Variant report
Variant | rs7792195 |
---|---|
Chromosome Location | chr7:26025068-26025069 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:26024108..26025764-chr7:26238840..26240758,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000122566 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11980825 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13239817 | 0.90[ASN][1000 genomes] |
rs17152959 | 0.90[ASN][1000 genomes] |
rs1986928 | 0.98[ASN][1000 genomes] |
rs2012224 | 0.91[ASN][1000 genomes] |
rs35055962 | 0.97[ASN][1000 genomes] |
rs35153396 | 0.90[ASN][1000 genomes] |
rs35797325 | 0.98[ASN][1000 genomes] |
rs35855074 | 0.97[ASN][1000 genomes] |
rs35931836 | 0.91[ASN][1000 genomes] |
rs4521656 | 0.91[ASN][1000 genomes] |
rs55704418 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56681948 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs57188228 | 0.94[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs57665417 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs59344953 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs61405107 | 0.97[EUR][1000 genomes] |
rs62446278 | 0.82[ASN][1000 genomes] |
rs6461901 | 0.98[ASN][1000 genomes] |
rs6461902 | 0.86[ASN][1000 genomes] |
rs6951118 | 0.98[ASN][1000 genomes] |
rs6972351 | 0.98[ASN][1000 genomes] |
rs6973562 | 0.98[ASN][1000 genomes] |
rs733645 | 0.91[ASN][1000 genomes] |
rs745580 | 0.82[ASN][1000 genomes] |
rs7786527 | 0.90[ASN][1000 genomes] |
rs7803271 | 0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1016813 | chr7:25405859-26150509 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 108 gene(s) | inside rSNPs | diseases |
2 | nsv538803 | chr7:25405859-26150509 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 108 gene(s) | inside rSNPs | diseases |
3 | nsv606432 | chr7:25988185-26223294 | Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 102 gene(s) | inside rSNPs | diseases |
4 | nsv887848 | chr7:26000137-26059739 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv606433 | chr7:26007582-26050920 | Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv470188 | chr7:26013958-26075094 | Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv464412 | chr7:26013959-26073411 | Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
8 | nsv606434 | chr7:26013959-26073411 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:26024200-26026000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr7:26024800-26025400 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |