Variant report
Variant | rs35060258 |
---|---|
Chromosome Location | chr5:90255753-90255754 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:90249044..90251772-chr5:90253923..90256613,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10074525 | 1.00[ASN][1000 genomes] |
rs10514342 | 1.00[ASN][1000 genomes] |
rs10514343 | 1.00[ASN][1000 genomes] |
rs11738573 | 1.00[ASN][1000 genomes] |
rs11743775 | 1.00[ASN][1000 genomes] |
rs11744033 | 1.00[ASN][1000 genomes] |
rs11744325 | 1.00[ASN][1000 genomes] |
rs11949884 | 1.00[ASN][1000 genomes] |
rs11951675 | 1.00[ASN][1000 genomes] |
rs11952993 | 1.00[ASN][1000 genomes] |
rs11955946 | 1.00[ASN][1000 genomes] |
rs12186968 | 1.00[ASN][1000 genomes] |
rs12187656 | 1.00[ASN][1000 genomes] |
rs12187790 | 1.00[ASN][1000 genomes] |
rs12188068 | 1.00[ASN][1000 genomes] |
rs12188094 | 1.00[ASN][1000 genomes] |
rs12188249 | 1.00[ASN][1000 genomes] |
rs12188655 | 1.00[ASN][1000 genomes] |
rs12189005 | 1.00[ASN][1000 genomes] |
rs17571029 | 1.00[ASN][1000 genomes] |
rs17572843 | 1.00[ASN][1000 genomes] |
rs17633498 | 1.00[ASN][1000 genomes] |
rs1976566 | 1.00[ASN][1000 genomes] |
rs2438348 | 1.00[ASN][1000 genomes] |
rs3114653 | 1.00[ASN][1000 genomes] |
rs34243354 | 1.00[ASN][1000 genomes] |
rs34381536 | 0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35299092 | 1.00[ASN][1000 genomes] |
rs55792004 | 1.00[ASN][1000 genomes] |
rs55941525 | 1.00[ASN][1000 genomes] |
rs56051320 | 1.00[ASN][1000 genomes] |
rs56099704 | 1.00[ASN][1000 genomes] |
rs56106025 | 1.00[ASN][1000 genomes] |
rs56258383 | 1.00[ASN][1000 genomes] |
rs62374052 | 1.00[ASN][1000 genomes] |
rs62376462 | 1.00[ASN][1000 genomes] |
rs62376463 | 1.00[ASN][1000 genomes] |
rs62376490 | 1.00[ASN][1000 genomes] |
rs62376491 | 1.00[ASN][1000 genomes] |
rs6452927 | 1.00[ASN][1000 genomes] |
rs66509877 | 1.00[ASN][1000 genomes] |
rs6860216 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6880626 | 1.00[ASN][1000 genomes] |
rs6886773 | 1.00[ASN][1000 genomes] |
rs6888672 | 1.00[ASN][1000 genomes] |
rs6888979 | 1.00[ASN][1000 genomes] |
rs6889138 | 1.00[ASN][1000 genomes] |
rs72784617 | 1.00[ASN][1000 genomes] |
rs72784624 | 1.00[ASN][1000 genomes] |
rs72784689 | 1.00[ASN][1000 genomes] |
rs7711168 | 1.00[ASN][1000 genomes] |
rs7721862 | 1.00[ASN][1000 genomes] |
rs7723305 | 1.00[ASN][1000 genomes] |
rs949789 | 0.87[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529544 | chr5:89523963-90412409 | Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 58 gene(s) | inside rSNPs | diseases |
2 | nsv517049 | chr5:90003131-90262475 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 9 gene(s) | inside rSNPs | diseases |
3 | nsv964781 | chr5:90249699-90256976 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv462247 | chr5:90249900-90298632 | Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv598928 | chr5:90249900-90298632 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:90230400-90265200 | Weak transcription | K562 | blood |
2 | chr5:90236800-90263200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr5:90242600-90261000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
4 | chr5:90253000-90265200 | Weak transcription | Fetal Brain Female | brain |
5 | chr5:90253200-90258000 | Weak transcription | Muscle Satellite Cultured Cells | -- |
6 | chr5:90253800-90258000 | Weak transcription | HUVEC | blood vessel |