Variant report
Variant | rs9877909 |
---|---|
Chromosome Location | chr3:158144264-158144265 |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:158136221..158139181-chr3:158142409..158144374,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1095626 | 0.89[EUR][1000 genomes] |
rs1095627 | 0.89[EUR][1000 genomes] |
rs1095628 | 0.89[EUR][1000 genomes] |
rs1095635 | 0.89[EUR][1000 genomes] |
rs1095637 | 0.89[EUR][1000 genomes] |
rs1095638 | 0.88[EUR][1000 genomes] |
rs1095639 | 0.89[EUR][1000 genomes] |
rs1095640 | 0.89[EUR][1000 genomes] |
rs1095641 | 0.88[EUR][1000 genomes] |
rs1095642 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1101158 | 0.89[EUR][1000 genomes] |
rs1104288 | 0.89[EUR][1000 genomes] |
rs1104289 | 0.89[EUR][1000 genomes] |
rs11717725 | 0.99[ASN][1000 genomes] |
rs11719188 | 0.98[ASN][1000 genomes] |
rs1193505 | 0.89[EUR][1000 genomes] |
rs1193506 | 0.89[EUR][1000 genomes] |
rs1193507 | 0.89[EUR][1000 genomes] |
rs1193508 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1193509 | 0.89[EUR][1000 genomes] |
rs1193510 | 0.89[EUR][1000 genomes] |
rs1193521 | 0.89[EUR][1000 genomes] |
rs1193534 | 0.88[EUR][1000 genomes] |
rs1193535 | 0.88[EUR][1000 genomes] |
rs1193537 | 0.89[EUR][1000 genomes] |
rs1204962 | 0.89[EUR][1000 genomes] |
rs12107103 | 0.99[ASN][1000 genomes] |
rs12107104 | 0.99[ASN][1000 genomes] |
rs1212739 | 0.88[EUR][1000 genomes] |
rs1213048 | 0.89[EUR][1000 genomes] |
rs12496767 | 0.88[ASN][1000 genomes] |
rs12629125 | 0.99[ASN][1000 genomes] |
rs12629587 | 0.85[ASN][1000 genomes] |
rs12631196 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12633594 | 0.99[ASN][1000 genomes] |
rs12638169 | 0.98[ASN][1000 genomes] |
rs13066362 | 0.89[EUR][1000 genomes] |
rs1526191 | 0.89[EUR][1000 genomes] |
rs1526192 | 0.89[EUR][1000 genomes] |
rs1526193 | 0.89[EUR][1000 genomes] |
rs1526194 | 0.89[EUR][1000 genomes] |
rs1618381 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1630304 | 0.89[EUR][1000 genomes] |
rs1724652 | 0.89[EUR][1000 genomes] |
rs1724654 | 0.89[EUR][1000 genomes] |
rs1724700 | 0.89[EUR][1000 genomes] |
rs1724704 | 0.89[EUR][1000 genomes] |
rs1730007 | 0.89[EUR][1000 genomes] |
rs1730020 | 0.89[EUR][1000 genomes] |
rs1730040 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1730042 | 0.89[EUR][1000 genomes] |
rs1730045 | 0.89[EUR][1000 genomes] |
rs1730058 | 0.86[EUR][1000 genomes] |
rs1730059 | 0.89[EUR][1000 genomes] |
rs1852285 | 0.89[EUR][1000 genomes] |
rs1983469 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2362965 | 0.83[ASN][1000 genomes] |
rs2362968 | 0.99[ASN][1000 genomes] |
rs2362969 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2362970 | 0.99[ASN][1000 genomes] |
rs2362972 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2682404 | 0.89[EUR][1000 genomes] |
rs2682405 | 0.89[EUR][1000 genomes] |
rs2682406 | 0.89[EUR][1000 genomes] |
rs2693527 | 0.90[EUR][1000 genomes] |
rs2693529 | 0.89[EUR][1000 genomes] |
rs2693530 | 0.84[EUR][1000 genomes] |
rs2693542 | 0.89[EUR][1000 genomes] |
rs2698322 | 0.89[EUR][1000 genomes] |
rs2698323 | 0.89[EUR][1000 genomes] |
rs28820925 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4289388 | 0.94[ASN][1000 genomes] |
rs4561872 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4679828 | 0.99[ASN][1000 genomes] |
rs4680433 | 0.99[ASN][1000 genomes] |
rs4680434 | 0.99[ASN][1000 genomes] |
rs4680436 | 0.96[ASN][1000 genomes] |
rs4680437 | 0.92[ASN][1000 genomes] |
rs6414388 | 0.85[ASN][1000 genomes] |
rs6414390 | 0.85[ASN][1000 genomes] |
rs6441182 | 0.89[EUR][1000 genomes] |
rs6441183 | 0.83[EUR][1000 genomes] |
rs6441184 | 0.84[EUR][1000 genomes] |
rs6441195 | 0.97[ASN][1000 genomes] |
rs6441197 | 0.98[ASN][1000 genomes] |
rs6441198 | 0.94[ASN][1000 genomes] |
rs6441200 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6441201 | 0.89[ASN][1000 genomes] |
rs67385174 | 0.98[ASN][1000 genomes] |
rs6800887 | 0.93[ASN][1000 genomes] |
rs6806702 | 0.97[ASN][1000 genomes] |
rs699927 | 0.82[EUR][1000 genomes] |
rs7426603 | 0.98[ASN][1000 genomes] |
rs7430565 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7610691 | 0.99[ASN][1000 genomes] |
rs7621674 | 0.89[EUR][1000 genomes] |
rs7621971 | 0.89[EUR][1000 genomes] |
rs7632059 | 0.99[ASN][1000 genomes] |
rs7636974 | 0.86[EUR][1000 genomes] |
rs7637291 | 0.89[EUR][1000 genomes] |
rs7641954 | 0.94[ASN][1000 genomes] |
rs7643792 | 0.89[EUR][1000 genomes] |
rs7648196 | 0.85[ASN][1000 genomes] |
rs827092 | 0.90[EUR][1000 genomes] |
rs827093 | 0.89[EUR][1000 genomes] |
rs827094 | 0.89[EUR][1000 genomes] |
rs827095 | 0.89[EUR][1000 genomes] |
rs827096 | 0.89[EUR][1000 genomes] |
rs827097 | 0.89[EUR][1000 genomes] |
rs827098 | 0.89[EUR][1000 genomes] |
rs827099 | 0.89[EUR][1000 genomes] |
rs827101 | 0.89[EUR][1000 genomes] |
rs827106 | 0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs827108 | 0.89[EUR][1000 genomes] |
rs827109 | 0.89[EUR][1000 genomes] |
rs827110 | 0.89[EUR][1000 genomes] |
rs827111 | 0.89[EUR][1000 genomes] |
rs827112 | 0.88[EUR][1000 genomes] |
rs827113 | 0.89[EUR][1000 genomes] |
rs827114 | 0.89[EUR][1000 genomes] |
rs827126 | 0.89[EUR][1000 genomes] |
rs827127 | 0.89[EUR][1000 genomes] |
rs827128 | 0.90[EUR][1000 genomes] |
rs827129 | 0.89[EUR][1000 genomes] |
rs827131 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs827132 | 0.89[EUR][1000 genomes] |
rs827134 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs827135 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs827137 | 0.89[EUR][1000 genomes] |
rs827140 | 0.89[EUR][1000 genomes] |
rs827163 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs827164 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs827166 | 0.89[EUR][1000 genomes] |
rs827171 | 0.88[EUR][1000 genomes] |
rs827176 | 0.88[EUR][1000 genomes] |
rs827177 | 0.88[EUR][1000 genomes] |
rs827178 | 0.88[EUR][1000 genomes] |
rs827179 | 0.88[EUR][1000 genomes] |
rs827180 | 0.88[EUR][1000 genomes] |
rs827181 | 0.86[EUR][1000 genomes] |
rs827184 | 0.85[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs844119 | 0.89[EUR][1000 genomes] |
rs864332 | 0.89[EUR][1000 genomes] |
rs865454 | 0.90[EUR][1000 genomes] |
rs865455 | 0.88[EUR][1000 genomes] |
rs9784311 | 0.90[EUR][1000 genomes] |
rs9810345 | 0.92[ASN][1000 genomes] |
rs9820370 | 0.90[EUR][1000 genomes] |
rs9823076 | 0.99[ASN][1000 genomes] |
rs9838399 | 0.86[EUR][1000 genomes] |
rs9843089 | 0.98[ASN][1000 genomes] |
rs9847045 | 0.98[ASN][1000 genomes] |
rs9847316 | 0.95[ASN][1000 genomes] |
rs9847460 | 0.99[ASN][1000 genomes] |
rs9850856 | 0.99[ASN][1000 genomes] |
rs9870802 | 0.99[ASN][1000 genomes] |
rs9872889 | 0.88[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 | nsv1000904 | chr3:158094357-158159317 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:158124600-158146600 | Weak transcription | Primary B cells from cord blood | blood |