Variant report
| Variant | rs13014995 |
|---|---|
| Chromosome Location | chr2:180729175-180729176 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:1)
- 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 | chr2:180724511..180728493-chr2:180729164..180732918,3 | MCF-7 | breast: |
(count:1 , 50 per page) page:
1
| No. | lncRNA name | Chromosome Location | lncRNA alias |
|---|---|---|---|
| 1 | lnc-UBE2E3-9 | chr2:180729067-180729484 | NONHSAT075835 |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000144331 | Chromatin interaction |
| ENSG00000221240 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:19)
| rs_ID | r2[population] |
|---|---|
| rs10153833 | 0.93[CEU][hapmap] |
| rs10930887 | 0.96[CEU][hapmap];0.84[YRI][hapmap] |
| rs1352111 | 0.93[CEU][hapmap] |
| rs1383413 | 0.84[CEU][hapmap];0.81[AMR][1000 genomes] |
| rs1383414 | 0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs165374 | 0.92[CEU][hapmap] |
| rs165379 | 0.96[CEU][hapmap] |
| rs165380 | 0.92[CEU][hapmap] |
| rs187745 | 0.93[CEU][hapmap] |
| rs194674 | 0.96[CEU][hapmap] |
| rs2367797 | 0.85[CEU][hapmap] |
| rs259833 | 0.96[CEU][hapmap] |
| rs357712 | 0.93[CEU][hapmap] |
| rs357714 | 0.92[CEU][hapmap] |
| rs6725456 | 0.93[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.90[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
| rs6752731 | 0.85[CEU][hapmap] |
| rs7557122 | 0.85[CEU][hapmap] |
| rs7588035 | 0.83[CEU][hapmap] |
| rs7597666 | 0.85[CEU][hapmap] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1002305 | chr2:180568558-180812846 | Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
| 2 | nsv428731 | chr2:180629389-180805171 | Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 5 gene(s) | inside rSNPs | diseases |
| 3 | nsv875472 | chr2:180696414-181024926 | Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 8 gene(s) | inside rSNPs | diseases |
| 4 | nsv875473 | chr2:180696414-181055597 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 8 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
