Variant report
Variant | rs13071985 |
---|---|
Chromosome Location | chr3:141541105-141541106 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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rs_ID | r2[population] |
---|---|
rs13065327 | 0.86[EUR][1000 genomes] |
rs13065862 | 0.81[CEU][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes] |
rs13076009 | 0.84[EUR][1000 genomes] |
rs13085196 | 1.00[YRI][hapmap];0.85[EUR][1000 genomes] |
rs16851803 | 0.81[ASN][1000 genomes] |
rs2138790 | 0.80[EUR][1000 genomes] |
rs2681692 | 0.81[EUR][1000 genomes] |
rs2681699 | 0.82[ASW][hapmap] |
rs2681700 | 0.82[ASW][hapmap];0.81[CEU][hapmap] |
rs33928105 | 0.85[EUR][1000 genomes] |
rs34212237 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs34902798 | 0.86[EUR][1000 genomes] |
rs35026516 | 0.84[EUR][1000 genomes] |
rs35204030 | 0.86[EUR][1000 genomes] |
rs35249682 | 0.85[EUR][1000 genomes] |
rs35355622 | 0.86[EUR][1000 genomes] |
rs35652193 | 0.86[EUR][1000 genomes] |
rs35805003 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36009541 | 0.82[EUR][1000 genomes] |
rs55769955 | 0.86[EUR][1000 genomes] |
rs56361763 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71304105 | 0.82[EUR][1000 genomes] |
rs73226676 | 0.84[EUR][1000 genomes] |
rs73872344 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949709 | chr3:141295050-142178144 | Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 61 gene(s) | inside rSNPs | diseases |
2 | nsv1013352 | chr3:141541105-141870293 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:141534800-141547800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr3:141539800-141547000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |