Variant report
Variant | rs11916269 |
---|---|
Chromosome Location | chr3:145987210-145987211 |
allele | C/G |
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 | chr3:145986622..145989134-chr3:145993598..145995580,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11919756 | 0.87[AFR][1000 genomes] |
rs11920604 | 0.84[AFR][1000 genomes] |
rs11927463 | 0.81[AFR][1000 genomes] |
rs11928255 | 0.85[AFR][1000 genomes] |
rs11928534 | 0.83[AFR][1000 genomes] |
rs11929382 | 0.83[AFR][1000 genomes] |
rs13062557 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs13063066 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13064230 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13071899 | 1.00[ASN][1000 genomes] |
rs13072399 | 1.00[ASN][1000 genomes] |
rs13073749 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13082942 | 0.86[EUR][1000 genomes] |
rs13085381 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13092543 | 1.00[ASN][1000 genomes] |
rs13097291 | 1.00[ASN][1000 genomes] |
rs1398124 | 1.00[ASN][1000 genomes] |
rs16858193 | 0.88[AFR][1000 genomes] |
rs16858200 | 0.87[AFR][1000 genomes] |
rs2175666 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2175667 | 0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34100380 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34286112 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34287919 | 0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34363776 | 0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34370775 | 1.00[ASN][1000 genomes] |
rs34522376 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34839095 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs34901415 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34965829 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35045356 | 0.88[AFR][1000 genomes] |
rs35054584 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35110814 | 0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35231667 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35366505 | 0.84[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35403397 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35466414 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35632120 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35655354 | 1.00[ASN][1000 genomes] |
rs35658240 | 1.00[ASN][1000 genomes] |
rs35723694 | 0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs35969224 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs3804655 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs3804656 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs3828380 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6440424 | 0.87[AFR][1000 genomes] |
rs6440425 | 0.87[AFR][1000 genomes] |
rs6766764 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6780223 | 0.87[AFR][1000 genomes] |
rs6780240 | 0.87[AFR][1000 genomes] |
rs6782950 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6788357 | 0.83[AFR][1000 genomes] |
rs6793309 | 0.87[AFR][1000 genomes] |
rs6794565 | 0.86[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs71300385 | 0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs71300386 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71300388 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71300389 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71300390 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71300391 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72997087 | 0.88[AFR][1000 genomes] |
rs72997096 | 0.86[AFR][1000 genomes] |
rs72997098 | 0.88[AFR][1000 genomes] |
rs72999112 | 0.87[AFR][1000 genomes] |
rs72999115 | 0.82[AFR][1000 genomes] |
rs72999117 | 0.87[AFR][1000 genomes] |
rs72999118 | 0.84[AFR][1000 genomes] |
rs72999119 | 0.83[AFR][1000 genomes] |
rs73867526 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7614839 | 0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7623124 | 0.87[AFR][1000 genomes] |
rs7634946 | 0.87[AFR][1000 genomes] |
rs7642484 | 1.00[ASN][1000 genomes] |
rs7652376 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877614 | chr3:145903426-146025896 | ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
2 | nsv877615 | chr3:145910430-145988231 | ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
3 | esv3333601 | chr3:145940702-146068210 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | esv3416330 | chr3:145941029-146068457 | Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv998388 | chr3:145960954-146087749 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:145983800-145998800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr3:145984600-145990000 | Weak transcription | H9 Cell Line | embryonic stem cell |
3 | chr3:145987000-145991800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr3:145987000-145992000 | Weak transcription | Muscle Satellite Cultured Cells | -- |