Variant report
Variant | rs60636413 |
---|---|
Chromosome Location | chr7:27764768-27764769 |
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 |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000229893 | Chromatin interaction |
ENSG00000106052 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17155954 | 0.81[ASN][1000 genomes] |
rs2299105 | 1.00[ASN][1000 genomes] |
rs55901354 | 0.89[ASN][1000 genomes] |
rs56916239 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56995723 | 1.00[ASN][1000 genomes] |
rs58546705 | 0.91[ASN][1000 genomes] |
rs58651394 | 0.89[ASN][1000 genomes] |
rs59041966 | 0.89[ASN][1000 genomes] |
rs59614135 | 0.82[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs73684028 | 0.96[ASN][1000 genomes] |
rs73684030 | 0.97[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs73684035 | 0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73684037 | 0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73684045 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73684048 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73684050 | 1.00[ASN][1000 genomes] |
rs73684052 | 1.00[ASN][1000 genomes] |
rs73684053 | 0.96[ASN][1000 genomes] |
rs73684055 | 1.00[ASN][1000 genomes] |
rs73684057 | 1.00[ASN][1000 genomes] |
rs73684058 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949025 | chr7:27578167-28075172 | Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:27760000-27778800 | Weak transcription | HSMMtube | muscle |