Variant report
Variant | rs12233848 |
---|---|
Chromosome Location | chr4:175277948-175277949 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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rs_ID | r2[population] |
---|---|
rs11725800 | 0.88[ASN][1000 genomes] |
rs11727574 | 0.89[ASN][1000 genomes] |
rs11732586 | 0.89[ASN][1000 genomes] |
rs11735455 | 0.89[ASN][1000 genomes] |
rs13101376 | 0.89[ASN][1000 genomes] |
rs13102962 | 0.85[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs13107351 | 0.88[ASN][1000 genomes] |
rs13108930 | 0.88[ASN][1000 genomes] |
rs13109756 | 0.89[ASN][1000 genomes] |
rs13120534 | 0.89[ASN][1000 genomes] |
rs13122946 | 0.88[ASN][1000 genomes] |
rs13126536 | 0.87[ASN][1000 genomes] |
rs13132617 | 0.88[ASN][1000 genomes] |
rs13135662 | 0.83[ASN][1000 genomes] |
rs13140627 | 0.88[ASN][1000 genomes] |
rs13142395 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs13145787 | 0.87[ASN][1000 genomes] |
rs13146439 | 0.88[ASN][1000 genomes] |
rs13149585 | 0.83[ASN][1000 genomes] |
rs13149810 | 0.88[ASN][1000 genomes] |
rs13150656 | 0.88[ASN][1000 genomes] |
rs13152348 | 0.81[ASN][1000 genomes] |
rs1922383 | 0.89[ASN][1000 genomes] |
rs1922384 | 0.88[ASN][1000 genomes] |
rs28519075 | 0.89[ASN][1000 genomes] |
rs28657489 | 0.90[ASN][1000 genomes] |
rs34037587 | 0.88[ASN][1000 genomes] |
rs34054930 | 0.85[ASN][1000 genomes] |
rs34135350 | 0.85[ASN][1000 genomes] |
rs34175211 | 0.86[ASN][1000 genomes] |
rs34261835 | 0.88[AFR][1000 genomes];0.94[AMR][1000 genomes] |
rs34400328 | 0.91[ASN][1000 genomes] |
rs34421418 | 0.90[ASN][1000 genomes] |
rs34425026 | 0.91[ASN][1000 genomes] |
rs34572193 | 0.87[ASN][1000 genomes] |
rs34592304 | 0.85[ASN][1000 genomes] |
rs34604934 | 0.88[ASN][1000 genomes] |
rs34609084 | 0.89[ASN][1000 genomes] |
rs34674779 | 0.81[ASN][1000 genomes] |
rs34717346 | 0.91[ASN][1000 genomes] |
rs34795808 | 0.89[ASN][1000 genomes] |
rs34833822 | 0.87[ASN][1000 genomes] |
rs35078417 | 0.89[ASN][1000 genomes] |
rs35211627 | 0.85[ASN][1000 genomes] |
rs35216513 | 0.80[ASN][1000 genomes] |
rs35263478 | 0.88[ASN][1000 genomes] |
rs35295528 | 0.87[ASN][1000 genomes] |
rs35326753 | 0.83[ASN][1000 genomes] |
rs35347093 | 0.89[ASN][1000 genomes] |
rs35423027 | 0.86[ASN][1000 genomes] |
rs35539859 | 0.86[ASN][1000 genomes] |
rs35635103 | 0.91[ASN][1000 genomes] |
rs35663303 | 0.87[ASN][1000 genomes] |
rs35697391 | 0.85[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs35706347 | 0.81[ASN][1000 genomes] |
rs35760448 | 0.89[ASN][1000 genomes] |
rs35794791 | 0.83[ASN][1000 genomes] |
rs35920928 | 0.88[ASN][1000 genomes] |
rs35978128 | 0.88[ASN][1000 genomes] |
rs36122870 | 0.88[ASN][1000 genomes] |
rs3980460 | 0.83[ASN][1000 genomes] |
rs4131102 | 0.90[ASN][1000 genomes] |
rs4131103 | 0.89[ASN][1000 genomes] |
rs4273447 | 0.89[ASN][1000 genomes] |
rs4568217 | 0.89[ASN][1000 genomes] |
rs4695776 | 0.92[ASN][1000 genomes] |
rs4695929 | 0.83[ASN][1000 genomes] |
rs62335849 | 0.90[ASN][1000 genomes] |
rs62335856 | 0.85[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs62335857 | 0.91[ASN][1000 genomes] |
rs62337061 | 0.89[ASN][1000 genomes] |
rs62337062 | 0.89[ASN][1000 genomes] |
rs62337063 | 0.89[ASN][1000 genomes] |
rs62337086 | 0.88[ASN][1000 genomes] |
rs62337087 | 0.88[ASN][1000 genomes] |
rs6553785 | 0.91[ASN][1000 genomes] |
rs6553786 | 0.91[ASN][1000 genomes] |
rs6553789 | 0.89[ASN][1000 genomes] |
rs6553790 | 0.89[ASN][1000 genomes] |
rs6553791 | 0.89[ASN][1000 genomes] |
rs67728476 | 0.89[ASN][1000 genomes] |
rs6812366 | 0.84[ASN][1000 genomes] |
rs6822535 | 0.96[ASN][1000 genomes] |
rs6827853 | 0.87[ASN][1000 genomes] |
rs6835446 | 0.91[ASN][1000 genomes] |
rs6852435 | 0.91[ASN][1000 genomes] |
rs6853004 | 0.89[ASN][1000 genomes] |
rs6853166 | 0.89[ASN][1000 genomes] |
rs6853181 | 0.89[ASN][1000 genomes] |
rs7654427 | 0.89[ASN][1000 genomes] |
rs7655606 | 0.89[ASN][1000 genomes] |
rs7656628 | 0.91[ASN][1000 genomes] |
rs7665426 | 0.88[ASN][1000 genomes] |
rs7665708 | 0.89[ASN][1000 genomes] |
rs7667325 | 0.89[ASN][1000 genomes] |
rs7667374 | 0.89[ASN][1000 genomes] |
rs7667642 | 0.81[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs7671492 | 0.91[ASN][1000 genomes] |
rs7672838 | 0.85[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs7677994 | 0.83[ASN][1000 genomes] |
rs7680564 | 0.89[ASN][1000 genomes] |
rs7687802 | 0.89[ASN][1000 genomes] |
rs7688229 | 0.87[ASN][1000 genomes] |
rs7689422 | 0.89[ASN][1000 genomes] |
rs7689484 | 0.90[ASN][1000 genomes] |
rs7691061 | 0.89[ASN][1000 genomes] |
rs7695912 | 0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1016910 | chr4:174952788-175349057 | Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv537363 | chr4:174952788-175349057 | Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | nsv596234 | chr4:175053051-175361437 | Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
4 | nsv869116 | chr4:175231090-175801761 | Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:175274200-175279600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
2 | chr4:175274400-175279600 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
3 | chr4:175277400-175278400 | Weak transcription | Left Ventricle | heart |