Variant report
Variant | rs35074129 |
---|---|
Chromosome Location | chr22:30866471-30866472 |
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] |
---|---|
rs1131603 | 1.00[ASN][1000 genomes] |
rs13053196 | 1.00[ASN][1000 genomes] |
rs13056562 | 1.00[ASN][1000 genomes] |
rs13058084 | 1.00[ASN][1000 genomes] |
rs13058399 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs13058535 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs17730748 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17738020 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34102711 | 1.00[ASN][1000 genomes] |
rs34318316 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs34471369 | 1.00[ASN][1000 genomes] |
rs34886169 | 1.00[ASN][1000 genomes] |
rs34911581 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs34964064 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs35057984 | 1.00[ASN][1000 genomes] |
rs35246430 | 1.00[ASN][1000 genomes] |
rs35617977 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35765517 | 1.00[ASN][1000 genomes] |
rs35960997 | 1.00[ASN][1000 genomes] |
rs4449240 | 1.00[ASN][1000 genomes] |
rs4820002 | 1.00[ASN][1000 genomes] |
rs4820834 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4820840 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4823086 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs4823087 | 1.00[ASN][1000 genomes] |
rs67384221 | 1.00[ASN][1000 genomes] |
rs67401267 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs68042293 | 1.00[ASN][1000 genomes] |
rs7292248 | 1.00[ASN][1000 genomes] |
rs73168654 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv829171 | chr22:30598030-31043578 | Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 66 gene(s) | inside rSNPs | diseases |
2 | nsv915818 | chr22:30708245-31346302 | Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 82 gene(s) | inside rSNPs | diseases |
3 | nsv459870 | chr22:30836313-30868418 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv588886 | chr22:30836313-30868418 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr22:30857800-30867600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr22:30858200-30866800 | Weak transcription | Liver | Liver |
3 | chr22:30866400-30866600 | Bivalent Enhancer | Primary T cells fromperipheralblood | blood |