Variant report
Variant | rs10505207 |
---|---|
Chromosome Location | chr8:114700007-114700008 |
allele | A/G |
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] |
---|---|
rs10088331 | 0.87[ASN][1000 genomes] |
rs10088339 | 0.84[ASN][1000 genomes] |
rs10102855 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs10105039 | 0.85[ASN][1000 genomes] |
rs10105221 | 0.85[ASN][1000 genomes] |
rs10113088 | 0.83[ASN][1000 genomes] |
rs1025894 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs10505206 | 0.85[ASN][1000 genomes] |
rs10955672 | 0.83[ASN][1000 genomes] |
rs12335168 | 0.93[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12386865 | 0.84[ASN][1000 genomes] |
rs12386964 | 0.85[ASN][1000 genomes] |
rs12677871 | 0.82[ASN][1000 genomes] |
rs12681503 | 0.83[ASN][1000 genomes] |
rs1348382 | 0.87[ASN][1000 genomes] |
rs1452755 | 0.92[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1597862 | 0.85[ASN][1000 genomes] |
rs16884960 | 0.86[ASN][1000 genomes] |
rs16884999 | 0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28477627 | 0.83[ASN][1000 genomes] |
rs28579378 | 0.83[ASN][1000 genomes] |
rs28825376 | 0.83[ASN][1000 genomes] |
rs62522065 | 0.83[ASN][1000 genomes] |
rs734621 | 0.93[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs734622 | 0.84[ASN][1000 genomes] |
rs7816794 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7825903 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7826236 | 0.83[ASN][1000 genomes] |
rs7826446 | 0.83[ASN][1000 genomes] |
rs7831447 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7833423 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817379 | chr8:114338391-115011632 | Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv818650 | chr8:114574863-115477600 | Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | esv2758168 | chr8:114575703-115321957 | Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | esv2759636 | chr8:114575703-115321957 | Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
5 | nsv891335 | chr8:114589007-114725064 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv891336 | chr8:114667112-114753522 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | esv1851155 | chr8:114673166-114773729 | Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | esv3327619 | chr8:114698979-114741570 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:114698200-114703400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
2 | chr8:114698200-114703600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |