Variant report
Variant | rs73367231 |
---|---|
Chromosome Location | chr14:84638970-84638971 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:5)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:5 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | BHLHE40 | chr14:84638838-84639014 | HepG2 | liver: | n/a | n/a |
2 | HEY1 | chr14:84638840-84639089 | HepG2 | liver: | n/a | n/a |
3 | BCL11A | chr14:84638802-84639015 | GM12878 | blood: | n/a | n/a |
4 | JUND | chr14:84638874-84638976 | HepG2 | liver: | n/a | n/a |
5 | RXRA | chr14:84638820-84639035 | GM12878 | blood: | n/a | n/a |
No data |
No data |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-RP11-497E19.2.1-11 | chr14:84638664-84638970 | NONHSAT038100 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000258762 | TF binding region |
ENSG00000258923 | TF binding region |
ENSG00000259012 | TF binding region |
rs_ID | r2[population] |
---|---|
rs41519447 | 1.00[AMR][1000 genomes] |
rs59321128 | 1.00[AMR][1000 genomes] |
rs73365597 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73378984 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv565376 | chr14:84612088-84644822 | Enhancers Weak transcription | TF binding regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv976360 | chr14:84637552-84639420 | Inactive region | TF binding regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
No data |