Variant report
Variant | rs7782148 |
---|---|
Chromosome Location | chr7:15953786-15953787 |
allele | C/T |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:15948178..15950643-chr7:15952055..15954693,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10253795 | 0.92[ASN][1000 genomes] |
rs10255820 | 0.83[EUR][1000 genomes] |
rs12699757 | 0.92[ASN][1000 genomes] |
rs1298311 | 0.93[ASN][1000 genomes] |
rs38220 | 0.80[ASN][1000 genomes] |
rs38222 | 0.80[ASN][1000 genomes] |
rs38223 | 0.88[ASN][1000 genomes] |
rs38226 | 0.86[ASN][1000 genomes] |
rs38231 | 0.88[ASN][1000 genomes] |
rs38233 | 0.88[ASN][1000 genomes] |
rs38236 | 0.86[ASN][1000 genomes] |
rs38238 | 0.89[ASN][1000 genomes] |
rs38239 | 0.89[ASN][1000 genomes] |
rs38251 | 0.90[ASN][1000 genomes] |
rs38252 | 0.90[ASN][1000 genomes] |
rs38258 | 0.92[ASN][1000 genomes] |
rs6943089 | 0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6949049 | 0.93[ASN][1000 genomes] |
rs6965426 | 0.92[ASN][1000 genomes] |
rs6970657 | 0.88[ASN][1000 genomes] |
rs768667 | 0.92[ASN][1000 genomes] |
rs768668 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs800713 | 0.89[ASN][1000 genomes] |
rs800715 | 0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv523199 | chr7:15582208-16042596 | Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
2 | nsv1016642 | chr7:15884061-16799788 | Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
3 | nsv1017958 | chr7:15910153-15956470 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:15946400-15955400 | Weak transcription | Rectal Smooth Muscle | rectum |
2 | chr7:15953400-15955400 | Weak transcription | Colon Smooth Muscle | Colon |