Variant report
Variant | rs244698 |
---|---|
Chromosome Location | chr5:57664525-57664526 |
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 | chr5:57660346..57663581-chr5:57663913..57666840,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs151915 | 0.97[EUR][1000 genomes] |
rs151921 | 0.89[EUR][1000 genomes] |
rs151922 | 0.88[EUR][1000 genomes] |
rs151923 | 0.89[EUR][1000 genomes] |
rs154681 | 0.97[EUR][1000 genomes] |
rs244700 | 0.97[EUR][1000 genomes] |
rs245491 | 0.82[YRI][hapmap] |
rs2548599 | 0.96[EUR][1000 genomes] |
rs2652499 | 0.95[EUR][1000 genomes] |
rs2662618 | 0.95[EUR][1000 genomes] |
rs26976 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs26979 | 0.96[EUR][1000 genomes] |
rs27212 | 0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs27604 | 0.96[EUR][1000 genomes] |
rs27917 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs36645 | 0.86[EUR][1000 genomes] |
rs399282 | 0.97[EUR][1000 genomes] |
rs412028 | 0.97[EUR][1000 genomes] |
rs451022 | 0.95[CEU][hapmap];0.97[EUR][1000 genomes] |
rs696189 | 0.92[EUR][1000 genomes] |
rs697087 | 0.95[EUR][1000 genomes] |
rs697088 | 0.96[EUR][1000 genomes] |
rs702586 | 0.95[EUR][1000 genomes] |
rs834935 | 0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3489100 | chr5:57545689-57669673 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | esv3489101 | chr5:57545689-57669673 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv4842 | chr5:57653257-57694850 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:57664400-57666400 | Enhancers | Fetal Heart | heart |