Variant report
Variant | rs10008431 |
---|---|
Chromosome Location | chr4:18934125-18934126 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10005486 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10008054 | 0.87[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs10489055 | 0.87[EUR][1000 genomes] |
rs1079811 | 0.86[EUR][1000 genomes] |
rs1079812 | 0.85[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs11728202 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11736810 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs13119001 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs13129810 | 0.89[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs13142105 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1452555 | 0.87[EUR][1000 genomes] |
rs1452556 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs1990495 | 0.86[EUR][1000 genomes] |
rs2067979 | 0.85[ASN][1000 genomes] |
rs28377112 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs34295055 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6818287 | 0.89[EUR][1000 genomes] |
rs6839469 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs7680497 | 0.92[EUR][1000 genomes] |
rs7685547 | 0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9992468 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9992560 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9995472 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9996485 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533087 | chr4:18362040-19176896 | Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv532708 | chr4:18596861-19176896 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | Chromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv878723 | chr4:18668957-19005988 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1000054 | chr4:18839588-19271261 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv537051 | chr4:18839588-19271261 | Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1008625 | chr4:18880048-19148705 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1010560 | chr4:18892570-18968334 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv1000563 | chr4:18924475-19246818 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv1006775 | chr4:18932671-18988369 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:18932400-18937400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr4:18933600-18934600 | Enhancers | Fetal Kidney | kidney |
3 | chr4:18933800-18936000 | Enhancers | Fetal Heart | heart |