Variant report
Variant | rs10280055 |
---|---|
Chromosome Location | chr7:78750133-78750134 |
allele | G/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 | chr7:78749811..78752141-chr7:78766151..78767665,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10255710 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.98[LWK][hapmap];0.97[MKK][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10255742 | 0.89[GIH][hapmap] |
rs10953783 | 0.83[MEX][hapmap] |
rs11760355 | 0.80[GIH][hapmap];0.83[MEX][hapmap] |
rs11767464 | 0.90[CEU][hapmap];0.82[CHD][hapmap];0.89[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12112164 | 0.82[GIH][hapmap] |
rs12531031 | 0.94[ASW][hapmap];0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.96[YRI][hapmap] |
rs12674038 | 0.85[CEU][hapmap];0.82[TSI][hapmap] |
rs12706007 | 0.95[CHB][hapmap];0.95[JPT][hapmap] |
rs13243641 | 0.85[CEU][hapmap] |
rs1990432 | 0.82[GIH][hapmap];0.83[MEX][hapmap] |
rs1990433 | 0.82[GIH][hapmap] |
rs2191806 | 0.85[CEU][hapmap];0.82[TSI][hapmap] |
rs2215581 | 0.80[CEU][hapmap] |
rs2215585 | 1.00[ASW][hapmap];0.80[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];0.94[MKK][hapmap];0.89[TSI][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4020771 | 0.82[GIH][hapmap];0.83[MEX][hapmap] |
rs6466510 | 0.90[CEU][hapmap] |
rs6466533 | 0.83[MEX][hapmap] |
rs6957950 | 0.84[GIH][hapmap] |
rs740967 | 1.00[CEU][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7787597 | 0.82[GIH][hapmap];0.87[MEX][hapmap] |
rs7789016 | 1.00[CEU][hapmap];0.91[CHB][hapmap];0.96[YRI][hapmap] |
rs7790562 | 0.85[CEU][hapmap];0.82[TSI][hapmap] |
rs7790650 | 0.82[GIH][hapmap] |
rs7793056 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7810534 | 0.90[CEU][hapmap];0.86[CHB][hapmap];0.93[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv464598 | chr7:78492642-79483480 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
2 | nsv607659 | chr7:78492642-79483480 | Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
3 | nsv1029799 | chr7:78608097-79061737 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv831040 | chr7:78623195-78831998 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv888510 | chr7:78742376-78865618 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:78748400-78751400 | Weak transcription | HUVEC | blood vessel |
2 | chr7:78749600-78750400 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |