Variant report
Variant | rs56197713 |
---|---|
Chromosome Location | chr4:95091790-95091791 |
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 | chr4:95089461..95092214-chr4:95128787..95131060,3 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000163104 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10008044 | 0.95[ASN][1000 genomes] |
rs10016806 | 0.88[ASN][1000 genomes] |
rs10023115 | 0.95[ASN][1000 genomes] |
rs10024642 | 0.86[ASN][1000 genomes] |
rs10030586 | 0.90[ASN][1000 genomes] |
rs10034781 | 0.86[ASN][1000 genomes] |
rs10433970 | 0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10516947 | 0.93[ASN][1000 genomes] |
rs10856908 | 0.86[ASN][1000 genomes] |
rs11097406 | 0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11097407 | 0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11097408 | 0.86[ASN][1000 genomes] |
rs11097411 | 0.86[ASN][1000 genomes] |
rs11722476 | 0.83[AFR][1000 genomes] |
rs11724791 | 0.91[EUR][1000 genomes] |
rs11943926 | 0.91[ASN][1000 genomes] |
rs12499309 | 0.86[ASN][1000 genomes] |
rs12501138 | 0.93[ASN][1000 genomes] |
rs12501826 | 0.91[EUR][1000 genomes] |
rs12502310 | 0.86[EUR][1000 genomes] |
rs12505596 | 0.93[ASN][1000 genomes] |
rs12510326 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12511433 | 0.86[ASN][1000 genomes] |
rs12513267 | 0.93[ASN][1000 genomes] |
rs12643901 | 0.85[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs12645192 | 0.83[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs12646184 | 0.86[ASN][1000 genomes] |
rs13111083 | 0.86[ASN][1000 genomes] |
rs13112528 | 0.86[ASN][1000 genomes] |
rs13132963 | 0.86[ASN][1000 genomes] |
rs13135934 | 0.86[ASN][1000 genomes] |
rs13142645 | 0.86[ASN][1000 genomes] |
rs13434570 | 0.86[ASN][1000 genomes] |
rs13435702 | 0.86[ASN][1000 genomes] |
rs1565062 | 0.86[ASN][1000 genomes] |
rs1605923 | 0.89[EUR][1000 genomes] |
rs17021364 | 0.87[EUR][1000 genomes] |
rs17021463 | 0.86[ASN][1000 genomes] |
rs17302300 | 0.91[ASN][1000 genomes] |
rs17310266 | 0.82[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs17310526 | 0.86[ASN][1000 genomes] |
rs17374832 | 0.93[ASN][1000 genomes] |
rs17376404 | 0.86[ASN][1000 genomes] |
rs17376488 | 0.86[ASN][1000 genomes] |
rs17623135 | 0.86[ASN][1000 genomes] |
rs1828324 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs183993 | 0.91[ASN][1000 genomes] |
rs1876917 | 0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1876918 | 0.95[ASN][1000 genomes] |
rs2087170 | 0.86[ASN][1000 genomes] |
rs2129595 | 0.86[ASN][1000 genomes] |
rs2169719 | 0.91[EUR][1000 genomes] |
rs2171381 | 0.86[ASN][1000 genomes] |
rs2171384 | 0.93[ASN][1000 genomes] |
rs2199602 | 0.92[EUR][1000 genomes] |
rs2276910 | 0.91[ASN][1000 genomes] |
rs2632399 | 0.85[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs2632401 | 0.90[ASN][1000 genomes] |
rs2632405 | 0.90[ASN][1000 genomes] |
rs2632410 | 0.90[ASN][1000 genomes] |
rs2632411 | 0.90[ASN][1000 genomes] |
rs2632417 | 0.91[ASN][1000 genomes] |
rs2664871 | 0.85[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs2664872 | 0.90[ASN][1000 genomes] |
rs2664880 | 0.90[ASN][1000 genomes] |
rs2664881 | 0.90[ASN][1000 genomes] |
rs2664892 | 0.88[ASN][1000 genomes] |
rs2664894 | 0.88[ASN][1000 genomes] |
rs282447 | 0.89[ASN][1000 genomes] |
rs282448 | 0.85[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs282449 | 0.83[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs282450 | 0.90[ASN][1000 genomes] |
rs28398254 | 0.90[EUR][1000 genomes] |
rs28408270 | 0.93[ASN][1000 genomes] |
rs28417458 | 0.91[EUR][1000 genomes] |
rs28469860 | 0.88[ASN][1000 genomes] |
rs28474924 | 0.91[EUR][1000 genomes] |
rs28613890 | 0.91[EUR][1000 genomes] |
rs2865343 | 0.93[ASN][1000 genomes] |
rs2865344 | 0.93[ASN][1000 genomes] |
rs2865345 | 0.88[ASN][1000 genomes] |
rs28696050 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs2883 | 0.88[ASN][1000 genomes] |
rs2902979 | 0.82[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs3106133 | 0.90[ASN][1000 genomes] |
rs3106134 | 0.91[ASN][1000 genomes] |
rs3106135 | 0.88[AFR][1000 genomes];0.90[ASN][1000 genomes] |
rs3106136 | 0.88[ASN][1000 genomes] |
rs3113862 | 0.90[ASN][1000 genomes] |
rs3113863 | 0.90[ASN][1000 genomes] |
rs34145031 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs34383543 | 0.83[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs34396894 | 0.95[ASN][1000 genomes] |
rs34711938 | 0.86[ASN][1000 genomes] |
rs35361491 | 0.86[ASN][1000 genomes] |
rs35670996 | 0.86[ASN][1000 genomes] |
rs35995707 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs4235050 | 0.88[ASN][1000 genomes] |
rs4438731 | 0.95[ASN][1000 genomes] |
rs4558832 | 0.87[ASN][1000 genomes] |
rs4560373 | 0.93[ASN][1000 genomes] |
rs4692999 | 0.89[ASN][1000 genomes] |
rs4693000 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4693003 | 0.90[ASN][1000 genomes] |
rs4693004 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs4693375 | 0.91[ASN][1000 genomes] |
rs4693377 | 0.87[ASN][1000 genomes] |
rs4693378 | 0.86[ASN][1000 genomes] |
rs4693381 | 0.86[ASN][1000 genomes] |
rs56161035 | 0.90[EUR][1000 genomes] |
rs60428594 | 0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs61004493 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs61069704 | 0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs61514245 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs6532469 | 0.92[ASN][1000 genomes] |
rs6532472 | 0.93[ASN][1000 genomes] |
rs6532476 | 0.86[ASN][1000 genomes] |
rs66581998 | 0.84[ASN][1000 genomes] |
rs67552174 | 0.83[ASN][1000 genomes] |
rs6817795 | 0.93[ASN][1000 genomes] |
rs6821438 | 0.95[ASN][1000 genomes] |
rs6821638 | 0.94[ASN][1000 genomes] |
rs6823404 | 0.86[ASN][1000 genomes] |
rs6840674 | 0.86[ASN][1000 genomes] |
rs6841121 | 0.86[ASN][1000 genomes] |
rs6857967 | 0.93[ASN][1000 genomes] |
rs6858265 | 0.91[ASN][1000 genomes] |
rs6858342 | 0.93[ASN][1000 genomes] |
rs722486 | 0.95[ASN][1000 genomes] |
rs72663782 | 0.89[EUR][1000 genomes] |
rs72663785 | 0.92[EUR][1000 genomes] |
rs72663787 | 0.92[EUR][1000 genomes] |
rs72663802 | 0.91[EUR][1000 genomes] |
rs72665608 | 0.92[ASN][1000 genomes] |
rs72665629 | 0.93[ASN][1000 genomes] |
rs72665658 | 0.90[ASN][1000 genomes] |
rs7435106 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs7437089 | 0.84[ASN][1000 genomes] |
rs7439869 | 0.86[ASN][1000 genomes] |
rs7442254 | 0.83[ASN][1000 genomes] |
rs7654565 | 0.93[ASN][1000 genomes] |
rs7654919 | 0.91[ASN][1000 genomes] |
rs7657789 | 0.86[ASN][1000 genomes] |
rs7669168 | 0.93[ASN][1000 genomes] |
rs7678054 | 0.97[ASN][1000 genomes] |
rs7680953 | 0.85[ASN][1000 genomes] |
rs7685121 | 0.86[ASN][1000 genomes] |
rs7697827 | 0.86[ASN][1000 genomes] |
rs8026 | 0.86[ASN][1000 genomes] |
rs8336 | 0.86[ASN][1000 genomes] |
rs9307136 | 0.91[ASN][1000 genomes] |
rs9307137 | 0.90[ASN][1000 genomes] |
rs9884209 | 0.86[ASN][1000 genomes] |
rs9884431 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv931979 | chr4:94289958-95121723 | Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv821636 | chr4:94439636-95116590 | Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv879618 | chr4:94980768-95136164 | Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv993495 | chr4:94992315-95482578 | Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
5 | nsv879621 | chr4:95046907-95099194 | Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
6 | nsv966205 | chr4:95090307-95094146 | Enhancers ZNF genes & repeats Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:95089800-95099600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr4:95090200-95094800 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
3 | chr4:95091600-95092000 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |