425805 | ||||||
chr6:36425805
|
A | ACAAACAA others(11): Show |
5 | a0001c0003t0001g0303a0001c0003t0001g0304a0001c0003t0001g0305others(2): Show | 5 | HG00738.hp2 NA18942.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+108_169+109ins others(18): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425805 | ||||||
chr6:36425805
|
A | ACAAACAA others(13): Show |
2 | a0001c0003t0001g0306a0001c0003t0001g0307 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.169+108_169+109ins others(20): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425805 | ||||||
chr6:36425805
|
A | T | 2 | a0001c0001t0009g0363a0002c0002t0001g0288 | 2 | HG03471.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.169+109T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425805 | ||||||
chr6:36425805
|
AAT | A | 4 | a0002c0002t0001g0023a0002c0002t0001g0196a0002c0002t0001g0214others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+107_169+108del others(2): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425805 | ||||||
chr6:36425805
|
AATAT | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 121 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.169+105_169+108del others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425805 | ||||||
chr6:36425807
|
T | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(91): Show | 100 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.169+107A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425807 | ||||||
chr6:36425808
|
A | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.169+106T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425808 | ||||||
chr6:36425809
|
T | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(72): Show | 81 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.169+105A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425809 | ||||||
chr6:36425810
|
A | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.169+104T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425810 | ||||||
chr6:36425811
|
T | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(139): Show | 150 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.169+103A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425811 | ||||||
chr6:36425813
|
T | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(125): Show | 135 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.169+101A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425813 | ||||||
chr6:36425815
|
T | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(117): Show | 127 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.169+99A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425815 | ||||||
chr6:36425817
|
T | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.169+97A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 3/4 | chr6 | 36425817 | ||||||
chr6:36426125
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-9-34G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426125 | ||||||
chr6:36426214
|
A | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-123T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426214 | ||||||
chr6:36426257
|
C | T | 1 | a0001c0003t0001g0305 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9-166G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426257 | ||||||
chr6:36426258
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9-167C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426258 | ||||||
chr6:36426310
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-9-219C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426310 | ||||||
chr6:36426353
|
CGCTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-272_-9-263delAA others(8): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426353 | ||||||
chr6:36426355
|
C | CT | 46 | a0002c0002t0001g0150a0002c0002t0001g0162a0002c0002t0001g0164others(43): Show | 46 | HG00438.hp1 HG00597.hp1 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.-9-265dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
C | CTT | 16 | a0002c0002t0001g0174a0002c0002t0001g0182a0002c0002t0001g0183others(13): Show | 16 | HG01109.hp1 HG01255.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-266_-9-265dupAA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
CT | C | 15 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0013others(12): Show | 21 | HG01070.hp1 HG02273.hp1 HG02683.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9-265delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
CTTTTTTT others(4): Show |
C | 13 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0034others(10): Show | 13 | HG00544.hp1 HG01361.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-9-275_-9-265delAA others(9): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
CTTTTTTT others(5): Show |
C | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(114): Show | 125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-9-276_-9-265delAA others(10): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
CTTTTTTT others(6): Show |
C | 65 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(62): Show | 69 | HG00438.hp2 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-9-277_-9-265delAA others(11): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
CTTTTTTT others(7): Show |
C | 12 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0046others(9): Show | 13 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-278_-9-265delAA others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426355
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-279_-9-265delAA others(13): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426355 | ||||||
chr6:36426365
|
T | C | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-274A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426365 | ||||||
chr6:36426366
|
T | G | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-275A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426366 | ||||||
chr6:36426367
|
T | C | 1 | a0001c0001t0001g0005 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-276A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426367 | ||||||
chr6:36426392
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-9-301G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426392 | ||||||
chr6:36426394
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-303T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426394 | ||||||
chr6:36426519
|
C | T | 1 | a0001c0001t0008g0362 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9-428G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426519 | ||||||
chr6:36426528
|
G | A | 1 | a0001c0001t0007g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-437C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426528 | ||||||
chr6:36426540
|
T | C | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-449A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426540 | ||||||
chr6:36426559
|
A | C | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-468T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426559 | ||||||
chr6:36426574
|
C | T | 1 | a0002c0002t0001g0256 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-9-483G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426574 | ||||||
chr6:36426649
|
C | T | 2 | a0002c0002t0001g0297a0002c0002t0001g0298 | 2 | NA18965.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-9-558G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426649 | ||||||
chr6:36426802
|
A | C | 1 | a0002c0002t0001g0279 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-9-711T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426802 | ||||||
chr6:36426831
|
CAT | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 221 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.-9-742_-9-741delAT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36426831 | ||||||
chr6:36427015
|
C | CT | 11 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(8): Show | 11 | HG01255.hp1 HG01255.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-925dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427015 | ||||||
chr6:36427015
|
C | CTT | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(84): Show | 95 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-9-926_-9-925dupAA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427015 | ||||||
chr6:36427028
|
G | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(108): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-937C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427028 | ||||||
chr6:36427029
|
A | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(108): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-938T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427029 | ||||||
chr6:36427032
|
C | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(108): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-941G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427032 | ||||||
chr6:36427034
|
G | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(108): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-943C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427034 | ||||||
chr6:36427118
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9-1027A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427118 | ||||||
chr6:36427149
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-1058G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427149 | ||||||
chr6:36427301
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-9-1210C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427301 | ||||||
chr6:36427328
|
AT | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-1238delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427328 | ||||||
chr6:36427571
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-1480T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427571 | ||||||
chr6:36427603
|
ATATTT | A | 7 | a0001c0003t0001g0303a0001c0003t0001g0304a0001c0003t0001g0305others(4): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1517_-9-1513del others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427603 | ||||||
chr6:36427660
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-1569C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427660 | ||||||
chr6:36427670
|
TA | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1580delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427670 | ||||||
chr6:36427713
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1622C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427713 | ||||||
chr6:36427742
|
TGCACTTA others(2): Show |
T | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-1660_-9-1652del others(9): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427742 | ||||||
chr6:36427840
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0112a0001c0001t0001g0136others(1): Show | 5 | HG02922.hp1 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1749T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427840 | ||||||
chr6:36427891
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-1800C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427891 | ||||||
chr6:36427984
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(70): Show | 79 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9-1893C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427984 | ||||||
chr6:36427994
|
G | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-1903C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36427994 | ||||||
chr6:36428053
|
C | T | 18 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-1962G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428053 | ||||||
chr6:36428220
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-2129G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428220 | ||||||
chr6:36428259
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-9-2168G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428259 | ||||||
chr6:36428316
|
G | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0331a0001c0001t0001g0356 | 3 | HG00642.hp2 HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-2225C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428316 | ||||||
chr6:36428416
|
G | GAAAAAAA others(5): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-2326_-9-2325ins others(12): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428416 | ||||||
chr6:36428416
|
G | GAAAAAAA others(6): Show |
36 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(33): Show | 38 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-9-2326_-9-2325ins others(13): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428416 | ||||||
chr6:36428416
|
G | GAAAAAAA others(7): Show |
152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 165 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.-9-2326_-9-2325ins others(14): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428416 | ||||||
chr6:36428416
|
G | GAAAAAAA others(8): Show |
16 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(13): Show | 16 | HG00673.hp2 HG00735.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-2326_-9-2325ins others(15): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428416 | ||||||
chr6:36428416
|
G | GAAAAAAA others(9): Show |
1 | a0001c0001t0001g0133 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-9-2326_-9-2325ins others(16): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428416 | ||||||
chr6:36428432
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-9-2341T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428432 | ||||||
chr6:36428450
|
T | C | 1 | a0001c0001t0007g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-2359A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428450 | ||||||
chr6:36428746
|
CT | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 187 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.-9-2656delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428746 | ||||||
chr6:36428759
|
TG | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(13): Show | 18 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-2669delC | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428759 | ||||||
chr6:36428844
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-9-2753G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428844 | ||||||
chr6:36428861
|
G | T | 1 | a0002c0002t0001g0296 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-9-2770C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428861 | ||||||
chr6:36428862
|
T | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 230 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.-9-2771A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428862 | ||||||
chr6:36428990
|
A | G | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-2899T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36428990 | ||||||
chr6:36429126
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3035T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429126 | ||||||
chr6:36429131
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3040A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429131 | ||||||
chr6:36429132
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3041A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429132 | ||||||
chr6:36429163
|
A | T | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-3072T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429163 | ||||||
chr6:36429253
|
G | GAGAGTGA others(394): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0115 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(401): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(393): Show |
2 | a0002c0002t0001g0086a0002c0002t0001g0295 | 2 | HG02602.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(400): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(431): Show |
1 | a0001c0001t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(438): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(393): Show |
113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 122 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(400): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(392): Show |
2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(399): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(392): Show |
2 | a0002c0002t0001g0249a0002c0002t0001g0250 | 2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(399): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(392): Show |
1 | a0002c0002t0001g0251 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(399): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(392): Show |
146 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(143): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(399): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(430): Show |
1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(437): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(392): Show |
16 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(13): Show | 16 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(399): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(383): Show |
1 | a0002c0002t0001g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(390): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(391): Show |
1 | a0002c0002t0001g0255 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(398): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429253
|
G | GAGAGTGA others(383): Show |
1 | a0002c0002t0001g0269 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-9-3163_-9-3162ins others(390): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429253 | ||||||
chr6:36429271
|
C | CAAAAAAA others(394): Show |
20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-3181_-9-3180ins others(401): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429271 | ||||||
chr6:36429271
|
C | CAAAAAAA others(393): Show |
1 | a0002c0002t0001g0188 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-9-3181_-9-3180ins others(400): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429271 | ||||||
chr6:36429271
|
C | CAAAAAAA others(393): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(48): Show | 57 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.-9-3181_-9-3180ins others(400): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429271 | ||||||
chr6:36429271
|
C | CAAAAAAA others(394): Show |
1 | a0001c0001t0001g0319 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-9-3181_-9-3180ins others(401): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429271 | ||||||
chr6:36429272
|
A | AAAAAAAA others(392): Show |
2 | a0001c0001t0001g0119a0001c0001t0001g0155 | 2 | HG01070.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9-3182_-9-3181ins others(399): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429272 | ||||||
chr6:36429452
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3361C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429452 | ||||||
chr6:36429508
|
C | CT | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(108): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-3418dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429508 | ||||||
chr6:36429508
|
C | CTTT | 67 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(64): Show | 73 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-9-3420_-9-3418dup others(3): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429508 | ||||||
chr6:36429508
|
C | CTTTT | 20 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0155others(17): Show | 20 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-3421_-9-3418dup others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429508 | ||||||
chr6:36429508
|
C | CTTTTT | 7 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0050others(4): Show | 9 | HG01891.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-3422_-9-3418dup others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429508 | ||||||
chr6:36429591
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-3500G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429591 | ||||||
chr6:36429660
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 8 | HG00741.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-3569G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429660 | ||||||
chr6:36429697
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3606C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429697 | ||||||
chr6:36429715
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3624A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429715 | ||||||
chr6:36429756
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-3665G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429756 | ||||||
chr6:36429768
|
G | T | 1 | a0001c0001t0007g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-3677C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429768 | ||||||
chr6:36429785
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-9-3694C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429785 | ||||||
chr6:36429861
|
T | TC | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3771_-9-3770ins others(1): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429861 | ||||||
chr6:36429911
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(86): Show | 97 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-9-3820C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429911 | ||||||
chr6:36429979
|
G | T | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | NA18946.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-9-3888C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429979 | ||||||
chr6:36429998
|
G | C | 1 | a0002c0002t0002g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-9-3907C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36429998 | ||||||
chr6:36430009
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-3918C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430009 | ||||||
chr6:36430057
|
C | T | 1 | a0002c0002t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-9-3966G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430057 | ||||||
chr6:36430121
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-4030A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430121 | ||||||
chr6:36430162
|
G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-9-4071C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430162 | ||||||
chr6:36430219
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-9-4128T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430219 | ||||||
chr6:36430363
|
A | C | 1 | a0002c0002t0001g0188 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-9-4272T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430363 | ||||||
chr6:36430369
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.-9-4278G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430369 | ||||||
chr6:36430382
|
G | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-4291C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430382 | ||||||
chr6:36430452
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-4361A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430452 | ||||||
chr6:36430525
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-4434T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430525 | ||||||
chr6:36430580
|
C | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-4489G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430580 | ||||||
chr6:36430727
|
C | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-4636G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430727 | ||||||
chr6:36430748
|
C | T | 1 | a0002c0002t0001g0360 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9-4657G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430748 | ||||||
chr6:36430785
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 230 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.-9-4694C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430785 | ||||||
chr6:36430820
|
C | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.-9-4729G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430820 | ||||||
chr6:36430839
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 222 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.-9-4748C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430839 | ||||||
chr6:36430944
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 228 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.-9-4853C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36430944 | ||||||
chr6:36431089
|
T | C | 1 | a0002c0002t0001g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-4998A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431089 | ||||||
chr6:36431309
|
G | A | 155 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(152): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-5218C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431309 | ||||||
chr6:36431343
|
T | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(272): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.-9-5252A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431343 | ||||||
chr6:36431421
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-9-5330T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431421 | ||||||
chr6:36431462
|
G | A | 155 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0011others(152): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-9-5371C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431462 | ||||||
chr6:36431566
|
G | A | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-5475C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431566 | ||||||
chr6:36431567
|
G | A | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-5476C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431567 | ||||||
chr6:36431592
|
C | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5501G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431592 | ||||||
chr6:36431601
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5510A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431601 | ||||||
chr6:36431769
|
A | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5678T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431769 | ||||||
chr6:36431778
|
C | A | 5 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0023others(2): Show | 6 | HG02451.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5687G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431778 | ||||||
chr6:36431837
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-9-5746C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431837 | ||||||
chr6:36431896
|
G | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(360): Show | 386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.-9-5805C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431896 | ||||||
chr6:36431900
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5809C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36431900 | ||||||
chr6:36432050
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-5959G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432050 | ||||||
chr6:36432055
|
C | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5964G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432055 | ||||||
chr6:36432063
|
T | C | 4 | a0001c0001t0001g0348a0001c0001t0001g0358a0001c0001t0001g0359others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5972A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432063 | ||||||
chr6:36432105
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-6014C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432105 | ||||||
chr6:36432165
|
A | C | 2 | a0002c0002t0001g0166a0002c0002t0001g0187 | 2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-9-6074T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432165 | ||||||
chr6:36432225
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-6134C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432225 | ||||||
chr6:36432258
|
G | A | 10 | a0002c0002t0001g0008a0002c0002t0001g0012a0002c0002t0001g0013others(7): Show | 13 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6167C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432258 | ||||||
chr6:36432265
|
C | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-6174G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432265 | ||||||
chr6:36432390
|
A | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-6299T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432390 | ||||||
chr6:36432392
|
T | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-6301A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432392 | ||||||
chr6:36432418
|
A | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-6327T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432418 | ||||||
chr6:36432535
|
G | T | 1 | a0002c0002t0001g0276 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-10+6232C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432535 | ||||||
chr6:36432545
|
A | C | 5 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0023others(2): Show | 6 | HG02451.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+6222T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432545 | ||||||
chr6:36432684
|
A | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(95): Show | 104 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-10+6083T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432684 | ||||||
chr6:36432686
|
C | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+6081G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432686 | ||||||
chr6:36432696
|
A | G | 1 | a0002c0002t0001g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10+6071T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432696 | ||||||
chr6:36432765
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+6002A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432765 | ||||||
chr6:36432856
|
TGAAAA | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5906_-10+5910d others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36432856 | ||||||
chr6:36433157
|
CAG | C | 7 | a0002c0002t0001g0270a0002c0002t0001g0296a0002c0002t0001g0297others(4): Show | 7 | NA18747.hp2 NA18941.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+5608_-10+5609d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433157 | ||||||
chr6:36433167
|
AAGAATCA others(1): Show |
A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5592_-10+5599d others(10): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433167 | ||||||
chr6:36433410
|
T | C | 1 | a0001c0001t0001g0350 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-10+5357A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433410 | ||||||
chr6:36433418
|
GA | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5348delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433418 | ||||||
chr6:36433518
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5249G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433518 | ||||||
chr6:36433594
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5173A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433594 | ||||||
chr6:36433604
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0089others(17): Show | 21 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-10+5163C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433604 | ||||||
chr6:36433605
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+5162C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433605 | ||||||
chr6:36433637
|
A | G | 5 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0023others(2): Show | 6 | HG02451.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+5130T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433637 | ||||||
chr6:36433837
|
A | AAAAAAG | 153 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(150): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.-10+4929_-10+4930i others(8): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433837 | ||||||
chr6:36433837
|
A | AAAAAG | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 209 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.-10+4929_-10+4930i others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433837 | ||||||
chr6:36433837
|
A | AAAAG | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(5): Show | 9 | HG02132.hp2 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+4926_-10+4929d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433837 | ||||||
chr6:36433884
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4883G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433884 | ||||||
chr6:36433907
|
C | T | 1 | a0001c0003t0001g0305 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-10+4860G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433907 | ||||||
chr6:36433985
|
T | G | 1 | a0001c0001t0001g0351 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-10+4782A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36433985 | ||||||
chr6:36434166
|
TA | T | 4 | a0002c0002t0001g0023a0002c0002t0001g0196a0002c0002t0001g0360others(1): Show | 5 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+4600delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434166 | ||||||
chr6:36434334
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4433C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434334 | ||||||
chr6:36434450
|
TTA | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4315_-10+4316d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434450 | ||||||
chr6:36434527
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-10+4240T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434527 | ||||||
chr6:36434531
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-10+4236T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434531 | ||||||
chr6:36434548
|
T | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4219A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434548 | ||||||
chr6:36434657
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4110A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434657 | ||||||
chr6:36434658
|
C | T | 8 | a0002c0002t0001g0023a0002c0002t0001g0150a0002c0002t0001g0162others(5): Show | 9 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10+4109G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434658 | ||||||
chr6:36434811
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-10+3956G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36434811 | ||||||
chr6:36435071
|
T | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3696A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435071 | ||||||
chr6:36435126
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3641A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435126 | ||||||
chr6:36435128
|
T | G | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3639A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435128 | ||||||
chr6:36435157
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3610A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435157 | ||||||
chr6:36435189
|
C | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3578G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435189 | ||||||
chr6:36435208
|
G | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+3559C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435208 | ||||||
chr6:36435320
|
G | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+3447C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435320 | ||||||
chr6:36435392
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3375G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435392 | ||||||
chr6:36435399
|
AAT | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3366_-10+3367d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435399 | ||||||
chr6:36435401
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-10+3366A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435401 | ||||||
chr6:36435583
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-10+3184G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435583 | ||||||
chr6:36435601
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-10+3166C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435601 | ||||||
chr6:36435617
|
A | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 131 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-10+3150T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435617 | ||||||
chr6:36435634
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+3133C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435634 | ||||||
chr6:36435796
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2971G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435796 | ||||||
chr6:36435813
|
G | A | 2 | a0002c0002t0001g0174a0002c0002t0001g0254 | 2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-10+2954C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435813 | ||||||
chr6:36435845
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+2922G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36435845 | ||||||
chr6:36436092
|
T | A | 1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10+2675A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436092 | ||||||
chr6:36436096
|
TA | T | 4 | a0002c0002t0001g0023a0002c0002t0001g0194a0002c0002t0001g0360others(1): Show | 5 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2670delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436096 | ||||||
chr6:36436097
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(47): Show | 56 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-10+2670T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436097 | ||||||
chr6:36436098
|
A | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2669T>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436098 | ||||||
chr6:36436113
|
C | CA | 6 | a0001c0001t0001g0082a0001c0001t0001g0159a0001c0001t0001g0325others(3): Show | 6 | HG01943.hp1 HG02145.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+2653dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436113 | ||||||
chr6:36436113
|
CA | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(226): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-10+2653delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436113 | ||||||
chr6:36436113
|
CAA | C | 53 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 54 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+2652_-10+2653d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436113 | ||||||
chr6:36436203
|
C | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0360a0002c0002t0002g0006 | 4 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+2564G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436203 | ||||||
chr6:36436323
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2444C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436323 | ||||||
chr6:36436686
|
T | C | 10 | a0001c0001t0001g0159a0001c0001t0001g0264a0001c0001t0005g0160others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+2081A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436686 | ||||||
chr6:36436748
|
A | G | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-10+2019T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36436748 | ||||||
chr6:36437103
|
C | T | 7 | a0001c0003t0001g0303a0001c0003t0001g0304a0001c0003t0001g0305others(4): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+1664G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437103 | ||||||
chr6:36437148
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-10+1619C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437148 | ||||||
chr6:36437173
|
G | A | 156 | a0001c0001t0001g0177a0001c0001t0001g0197a0001c0001t0002g0266others(153): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-10+1594C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437173 | ||||||
chr6:36437265
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 5 | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1502G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437265 | ||||||
chr6:36437266
|
G | A | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+1501C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437266 | ||||||
chr6:36437272
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10+1495C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437272 | ||||||
chr6:36437287
|
AAAAC | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-10+1476_-10+1479d others(6): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437287 | ||||||
chr6:36437295
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10+1472G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437295 | ||||||
chr6:36437313
|
A | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(360): Show | 386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.-10+1454T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437313 | ||||||
chr6:36437341
|
T | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 19 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10+1426A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437341 | ||||||
chr6:36437389
|
A | G | 1 | a0002c0002t0001g0186 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-10+1378T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437389 | ||||||
chr6:36437454
|
A | C | 1 | a0002c0002t0001g0185 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10+1313T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437454 | ||||||
chr6:36437514
|
GT | G | 292 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(289): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-10+1252delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437514 | ||||||
chr6:36437552
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG00639.hp1 HG00735.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1215G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437552 | ||||||
chr6:36437575
|
G | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+1192C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437575 | ||||||
chr6:36437604
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-10+1163G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437604 | ||||||
chr6:36437717
|
C | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0264 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-10+1050G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437717 | ||||||
chr6:36437763
|
T | G | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+1004A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437763 | ||||||
chr6:36437778
|
T | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 226 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.-10+989A>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437778 | ||||||
chr6:36437820
|
C | CT | 16 | a0001c0001t0001g0049a0001c0001t0001g0153a0002c0002t0001g0162others(13): Show | 16 | HG00438.hp1 HG02027.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10+946dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437820 | ||||||
chr6:36437820
|
CT | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 160 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-10+946delA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437820 | ||||||
chr6:36437820
|
CTT | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0003g0018others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+945_-10+946del others(2): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437820 | ||||||
chr6:36437827
|
T | C | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-10+940A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36437827 | ||||||
chr6:36438084
|
T | C | 36 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0268others(33): Show | 38 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-10+683A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438084 | ||||||
chr6:36438099
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(47): Show | 56 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-10+668G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438099 | ||||||
chr6:36438526
|
C | T | 1 | a0001c0001t0001g0320 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-10+241G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438526 | ||||||
chr6:36438578
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01243.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-10+189T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438578 | ||||||
chr6:36438580
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01243.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-10+187C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438580 | ||||||
chr6:36438581
|
C | A | 1 | a0002c0002t0001g0302 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10+186G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438581 | ||||||
chr6:36438645
|
A | C | 4 | a0002c0002t0001g0162a0002c0002t0001g0163a0002c0002t0001g0164others(1): Show | 4 | NA18940.hp2 NA18974.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+122T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438645 | ||||||
chr6:36438665
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-10+102C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438665 | ||||||
chr6:36438755
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-10+12C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 2/4 | chr6 | 36438755 | ||||||
chr6:36438914
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-129-28C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36438914 | ||||||
chr6:36438927
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-129-41A>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36438927 | ||||||
chr6:36439008
|
C | CT | 49 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0084others(46): Show | 55 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-129-123dupA | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439008 | ||||||
chr6:36439075
|
T | C | 1 | a0001c0001t0001g0361 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-129-189A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439075 | ||||||
chr6:36439115
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-129-229G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439115 | ||||||
chr6:36439160
|
C | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-274G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439160 | ||||||
chr6:36439245
|
G | A | 8 | a0001c0001t0005g0160a0001c0003t0001g0303a0001c0003t0001g0304others(5): Show | 8 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129-359C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439245 | ||||||
chr6:36439279
|
T | C | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-129-393A>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439279 | ||||||
chr6:36439297
|
C | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 19 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.-129-411G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439297 | ||||||
chr6:36439323
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-129-437T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439323 | ||||||
chr6:36439350
|
G | T | 18 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-129-464C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439350 | ||||||
chr6:36439380
|
G | A | 1 | a0002c0002t0001g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-129-494C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439380 | ||||||
chr6:36439439
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-129-553G>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439439 | ||||||
chr6:36439481
|
C | T | 1 | a0002c0002t0001g0360 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-129-595G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439481 | ||||||
chr6:36439644
|
GA | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(232): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.-129-759delT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439644 | ||||||
chr6:36439644
|
GAA | G | 15 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0050others(12): Show | 16 | HG01361.hp2 HG01891.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-129-760_-129-759d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439644 | ||||||
chr6:36439662
|
AC | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-129-777delG | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439662 | ||||||
chr6:36439663
|
C | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG03540.hp1 NA19001.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129-777G>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36439663 | ||||||
chr6:36440136
|
A | AC | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 131 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-129-1251_-129-125 others(5): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440136 | ||||||
chr6:36440217
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 131 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.-129-1331C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440217 | ||||||
chr6:36440284
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-129-1398T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440284 | ||||||
chr6:36440293
|
G | A | 3 | a0001c0001t0001g0358a0001c0001t0001g0359a0002c0002t0001g0312 | 3 | HG02647.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-129-1407C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440293 | ||||||
chr6:36440308
|
C | T | 2 | a0001c0001t0008g0362a0001c0001t0009g0363 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-129-1422G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440308 | ||||||
chr6:36440337
|
G | A | 5 | a0001c0001t0008g0362a0001c0001t0009g0363a0002c0002t0001g0023others(2): Show | 6 | HG02451.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129-1451C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440337 | ||||||
chr6:36440429
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-129-1543C>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440429 | ||||||
chr6:36440443
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0054others(28): Show | 33 | HG00423.hp2 HG00544.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.-129-1557C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440443 | ||||||
chr6:36440971
|
A | G | 4 | a0001c0001t0008g0362a0001c0001t0009g0363a0001c0001t0010g0365others(1): Show | 4 | HG02886.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130+1564T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36440971 | ||||||
chr6:36441111
|
G | GA | 25 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.-130+1423dupT | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441111 | ||||||
chr6:36441354
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-130+1181G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441354 | ||||||
chr6:36441517
|
G | C | 1 | a0002c0002t0001g0314 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-130+1018C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441517 | ||||||
chr6:36441729
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-130+806T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441729 | ||||||
chr6:36441754
|
C | T | 1 | a0002c0002t0001g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-130+781G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441754 | ||||||
chr6:36441800
|
A | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130+735T>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441800 | ||||||
chr6:36441814
|
G | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-130+721C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441814 | ||||||
chr6:36441868
|
C | CTGAAA | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 133 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-130+666_-130+667i others(7): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441868 | ||||||
chr6:36441964
|
G | A | 358 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(355): Show | 381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.-130+571C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36441964 | ||||||
chr6:36442053
|
A | G | 1 | a0001c0001t0001g0007 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-130+482T>C | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442053 | ||||||
chr6:36442068
|
C | CAT | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(78): Show | 89 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-130+465_-130+466d others(4): Show |
PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442068 | ||||||
chr6:36442275
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-130+260G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442275 | ||||||
chr6:36442413
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 112 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-130+122C>T | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442413 | ||||||
chr6:36442422
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-130+113G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442422 | ||||||
chr6:36442446
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 208 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.-130+89G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442446 | ||||||
chr6:36442516
|
C | T | 2 | a0002c0002t0001g0023a0002c0002t0002g0006 | 3 | HG02451.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-130+19G>A | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442516 | ||||||
chr6:36442531
|
G | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0315others(46): Show | 55 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.-130+4C>G | PXT1 | ENSG00000179165.12 | transcript | ENST00000454782.3 | protein_coding | 1/4 | chr6 | 36442531 |