Variant report
Variant | rs62488405 |
---|---|
Chromosome Location | chr7:86234000-86234001 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10241183 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs200839 | 0.86[EUR][1000 genomes] |
rs2204638 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2526952 | 0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs274616 | 0.86[EUR][1000 genomes] |
rs274617 | 0.86[EUR][1000 genomes] |
rs274618 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs274619 | 0.86[EUR][1000 genomes] |
rs274620 | 0.86[EUR][1000 genomes] |
rs274621 | 0.86[EUR][1000 genomes] |
rs274622 | 0.88[EUR][1000 genomes] |
rs274624 | 0.82[AMR][1000 genomes] |
rs274628 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs274629 | 0.86[EUR][1000 genomes] |
rs274630 | 0.86[EUR][1000 genomes] |
rs274631 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs274633 | 0.86[EUR][1000 genomes] |
rs274634 | 0.86[EUR][1000 genomes] |
rs274636 | 0.86[EUR][1000 genomes] |
rs274637 | 0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1025032 | chr7:86032479-86642973 | Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv1017470 | chr7:86221308-86263909 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv526622 | chr7:86222259-86260816 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | esv2764034 | chr7:86227204-86245054 | Enhancers Flanking Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv3477373 | chr7:86231201-86245406 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
6 | esv3477375 | chr7:86231318-86245286 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
7 | nsv819490 | chr7:86231368-86245850 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:86231000-86235000 | Weak transcription | Brain Angular Gyrus | brain |