Variant report
Variant | rs2936010 |
---|---|
Chromosome Location | chr1:213213567-213213568 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:3 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000174606 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10465694 | 0.81[EUR][1000 genomes] |
rs1976333 | 0.82[EUR][1000 genomes] |
rs2172982 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2935209 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2935219 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2936011 | 0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs3002285 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs3010779 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs3010787 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs3010789 | 0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs3124668 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4543872 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4951475 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4951476 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1008594 | chr1:213110654-213236750 | Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:213212600-213214600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |