Variant report
Variant | rs10485928 |
---|---|
Chromosome Location | chr7:78686825-78686826 |
allele | A/C |
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 | chr7:78680321..78683272-chr7:78686502..78688648,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1014797 | 1.00[ASN][1000 genomes] |
rs10225940 | 1.00[CEU][hapmap] |
rs10226562 | 1.00[CEU][hapmap] |
rs10226710 | 1.00[CEU][hapmap] |
rs10228655 | 0.89[CEU][hapmap] |
rs10232513 | 1.00[CEU][hapmap] |
rs10232994 | 1.00[CEU][hapmap] |
rs10233023 | 1.00[CEU][hapmap] |
rs10236869 | 1.00[CEU][hapmap] |
rs10237768 | 1.00[CEU][hapmap] |
rs10241786 | 1.00[CEU][hapmap] |
rs10244720 | 1.00[CEU][hapmap] |
rs10249662 | 1.00[CEU][hapmap] |
rs10250886 | 1.00[CEU][hapmap] |
rs10254541 | 1.00[CEU][hapmap] |
rs10254557 | 1.00[CEU][hapmap] |
rs10255028 | 1.00[CEU][hapmap] |
rs10268461 | 1.00[CEU][hapmap] |
rs10281393 | 1.00[CEU][hapmap] |
rs10485922 | 1.00[ASN][1000 genomes] |
rs10485927 | 1.00[CEU][hapmap] |
rs17151853 | 1.00[CEU][hapmap] |
rs17151861 | 1.00[CEU][hapmap] |
rs17151887 | 1.00[CEU][hapmap] |
rs17406392 | 0.80[CEU][hapmap] |
rs17471316 | 1.00[ASN][1000 genomes] |
rs2363929 | 1.00[ASN][1000 genomes] |
rs41435246 | 1.00[ASN][1000 genomes] |
rs7787164 | 1.00[CEU][hapmap] |

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 | nsv482826 | chr7:78548319-78717605 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv471642 | chr7:78548320-78717605 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | 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 |
6 | 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:78680800-78690800 | Weak transcription | Brain Substantia Nigra | brain |