Variant report
Variant | rs6935032 |
---|---|
Chromosome Location | chr6:70735586-70735587 |
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 | chr6:70733478..70735674-chr6:111948074..111949663,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10485244 | 0.86[CHB][hapmap] |
rs2273426 | 0.90[CEU][hapmap];0.81[EUR][1000 genomes] |
rs3793038 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs3805961 | 0.81[CHB][hapmap] |
rs3805962 | 0.81[CHB][hapmap] |
rs3805968 | 0.81[CHB][hapmap] |
rs3805973 | 0.86[CHB][hapmap] |
rs3805977 | 0.81[CHB][hapmap] |
rs3805986 | 0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs3805987 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6906337 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9346367 | 1.00[CEU][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9346368 | 0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9354904 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9364070 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9364071 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs9446169 | 0.86[CHB][hapmap] |
rs9446170 | 0.86[CHB][hapmap] |
rs9446178 | 0.88[ASN][1000 genomes] |
rs9454944 | 0.90[CEU][hapmap];0.89[EUR][1000 genomes] |
rs978290 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs978291 | 1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1026151 | chr6:70621616-70946967 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv470832 | chr6:70654657-70767756 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv603637 | chr6:70658432-70740151 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
4 | nsv603638 | chr6:70658432-70740306 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
5 | nsv933674 | chr6:70663616-70973112 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
6 | nsv1026836 | chr6:70727747-70849014 | Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv525985 | chr6:70728202-70766504 | Strong transcription Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:70733000-70748600 | Weak transcription | GM12878-XiMat | blood |
2 | chr6:70733400-70737000 | Strong transcription | Primary B cells from peripheral blood | blood |
3 | chr6:70734000-70735600 | Strong transcription | Primary B cells from cord blood | blood |