Variant report
Variant | rs12631196 |
---|---|
Chromosome Location | chr3:158171455-158171456 |
allele | A/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 | chr15:72523089..72524657-chr3:158169373..158172267,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000067225 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1095626 | 0.86[EUR][1000 genomes] |
rs1095627 | 0.86[EUR][1000 genomes] |
rs1095628 | 0.86[EUR][1000 genomes] |
rs1095635 | 0.86[EUR][1000 genomes] |
rs1095637 | 0.86[EUR][1000 genomes] |
rs1095638 | 0.85[EUR][1000 genomes] |
rs1095639 | 0.86[EUR][1000 genomes] |
rs1095640 | 0.86[EUR][1000 genomes] |
rs1095641 | 0.85[EUR][1000 genomes] |
rs1095642 | 0.91[EUR][1000 genomes] |
rs1101158 | 0.86[EUR][1000 genomes] |
rs1104288 | 0.86[EUR][1000 genomes] |
rs1104289 | 0.86[EUR][1000 genomes] |
rs11717725 | 0.83[ASN][1000 genomes] |
rs11719188 | 0.83[ASN][1000 genomes] |
rs1193505 | 0.86[EUR][1000 genomes] |
rs1193506 | 0.86[EUR][1000 genomes] |
rs1193507 | 0.86[EUR][1000 genomes] |
rs1193508 | 0.87[EUR][1000 genomes] |
rs1193509 | 0.86[EUR][1000 genomes] |
rs1193510 | 0.86[EUR][1000 genomes] |
rs1193521 | 0.86[EUR][1000 genomes] |
rs1193534 | 0.85[EUR][1000 genomes] |
rs1193535 | 0.85[EUR][1000 genomes] |
rs1193537 | 0.86[EUR][1000 genomes] |
rs1204962 | 0.86[EUR][1000 genomes] |
rs12107103 | 0.83[ASN][1000 genomes] |
rs12107104 | 0.83[ASN][1000 genomes] |
rs1212739 | 0.85[EUR][1000 genomes] |
rs1213048 | 0.86[EUR][1000 genomes] |
rs12496767 | 0.85[ASN][1000 genomes] |
rs12629125 | 0.83[ASN][1000 genomes] |
rs12633594 | 0.83[ASN][1000 genomes] |
rs12638169 | 0.85[ASN][1000 genomes] |
rs13066362 | 0.86[EUR][1000 genomes] |
rs1526191 | 0.86[EUR][1000 genomes] |
rs1526192 | 0.86[EUR][1000 genomes] |
rs1526193 | 0.86[EUR][1000 genomes] |
rs1526194 | 0.86[EUR][1000 genomes] |
rs1618381 | 0.86[EUR][1000 genomes] |
rs1630304 | 0.86[EUR][1000 genomes] |
rs1724652 | 0.86[EUR][1000 genomes] |
rs1724654 | 0.86[EUR][1000 genomes] |
rs1724700 | 0.86[EUR][1000 genomes] |
rs1724704 | 0.86[EUR][1000 genomes] |
rs1730007 | 0.86[EUR][1000 genomes] |
rs1730020 | 0.86[EUR][1000 genomes] |
rs1730040 | 0.87[EUR][1000 genomes] |
rs1730042 | 0.86[EUR][1000 genomes] |
rs1730045 | 0.86[EUR][1000 genomes] |
rs1730058 | 0.82[EUR][1000 genomes] |
rs1730059 | 0.85[EUR][1000 genomes] |
rs1852285 | 0.86[EUR][1000 genomes] |
rs1983469 | 0.87[EUR][1000 genomes] |
rs2362968 | 0.83[ASN][1000 genomes] |
rs2362969 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs2362970 | 0.83[ASN][1000 genomes] |
rs2362972 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2682404 | 0.86[EUR][1000 genomes] |
rs2682405 | 0.86[EUR][1000 genomes] |
rs2682406 | 0.86[EUR][1000 genomes] |
rs2693527 | 0.87[EUR][1000 genomes] |
rs2693529 | 0.86[EUR][1000 genomes] |
rs2693530 | 0.81[EUR][1000 genomes] |
rs2693542 | 0.86[EUR][1000 genomes] |
rs2698322 | 0.86[EUR][1000 genomes] |
rs2698323 | 0.86[EUR][1000 genomes] |
rs28820925 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4289388 | 0.89[ASN][1000 genomes] |
rs4561872 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4679828 | 0.83[ASN][1000 genomes] |
rs4680433 | 0.83[ASN][1000 genomes] |
rs4680434 | 0.83[ASN][1000 genomes] |
rs4680436 | 0.86[ASN][1000 genomes] |
rs4680437 | 0.89[ASN][1000 genomes] |
rs6441182 | 0.86[EUR][1000 genomes] |
rs6441195 | 0.84[ASN][1000 genomes] |
rs6441197 | 0.85[ASN][1000 genomes] |
rs6441198 | 0.89[ASN][1000 genomes] |
rs6441200 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6441201 | 0.87[ASN][1000 genomes] |
rs67385174 | 0.83[ASN][1000 genomes] |
rs6800887 | 0.88[ASN][1000 genomes] |
rs6806702 | 0.81[ASN][1000 genomes] |
rs7426603 | 0.83[ASN][1000 genomes] |
rs7430565 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7610691 | 0.83[ASN][1000 genomes] |
rs7621674 | 0.86[EUR][1000 genomes] |
rs7621971 | 0.86[EUR][1000 genomes] |
rs7632059 | 0.83[ASN][1000 genomes] |
rs7636974 | 0.83[EUR][1000 genomes] |
rs7637291 | 0.86[EUR][1000 genomes] |
rs7641954 | 0.89[ASN][1000 genomes] |
rs7643792 | 0.86[EUR][1000 genomes] |
rs827092 | 0.87[EUR][1000 genomes] |
rs827093 | 0.86[EUR][1000 genomes] |
rs827094 | 0.86[EUR][1000 genomes] |
rs827095 | 0.86[EUR][1000 genomes] |
rs827096 | 0.86[EUR][1000 genomes] |
rs827097 | 0.86[EUR][1000 genomes] |
rs827098 | 0.86[EUR][1000 genomes] |
rs827099 | 0.86[EUR][1000 genomes] |
rs827101 | 0.86[EUR][1000 genomes] |
rs827106 | 0.91[EUR][1000 genomes] |
rs827108 | 0.86[EUR][1000 genomes] |
rs827109 | 0.86[EUR][1000 genomes] |
rs827110 | 0.86[EUR][1000 genomes] |
rs827111 | 0.86[EUR][1000 genomes] |
rs827112 | 0.85[EUR][1000 genomes] |
rs827113 | 0.86[EUR][1000 genomes] |
rs827114 | 0.86[EUR][1000 genomes] |
rs827126 | 0.86[EUR][1000 genomes] |
rs827127 | 0.86[EUR][1000 genomes] |
rs827128 | 0.87[EUR][1000 genomes] |
rs827129 | 0.86[EUR][1000 genomes] |
rs827131 | 0.86[EUR][1000 genomes] |
rs827132 | 0.86[EUR][1000 genomes] |
rs827134 | 0.91[EUR][1000 genomes] |
rs827135 | 0.91[EUR][1000 genomes] |
rs827137 | 0.86[EUR][1000 genomes] |
rs827140 | 0.86[EUR][1000 genomes] |
rs827163 | 0.86[EUR][1000 genomes] |
rs827164 | 0.86[EUR][1000 genomes] |
rs827166 | 0.86[EUR][1000 genomes] |
rs827171 | 0.85[EUR][1000 genomes] |
rs827176 | 0.85[EUR][1000 genomes] |
rs827177 | 0.85[EUR][1000 genomes] |
rs827178 | 0.85[EUR][1000 genomes] |
rs827179 | 0.85[EUR][1000 genomes] |
rs827180 | 0.85[EUR][1000 genomes] |
rs827181 | 0.83[EUR][1000 genomes] |
rs827184 | 0.90[EUR][1000 genomes] |
rs844119 | 0.86[EUR][1000 genomes] |
rs864332 | 0.86[EUR][1000 genomes] |
rs865454 | 0.87[EUR][1000 genomes] |
rs865455 | 0.85[EUR][1000 genomes] |
rs9784311 | 0.87[EUR][1000 genomes] |
rs9810345 | 0.87[ASN][1000 genomes] |
rs9820370 | 0.87[EUR][1000 genomes] |
rs9823076 | 0.83[ASN][1000 genomes] |
rs9838399 | 0.83[EUR][1000 genomes] |
rs9843089 | 0.82[ASN][1000 genomes] |
rs9847045 | 0.82[ASN][1000 genomes] |
rs9847316 | 0.85[ASN][1000 genomes] |
rs9847460 | 0.83[ASN][1000 genomes] |
rs9850856 | 0.83[ASN][1000 genomes] |
rs9870802 | 0.83[ASN][1000 genomes] |
rs9872889 | 0.85[ASN][1000 genomes] |
rs9877909 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1002378 | chr3:157715428-158673414 | Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
2 | nsv916910 | chr3:157926799-158183372 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv1014381 | chr3:158070451-158350118 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv1004124 | chr3:158146715-158808638 | Genic enhancers Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
5 | nsv967206 | chr3:158149860-158176292 | Flanking Active TSS Enhancers Weak transcription Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:158156400-158176200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr3:158161800-158171800 | Weak transcription | GM12878-XiMat | blood |
3 | chr3:158165600-158172600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
4 | chr3:158169200-158176000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr3:158169600-158182400 | Weak transcription | Primary B cells from cord blood | blood |
6 | chr3:158171400-158177800 | Weak transcription | Primary neutrophils fromperipheralblood | blood |