Variant report
Variant | rs2432969 |
---|---|
Chromosome Location | chr8:120294297-120294298 |
allele | C/T |
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 | chr8:120288326..120291093-chr8:120293809..120295588,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1154819 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs11777159 | 0.81[AMR][1000 genomes] |
rs1364704 | 1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs1425048 | 0.94[AMR][1000 genomes] |
rs1425049 | 1.00[CEU][hapmap] |
rs1425068 | 1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes] |
rs1579353 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs1582675 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16892528 | 1.00[CHB][hapmap] |
rs1895706 | 1.00[CEU][hapmap];0.88[AMR][1000 genomes] |
rs2432970 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs2432971 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs2432976 | 0.91[ASN][1000 genomes] |
rs2432978 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2432984 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes] |
rs2432985 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2468164 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2469989 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2469993 | 0.96[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2470041 | 1.00[CEU][hapmap];0.81[EUR][1000 genomes] |
rs2470042 | 1.00[CEU][hapmap];0.81[EUR][1000 genomes] |
rs2875872 | 1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs764292 | 0.93[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv868916 | chr8:119911943-120762250 | Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
2 | nsv1026655 | chr8:120282929-120522329 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:120291200-120302800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |