geneid | 55209 |
---|---|
ensemblid | ENSG00000168137.20 |
hgncid | 25566 |
symbol | SETD5 |
name | SET domain containing 5 |
refseq_nuc | NM_001080517.3 |
refseq_prot | NP_001073986.1 |
ensembl_nuc | ENST00000402198.7 |
ensembl_prot | ENSP00000385852.2 |
mane_status | MANE Select |
chr | chr3 |
start | 9397615 |
end | 9478154 |
strand | + |
ver | v1.2 |
region | chr3:9397615-9478154 |
region5000 | chr3:9392615-9483154 |
regionname0 | SETD5_chr3_9397615_9478154 |
regionname5000 | SETD5_chr3_9392615_9483154 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1442 | 217 | 76 | 41 | 73 | 12 | 13 | 51 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0002 | 0/0 | 1442 | 11 | 2 | 4 | 0 | 0 | 5 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003 | 0/0 | 1442 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0004 | 0/0 | 1442 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0005 | 0/0 | 1442 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0006 | 0/0 | 1442 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4329 | 203 | 67 | 39 | 71 | 11 | 13 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0002 | 0/0 | 4329 | 11 | 2 | 4 | 0 | 0 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0003 | 0/0 | 4329 | 9 | 8 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0004 | 0/0 | 4329 | 4 | 0 | 0 | 4 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0005 | 0/0 | 4329 | 3 | 0 | 3 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0006 | 0/0 | 4329 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0007 | 0/0 | 4329 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0008 | 0/0 | 4329 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0009 | 0/0 | 4329 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0010 | 0/0 | 4329 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0011 | 0/0 | 4329 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
c0012 | 0/0 | 4329 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2600 | 60 | 10 | 13 | 24 | 7 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0002 | 0/0 | 2601 | 34 | 8 | 6 | 13 | 2 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0003 | 0/0 | 2597 | 13 | 0 | 4 | 8 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0004 | 1/0 | 2603 | 10 | 2 | 2 | 4 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0005 | 0/0 | 2599 | 10 | 1 | 1 | 7 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0006 | 0/0 | 2602 | 7 | 5 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0007 | 0/0 | 2599 | 7 | 3 | 1 | 0 | 0 | 3 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0008 | 0/0 | 2600 | 6 | 6 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0009 | 0/0 | 2599 | 5 | 2 | 2 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0010 | 0/0 | 2597 | 5 | 4 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0011 | 0/0 | 2596 | 5 | 0 | 2 | 0 | 2 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0012 | 0/0 | 2603 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0013 | 0/0 | 2604 | 4 | 2 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0014 | 0/0 | 2603 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0015 | 0/0 | 2600 | 4 | 0 | 0 | 4 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0016 | 0/0 | 2598 | 4 | 2 | 2 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0017 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0018 | 0/0 | 2600 | 3 | 0 | 2 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0019 | 0/0 | 2600 | 3 | 0 | 2 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0020 | 0/0 | 2611 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0021 | 0/0 | 2605 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0022 | 0/0 | 2606 | 2 | 1 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0023 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0024 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0025 | 0/0 | 2603 | 2 | 0 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0026 | 0/0 | 2603 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0027 | 0/0 | 2601 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0028 | 0/0 | 2598 | 2 | 0 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0029 | 0/0 | 2597 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0030 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0031 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0032 | 0/0 | 2606 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0033 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0034 | 0/0 | 2606 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0035 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0036 | 0/0 | 2603 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0037 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0038 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0039 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0040 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0041 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0042 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0043 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0044 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0045 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0046 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0047 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0048 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0049 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0050 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0051 | 0/0 | 2596 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0052 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0053 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0054 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0055 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0056 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0057 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
t0058 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4329 | 203 | 67 | 39 | 71 | 11 | 13 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0003 | 0/0 | 4329 | 9 | 8 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0007 | 0/0 | 4329 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0009 | 0/0 | 4329 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0010 | 0/0 | 4329 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0012 | 0/0 | 4329 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0002c0002 | 0/0 | 4329 | 11 | 2 | 4 | 0 | 0 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003c0005 | 0/0 | 4329 | 3 | 0 | 3 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003c0008 | 0/0 | 4329 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0004c0004 | 0/0 | 4329 | 4 | 0 | 0 | 4 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0005c0006 | 0/0 | 4329 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0006c0011 | 0/0 | 4329 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6928 | 57 | 9 | 12 | 23 | 7 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0002 | 0/0 | 6929 | 31 | 6 | 6 | 13 | 1 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0003 | 0/0 | 6925 | 13 | 0 | 4 | 8 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0004 | 1/0 | 6931 | 10 | 2 | 2 | 4 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0005 | 0/0 | 6927 | 10 | 1 | 1 | 7 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0006 | 0/0 | 6930 | 7 | 5 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0007 | 0/0 | 6927 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0008 | 0/0 | 6928 | 6 | 6 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0009 | 0/0 | 6927 | 5 | 2 | 2 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0011 | 0/0 | 6924 | 5 | 0 | 2 | 0 | 2 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0012 | 0/0 | 6931 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0013 | 0/0 | 6932 | 4 | 2 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0014 | 0/0 | 6931 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0015 | 0/0 | 6928 | 4 | 0 | 0 | 4 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0017 | 0/0 | 6929 | 3 | 3 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0018 | 0/0 | 6928 | 3 | 0 | 2 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0020 | 0/0 | 6939 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0021 | 0/0 | 6933 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0022 | 0/0 | 6934 | 2 | 1 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0023 | 0/0 | 6932 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0024 | 0/0 | 6929 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0025 | 0/0 | 6931 | 2 | 0 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0028 | 0/0 | 6926 | 2 | 0 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0030 | 0/0 | 6939 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0031 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0032 | 0/0 | 6934 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0033 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0034 | 0/0 | 6934 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0035 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0036 | 0/0 | 6931 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0038 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0040 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0041 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0043 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0044 | 0/0 | 6927 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0046 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0047 | 0/0 | 6928 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0049 | 0/0 | 6928 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0050 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0051 | 0/0 | 6924 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0052 | 0/0 | 6924 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0054 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0055 | 0/0 | 6924 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0056 | 0/0 | 6923 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0001t0057 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0003t0010 | 0/0 | 6925 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0003t0016 | 0/0 | 6926 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0003t0029 | 0/0 | 6925 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0003t0053 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0007t0037 | 0/0 | 6929 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0007t0058 | 0/0 | 6917 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0009t0002 | 0/0 | 6929 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0010t0001 | 0/0 | 6928 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0001c0012t0048 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0002c0002t0007 | 0/0 | 6927 | 6 | 2 | 1 | 0 | 0 | 3 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0002c0002t0019 | 0/0 | 6928 | 3 | 0 | 2 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0002c0002t0042 | 0/0 | 6929 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0002c0002t0045 | 0/0 | 6926 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003c0005t0010 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003c0005t0016 | 0/0 | 6926 | 2 | 0 | 2 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003c0008t0001 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0003c0008t0002 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0004c0004t0026 | 0/0 | 6931 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0004c0004t0027 | 0/0 | 6929 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0005c0006t0002 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0005c0006t0039 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
a0006c0011t0001 | 0/0 | 6928 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | copy fasta | chr3 | 9392615 | 9483154 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0009g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0011g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0011g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0013g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0013g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0014g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0015g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0015g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0015g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0017g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0018g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0018g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0020g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0021g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0021g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0022g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0022g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0023g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0023g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0024g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0024g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0025g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0025g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0028g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0028g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0030g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0031g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0032g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0033g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0034g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0035g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0036g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0038g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0040g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0041g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0043g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0044g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0046g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0047g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0049g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0050g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0051g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0052g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0054g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0055g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0056g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0001t0057g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0016g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0029g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0029g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0003t0053g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0007t0037g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0007t0058g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0009t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0010t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0001c0012t0048g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0007g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0007g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0019g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0019g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0019g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0042g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0002c0002t0045g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0003c0005t0010g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0003c0005t0016g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0003c0005t0016g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0003c0008t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0003c0008t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0004c0004t0026g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0004c0004t0026g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0004c0004t0027g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0004c0004t0027g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0005c0006t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0005c0006t0039g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
a0006c0011t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00544 | hp1 | a0001 | c0001 | t0030 | g0019 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00621 | hp1 | a0001 | c0001 | t0050 | g0223 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0222 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00673 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00735 | hp1 | a0002 | c0002 | t0007 | g0182 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00735 | hp2 | a0001 | c0001 | t0022 | g0018 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG00741 | hp2 | a0002 | c0002 | t0019 | g0180 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01069 | hp1 | a0003 | c0005 | t0010 | g0200 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01069 | hp2 | a0001 | c0001 | t0036 | g0025 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01070 | hp1 | a0001 | c0001 | t0056 | g0229 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0136 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01071 | hp1 | a0003 | c0005 | t0016 | g0201 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01074 | hp2 | a0001 | c0010 | t0001 | g0042 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0119 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01099 | hp1 | a0001 | c0003 | t0053 | g0198 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0149 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01169 | hp2 | a0001 | c0001 | t0018 | g0123 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01175 | hp2 | a0003 | c0005 | t0016 | g0202 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01255 | hp1 | a0001 | c0001 | t0011 | g0226 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01346 | hp1 | a0002 | c0002 | t0045 | g0187 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01346 | hp2 | a0001 | c0001 | t0009 | g0040 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01433 | hp2 | a0001 | c0001 | t0028 | g0212 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01496 | hp1 | a0001 | c0001 | t0025 | g0002 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01496 | hp2 | a0001 | c0001 | t0018 | g0124 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0185 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01516 | hp1 | a0001 | c0001 | t0011 | g0228 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01517 | hp1 | a0001 | c0001 | t0011 | g0227 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01884 | hp1 | a0001 | c0001 | t0023 | g0167 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01884 | hp2 | a0005 | c0006 | t0002 | g0101 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02004 | hp1 | a0001 | c0001 | t0051 | g0231 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02004 | hp2 | a0001 | c0001 | t0013 | g0133 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02040 | hp2 | a0001 | c0001 | t0015 | g0089 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02055 | hp2 | a0001 | c0001 | t0038 | g0235 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02080 | hp2 | a0001 | c0001 | t0015 | g0075 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02129 | hp1 | a0001 | c0001 | t0025 | g0111 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02129 | hp2 | a0001 | c0007 | t0058 | g0006 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02145 | hp1 | a0005 | c0006 | t0039 | g0102 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02145 | hp2 | a0001 | c0001 | t0020 | g0153 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02572 | hp1 | a0001 | c0003 | t0016 | g0203 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02615 | hp1 | a0001 | c0003 | t0010 | g0196 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0234 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02622 | hp1 | a0001 | c0001 | t0057 | g0178 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02622 | hp2 | a0001 | c0001 | t0013 | g0079 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0039 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02630 | hp2 | a0001 | c0001 | t0017 | g0161 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0121 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02647 | hp2 | a0001 | c0003 | t0010 | g0199 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02717 | hp2 | a0001 | c0003 | t0010 | g0204 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02723 | hp1 | a0001 | c0001 | t0046 | g0206 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02723 | hp2 | a0001 | c0001 | t0054 | g0208 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02809 | hp1 | a0001 | c0001 | t0023 | g0169 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02818 | hp2 | a0001 | c0001 | t0022 | g0171 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0116 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02895 | hp1 | a0001 | c0003 | t0029 | g0194 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02897 | hp2 | a0001 | c0003 | t0010 | g0195 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0163 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02970 | hp1 | a0001 | c0003 | t0016 | g0193 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0155 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02976 | hp1 | a0001 | c0001 | t0035 | g0177 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02976 | hp2 | a0001 | c0001 | t0024 | g0117 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03017 | hp1 | a0002 | c0002 | t0007 | g0181 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03041 | hp2 | a0001 | c0003 | t0029 | g0197 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03098 | hp1 | a0001 | c0001 | t0055 | g0225 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03098 | hp2 | a0003 | c0008 | t0002 | g0095 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0162 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03130 | hp2 | a0001 | c0012 | t0048 | g0207 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0112 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03139 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03195 | hp1 | a0003 | c0008 | t0001 | g0081 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0174 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03453 | hp2 | a0001 | c0001 | t0052 | g0175 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03491 | hp2 | a0002 | c0002 | t0007 | g0004 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03492 | hp2 | a0002 | c0002 | t0007 | g0004 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0156 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03540 | hp1 | a0002 | c0002 | t0007 | g0191 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0172 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0233 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03688 | hp1 | a0002 | c0002 | t0019 | g0183 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03831 | hp2 | a0002 | c0002 | t0042 | g0179 | SAS | BEB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG04115 | hp2 | a0001 | c0001 | t0011 | g0230 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18906 | hp2 | a0001 | c0001 | t0040 | g0090 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18940 | hp2 | a0004 | c0004 | t0027 | g0022 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18942 | hp1 | a0001 | c0001 | t0043 | g0026 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18942 | hp2 | a0001 | c0001 | t0034 | g0028 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18950 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18950 | hp2 | a0004 | c0004 | t0026 | g0060 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18952 | hp1 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18957 | hp1 | a0004 | c0004 | t0026 | g0037 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18957 | hp2 | a0001 | c0001 | t0028 | g0217 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18973 | hp2 | a0001 | c0001 | t0047 | g0017 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18983 | hp2 | a0001 | c0001 | t0049 | g0044 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18991 | hp1 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18991 | hp2 | a0001 | c0007 | t0037 | g0005 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19000 | hp2 | a0004 | c0004 | t0027 | g0078 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0173 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19043 | hp1 | a0001 | c0001 | t0021 | g0120 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19043 | hp2 | a0001 | c0001 | t0041 | g0073 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19074 | hp2 | a0001 | c0001 | t0015 | g0031 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19084 | hp1 | a0006 | c0011 | t0001 | g0034 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19089 | hp2 | a0001 | c0001 | t0013 | g0080 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19240 | hp1 | a0001 | c0001 | t0024 | g0157 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA19240 | hp2 | a0002 | c0002 | t0007 | g0184 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA20805 | hp1 | a0001 | c0009 | t0002 | g0135 | EUR | TSI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01123 | hp1 | a0002 | c0002 | t0019 | g0192 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02486 | hp1 | a0001 | c0001 | t0014 | g0170 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02486 | hp2 | a0001 | c0001 | t0032 | g0189 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0158 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG02559 | hp2 | a0001 | c0001 | t0044 | g0074 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03471 | hp1 | a0001 | c0001 | t0031 | g0077 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG03471 | hp2 | a0001 | c0001 | t0033 | g0165 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0159 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0109 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA20300 | hp2 | a0001 | c0001 | t0021 | g0118 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0014 | REF | REF | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:9434386
|
G | A | 1 | a0005 | 2 | HG01884.hp2 HG02145.hp1 |
missense_variant | MODERATE | c.230G>A | p.Arg77His | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 5/23 | 769/6931 | 230/4329 | 77/1442 | chr3 | 9434386 | ||
chr3:9464601
|
T | C | 1 | a0004 | 4 | NA18940.hp2 NA18950.hp2 NA18957.hp1 others(1): Show |
missense_variant | MODERATE | c.2653T>C | p.Tyr885His | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/23 | 3192/6931 | 2653/4329 | 885/1442 | chr3 | 9464601 | ||
chr3:9470658
|
A | G | 1 | a0006 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.2924A>G | p.Gln975Arg | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/23 | 3463/6931 | 2924/4329 | 975/1442 | chr3 | 9470658 | ||
chr3:9473449
|
A | G | 1 | a0003 | 5 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(2): Show |
missense_variant | MODERATE | c.3409A>G | p.Met1137Val | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/23 | 3948/6931 | 3409/4329 | 1137/1442 | chr3 | 9473449 | ||
chr3:9475685
|
C | T | 1 | a0002 | 11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
missense_variant | MODERATE | c.3923C>T | p.Thr1308Ile | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 4462/6931 | 3923/4329 | 1308/1442 | chr3 | 9475685 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:9434483
|
C | T | 1 | a0001c0012 | 1 | HG03130.hp2 | splice_region_variant&synonymous_variant | LOW | c.327C>T | p.Cys109Cys | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 5/23 | 866/6931 | 327/4329 | 109/1442 | chr3 | 9434483 | ||
chr3:9464492
|
T | G | 1 | a0001c0007 | 2 | HG02129.hp2 NA18991.hp2 |
synonymous_variant | LOW | c.2544T>G | p.Leu848Leu | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/23 | 3083/6931 | 2544/4329 | 848/1442 | chr3 | 9464492 | ||
chr3:9473370
|
T | C | 1 | a0001c0009 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.3330T>C | p.Thr1110Thr | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/23 | 3869/6931 | 3330/4329 | 1110/1442 | chr3 | 9473370 | ||
chr3:9474515
|
C | T | 2 | a0001c0003a0003c0005 | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
synonymous_variant | LOW | c.3564C>T | p.Ser1188Ser | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/23 | 4103/6931 | 3564/4329 | 1188/1442 | chr3 | 9474515 | ||
chr3:9475893
|
C | T | 1 | a0001c0010 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.4131C>T | p.Asn1377Asn | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 4670/6931 | 4131/4329 | 1377/1442 | chr3 | 9475893 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:9397651
|
T | TGCC | 6 | a0001c0001t0021a0001c0001t0022a0001c0001t0031others(3): Show | 8 | HG00735.hp2 HG02486.hp2 HG02818.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-470_-468dupCGC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31252 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | ||||
chr3:9397651
|
T | TGCCGCCG others(2): Show |
2 | a0001c0001t0020a0001c0001t0030 | 3 | HG00544.hp1 HG02145.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-476_-468dupCGCCGC others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31252 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | ||||
chr3:9397651
|
TGCC | T | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(26): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(138): Show |
5_prime_UTR_variant | MODIFIER | c.-470_-468delCGC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | ||||
chr3:9397651
|
TGCCGCC | T | 15 | a0001c0001t0003a0001c0001t0011a0001c0001t0028others(12): Show | 38 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-473_-468delCGCCGC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | ||||
chr3:9397651
|
TGCCGCCG others(5): Show |
T | 1 | a0001c0007t0058 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-479_-468delCGCCGC others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | ||||
chr3:9397684
|
C | T | 1 | a0001c0001t0057 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-470C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | chr3 | 9397684 | ||||||
chr3:9397781
|
C | G | 4 | a0001c0001t0015a0001c0001t0034a0004c0004t0026others(1): Show | 9 | HG02040.hp2 HG02080.hp2 NA18940.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-373C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | chr3 | 9397781 | ||||||
chr3:9397857
|
C | G | 1 | a0001c0001t0049 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-297C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31082 | chr3 | 9397857 | |||||
chr3:9424519
|
A | G | 1 | a0001c0012t0048 | 1 | HG03130.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-124A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/23 | chr3 | 9424519 | ||||||
chr3:9428907
|
C | T | 1 | a0001c0001t0047 | 1 | NA18973.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/23 | chr3 | 9428907 | ||||||
chr3:9476210
|
T | C | 1 | a0001c0001t0050 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 119 | chr3 | 9476210 | |||||
chr3:9476399
|
G | A | 1 | a0001c0001t0051 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 308 | chr3 | 9476399 | |||||
chr3:9476422
|
C | T | 3 | a0001c0001t0046a0001c0007t0037a0001c0007t0058 | 3 | HG02129.hp2 HG02723.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*331C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 331 | chr3 | 9476422 | |||||
chr3:9476459
|
TA | T | 17 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(14): Show | 43 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*387delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 387 | INFO_REALIGN_3_PRIME | chr3 | 9476459 | ||||
chr3:9476459
|
TAA | T | 5 | a0001c0001t0008a0001c0001t0017a0001c0001t0033others(2): Show | 12 | HG02129.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*386_*387delAA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 386 | INFO_REALIGN_3_PRIME | chr3 | 9476459 | ||||
chr3:9476563
|
A | G | 1 | a0001c0001t0034 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 472 | chr3 | 9476563 | |||||
chr3:9476646
|
G | A | 1 | a0001c0001t0043 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 555 | chr3 | 9476646 | |||||
chr3:9476764
|
C | T | 2 | a0001c0001t0014a0001c0001t0023 | 6 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*673C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 673 | chr3 | 9476764 | |||||
chr3:9476827
|
C | T | 21 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(18): Show | 50 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 736 | chr3 | 9476827 | |||||
chr3:9476955
|
G | A | 1 | a0001c0001t0046 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 864 | chr3 | 9476955 | |||||
chr3:9477123
|
G | C | 16 | a0001c0001t0003a0001c0001t0011a0001c0001t0014others(13): Show | 38 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1032G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1032 | chr3 | 9477123 | |||||
chr3:9477178
|
G | C | 1 | a0001c0001t0036 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1087 | chr3 | 9477178 | |||||
chr3:9477521
|
C | G | 1 | a0005c0006t0039 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1430 | chr3 | 9477521 | |||||
chr3:9477679
|
AT | A | 17 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(14): Show | 40 | HG01070.hp1 HG01081.hp2 HG01099.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1610delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1610 | INFO_REALIGN_3_PRIME | chr3 | 9477679 | ||||
chr3:9477864
|
T | A | 1 | a0001c0001t0052 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1773T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1773 | chr3 | 9477864 | |||||
chr3:9477906
|
G | A | 1 | a0001c0001t0036 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1815G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1815 | chr3 | 9477906 | |||||
chr3:9478004
|
C | CG | 25 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(22): Show | 75 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1920dupG | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1921 | INFO_REALIGN_3_PRIME | chr3 | 9478004 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:9398070
|
T | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+93T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398070 | ||||||
chr3:9398129
|
C | T | 4 | a0001c0001t0006g0236a0001c0001t0009g0234a0001c0001t0012g0233others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+152C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398129 | ||||||
chr3:9398204
|
A | G | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-177+227A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398204 | ||||||
chr3:9398211
|
C | T | 1 | a0001c0012t0048g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-177+234C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398211 | ||||||
chr3:9398373
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+396C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398373 | ||||||
chr3:9398444
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+467C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398444 | ||||||
chr3:9398719
|
C | T | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-177+742C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398719 | ||||||
chr3:9398729
|
G | C | 2 | a0001c0001t0002g0001a0001c0001t0005g0001 | 2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-177+752G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398729 | ||||||
chr3:9399389
|
C | T | 86 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(83): Show | 87 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-177+1412C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399389 | ||||||
chr3:9399399
|
A | G | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+1422A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399399 | ||||||
chr3:9399496
|
A | T | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(13): Show | 17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-177+1519A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399496 | ||||||
chr3:9399827
|
CA | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-177+1867delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9399827 | |||||
chr3:9399858
|
G | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+1881G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399858 | ||||||
chr3:9399902
|
CAG | C | 29 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-177+1926_-177+192 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399902 | ||||||
chr3:9400035
|
A | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0018g0123others(1): Show | 4 | HG00099.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+2058A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400035 | ||||||
chr3:9400053
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-177+2076G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400053 | ||||||
chr3:9400081
|
C | T | 1 | a0002c0002t0007g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-177+2104C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400081 | ||||||
chr3:9400294
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+2317C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400294 | ||||||
chr3:9400840
|
C | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+2863C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400840 | ||||||
chr3:9400977
|
A | G | 1 | a0001c0001t0025g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-177+3000A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400977 | ||||||
chr3:9400985
|
C | A | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+3008C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400985 | ||||||
chr3:9401051
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-177+3074A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401051 | ||||||
chr3:9401206
|
A | G | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-177+3229A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401206 | ||||||
chr3:9401319
|
C | G | 1 | a0001c0001t0006g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177+3342C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401319 | ||||||
chr3:9401370
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-177+3393G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401370 | ||||||
chr3:9401413
|
A | G | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+3436A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401413 | ||||||
chr3:9401565
|
T | C | 1 | a0001c0001t0047g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-177+3588T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401565 | ||||||
chr3:9401734
|
T | C | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-177+3757T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401734 | ||||||
chr3:9401870
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-177+3893T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401870 | ||||||
chr3:9402572
|
C | G | 1 | a0001c0001t0009g0013 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-177+4595C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402572 | ||||||
chr3:9402616
|
C | G | 1 | a0001c0001t0009g0013 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-177+4639C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402616 | ||||||
chr3:9402743
|
G | A | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-177+4766G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402743 | ||||||
chr3:9402974
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0030g0019 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-177+4997T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402974 | ||||||
chr3:9403001
|
C | T | 1 | a0001c0003t0010g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-177+5024C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403001 | ||||||
chr3:9403143
|
G | T | 1 | a0001c0001t0003g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-177+5166G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403143 | ||||||
chr3:9403225
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0002g0012 | 2 | HG01258.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-177+5248A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403225 | ||||||
chr3:9403489
|
G | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+5512G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403489 | ||||||
chr3:9403564
|
G | A | 1 | a0001c0001t0012g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-177+5587G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403564 | ||||||
chr3:9404018
|
T | C | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-177+6041T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404018 | ||||||
chr3:9404067
|
A | G | 1 | a0001c0001t0006g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-177+6090A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404067 | ||||||
chr3:9404312
|
T | C | 3 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0057g0178 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-177+6335T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404312 | ||||||
chr3:9404321
|
TAAAG | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+6348_-177+635 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9404321 | |||||
chr3:9404643
|
C | A | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-177+6666C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404643 | ||||||
chr3:9404714
|
A | G | 1 | a0001c0001t0005g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-177+6737A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404714 | ||||||
chr3:9404860
|
C | T | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+6883C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404860 | ||||||
chr3:9405139
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-177+7162A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405139 | ||||||
chr3:9405218
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-177+7241C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405218 | ||||||
chr3:9405369
|
C | T | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-177+7392C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405369 | ||||||
chr3:9405403
|
G | A | 25 | a0001c0001t0004g0168a0001c0001t0006g0164a0001c0001t0006g0176others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+7426G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405403 | ||||||
chr3:9405958
|
T | A | 6 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(3): Show | 6 | HG01074.hp1 HG01192.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+7981T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405958 | ||||||
chr3:9406062
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-177+8085G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406062 | ||||||
chr3:9406065
|
T | G | 1 | a0001c0001t0003g0215 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-177+8088T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406065 | ||||||
chr3:9406285
|
G | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+8308G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406285 | ||||||
chr3:9406431
|
C | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+8454C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406431 | ||||||
chr3:9406540
|
G | A | 18 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177+8563G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406540 | ||||||
chr3:9406578
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-177+8601A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406578 | ||||||
chr3:9406607
|
C | CAA | 6 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228others(3): Show | 6 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+8643_-177+864 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAA | 8 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(5): Show | 8 | HG01099.hp1 HG02615.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-177+8641_-177+864 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAA | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+8639_-177+864 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(3): Show |
23 | a0001c0001t0004g0168a0001c0001t0006g0164a0001c0001t0006g0176others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-177+8635_-177+864 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0007g0205a0001c0001t0017g0155a0001c0001t0017g0156 | 3 | HG02970.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-177+8634_-177+864 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(6): Show |
1 | a0001c0007t0058g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-177+8632_-177+864 others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(7): Show |
1 | a0001c0007t0037g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-177+8631_-177+864 others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(9): Show |
16 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0214others(13): Show | 16 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177+8644_-177+864 others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0216others(2): Show | 5 | HG01192.hp2 HG01978.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+8644_-177+864 others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0020g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(23): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0020g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(24): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406607
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(25): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | |||||
chr3:9406681
|
C | T | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+8704C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406681 | ||||||
chr3:9406957
|
A | G | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-177+8980A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406957 | ||||||
chr3:9406983
|
G | A | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-177+9006G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406983 | ||||||
chr3:9407054
|
G | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+9077G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407054 | ||||||
chr3:9407090
|
G | A | 1 | a0001c0001t0024g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-177+9113G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407090 | ||||||
chr3:9407144
|
A | G | 1 | a0001c0001t0004g0151 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-177+9167A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407144 | ||||||
chr3:9407195
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-177+9218G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407195 | ||||||
chr3:9407283
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-177+9306G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407283 | ||||||
chr3:9407371
|
C | T | 34 | a0001c0001t0004g0168a0001c0001t0006g0114a0001c0001t0006g0115others(31): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-177+9394C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407371 | ||||||
chr3:9407381
|
A | G | 7 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0148others(4): Show | 7 | HG00597.hp2 HG01109.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+9404A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407381 | ||||||
chr3:9407386
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0002g0105 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-177+9409A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407386 | ||||||
chr3:9407726
|
T | C | 95 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(92): Show | 96 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-177+9749T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407726 | ||||||
chr3:9407758
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+9781T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407758 | ||||||
chr3:9407912
|
A | C | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(13): Show | 17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-177+9935A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407912 | ||||||
chr3:9407914
|
C | G | 1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-177+9937C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407914 | ||||||
chr3:9407949
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-177+9972G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407949 | ||||||
chr3:9407956
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-177+9979C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407956 | ||||||
chr3:9407980
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-177+10003A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407980 | ||||||
chr3:9408000
|
C | CA | 225 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-177+10035dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9408000 | |||||
chr3:9408000
|
C | CAA | 12 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+10034_-177+10 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9408000 | |||||
chr3:9408062
|
T | C | 4 | a0001c0001t0004g0168a0001c0001t0014g0170a0001c0001t0023g0167others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+10085T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408062 | ||||||
chr3:9408131
|
G | T | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+10154G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408131 | ||||||
chr3:9408228
|
C | G | 2 | a0005c0006t0002g0101a0005c0006t0039g0102 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-177+10251C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408228 | ||||||
chr3:9408511
|
T | C | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-177+10534T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408511 | ||||||
chr3:9408617
|
TC | T | 25 | a0001c0001t0004g0168a0001c0001t0006g0164a0001c0001t0006g0176others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+10646delC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9408617 | |||||
chr3:9408621
|
C | T | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+10644C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408621 | ||||||
chr3:9408928
|
A | G | 1 | a0001c0001t0006g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177+10951A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408928 | ||||||
chr3:9409084
|
C | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+11107C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409084 | ||||||
chr3:9409092
|
A | T | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+11115A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409092 | ||||||
chr3:9409155
|
G | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+11178G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409155 | ||||||
chr3:9409528
|
C | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+11551C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409528 | ||||||
chr3:9409554
|
T | C | 1 | a0001c0003t0010g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-177+11577T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409554 | ||||||
chr3:9409599
|
C | G | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+11622C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409599 | ||||||
chr3:9409603
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0005g0001 | 2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-177+11626C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409603 | ||||||
chr3:9409693
|
T | A | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-177+11716T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409693 | ||||||
chr3:9409801
|
C | T | 1 | a0001c0001t0018g0010 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-177+11824C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409801 | ||||||
chr3:9409841
|
C | T | 7 | a0001c0001t0004g0168a0001c0001t0014g0170a0001c0001t0014g0172others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+11864C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409841 | ||||||
chr3:9410023
|
T | G | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+12046T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410023 | ||||||
chr3:9410157
|
C | G | 2 | a0001c0001t0004g0099a0001c0001t0004g0100 | 2 | NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-177+12180C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410157 | ||||||
chr3:9410219
|
G | A | 1 | a0004c0004t0027g0022 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-177+12242G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410219 | ||||||
chr3:9410225
|
A | G | 1 | a0004c0004t0027g0022 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-177+12248A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410225 | ||||||
chr3:9410262
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+12285T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410262 | ||||||
chr3:9410336
|
T | C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+12359T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410336 | ||||||
chr3:9410453
|
C | T | 1 | a0001c0001t0024g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-177+12476C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410453 | ||||||
chr3:9410474
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0098 | 2 | HG00673.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-177+12497C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410474 | ||||||
chr3:9410504
|
G | A | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+12527G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410504 | ||||||
chr3:9410560
|
G | C | 1 | a0001c0001t0003g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-177+12583G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410560 | ||||||
chr3:9410804
|
C | CTTTT | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+12830_-177+12 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9410804 | |||||
chr3:9410877
|
C | CT | 68 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(65): Show | 69 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.-177+12911dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9410877 | |||||
chr3:9410877
|
C | CTT | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-177+12910_-177+12 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9410877 | |||||
chr3:9410919
|
C | T | 10 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(7): Show | 10 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177+12942C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410919 | ||||||
chr3:9411453
|
G | A | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-13014G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411453 | ||||||
chr3:9411761
|
C | G | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-12706C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411761 | ||||||
chr3:9411772
|
T | C | 2 | a0001c0001t0003g0218a0001c0001t0028g0217 | 2 | NA18940.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-176-12695T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411772 | ||||||
chr3:9411776
|
T | G | 1 | a0001c0001t0024g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-176-12691T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411776 | ||||||
chr3:9411976
|
T | C | 45 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(42): Show | 46 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-176-12491T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411976 | ||||||
chr3:9412387
|
G | GT | 51 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0072others(48): Show | 51 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-176-12050dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | |||||
chr3:9412387
|
G | GTT | 11 | a0001c0001t0001g0008a0001c0001t0001g0097a0001c0001t0005g0185others(8): Show | 11 | HG01099.hp1 HG01175.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.-176-12051_-176-12 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | |||||
chr3:9412387
|
G | GTTT | 10 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(7): Show | 10 | HG00323.hp2 HG00735.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-176-12052_-176-12 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | |||||
chr3:9412387
|
GT | G | 33 | a0001c0001t0001g0027a0001c0001t0001g0127a0001c0001t0004g0168others(30): Show | 33 | HG01069.hp2 HG01517.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-176-12050delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | |||||
chr3:9412390
|
T | G | 1 | a0001c0001t0001g0023 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-176-12077T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412390 | ||||||
chr3:9412399
|
T | G | 2 | a0001c0001t0017g0156a0001c0001t0038g0235 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-176-12068T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412399 | ||||||
chr3:9412400
|
T | G | 26 | a0001c0001t0004g0168a0001c0001t0006g0164a0001c0001t0006g0176others(23): Show | 26 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-176-12067T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412400 | ||||||
chr3:9412408
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-176-12059T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412408 | ||||||
chr3:9412414
|
TTTTA | T | 21 | a0001c0001t0003g0209a0001c0001t0003g0213a0001c0001t0003g0214others(18): Show | 21 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-176-12052_-176-12 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412414 | ||||||
chr3:9412471
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-11996T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412471 | ||||||
chr3:9412661
|
T | G | 1 | a0001c0003t0010g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-176-11806T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412661 | ||||||
chr3:9412819
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-11648T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412819 | ||||||
chr3:9412973
|
A | G | 1 | a0001c0001t0006g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-176-11494A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412973 | ||||||
chr3:9412976
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0002g0093 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-176-11491C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412976 | ||||||
chr3:9413078
|
A | G | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-11389A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413078 | ||||||
chr3:9413225
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-176-11242T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413225 | ||||||
chr3:9413238
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-176-11229T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413238 | ||||||
chr3:9413327
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-11140A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413327 | ||||||
chr3:9413367
|
T | A | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-11100T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413367 | ||||||
chr3:9413646
|
CG | C | 5 | a0001c0001t0001g0069a0001c0001t0002g0068a0001c0001t0004g0147others(2): Show | 5 | HG02074.hp2 NA18906.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-10817delG | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413646 | |||||
chr3:9413649
|
G | GGGTGTGT | 11 | a0001c0001t0001g0188a0001c0001t0002g0190a0001c0001t0032g0189others(8): Show | 11 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-176-10817_-176-10 others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | GGGTGTGT others(4): Show |
1 | a0002c0002t0007g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-176-10817_-176-10 others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | GGT | 31 | a0001c0001t0001g0003a0001c0001t0001g0067a0001c0001t0001g0087others(28): Show | 32 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-176-10783_-176-10 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | GGTGT | 26 | a0001c0001t0006g0164a0001c0001t0006g0176a0001c0001t0006g0236others(23): Show | 26 | HG01099.hp1 HG01255.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-10785_-176-10 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | GGTGTGT | 11 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0213others(8): Show | 11 | HG01070.hp1 HG01074.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-176-10787_-176-10 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | GGTGTGTG others(1): Show |
13 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0218others(10): Show | 13 | HG00621.hp1 HG00639.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-176-10789_-176-10 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | GGTGTGTG others(3): Show |
4 | a0001c0001t0003g0211a0001c0001t0007g0205a0001c0001t0011g0230others(1): Show | 4 | HG02004.hp1 HG03688.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-10791_-176-10 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413649
|
G | T | 2 | a0001c0001t0005g0091a0001c0001t0005g0092 | 2 | NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-176-10818G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413649 | ||||||
chr3:9413649
|
GGT | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-176-10783_-176-10 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | |||||
chr3:9413770
|
TTTTTG | T | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-10677_-176-10 others(11): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413770 | |||||
chr3:9413840
|
T | A | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-176-10627T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413840 | ||||||
chr3:9413882
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-176-10585A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413882 | ||||||
chr3:9413912
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-176-10555G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413912 | ||||||
chr3:9414027
|
G | A | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-10440G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414027 | ||||||
chr3:9414194
|
G | A | 1 | a0001c0001t0022g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-176-10273G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414194 | ||||||
chr3:9414236
|
G | T | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-10231G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414236 | ||||||
chr3:9414395
|
GTGTTGT | G | 3 | a0001c0001t0002g0029a0003c0008t0001g0081a0003c0008t0002g0095 | 3 | HG03098.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-176-10064_-176-10 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9414395 | |||||
chr3:9414417
|
G | C | 18 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176-10050G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414417 | ||||||
chr3:9414540
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-176-9927A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414540 | ||||||
chr3:9414603
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-9864T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414603 | ||||||
chr3:9414658
|
C | A | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-176-9809C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414658 | ||||||
chr3:9414680
|
T | A | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-176-9787T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414680 | ||||||
chr3:9414796
|
T | C | 1 | a0001c0001t0006g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-176-9671T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414796 | ||||||
chr3:9414936
|
A | G | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-9531A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414936 | ||||||
chr3:9415021
|
A | C | 34 | a0001c0001t0004g0168a0001c0001t0006g0114a0001c0001t0006g0115others(31): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-176-9446A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415021 | ||||||
chr3:9415068
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-176-9399A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415068 | ||||||
chr3:9415270
|
T | C | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-176-9197T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415270 | ||||||
chr3:9415577
|
A | T | 82 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(79): Show | 83 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-176-8890A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415577 | ||||||
chr3:9415586
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-176-8881A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415586 | ||||||
chr3:9415588
|
T | A | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-8879T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415588 | ||||||
chr3:9415589
|
T | A | 1 | a0001c0001t0003g0221 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-176-8878T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415589 | ||||||
chr3:9415621
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-176-8846C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415621 | ||||||
chr3:9415674
|
A | G | 82 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(79): Show | 83 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-176-8793A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415674 | ||||||
chr3:9415682
|
C | T | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-8785C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415682 | ||||||
chr3:9415802
|
G | C | 1 | a0001c0001t0011g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-176-8665G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415802 | ||||||
chr3:9416129
|
C | G | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-8338C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416129 | ||||||
chr3:9416183
|
GTCT | G | 95 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(92): Show | 96 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-176-8280_-176-827 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9416183 | |||||
chr3:9416312
|
C | A | 1 | a0001c0001t0002g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-176-8155C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416312 | ||||||
chr3:9416388
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0009g0071a0001c0001t0040g0090 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-176-8079G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416388 | ||||||
chr3:9416545
|
A | G | 1 | a0001c0003t0010g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-176-7922A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416545 | ||||||
chr3:9416565
|
G | A | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-7902G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416565 | ||||||
chr3:9416623
|
A | G | 34 | a0001c0001t0004g0168a0001c0001t0006g0114a0001c0001t0006g0115others(31): Show | 34 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-176-7844A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416623 | ||||||
chr3:9416940
|
T | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0001g0143 | 3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-176-7527T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416940 | ||||||
chr3:9417026
|
A | T | 37 | a0001c0001t0004g0168a0001c0001t0006g0114a0001c0001t0006g0115others(34): Show | 37 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.-176-7441A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417026 | ||||||
chr3:9417178
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176-7289G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417178 | ||||||
chr3:9417224
|
T | C | 1 | a0001c0001t0018g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-176-7243T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417224 | ||||||
chr3:9417483
|
C | CT | 7 | a0001c0001t0003g0221a0001c0001t0007g0205a0001c0001t0013g0080others(4): Show | 7 | HG02129.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-6970dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417483 | |||||
chr3:9417483
|
CT | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0098a0001c0001t0004g0099others(35): Show | 38 | HG00673.hp1 HG01081.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-176-6970delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417483 | |||||
chr3:9417497
|
T | C | 1 | a0001c0001t0024g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-176-6970T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417497 | ||||||
chr3:9417498
|
C | T | 27 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(24): Show | 27 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-176-6969C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417498 | ||||||
chr3:9417522
|
A | G | 95 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(92): Show | 96 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-176-6945A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417522 | ||||||
chr3:9417578
|
C | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-6889C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417578 | ||||||
chr3:9417611
|
A | G | 83 | a0001c0001t0001g0113a0001c0001t0001g0186a0001c0001t0001g0188others(80): Show | 84 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.-176-6856A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417611 | ||||||
chr3:9417638
|
A | G | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-6829A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417638 | ||||||
chr3:9417741
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0009g0071 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-176-6726T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417741 | ||||||
chr3:9417942
|
G | GT | 27 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0001t0001g0188others(24): Show | 28 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-176-6509dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417942 | |||||
chr3:9417942
|
G | GTT | 5 | a0001c0001t0051g0231a0001c0001t0055g0225a0001c0007t0058g0006others(2): Show | 5 | HG01123.hp1 HG02004.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-6510_-176-650 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417942 | |||||
chr3:9417947
|
T | TG | 18 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(15): Show | 18 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176-6520_-176-651 others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417947 | ||||||
chr3:9418003
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-176-6464C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418003 | ||||||
chr3:9418107
|
AT | A | 9 | a0001c0001t0001g0072a0001c0001t0001g0106a0001c0001t0002g0105others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-176-6346delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9418107 | |||||
chr3:9418194
|
C | T | 3 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0057g0178 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-176-6273C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418194 | ||||||
chr3:9418194
|
CGCCTCG | C | 9 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG01109.hp1 HG02809.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.-176-6270_-176-626 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9418194 | |||||
chr3:9418322
|
G | A | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-176-6145G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418322 | ||||||
chr3:9418557
|
A | G | 1 | a0001c0001t0034g0028 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-176-5910A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418557 | ||||||
chr3:9418732
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176-5735G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418732 | ||||||
chr3:9418743
|
C | T | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-5724C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418743 | ||||||
chr3:9418803
|
CA | C | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0104others(13): Show | 17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-176-5651delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9418803 | |||||
chr3:9418839
|
T | C | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-176-5628T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418839 | ||||||
chr3:9418890
|
A | C | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-176-5577A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418890 | ||||||
chr3:9419073
|
C | T | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-5394C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419073 | ||||||
chr3:9419098
|
A | G | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-176-5369A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419098 | ||||||
chr3:9419206
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176-5261G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419206 | ||||||
chr3:9419269
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-5198A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419269 | ||||||
chr3:9420238
|
GATAATA | G | 9 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176-4217_-176-421 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9420238 | |||||
chr3:9420241
|
A | G | 11 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.-176-4226A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420241 | ||||||
chr3:9420315
|
C | G | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-4152C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420315 | ||||||
chr3:9420362
|
T | C | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-4105T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420362 | ||||||
chr3:9420392
|
C | G | 28 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(25): Show | 28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-4075C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420392 | ||||||
chr3:9420433
|
T | C | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-176-4034T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420433 | ||||||
chr3:9420832
|
A | AT | 45 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(42): Show | 46 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-176-3624dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9420832 | |||||
chr3:9420832
|
A | ATT | 46 | a0001c0001t0004g0168a0001c0001t0006g0114a0001c0001t0006g0115others(43): Show | 46 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-176-3625_-176-362 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9420832 | |||||
chr3:9421137
|
A | C | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-3330A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421137 | ||||||
chr3:9421352
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-176-3115G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421352 | ||||||
chr3:9421387
|
C | G | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-3080C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421387 | ||||||
chr3:9421446
|
T | C | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-176-3021T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421446 | ||||||
chr3:9421508
|
C | T | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-176-2959C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421508 | ||||||
chr3:9421778
|
A | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(88): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-176-2689A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421778 | ||||||
chr3:9422004
|
A | G | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-2463A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422004 | ||||||
chr3:9422296
|
G | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-2171G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422296 | ||||||
chr3:9422299
|
T | G | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-176-2168T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422299 | ||||||
chr3:9422408
|
A | G | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-2059A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422408 | ||||||
chr3:9422474
|
G | A | 1 | a0001c0001t0018g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-176-1993G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422474 | ||||||
chr3:9422753
|
G | T | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-1714G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422753 | ||||||
chr3:9422827
|
A | G | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-176-1640A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422827 | ||||||
chr3:9422828
|
A | G | 1 | a0001c0010t0001g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-176-1639A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422828 | ||||||
chr3:9423041
|
T | C | 82 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(79): Show | 83 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-176-1426T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423041 | ||||||
chr3:9423287
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-176-1180A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423287 | ||||||
chr3:9423317
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-176-1150G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423317 | ||||||
chr3:9423708
|
G | A | 2 | a0001c0001t0003g0219a0001c0001t0003g0220 | 2 | NA19070.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-176-759G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423708 | ||||||
chr3:9423845
|
G | A | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-176-622G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423845 | ||||||
chr3:9423980
|
A | G | 7 | a0001c0001t0001g0072a0001c0001t0009g0071a0001c0001t0022g0018others(4): Show | 7 | HG00735.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-487A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423980 | ||||||
chr3:9424095
|
A | T | 97 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0186others(94): Show | 98 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.-176-372A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9424095 | ||||||
chr3:9424357
|
GA | G | 3 | a0003c0005t0010g0200a0003c0005t0016g0201a0003c0005t0016g0202 | 3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-176-109delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9424357 | ||||||
chr3:9424562
|
T | C | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-117+36T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9424562 | ||||||
chr3:9424651
|
C | T | 1 | a0001c0001t0005g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-117+125C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9424651 | ||||||
chr3:9424766
|
A | G | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-117+240A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9424766 | ||||||
chr3:9425036
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-117+510A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425036 | ||||||
chr3:9425038
|
A | G | 2 | a0001c0001t0002g0190a0002c0002t0007g0191 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-117+512A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425038 | ||||||
chr3:9425051
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-117+528_-117+529i others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425051 | |||||
chr3:9425054
|
T | G | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-117+528T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425054 | ||||||
chr3:9425055
|
C | CT | 18 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(15): Show | 18 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-117+552dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTT | 6 | a0001c0001t0001g0007a0001c0001t0007g0205a0001c0003t0010g0204others(3): Show | 6 | HG01071.hp1 HG01099.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-117+550_-117+552d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTTT | 7 | a0001c0001t0055g0225a0001c0003t0010g0196a0001c0003t0010g0199others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-117+549_-117+552d others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTTTT | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-117+548_-117+552d others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTTTTT | 18 | a0001c0001t0001g0188a0001c0001t0002g0190a0001c0001t0003g0232others(15): Show | 19 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-117+547_-117+552d others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0006g0236a0001c0001t0038g0235 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-117+530_-117+552d others(25): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0012g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-117+552_-117+553i others(29): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0009g0234 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-117+552_-117+553i others(30): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-117+529C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425055 | ||||||
chr3:9425055
|
C | T | 3 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0057g0178 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-117+529C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425055 | ||||||
chr3:9425055
|
CT | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0002g0030others(10): Show | 13 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-117+552delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425055
|
CTTT | C | 11 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(8): Show | 11 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-117+550_-117+552d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | |||||
chr3:9425062
|
T | TTTTTTTT others(6): Show |
2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-117+548_-117+549i others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425062 | |||||
chr3:9425102
|
T | C | 36 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(33): Show | 36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-117+576T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425102 | ||||||
chr3:9425118
|
A | G | 1 | a0001c0001t0003g0209 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-117+592A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425118 | ||||||
chr3:9425207
|
G | A | 26 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(23): Show | 26 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-117+681G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425207 | ||||||
chr3:9425253
|
A | G | 36 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(33): Show | 36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-117+727A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425253 | ||||||
chr3:9425264
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-117+738G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425264 | ||||||
chr3:9425377
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-117+851T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425377 | ||||||
chr3:9425388
|
T | C | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(13): Show | 17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-117+862T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425388 | ||||||
chr3:9425575
|
C | CT | 17 | a0001c0001t0001g0138a0001c0001t0002g0150a0001c0001t0013g0039others(14): Show | 17 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-117+1068dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425575 | |||||
chr3:9425575
|
CT | C | 26 | a0001c0001t0001g0008a0001c0001t0001g0186a0001c0001t0001g0188others(23): Show | 27 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-117+1068delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425575 | |||||
chr3:9425635
|
G | T | 1 | a0002c0002t0007g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-117+1109G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425635 | ||||||
chr3:9425776
|
G | A | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-117+1250G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425776 | ||||||
chr3:9425922
|
G | A | 1 | a0001c0007t0058g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-117+1396G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425922 | ||||||
chr3:9425942
|
A | G | 1 | a0001c0003t0053g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-117+1416A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425942 | ||||||
chr3:9426005
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-117+1479T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426005 | ||||||
chr3:9426015
|
A | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-117+1489A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426015 | ||||||
chr3:9426172
|
A | G | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-117+1646A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426172 | ||||||
chr3:9426210
|
TC | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0083a0001c0001t0002g0012others(1): Show | 4 | HG01258.hp2 HG01934.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-117+1687delC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9426210 | |||||
chr3:9426212
|
C | CT | 27 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0020others(24): Show | 27 | HG00099.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTT | 19 | a0001c0001t0001g0007a0001c0001t0001g0103a0001c0001t0001g0110others(16): Show | 19 | HG00597.hp2 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTT | 18 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0049others(15): Show | 18 | HG00639.hp2 HG01071.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTT | 12 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG00099.hp1 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTT | 14 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0054others(11): Show | 14 | HG00323.hp1 HG00438.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTT | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0005c0006t0039g0102 | 3 | HG00621.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT | 3 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0005g0066 | 3 | HG03516.hp2 NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(11): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0036a0001c0001t0001g0098a0001c0001t0001g0126others(2): Show | 5 | HG01928.hp2 NA18942.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(3): Show |
9 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0062others(6): Show | 9 | HG00544.hp1 HG00673.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0113a0001c0001t0005g0041 | 2 | HG00544.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0146a0001c0001t0002g0056a0004c0004t0027g0022 | 3 | HG02132.hp1 NA18940.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0046a0004c0004t0026g0060 | 2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-117+1686_-117+168 others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
C | CTTTTTTT others(14): Show |
1 | a0004c0004t0027g0078 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-117+1686_-117+168 others(25): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCT | C | 4 | a0001c0001t0002g0048a0001c0001t0009g0013a0001c0001t0043g0026others(1): Show | 4 | HG02683.hp1 HG02970.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-117+1687_-117+168 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(1): Show |
C | 3 | a0001c0003t0016g0203a0003c0005t0010g0200a0003c0005t0016g0201 | 3 | HG01069.hp1 HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-117+1687_-117+169 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(2): Show |
C | 4 | a0001c0003t0010g0196a0001c0003t0010g0199a0001c0003t0029g0197others(1): Show | 4 | HG01099.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-117+1687_-117+169 others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(3): Show |
C | 3 | a0001c0003t0010g0195a0001c0003t0010g0204a0001c0003t0029g0194 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-117+1687_-117+169 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(4): Show |
C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-117+1687_-117+169 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-117+1687_-117+169 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-117+1687_-117+169 others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(7): Show |
C | 8 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0005g0091others(5): Show | 8 | HG01192.hp2 HG01433.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(8): Show |
C | 23 | a0001c0001t0003g0211a0001c0001t0003g0213a0001c0001t0003g0214others(20): Show | 23 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(9): Show |
C | 19 | a0001c0001t0001g0129a0001c0001t0001g0186a0001c0001t0001g0188others(16): Show | 20 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(11): Show |
C | 2 | a0001c0001t0002g0104a0001c0001t0007g0205 | 2 | HG02071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(22): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(15): Show |
C | 3 | a0001c0001t0004g0100a0001c0001t0020g0153a0001c0001t0020g0154 | 3 | HG02145.hp2 HG03139.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(26): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426212
|
CCTTTTTT others(16): Show |
C | 27 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(24): Show | 27 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(27): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | ||||||
chr3:9426213
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-117+1687C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426213 | ||||||
chr3:9426275
|
G | T | 1 | a0001c0003t0010g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-117+1749G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426275 | ||||||
chr3:9426343
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-117+1817T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426343 | ||||||
chr3:9426593
|
A | C | 1 | a0001c0007t0037g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-117+2067A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426593 | ||||||
chr3:9427519
|
C | G | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-116-1304C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427519 | ||||||
chr3:9427543
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-116-1280T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427543 | ||||||
chr3:9427544
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-116-1279G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427544 | ||||||
chr3:9427595
|
C | T | 8 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0129others(5): Show | 8 | HG00099.hp2 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-116-1228C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427595 | ||||||
chr3:9427603
|
T | C | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-116-1220T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427603 | ||||||
chr3:9427620
|
T | C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-116-1203T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427620 | ||||||
chr3:9427711
|
C | G | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-116-1112C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427711 | ||||||
chr3:9427822
|
A | G | 2 | a0001c0003t0010g0195a0001c0003t0029g0194 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-116-1001A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427822 | ||||||
chr3:9427937
|
T | C | 1 | a0001c0001t0011g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-116-886T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427937 | ||||||
chr3:9427971
|
G | A | 29 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-116-852G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427971 | ||||||
chr3:9428020
|
G | A | 1 | a0001c0001t0043g0026 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-116-803G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428020 | ||||||
chr3:9428032
|
G | T | 13 | a0001c0001t0035g0177a0001c0003t0010g0195a0001c0003t0010g0196others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-116-791G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428032 | ||||||
chr3:9428139
|
C | T | 1 | a0001c0001t0021g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-116-684C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428139 | ||||||
chr3:9428140
|
G | A | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-116-683G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428140 | ||||||
chr3:9428271
|
A | G | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-116-552A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428271 | ||||||
chr3:9428307
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-116-516G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428307 | ||||||
chr3:9428507
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-116-316A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428507 | ||||||
chr3:9429493
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.71+484G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9429493 | ||||||
chr3:9429502
|
T | G | 2 | a0001c0001t0001g0106a0001c0001t0002g0105 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.71+493T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9429502 | ||||||
chr3:9429548
|
G | T | 6 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228others(3): Show | 6 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+539G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9429548 | ||||||
chr3:9429616
|
TA | T | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.71+611delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr3 | 9429616 | |||||
chr3:9430095
|
A | C | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+1086A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430095 | ||||||
chr3:9430216
|
T | C | 2 | a0001c0001t0002g0068a0001c0001t0013g0080 | 2 | HG02074.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.71+1207T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430216 | ||||||
chr3:9430317
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.71+1308T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430317 | ||||||
chr3:9430564
|
C | A | 1 | a0001c0001t0005g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.71+1555C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430564 | ||||||
chr3:9430773
|
C | T | 1 | a0001c0001t0033g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.71+1764C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430773 | ||||||
chr3:9431044
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.71+2035C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431044 | ||||||
chr3:9431237
|
A | G | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71+2228A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431237 | ||||||
chr3:9431518
|
A | C | 36 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(33): Show | 36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-2327A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431518 | ||||||
chr3:9431618
|
A | G | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.72-2227A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431618 | ||||||
chr3:9431950
|
G | A | 1 | a0001c0001t0006g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.72-1895G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431950 | ||||||
chr3:9431985
|
T | C | 26 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-1860T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431985 | ||||||
chr3:9432167
|
C | T | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.72-1678C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432167 | ||||||
chr3:9432176
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.72-1669C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432176 | ||||||
chr3:9432253
|
G | GTTC | 36 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(33): Show | 36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-1588_72-1586dup others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr3 | 9432253 | |||||
chr3:9432278
|
C | G | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72-1567C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432278 | ||||||
chr3:9432377
|
A | G | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.72-1468A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432377 | ||||||
chr3:9432466
|
C | T | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-1379C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432466 | ||||||
chr3:9432987
|
G | A | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.72-858G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432987 | ||||||
chr3:9433076
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.72-769T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433076 | ||||||
chr3:9433158
|
C | G | 1 | a0001c0001t0032g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.72-687C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433158 | ||||||
chr3:9433298
|
T | C | 2 | a0002c0002t0019g0183a0002c0002t0042g0179 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.72-547T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433298 | ||||||
chr3:9433434
|
G | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.72-411G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433434 | ||||||
chr3:9433630
|
C | G | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.72-215C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433630 | ||||||
chr3:9433732
|
T | A | 1 | a0001c0001t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.72-113T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433732 | ||||||
chr3:9434011
|
T | C | 2 | a0001c0001t0002g0001a0001c0001t0005g0001 | 2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.177+61T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 4/22 | chr3 | 9434011 | ||||||
chr3:9434601
|
G | T | 1 | a0001c0012t0048g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.329+116G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 5/22 | chr3 | 9434601 | ||||||
chr3:9435243
|
C | CA | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0001others(4): Show | 7 | HG02080.hp2 HG02895.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.388+383dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | |||||
chr3:9435243
|
CA | C | 20 | a0001c0001t0001g0072a0001c0001t0001g0143a0001c0001t0001g0186others(17): Show | 21 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+383delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | |||||
chr3:9435243
|
CAA | C | 72 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0003g0210others(69): Show | 72 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.388+382_388+383del others(2): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | |||||
chr3:9435243
|
CAAA | C | 5 | a0001c0001t0006g0119a0001c0001t0008g0163a0001c0001t0012g0112others(2): Show | 5 | HG01070.hp1 HG01081.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+381_388+383del others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | |||||
chr3:9435245
|
A | C | 1 | a0002c0002t0007g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.388+363A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435245 | ||||||
chr3:9435278
|
C | G | 26 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(23): Show | 26 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.388+396C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435278 | ||||||
chr3:9435350
|
TTC | T | 3 | a0001c0001t0012g0116a0001c0001t0021g0120a0001c0001t0024g0117 | 3 | HG02886.hp2 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.389-373_389-372del others(2): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435350 | |||||
chr3:9435366
|
G | A | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.389-362G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435366 | ||||||
chr3:9435466
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.389-262T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435466 | ||||||
chr3:9435540
|
C | G | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.389-188C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435540 | ||||||
chr3:9435546
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.389-182G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435546 | ||||||
chr3:9435547
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.389-181C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435547 | ||||||
chr3:9435549
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.389-179A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435549 | ||||||
chr3:9435621
|
G | C | 2 | a0001c0001t0002g0001a0001c0001t0005g0001 | 2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.389-107G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435621 | ||||||
chr3:9436153
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.567+247A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9436153 | ||||||
chr3:9436661
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.567+755A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9436661 | ||||||
chr3:9436837
|
C | T | 1 | a0001c0001t0003g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.567+931C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9436837 | ||||||
chr3:9437205
|
G | A | 1 | a0001c0001t0014g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.567+1299G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437205 | ||||||
chr3:9437458
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(48): Show | 52 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.567+1552G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437458 | ||||||
chr3:9437516
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.567+1610C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437516 | ||||||
chr3:9437520
|
T | G | 14 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(11): Show | 14 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.567+1614T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437520 | ||||||
chr3:9437522
|
C | CGT | 25 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0186others(22): Show | 26 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.567+1643_567+1644d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGT | 10 | a0001c0001t0001g0106a0001c0001t0002g0105a0001c0001t0032g0189others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.567+1641_567+1644d others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0003g0209a0001c0001t0007g0205 | 2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.567+1635_567+1644d others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(5): Show |
20 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0213others(17): Show | 20 | HG00621.hp1 HG01074.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.567+1633_567+1644d others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(7): Show |
13 | a0001c0001t0003g0232a0001c0001t0011g0222a0001c0001t0011g0226others(10): Show | 13 | HG00639.hp1 HG01070.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.567+1631_567+1644d others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(9): Show |
3 | a0001c0001t0006g0236a0001c0001t0024g0157a0001c0001t0055g0225 | 3 | HG02572.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.567+1629_567+1644d others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(11): Show |
9 | a0001c0001t0006g0114a0001c0001t0006g0119a0001c0001t0006g0164others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+1627_567+1644d others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(13): Show |
3 | a0001c0001t0006g0115a0001c0001t0012g0112a0001c0001t0021g0120 | 3 | HG02818.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.567+1625_567+1644d others(22): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(15): Show |
8 | a0001c0001t0008g0159a0001c0001t0008g0160a0001c0001t0008g0163others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.567+1623_567+1644d others(24): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(17): Show |
5 | a0001c0001t0008g0158a0001c0001t0008g0162a0001c0001t0017g0155others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+1621_567+1644d others(26): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437522
|
C | CGTGTGTG others(19): Show |
1 | a0001c0001t0008g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.567+1619_567+1644d others(28): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | |||||
chr3:9437671
|
G | A | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.567+1765G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437671 | ||||||
chr3:9437729
|
G | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0005g0185 | 3 | HG00323.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.567+1823G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437729 | ||||||
chr3:9437819
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.567+1913A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437819 | ||||||
chr3:9438002
|
CA | C | 91 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0137others(88): Show | 92 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.567+2111delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9438002 | |||||
chr3:9438018
|
T | A | 4 | a0001c0001t0005g0002a0001c0001t0018g0010a0001c0001t0025g0002others(1): Show | 4 | HG00673.hp2 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+2112T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438018 | ||||||
chr3:9438061
|
C | T | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567+2155C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438061 | ||||||
chr3:9438128
|
A | T | 2 | a0001c0001t0001g0054a0001c0001t0002g0046 | 2 | NA18990.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.567+2222A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438128 | ||||||
chr3:9438287
|
T | G | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.568-2169T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438287 | ||||||
chr3:9438393
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.568-2063A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438393 | ||||||
chr3:9438417
|
G | A | 6 | a0001c0001t0014g0170a0001c0001t0014g0172a0001c0001t0014g0173others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.568-2039G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438417 | ||||||
chr3:9438651
|
T | A | 1 | a0001c0001t0012g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.568-1805T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438651 | ||||||
chr3:9439199
|
A | G | 2 | a0002c0002t0007g0182a0002c0002t0019g0180 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.568-1257A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439199 | ||||||
chr3:9439200
|
C | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.568-1256C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439200 | ||||||
chr3:9439222
|
T | C | 83 | a0001c0001t0001g0069a0001c0001t0001g0186a0001c0001t0001g0188others(80): Show | 84 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.568-1234T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439222 | ||||||
chr3:9439320
|
C | T | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.568-1136C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439320 | ||||||
chr3:9439352
|
ATCAG | A | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.568-1099_568-1096d others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9439352 | |||||
chr3:9439363
|
A | G | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.568-1093A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439363 | ||||||
chr3:9439373
|
A | G | 26 | a0001c0001t0002g0033a0001c0001t0003g0209a0001c0001t0003g0210others(23): Show | 26 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.568-1083A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439373 | ||||||
chr3:9439429
|
G | T | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.568-1027G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439429 | ||||||
chr3:9439711
|
A | G | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.568-745A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439711 | ||||||
chr3:9439909
|
A | G | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.568-547A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439909 | ||||||
chr3:9440087
|
G | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.568-369G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9440087 | ||||||
chr3:9440109
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.568-347T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9440109 | ||||||
chr3:9440225
|
A | T | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.568-231A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9440225 | ||||||
chr3:9440725
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.810+27C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9440725 | ||||||
chr3:9441226
|
G | A | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.811-367G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9441226 | ||||||
chr3:9441352
|
AT | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0002g0068others(5): Show | 8 | HG02055.hp1 HG02074.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-225delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr3 | 9441352 | |||||
chr3:9441415
|
A | G | 1 | a0001c0001t0015g0032 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.811-178A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9441415 | ||||||
chr3:9441435
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.811-158G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9441435 | ||||||
chr3:9442081
|
C | T | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.960-47C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 9/22 | chr3 | 9442081 | ||||||
chr3:9442280
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+35A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442280 | ||||||
chr3:9442472
|
T | A | 3 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0057g0178 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1077+227T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442472 | ||||||
chr3:9442545
|
A | G | 1 | a0001c0001t0006g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1077+300A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442545 | ||||||
chr3:9442748
|
G | A | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1077+503G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442748 | ||||||
chr3:9442796
|
G | A | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(13): Show | 17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-512G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442796 | ||||||
chr3:9442979
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0002g0105 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1078-329G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442979 | ||||||
chr3:9442998
|
C | G | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1078-310C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442998 | ||||||
chr3:9443220
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1078-88C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9443220 | ||||||
chr3:9443235
|
G | C | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1078-73G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9443235 | ||||||
chr3:9443266
|
A | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1078-42A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9443266 | ||||||
chr3:9443638
|
CAG | C | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(13): Show | 17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1187+223_1187+224d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | 9443638 | |||||
chr3:9443805
|
C | A | 1 | a0003c0008t0002g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1187+388C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443805 | ||||||
chr3:9443836
|
C | G | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1187+419C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443836 | ||||||
chr3:9443893
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1187+476C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443893 | ||||||
chr3:9443929
|
G | A | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1187+512G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443929 | ||||||
chr3:9444047
|
G | A | 1 | a0001c0001t0055g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1187+630G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444047 | ||||||
chr3:9444091
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1187+674C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444091 | ||||||
chr3:9444282
|
T | C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1188-766T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444282 | ||||||
chr3:9444319
|
T | G | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1188-729T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444319 | ||||||
chr3:9444537
|
C | CT | 34 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(31): Show | 34 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1188-501dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | 9444537 | |||||
chr3:9444545
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1188-503T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444545 | ||||||
chr3:9444617
|
G | A | 2 | a0001c0001t0031g0077a0001c0001t0056g0229 | 2 | HG01070.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1188-431G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444617 | ||||||
chr3:9444699
|
T | C | 1 | a0001c0001t0005g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1188-349T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444699 | ||||||
chr3:9444763
|
G | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1188-285G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444763 | ||||||
chr3:9444819
|
G | A | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1188-229G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444819 | ||||||
chr3:9444841
|
A | C | 1 | a0001c0001t0001g0011 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1188-207A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444841 | ||||||
chr3:9444857
|
C | T | 3 | a0001c0001t0002g0088a0001c0001t0009g0013a0001c0001t0043g0026 | 3 | HG00597.hp1 NA18942.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1188-191C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444857 | ||||||
chr3:9445009
|
G | T | 14 | a0001c0001t0031g0077a0001c0001t0035g0177a0001c0003t0010g0195others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1188-39G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9445009 | ||||||
chr3:9445464
|
T | C | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1440+164T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 12/22 | chr3 | 9445464 | ||||||
chr3:9445937
|
T | G | 1 | a0001c0001t0049g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1524+197T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445937 | ||||||
chr3:9445962
|
G | GTT | 4 | a0001c0001t0007g0205a0001c0001t0011g0230a0001c0007t0037g0005others(1): Show | 4 | HG02129.hp2 HG04115.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+223_1524+224d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445962
|
G | GTTTTTTT others(9): Show |
3 | a0001c0001t0028g0217a0001c0001t0051g0231a0001c0001t0054g0208 | 3 | HG02004.hp1 HG02723.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1524+224_1524+225i others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445962
|
G | GTTTTTTT others(10): Show |
8 | a0001c0001t0003g0213a0001c0001t0003g0224a0001c0001t0004g0168others(5): Show | 8 | HG01070.hp1 HG01255.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+224_1524+225i others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445962
|
G | GTTTTTTT others(11): Show |
10 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0214others(7): Show | 10 | HG01074.hp1 HG01192.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+224_1524+225i others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445962
|
G | GTTTTTTT others(12): Show |
7 | a0001c0001t0003g0210a0001c0001t0003g0216a0001c0001t0003g0220others(4): Show | 7 | HG00639.hp1 HG01978.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+224_1524+225i others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445962
|
G | GTTTTTTT others(25): Show |
1 | a0001c0001t0022g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1524+224_1524+225i others(34): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445962
|
GTTGTTTT others(3): Show |
G | 1 | a0001c0001t0055g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1524+225_1524+234d others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | |||||
chr3:9445963
|
T | C | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1524+223T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445963 | ||||||
chr3:9445964
|
T | TG | 3 | a0001c0001t0002g0029a0001c0001t0004g0085a0003c0008t0002g0095 | 3 | HG03098.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1524+225dupG | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445964 | |||||
chr3:9445965
|
G | GT | 30 | a0001c0001t0001g0009a0001c0001t0001g0052a0001c0001t0001g0069others(27): Show | 31 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1524+248dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0031g0077a0001c0003t0053g0198 | 2 | HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1524+235_1524+248d others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(8): Show |
1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+234_1524+248d others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(9): Show |
2 | a0001c0003t0010g0196a0001c0003t0016g0203 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1524+233_1524+248d others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(12): Show |
3 | a0001c0003t0010g0195a0001c0003t0010g0204a0001c0003t0029g0194 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1524+230_1524+248d others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(18): Show |
1 | a0003c0005t0010g0200 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1524+248_1524+249i others(27): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(19): Show |
1 | a0003c0005t0016g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1524+248_1524+249i others(28): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | GTTTTTTT others(20): Show |
1 | a0003c0005t0016g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1524+248_1524+249i others(29): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445965
|
G | T | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1524+225G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445965 | ||||||
chr3:9445965
|
GT | G | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+248delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | |||||
chr3:9445966
|
T | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0024others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+226T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445966 | ||||||
chr3:9445968
|
T | TTTTTTTT others(8): Show |
1 | a0001c0003t0010g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1524+242_1524+243i others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445968 | |||||
chr3:9445971
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1524+231T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445971 | ||||||
chr3:9445974
|
T | TTTTTTTT others(11): Show |
1 | a0001c0001t0050g0223 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1524+248_1524+249i others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445974 | |||||
chr3:9445988
|
T | TTTTTTTT others(7): Show |
1 | a0001c0003t0029g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1524+248_1524+249i others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445988 | ||||||
chr3:9446011
|
G | A | 3 | a0003c0005t0010g0200a0003c0005t0016g0201a0003c0005t0016g0202 | 3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1524+271G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446011 | ||||||
chr3:9446026
|
G | A | 1 | a0001c0001t0024g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1524+286G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446026 | ||||||
chr3:9446069
|
C | T | 1 | a0001c0001t0023g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1524+329C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446069 | ||||||
chr3:9446095
|
C | G | 12 | a0001c0003t0010g0195a0001c0003t0010g0196a0001c0003t0010g0199others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+355C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446095 | ||||||
chr3:9446150
|
G | A | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1524+410G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446150 | ||||||
chr3:9446180
|
G | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1524+440G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446180 | ||||||
chr3:9446286
|
C | CA | 7 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0086others(4): Show | 7 | HG00597.hp1 HG00621.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+568dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9446286 | |||||
chr3:9446286
|
CAAA | C | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0213others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1524+566_1524+568d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9446286 | |||||
chr3:9446306
|
A | AAC | 32 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0127others(29): Show | 32 | HG00741.hp1 HG01109.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.1524+567_1524+568i others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9446306 | |||||
chr3:9446306
|
A | AC | 135 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1524+566_1524+567i others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446306 | ||||||
chr3:9446306
|
A | C | 37 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(34): Show | 37 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1524+566A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446306 | ||||||
chr3:9446318
|
C | T | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+578C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446318 | ||||||
chr3:9446499
|
T | G | 9 | a0001c0001t0008g0158a0001c0001t0008g0159a0001c0001t0008g0160others(6): Show | 9 | HG02258.hp2 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525-551T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446499 | ||||||
chr3:9446507
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1525-543T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446507 | ||||||
chr3:9446661
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0110 | 2 | HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1525-389T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446661 | ||||||
chr3:9446704
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0002g0053others(1): Show | 4 | HG00438.hp2 NA18948.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-346G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446704 | ||||||
chr3:9446720
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0108 | 2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1525-330C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446720 | ||||||
chr3:9446771
|
G | C | 1 | a0001c0001t0004g0063 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1525-279G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446771 | ||||||
chr3:9447031
|
C | A | 34 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(31): Show | 34 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1525-19C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9447031 | ||||||
chr3:9447481
|
A | G | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1782+174A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447481 | ||||||
chr3:9447504
|
CTAGCCTC others(13): Show |
C | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783-181_1783-162d others(22): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447504 | ||||||
chr3:9447525
|
A | G | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783-161A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447525 | ||||||
chr3:9447526
|
G | T | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783-160G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447526 | ||||||
chr3:9447650
|
A | ATTTC | 36 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(33): Show | 36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1783-34_1783-31dup others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr3 | 9447650 | |||||
chr3:9447656
|
G | A | 36 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(33): Show | 36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1783-30G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447656 | ||||||
chr3:9448053
|
T | A | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2103+47T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 15/22 | chr3 | 9448053 | ||||||
chr3:9448083
|
T | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2103+77T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 15/22 | chr3 | 9448083 | ||||||
chr3:9448164
|
G | A | 4 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228others(1): Show | 4 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+158G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 15/22 | chr3 | 9448164 | ||||||
chr3:9448747
|
C | T | 1 | a0001c0001t0005g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2346+117C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9448747 | ||||||
chr3:9448761
|
A | G | 1 | a0001c0001t0032g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2346+131A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9448761 | ||||||
chr3:9448834
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0005g0001 | 2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2346+204A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9448834 | ||||||
chr3:9449405
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2346+775A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449405 | ||||||
chr3:9449425
|
G | A | 17 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(14): Show | 17 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2346+795G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449425 | ||||||
chr3:9449444
|
T | C | 32 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(29): Show | 32 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.2346+814T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449444 | ||||||
chr3:9449947
|
G | A | 7 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(4): Show | 7 | HG00639.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2346+1317G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449947 | ||||||
chr3:9449973
|
A | T | 3 | a0004c0004t0026g0037a0004c0004t0026g0060a0004c0004t0027g0022 | 3 | NA18940.hp2 NA18950.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.2346+1343A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449973 | ||||||
chr3:9450256
|
C | T | 1 | a0001c0009t0002g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2346+1626C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450256 | ||||||
chr3:9450276
|
A | G | 1 | a0001c0001t0044g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2346+1646A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450276 | ||||||
chr3:9450311
|
A | T | 1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2346+1681A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450311 | ||||||
chr3:9450348
|
T | C | 4 | a0001c0001t0001g0020a0001c0001t0002g0070a0001c0001t0030g0019others(1): Show | 4 | HG00544.hp1 NA18970.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.2346+1718T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450348 | ||||||
chr3:9450422
|
A | T | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2346+1792A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450422 | ||||||
chr3:9450423
|
G | A | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2346+1793G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450423 | ||||||
chr3:9450583
|
A | G | 1 | a0001c0001t0004g0151 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2346+1953A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450583 | ||||||
chr3:9450592
|
T | C | 49 | a0001c0001t0001g0069a0001c0001t0001g0186a0001c0001t0001g0188others(46): Show | 50 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2346+1962T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450592 | ||||||
chr3:9450656
|
T | C | 17 | a0001c0001t0001g0069a0001c0001t0001g0186a0001c0001t0001g0188others(14): Show | 18 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.2346+2026T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450656 | ||||||
chr3:9450704
|
A | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2346+2074A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450704 | ||||||
chr3:9450749
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2346+2119A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450749 | ||||||
chr3:9450872
|
T | G | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2346+2242T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450872 | ||||||
chr3:9450923
|
T | C | 1 | a0001c0001t0051g0231 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2346+2293T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450923 | ||||||
chr3:9451559
|
T | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2347-2180T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451559 | ||||||
chr3:9451560
|
A | G | 31 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(28): Show | 31 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2347-2179A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451560 | ||||||
chr3:9451566
|
A | G | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2347-2173A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451566 | ||||||
chr3:9451578
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2347-2161G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451578 | ||||||
chr3:9451631
|
C | T | 18 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(15): Show | 19 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2347-2108C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451631 | ||||||
chr3:9451684
|
A | C | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2347-2055A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451684 | ||||||
chr3:9451727
|
C | T | 45 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(42): Show | 45 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.2347-2012C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451727 | ||||||
chr3:9451728
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2347-2011G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451728 | ||||||
chr3:9451789
|
G | A | 28 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(25): Show | 28 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.2347-1950G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451789 | ||||||
chr3:9451956
|
C | G | 1 | a0002c0002t0007g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2347-1783C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451956 | ||||||
chr3:9452201
|
A | T | 1 | a0001c0001t0008g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2347-1538A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452201 | ||||||
chr3:9452331
|
C | G | 1 | a0001c0001t0006g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2347-1408C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452331 | ||||||
chr3:9452590
|
TGTTTACA others(1): Show |
T | 81 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(78): Show | 82 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2347-1140_2347-113 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452590 | |||||
chr3:9452631
|
A | G | 30 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(27): Show | 30 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.2347-1108A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452631 | ||||||
chr3:9452659
|
A | AT | 17 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0086others(14): Show | 17 | HG01069.hp1 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2347-1055dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
A | ATT | 10 | a0001c0001t0006g0119a0001c0001t0035g0177a0001c0001t0052g0175others(7): Show | 10 | HG01071.hp1 HG01081.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.2347-1056_2347-105 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
A | ATTT | 21 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0164others(18): Show | 21 | HG01099.hp1 HG02451.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.2347-1057_2347-105 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
A | ATTTT | 8 | a0001c0001t0008g0158a0001c0001t0008g0160a0001c0001t0008g0162others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1058_2347-105 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
A | ATTTTT | 16 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(13): Show | 16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.2347-1059_2347-105 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
A | ATTTTTTT others(4): Show |
1 | a0001c0007t0058g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2347-1065_2347-105 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
A | ATTTTTTT others(5): Show |
1 | a0001c0007t0037g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2347-1066_2347-105 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
AT | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0020others(48): Show | 52 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.2347-1055delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452659
|
ATTTTT | A | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0213others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2347-1059_2347-105 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | |||||
chr3:9452704
|
G | A | 237 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2347-1035G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452704 | ||||||
chr3:9452726
|
A | G | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2347-1013A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452726 | ||||||
chr3:9452813
|
C | T | 1 | a0001c0010t0001g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2347-926C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452813 | ||||||
chr3:9452827
|
A | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(12): Show | 16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.2347-912A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452827 | ||||||
chr3:9452944
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2347-795A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452944 | ||||||
chr3:9453093
|
T | C | 1 | a0001c0001t0006g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2347-646T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453093 | ||||||
chr3:9453364
|
G | A | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2347-375G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453364 | ||||||
chr3:9453394
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2347-345C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453394 | ||||||
chr3:9453435
|
C | A | 81 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0002g0190others(78): Show | 82 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2347-304C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453435 | ||||||
chr3:9453659
|
C | G | 1 | a0001c0001t0004g0100 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2347-80C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453659 | ||||||
chr3:9453699
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2347-40A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453699 | ||||||
chr3:9453701
|
A | G | 106 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(103): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2347-38A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453701 | ||||||
chr3:9454243
|
G | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2476+375G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454243 | ||||||
chr3:9454260
|
G | T | 3 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0057g0178 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2476+392G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454260 | ||||||
chr3:9454293
|
T | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0045others(2): Show | 5 | HG01346.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476+425T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454293 | ||||||
chr3:9454478
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2476+610G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454478 | ||||||
chr3:9454524
|
G | T | 3 | a0001c0001t0001g0083a0001c0001t0002g0082a0001c0001t0047g0017 | 3 | NA18973.hp2 NA18999.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2476+656G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454524 | ||||||
chr3:9454546
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2476+678C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454546 | ||||||
chr3:9454564
|
G | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2476+696G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454564 | ||||||
chr3:9454576
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2476+708C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454576 | ||||||
chr3:9454622
|
C | CA | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0052others(21): Show | 24 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.2476+782dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
C | CAA | 5 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0002g0047others(2): Show | 5 | HG00621.hp2 HG02074.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476+781_2476+782d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0007g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2476+773_2476+782d others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
C | CAAAAAAA others(4): Show |
1 | a0002c0002t0019g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2476+772_2476+782d others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
CA | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(60): Show | 64 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2476+782delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
CAA | C | 6 | a0001c0001t0002g0024a0001c0001t0011g0226a0001c0001t0011g0230others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2476+781_2476+782d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
CAAA | C | 34 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(31): Show | 34 | HG01070.hp1 HG01081.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.2476+780_2476+782d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2476+772_2476+782d others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454622
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0188a0001c0001t0005g0185a0001c0001t0032g0189others(1): Show | 4 | HG00323.hp2 HG01515.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2476+771_2476+782d others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | |||||
chr3:9454637
|
A | C | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2476+769A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454637 | ||||||
chr3:9454638
|
A | C | 29 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(26): Show | 29 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.2476+770A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454638 | ||||||
chr3:9454639
|
A | C | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2476+771A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454639 | ||||||
chr3:9454644
|
A | C | 2 | a0001c0001t0013g0039a0001c0001t0013g0079 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2476+776A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454644 | ||||||
chr3:9455168
|
C | CT | 27 | a0001c0001t0001g0051a0001c0001t0001g0062a0001c0001t0001g0108others(24): Show | 27 | HG01099.hp2 HG01109.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.2476+1322dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | |||||
chr3:9455168
|
C | CTT | 5 | a0001c0001t0001g0138a0001c0001t0006g0119a0001c0001t0006g0236others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476+1321_2476+132 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | |||||
chr3:9455168
|
C | CTTT | 20 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0218others(17): Show | 20 | HG01884.hp1 HG02129.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.2476+1320_2476+132 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | |||||
chr3:9455168
|
C | CTTTT | 13 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(10): Show | 13 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2476+1319_2476+132 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | |||||
chr3:9455168
|
CT | C | 12 | a0001c0001t0002g0190a0001c0001t0040g0090a0002c0002t0007g0004others(9): Show | 13 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2476+1322delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | |||||
chr3:9455173
|
T | C | 11 | a0001c0001t0002g0190a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+1305T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455173 | ||||||
chr3:9455175
|
T | C | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2476+1307T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455175 | ||||||
chr3:9455193
|
A | G | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+1325A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455193 | ||||||
chr3:9455208
|
G | A | 1 | a0001c0001t0055g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2476+1340G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455208 | ||||||
chr3:9455230
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2476+1362C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455230 | ||||||
chr3:9455297
|
G | A | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2476+1429G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455297 | ||||||
chr3:9455359
|
G | T | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+1491G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455359 | ||||||
chr3:9455665
|
GT | G | 91 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0003g0210others(88): Show | 92 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.2476+1799delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455665 | |||||
chr3:9455709
|
G | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0045others(2): Show | 5 | HG01346.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476+1841G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455709 | ||||||
chr3:9455737
|
T | C | 3 | a0003c0005t0010g0200a0003c0005t0016g0201a0003c0005t0016g0202 | 3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2476+1869T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455737 | ||||||
chr3:9455915
|
A | G | 3 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0057g0178 | 3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2476+2047A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455915 | ||||||
chr3:9456198
|
G | A | 30 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(27): Show | 30 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.2476+2330G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456198 | ||||||
chr3:9456200
|
C | T | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2332C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456200 | ||||||
chr3:9456201
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2476+2333G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456201 | ||||||
chr3:9456201
|
GT | G | 76 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(73): Show | 77 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.2476+2335delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9456201 | |||||
chr3:9456211
|
C | G | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2476+2343C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456211 | ||||||
chr3:9456251
|
G | A | 3 | a0001c0003t0010g0195a0001c0003t0010g0204a0001c0003t0029g0194 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2476+2383G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456251 | ||||||
chr3:9456286
|
G | A | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2476+2418G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456286 | ||||||
chr3:9456336
|
C | T | 1 | a0002c0002t0007g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2476+2468C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456336 | ||||||
chr3:9456344
|
C | T | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+2476C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456344 | ||||||
chr3:9456346
|
T | C | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+2478T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456346 | ||||||
chr3:9456458
|
G | A | 12 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2590G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456458 | ||||||
chr3:9456459
|
G | A | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2591G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456459 | ||||||
chr3:9456480
|
T | TA | 65 | a0001c0001t0002g0142a0001c0001t0003g0209a0001c0001t0003g0210others(62): Show | 65 | HG00621.hp1 HG00639.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.2476+2629dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9456480 | |||||
chr3:9456480
|
T | TAA | 14 | a0001c0001t0020g0153a0001c0001t0020g0154a0001c0001t0046g0206others(11): Show | 15 | HG00735.hp1 HG00741.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.2476+2628_2476+262 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9456480 | |||||
chr3:9456562
|
A | G | 1 | a0001c0001t0040g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2476+2694A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456562 | ||||||
chr3:9456617
|
T | C | 1 | a0001c0001t0005g0065 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2476+2749T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456617 | ||||||
chr3:9456751
|
G | T | 1 | a0001c0001t0055g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2476+2883G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456751 | ||||||
chr3:9456835
|
G | A | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2967G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456835 | ||||||
chr3:9456890
|
T | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2476+3022T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456890 | ||||||
chr3:9456970
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0018g0124 | 2 | HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2476+3102G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456970 | ||||||
chr3:9457030
|
G | GAAGA | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+3169_2476+317 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9457030 | |||||
chr3:9457117
|
T | A | 1 | a0004c0004t0027g0078 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2476+3249T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457117 | ||||||
chr3:9457149
|
A | G | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+3281A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457149 | ||||||
chr3:9457190
|
TTAA | T | 2 | a0001c0001t0001g0106a0001c0001t0002g0105 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2476+3329_2476+333 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9457190 | |||||
chr3:9457372
|
C | A | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+3504C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457372 | ||||||
chr3:9457373
|
G | A | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2476+3505G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457373 | ||||||
chr3:9457376
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2476+3508A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457376 | ||||||
chr3:9457444
|
G | A | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2476+3576G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457444 | ||||||
chr3:9457566
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2476+3698G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457566 | ||||||
chr3:9457578
|
T | A | 1 | a0001c0001t0023g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2476+3710T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457578 | ||||||
chr3:9457579
|
A | T | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2476+3711A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457579 | ||||||
chr3:9457636
|
C | T | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+3768C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457636 | ||||||
chr3:9457764
|
A | G | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2476+3896A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457764 | ||||||
chr3:9457991
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2476+4123T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457991 | ||||||
chr3:9458066
|
G | A | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+4198G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458066 | ||||||
chr3:9458108
|
T | C | 2 | a0002c0002t0019g0183a0002c0002t0042g0179 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2476+4240T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458108 | ||||||
chr3:9458514
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2476+4646G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458514 | ||||||
chr3:9458517
|
G | A | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+4649G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458517 | ||||||
chr3:9458606
|
C | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2476+4738C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458606 | ||||||
chr3:9458661
|
A | G | 1 | a0001c0001t0044g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2476+4793A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458661 | ||||||
chr3:9459164
|
G | A | 9 | a0001c0001t0001g0084a0001c0001t0015g0031a0001c0001t0015g0032others(6): Show | 9 | HG02040.hp2 HG02080.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.2477-5261G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459164 | ||||||
chr3:9459263
|
G | C | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2477-5162G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459263 | ||||||
chr3:9459304
|
T | G | 1 | a0002c0002t0019g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2477-5121T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459304 | ||||||
chr3:9459419
|
G | A | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2477-5006G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459419 | ||||||
chr3:9459476
|
A | C | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-4949A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459476 | ||||||
chr3:9459629
|
A | C | 33 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(30): Show | 34 | HG00673.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.2477-4796A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459629 | ||||||
chr3:9459638
|
C | A | 1 | a0001c0001t0036g0025 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2477-4787C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459638 | ||||||
chr3:9459712
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2477-4713A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459712 | ||||||
chr3:9459714
|
C | CA | 46 | a0001c0001t0001g0086a0001c0001t0003g0209a0001c0001t0003g0211others(43): Show | 46 | HG00621.hp1 HG00639.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.2477-4693dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9459714 | |||||
chr3:9459714
|
C | CAA | 15 | a0001c0001t0003g0210a0001c0001t0006g0114a0001c0001t0006g0115others(12): Show | 15 | HG01081.hp2 HG01978.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-4694_2477-469 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9459714 | |||||
chr3:9459941
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2477-4484C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459941 | ||||||
chr3:9460025
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2477-4400A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460025 | ||||||
chr3:9460027
|
C | G | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2477-4398C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460027 | ||||||
chr3:9460089
|
C | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-4336C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460089 | ||||||
chr3:9460145
|
T | C | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-4280T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460145 | ||||||
chr3:9460170
|
A | G | 11 | a0001c0001t0006g0164a0001c0001t0008g0158a0001c0001t0008g0159others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2477-4255A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460170 | ||||||
chr3:9460204
|
T | C | 1 | a0001c0001t0013g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2477-4221T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460204 | ||||||
chr3:9460210
|
A | T | 1 | a0001c0001t0013g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2477-4215A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460210 | ||||||
chr3:9460245
|
A | G | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-4180A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460245 | ||||||
chr3:9460263
|
T | TA | 10 | a0001c0001t0032g0189a0002c0002t0007g0004a0002c0002t0007g0181others(7): Show | 11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2477-4150dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9460263 | |||||
chr3:9460395
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2477-4030C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460395 | ||||||
chr3:9460524
|
C | T | 35 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(32): Show | 35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2477-3901C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460524 | ||||||
chr3:9460643
|
A | G | 1 | a0001c0001t0022g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2477-3782A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460643 | ||||||
chr3:9460779
|
T | C | 92 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0003g0210others(89): Show | 93 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.2477-3646T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460779 | ||||||
chr3:9460813
|
C | T | 1 | a0002c0002t0007g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2477-3612C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460813 | ||||||
chr3:9461269
|
A | G | 1 | a0001c0001t0030g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2477-3156A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9461269 | ||||||
chr3:9461510
|
G | T | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-2915G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9461510 | ||||||
chr3:9461575
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-2850A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9461575 | ||||||
chr3:9462359
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2477-2066G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462359 | ||||||
chr3:9462415
|
G | A | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2477-2010G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462415 | ||||||
chr3:9462432
|
A | G | 1 | a0001c0001t0012g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2477-1993A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462432 | ||||||
chr3:9462575
|
A | G | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2477-1850A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462575 | ||||||
chr3:9462586
|
CA | C | 13 | a0001c0001t0007g0205a0001c0003t0010g0195a0001c0003t0053g0198others(10): Show | 14 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2477-1824delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9462586 | |||||
chr3:9462823
|
T | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-1602T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462823 | ||||||
chr3:9462838
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2477-1587A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462838 | ||||||
chr3:9462905
|
G | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-1520G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462905 | ||||||
chr3:9462948
|
T | A | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-1477T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462948 | ||||||
chr3:9463021
|
C | A | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-1404C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463021 | ||||||
chr3:9463163
|
G | A | 8 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01109.hp1 HG02809.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2477-1262G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463163 | ||||||
chr3:9463201
|
T | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0033others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-1224T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463201 | ||||||
chr3:9463275
|
G | C | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-1150G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463275 | ||||||
chr3:9463554
|
C | T | 93 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0003g0210others(90): Show | 94 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.2477-871C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463554 | ||||||
chr3:9463665
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0002g0012 | 2 | HG01258.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2477-760A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463665 | ||||||
chr3:9463778
|
T | C | 18 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(15): Show | 18 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2477-647T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463778 | ||||||
chr3:9463787
|
A | G | 4 | a0001c0001t0005g0002a0001c0001t0018g0010a0001c0001t0025g0002others(1): Show | 4 | HG00673.hp2 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2477-638A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463787 | ||||||
chr3:9463803
|
A | G | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-622A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463803 | ||||||
chr3:9463823
|
T | C | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-602T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463823 | ||||||
chr3:9464107
|
G | A | 1 | a0001c0001t0032g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2477-318G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9464107 | ||||||
chr3:9464367
|
G | A | 6 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0005g0002others(3): Show | 6 | HG00438.hp1 HG00673.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-58G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9464367 | ||||||
chr3:9464770
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2724+98T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464770 | ||||||
chr3:9464889
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2724+217A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464889 | ||||||
chr3:9464943
|
A | G | 1 | a0001c0001t0034g0028 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2724+271A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464943 | ||||||
chr3:9464966
|
G | A | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2724+294G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464966 | ||||||
chr3:9465024
|
A | T | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2724+352A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465024 | ||||||
chr3:9465054
|
T | C | 15 | a0001c0001t0002g0190a0001c0003t0010g0195a0001c0003t0010g0196others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2724+382T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465054 | ||||||
chr3:9465086
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2724+414A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465086 | ||||||
chr3:9465309
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2724+637A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465309 | ||||||
chr3:9465341
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2724+669T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465341 | ||||||
chr3:9465573
|
C | T | 10 | a0002c0002t0007g0004a0002c0002t0007g0181a0002c0002t0007g0182others(7): Show | 11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2724+901C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465573 | ||||||
chr3:9465587
|
C | G | 32 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0023others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.2724+915C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465587 | ||||||
chr3:9465630
|
T | A | 10 | a0002c0002t0007g0004a0002c0002t0007g0181a0002c0002t0007g0182others(7): Show | 11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2724+958T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465630 | ||||||
chr3:9465695
|
C | T | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2724+1023C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465695 | ||||||
chr3:9465715
|
T | C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2724+1043T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465715 | ||||||
chr3:9466170
|
C | G | 1 | a0001c0001t0007g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2724+1498C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466170 | ||||||
chr3:9466171
|
C | G | 1 | a0001c0001t0031g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2724+1499C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466171 | ||||||
chr3:9466224
|
C | G | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2724+1552C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466224 | ||||||
chr3:9466283
|
G | C | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2724+1611G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466283 | ||||||
chr3:9466287
|
C | CA | 13 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0056others(10): Show | 13 | HG00621.hp1 HG01934.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2724+1637dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9466287 | |||||
chr3:9466287
|
CA | C | 52 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0003g0209others(49): Show | 53 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.2724+1637delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9466287 | |||||
chr3:9466287
|
CAA | C | 23 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0024others(20): Show | 23 | HG01070.hp1 HG01109.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2724+1636_2724+163 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9466287 | |||||
chr3:9466304
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2724+1632A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466304 | ||||||
chr3:9466306
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2724+1634A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466306 | ||||||
chr3:9466473
|
A | C | 33 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(30): Show | 33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2724+1801A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466473 | ||||||
chr3:9466581
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2724+1909A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466581 | ||||||
chr3:9466613
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2724+1941T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466613 | ||||||
chr3:9466640
|
C | T | 10 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(7): Show | 10 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2724+1968C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466640 | ||||||
chr3:9466672
|
G | C | 6 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(3): Show | 6 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2724+2000G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466672 | ||||||
chr3:9466708
|
A | G | 10 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228others(7): Show | 10 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2724+2036A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466708 | ||||||
chr3:9466854
|
A | G | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2724+2182A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466854 | ||||||
chr3:9466994
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2724+2322A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466994 | ||||||
chr3:9467039
|
A | C | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2724+2367A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467039 | ||||||
chr3:9467120
|
G | A | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2724+2448G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467120 | ||||||
chr3:9467199
|
C | CA | 34 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0021others(31): Show | 35 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2724+2552dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | |||||
chr3:9467199
|
C | CAA | 11 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG00621.hp2 HG00741.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2724+2551_2724+255 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | |||||
chr3:9467199
|
C | CAAA | 5 | a0001c0003t0010g0204a0001c0003t0029g0197a0003c0005t0010g0200others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2724+2550_2724+255 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | |||||
chr3:9467199
|
C | CAAAA | 6 | a0001c0003t0010g0195a0001c0003t0016g0193a0001c0003t0016g0203others(3): Show | 6 | HG01175.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2724+2549_2724+255 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | |||||
chr3:9467199
|
CAA | C | 11 | a0001c0001t0003g0210a0001c0001t0003g0215a0001c0001t0008g0166others(8): Show | 11 | HG00621.hp1 HG01978.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2724+2551_2724+255 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | |||||
chr3:9467199
|
CAAA | C | 43 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0001t0003g0213others(40): Show | 43 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.2724+2550_2724+255 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | |||||
chr3:9467214
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0011g0228 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2724+2545_2724+255 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467214 | |||||
chr3:9467215
|
AAAAAAAA others(3): Show |
A | 7 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0230others(4): Show | 7 | HG01070.hp1 HG01255.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.2724+2546_2724+255 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467215 | |||||
chr3:9467263
|
G | A | 10 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228others(7): Show | 10 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2724+2591G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467263 | ||||||
chr3:9467451
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2724+2779A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467451 | ||||||
chr3:9467496
|
G | A | 15 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(12): Show | 15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2724+2824G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467496 | ||||||
chr3:9467514
|
C | T | 1 | a0001c0001t0052g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2724+2842C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467514 | ||||||
chr3:9467744
|
C | T | 15 | a0001c0001t0002g0190a0001c0003t0010g0195a0001c0003t0010g0196others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2725-2715C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467744 | ||||||
chr3:9467795
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2725-2664C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467795 | ||||||
chr3:9467799
|
C | T | 7 | a0001c0001t0014g0170a0001c0001t0014g0172a0001c0001t0014g0173others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2725-2660C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467799 | ||||||
chr3:9467869
|
G | C | 1 | a0001c0001t0049g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2725-2590G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467869 | ||||||
chr3:9467962
|
C | G | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2725-2497C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467962 | ||||||
chr3:9468392
|
C | T | 1 | a0001c0001t0005g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2725-2067C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468392 | ||||||
chr3:9468404
|
C | T | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2725-2055C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468404 | ||||||
chr3:9468405
|
C | T | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2725-2054C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468405 | ||||||
chr3:9468702
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2725-1757A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468702 | ||||||
chr3:9468788
|
G | A | 1 | a0002c0002t0045g0187 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2725-1671G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468788 | ||||||
chr3:9468806
|
G | A | 1 | a0001c0001t0031g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2725-1653G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468806 | ||||||
chr3:9468938
|
A | G | 3 | a0001c0001t0012g0116a0001c0001t0021g0120a0001c0001t0024g0117 | 3 | HG02886.hp2 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2725-1521A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468938 | ||||||
chr3:9469480
|
T | A | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2725-979T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469480 | ||||||
chr3:9469525
|
G | C | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2725-934G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469525 | ||||||
chr3:9469627
|
C | T | 25 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(22): Show | 25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2725-832C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469627 | ||||||
chr3:9469682
|
C | T | 1 | a0002c0002t0007g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2725-777C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469682 | ||||||
chr3:9469709
|
G | A | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2725-750G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469709 | ||||||
chr3:9469871
|
C | T | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2725-588C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469871 | ||||||
chr3:9469916
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2725-543G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469916 | ||||||
chr3:9469952
|
T | C | 1 | a0001c0001t0001g0129 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2725-507T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469952 | ||||||
chr3:9470008
|
C | T | 1 | a0001c0001t0051g0231 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2725-451C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470008 | ||||||
chr3:9470011
|
C | T | 32 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(29): Show | 32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2725-448C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470011 | ||||||
chr3:9470045
|
C | T | 2 | a0001c0001t0031g0077a0001c0001t0035g0177 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2725-414C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470045 | ||||||
chr3:9470052
|
C | T | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2725-407C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470052 | ||||||
chr3:9470291
|
G | A | 11 | a0001c0001t0007g0205a0002c0002t0007g0004a0002c0002t0007g0181others(8): Show | 12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2725-168G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470291 | ||||||
chr3:9470978
|
G | A | 1 | a0001c0001t0024g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3195+49G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9470978 | ||||||
chr3:9471023
|
A | G | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3195+94A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471023 | ||||||
chr3:9471098
|
T | C | 1 | a0004c0004t0026g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3195+169T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471098 | ||||||
chr3:9471435
|
G | C | 6 | a0001c0001t0011g0226a0001c0001t0011g0227a0001c0001t0011g0228others(3): Show | 6 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3195+506G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471435 | ||||||
chr3:9471728
|
G | A | 5 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0213others(2): Show | 5 | HG01074.hp1 HG01192.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.3195+799G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471728 | ||||||
chr3:9471785
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0002g0131 | 3 | HG00099.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3195+856G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471785 | ||||||
chr3:9471877
|
G | T | 1 | a0001c0001t0049g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3195+948G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471877 | ||||||
chr3:9472067
|
C | T | 1 | a0001c0001t0006g0119 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3195+1138C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472067 | ||||||
chr3:9472173
|
T | C | 9 | a0001c0001t0002g0190a0001c0003t0010g0195a0001c0003t0010g0196others(6): Show | 9 | HG01099.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3196-1063T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472173 | ||||||
chr3:9472190
|
A | ACACT | 3 | a0001c0001t0001g0146a0001c0001t0002g0046a0004c0004t0027g0078 | 3 | HG02132.hp1 NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3196-1046_3196-104 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472190 | ||||||
chr3:9472191
|
A | ACACTT | 38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(35): Show | 38 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.3196-1043_3196-103 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | 9472191 | |||||
chr3:9472191
|
A | T | 3 | a0001c0001t0001g0146a0001c0001t0002g0046a0004c0004t0027g0078 | 3 | HG02132.hp1 NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3196-1045A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472191 | ||||||
chr3:9472332
|
G | A | 61 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(58): Show | 62 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.3196-904G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472332 | ||||||
chr3:9472544
|
A | G | 2 | a0001c0007t0037g0005a0001c0007t0058g0006 | 2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.3196-692A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472544 | ||||||
chr3:9472644
|
A | G | 1 | a0002c0002t0007g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3196-592A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472644 | ||||||
chr3:9472724
|
C | CCACCTCC others(7): Show |
3 | a0001c0001t0046g0206a0001c0007t0037g0005a0001c0007t0058g0006 | 3 | HG02129.hp2 HG02723.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3196-510_3196-497d others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | 9472724 | |||||
chr3:9472752
|
C | T | 1 | a0001c0001t0008g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3196-484C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472752 | ||||||
chr3:9472791
|
G | A | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3196-445G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472791 | ||||||
chr3:9472896
|
G | A | 76 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(73): Show | 77 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.3196-340G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472896 | ||||||
chr3:9472907
|
C | T | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3196-329C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472907 | ||||||
chr3:9473024
|
A | G | 1 | a0001c0001t0044g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3196-212A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473024 | ||||||
chr3:9473153
|
T | C | 3 | a0001c0001t0046g0206a0001c0007t0037g0005a0001c0007t0058g0006 | 3 | HG02129.hp2 HG02723.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3196-83T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473153 | ||||||
chr3:9473172
|
G | A | 91 | a0001c0001t0002g0190a0001c0001t0003g0209a0001c0001t0003g0210others(88): Show | 92 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.3196-64G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473172 | ||||||
chr3:9473204
|
C | T | 1 | a0001c0001t0012g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3196-32C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473204 | ||||||
chr3:9473551
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3497+14T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473551 | ||||||
chr3:9473608
|
G | C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3497+71G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473608 | ||||||
chr3:9473711
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3497+174C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473711 | ||||||
chr3:9473910
|
C | T | 1 | a0001c0001t0035g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3497+373C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473910 | ||||||
chr3:9474101
|
A | C | 1 | a0001c0001t0046g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3498-348A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9474101 | ||||||
chr3:9474260
|
GGTT | G | 9 | a0001c0001t0006g0114a0001c0001t0006g0115a0001c0001t0006g0119others(6): Show | 9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3498-181_3498-179d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr3 | 9474260 | |||||
chr3:9474656
|
G | A | 7 | a0001c0001t0001g0072a0001c0001t0009g0071a0001c0001t0022g0018others(4): Show | 7 | HG00735.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3631+74G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474656 | ||||||
chr3:9474700
|
G | A | 1 | a0001c0001t0031g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3631+118G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474700 | ||||||
chr3:9474840
|
C | T | 1 | a0001c0001t0018g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3632-228C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474840 | ||||||
chr3:9474902
|
T | C | 12 | a0001c0001t0006g0164a0001c0001t0007g0205a0001c0001t0008g0158others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3632-166T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474902 | ||||||
chr3:9475245
|
C | G | 1 | a0001c0001t0006g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3720+89C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475245 | ||||||
chr3:9475389
|
A | G | 2 | a0001c0001t0020g0153a0001c0001t0020g0154 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3721-94A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475389 | ||||||
chr3:9475448
|
C | T | 1 | a0001c0003t0016g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3721-35C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475448 | ||||||
chr3:9475450
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3721-33C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475450 |