Variant report
Variant | rs7556220 |
---|---|
Chromosome Location | chr1:70280269-70280270 |
allele | C/T |
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] |
---|---|
rs10399623 | 0.95[YRI][hapmap];0.86[AFR][1000 genomes] |
rs10889863 | 1.00[GIH][hapmap];0.95[YRI][hapmap] |
rs11802766 | 0.95[YRI][hapmap] |
rs12062605 | 0.85[GIH][hapmap];1.00[TSI][hapmap] |
rs12074727 | 0.84[ASW][hapmap];0.85[GIH][hapmap] |
rs12075955 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12088269 | 0.85[GIH][hapmap] |
rs17131038 | 1.00[CEU][hapmap];0.95[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs17131039 | 1.00[GIH][hapmap] |
rs41440946 | 1.00[GIH][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap] |
rs61784020 | 0.84[EUR][1000 genomes] |
rs61784021 | 0.84[EUR][1000 genomes] |
rs7554827 | 1.00[GIH][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949691 | chr1:69749722-70302201 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv461784 | chr1:70231535-70306245 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv546452 | chr1:70231535-70306245 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | esv1842679 | chr1:70279860-70306245 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |