Variant report
Variant | rs7017705 |
---|---|
Chromosome Location | chr8:64982843-64982844 |
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)
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10504371 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12544687 | 0.84[EUR][1000 genomes] |
rs12549556 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12549559 | 0.93[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs13248395 | 0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13255222 | 0.95[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs13256546 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13273490 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs13280176 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1838420 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1838421 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1838424 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2018264 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2083995 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2356371 | 0.90[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2883915 | 0.83[EUR][1000 genomes] |
rs35152868 | 0.93[ASN][1000 genomes] |
rs35496690 | 0.85[AMR][1000 genomes] |
rs3910845 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4027777 | 0.83[AMR][1000 genomes] |
rs6981673 | 0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs6991156 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7014553 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs874777 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948343 | chr8:64804219-65328394 | Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv890969 | chr8:64807144-65047353 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv890970 | chr8:64975466-65125295 | ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:64982600-64992000 | Weak transcription | HUES6 Cell Line | embryonic stem cell |