Variant report
Variant | rs10515598 |
---|---|
Chromosome Location | chr5:147332895-147332896 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10036463 | 1.00[EUR][1000 genomes] |
rs10037068 | 1.00[EUR][1000 genomes] |
rs10037369 | 1.00[EUR][1000 genomes] |
rs10037673 | 1.00[EUR][1000 genomes] |
rs10038266 | 1.00[EUR][1000 genomes] |
rs10038968 | 1.00[EUR][1000 genomes] |
rs10041966 | 1.00[EUR][1000 genomes] |
rs10042754 | 1.00[EUR][1000 genomes] |
rs10044155 | 1.00[EUR][1000 genomes] |
rs10052920 | 1.00[EUR][1000 genomes] |
rs10054271 | 1.00[EUR][1000 genomes] |
rs10055303 | 1.00[EUR][1000 genomes] |
rs10056490 | 1.00[EUR][1000 genomes] |
rs10056793 | 1.00[EUR][1000 genomes] |
rs10057434 | 1.00[EUR][1000 genomes] |
rs10060456 | 1.00[EUR][1000 genomes] |
rs10062167 | 1.00[EUR][1000 genomes] |
rs10063124 | 1.00[EUR][1000 genomes] |
rs10063154 | 1.00[EUR][1000 genomes] |
rs10064440 | 1.00[EUR][1000 genomes] |
rs10065895 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10067543 | 1.00[EUR][1000 genomes] |
rs10067929 | 1.00[EUR][1000 genomes] |
rs10069389 | 1.00[EUR][1000 genomes] |
rs10070673 | 1.00[EUR][1000 genomes] |
rs10072814 | 1.00[EUR][1000 genomes] |
rs10074421 | 1.00[EUR][1000 genomes] |
rs10075087 | 1.00[EUR][1000 genomes] |
rs10075879 | 1.00[EUR][1000 genomes] |
rs10076722 | 1.00[EUR][1000 genomes] |
rs10076759 | 1.00[EUR][1000 genomes] |
rs10077349 | 1.00[EUR][1000 genomes] |
rs10078401 | 1.00[EUR][1000 genomes] |
rs10079585 | 1.00[EUR][1000 genomes] |
rs10079907 | 1.00[EUR][1000 genomes] |
rs10477356 | 1.00[EUR][1000 genomes] |
rs10477361 | 1.00[EUR][1000 genomes] |
rs10477362 | 1.00[EUR][1000 genomes] |
rs10515604 | 1.00[EUR][1000 genomes] |
rs11952390 | 1.00[EUR][1000 genomes] |
rs11956316 | 1.00[EUR][1000 genomes] |
rs11960859 | 1.00[EUR][1000 genomes] |
rs12171507 | 1.00[MEX][hapmap] |
rs13357089 | 1.00[EUR][1000 genomes] |
rs13360221 | 1.00[MEX][hapmap] |
rs13436290 | 1.00[EUR][1000 genomes] |
rs13436617 | 1.00[EUR][1000 genomes] |
rs13436756 | 1.00[EUR][1000 genomes] |
rs13436799 | 1.00[EUR][1000 genomes] |
rs13436800 | 1.00[EUR][1000 genomes] |
rs1422984 | 1.00[EUR][1000 genomes] |
rs1422999 | 1.00[MEX][hapmap] |
rs17096677 | 1.00[EUR][1000 genomes] |
rs17107495 | 1.00[EUR][1000 genomes] |
rs17107570 | 1.00[EUR][1000 genomes] |
rs17107730 | 1.00[EUR][1000 genomes] |
rs17107741 | 1.00[EUR][1000 genomes] |
rs28408445 | 1.00[EUR][1000 genomes] |
rs28433470 | 0.94[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs28449960 | 1.00[EUR][1000 genomes] |
rs28545137 | 1.00[EUR][1000 genomes] |
rs28573919 | 1.00[EUR][1000 genomes] |
rs28631785 | 1.00[EUR][1000 genomes] |
rs28732977 | 1.00[EUR][1000 genomes] |
rs28753859 | 1.00[EUR][1000 genomes] |
rs4502809 | 1.00[EUR][1000 genomes] |
rs4529179 | 1.00[EUR][1000 genomes] |
rs4994723 | 1.00[EUR][1000 genomes] |
rs56121007 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57186409 | 1.00[EUR][1000 genomes] |
rs57804951 | 1.00[EUR][1000 genomes] |
rs58069263 | 1.00[EUR][1000 genomes] |
rs58257443 | 1.00[EUR][1000 genomes] |
rs58888156 | 1.00[EUR][1000 genomes] |
rs60076377 | 1.00[EUR][1000 genomes] |
rs60206159 | 1.00[EUR][1000 genomes] |
rs60937504 | 1.00[EUR][1000 genomes] |
rs61331507 | 1.00[EUR][1000 genomes] |
rs6898139 | 1.00[EUR][1000 genomes] |
rs73265206 | 1.00[EUR][1000 genomes] |
rs73265249 | 1.00[EUR][1000 genomes] |
rs73265266 | 1.00[EUR][1000 genomes] |
rs73265280 | 1.00[EUR][1000 genomes] |
rs73265300 | 1.00[EUR][1000 genomes] |
rs73265302 | 1.00[EUR][1000 genomes] |
rs73271118 | 1.00[EUR][1000 genomes] |
rs73794605 | 1.00[EUR][1000 genomes] |
rs73797307 | 1.00[EUR][1000 genomes] |
rs73797311 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7700644 | 1.00[EUR][1000 genomes] |
rs9325051 | 1.00[EUR][1000 genomes] |
rs9325053 | 1.00[EUR][1000 genomes] |
rs9325054 | 1.00[EUR][1000 genomes] |
rs9325055 | 1.00[EUR][1000 genomes] |
rs9325056 | 1.00[EUR][1000 genomes] |
rs9325059 | 1.00[EUR][1000 genomes] |
rs9325060 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3334831 | chr5:147165950-147339765 | Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv1028477 | chr5:147255013-147416217 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | esv16820 | chr5:147320290-147337996 | Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | esv3692876 | chr5:147326902-147337164 | Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv2760927 | chr5:147327342-147343763 | Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv441968 | chr5:147327346-147337913 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv514328 | chr5:147329263-147337727 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:147326600-147345200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr5:147327000-147343200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr5:147327200-147343400 | Weak transcription | H9 Cell Line | embryonic stem cell |
4 | chr5:147327400-147335400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
5 | chr5:147327400-147335400 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
6 | chr5:147327600-147335200 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
7 | chr5:147328400-147334800 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
8 | chr5:147328400-147337600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
9 | chr5:147328400-147343400 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
10 | chr5:147330200-147335400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
11 | chr5:147330200-147335600 | Weak transcription | Hela-S3 | cervix |
12 | chr5:147331800-147343000 | Weak transcription | HUES64 Cell Line | embryonic stem cell |