Variant report
Variant | rs10000698 |
---|---|
Chromosome Location | chr4:74415939-74415940 |
allele | A/C |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:74405776..74408189-chr4:74414210..74416205,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10011693 | 1.00[AMR][1000 genomes] |
rs10015321 | 1.00[AMR][1000 genomes] |
rs10015884 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10032183 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10034509 | 1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10049835 | 0.95[YRI][hapmap];1.00[AMR][1000 genomes] |
rs1105321 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12331864 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1528922 | 0.83[AMR][1000 genomes] |
rs16849498 | 0.90[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2367164 | 1.00[AMR][1000 genomes] |
rs28533985 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28562313 | 1.00[AMR][1000 genomes] |
rs28570600 | 1.00[AMR][1000 genomes] |
rs28649464 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28651748 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28755465 | 1.00[AMR][1000 genomes] |
rs34123018 | 0.83[AFR][1000 genomes] |
rs3822100 | 0.81[YRI][hapmap] |
rs6831133 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7356389 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs9291186 | 1.00[AMR][1000 genomes] |
rs9995788 | 1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3430875 | chr4:74243646-74420354 | Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv1001725 | chr4:74354050-74860924 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
3 | nsv530126 | chr4:74376622-74843892 | Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:74415600-74416400 | Enhancers | HepG2 | liver |