Variant report
Variant | rs4462908 |
---|---|
Chromosome Location | chr3:139826751-139826752 |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:139818128..139821067-chr3:139825810..139829205,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10513099 | 1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs12494072 | 1.00[CHB][hapmap] |
rs16849957 | 1.00[CHB][hapmap] |
rs2280336 | 1.00[MEX][hapmap];0.88[TSI][hapmap];0.88[EUR][1000 genomes] |
rs2882425 | 0.82[TSI][hapmap];0.80[EUR][1000 genomes] |
rs4428137 | 1.00[CHB][hapmap] |
rs4600787 | 0.88[TSI][hapmap];0.88[EUR][1000 genomes] |
rs58656999 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60260333 | 0.85[EUR][1000 genomes] |
rs60313064 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6439896 | 1.00[CHB][hapmap] |
rs6767558 | 1.00[CHB][hapmap] |
rs6787267 | 0.87[YRI][hapmap] |
rs6799894 | 1.00[CHB][hapmap] |
rs6807785 | 1.00[CHB][hapmap] |
rs72984144 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs72984150 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs72984173 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72984176 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7619286 | 0.88[TSI][hapmap];0.88[EUR][1000 genomes] |
rs7624316 | 0.88[EUR][1000 genomes] |
rs7645419 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv998423 | chr3:139526446-139947336 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv829738 | chr3:139670836-139851945 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv829739 | chr3:139797496-140002685 | Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:139813800-139832600 | Weak transcription | Ovary | ovary |
2 | chr3:139822400-139834600 | Weak transcription | HSMMtube | muscle |