Variant report
Variant | rs7331776 |
---|---|
Chromosome Location | chr13:50465821-50465822 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | BATF | chr13:50465696-50465986 | GM12878 | blood: | n/a | chr13:50465875-50465886 |
2 | BATF | chr13:50465648-50465989 | GM12878 | blood: | n/a | chr13:50465875-50465886 |
No data |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-TRIM13-8 | chr13:50464545-50467516 | NR_003268 |
No data |
No data |
Variant related genes | Relation type |
---|---|
RNY4P30 | TF binding region |
ENSG00000258941 | Chromatin interaction |
ENSG00000150527 | Chromatin interaction |
ENSG00000258940 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs56215346 | 1.00[ASN][1000 genomes] |
rs7334755 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7338963 | 0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9591310 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3436655 | chr13:50462077-50472044 | Enhancers Weak transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv976113 | chr13:50464858-50466977 | Inactive region | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |