Variant report
Variant | rs9595815 |
---|---|
Chromosome Location | chr13:48502068-48502069 |
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 | chr13:48501618..48503669-chr13:48506224..48510200,3 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000260388 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1041070 | 0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11148100 | 0.89[ASN][1000 genomes] |
rs11618397 | 0.86[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs1185727 | 0.84[ASN][1000 genomes] |
rs12428259 | 0.86[CHB][hapmap];0.84[JPT][hapmap] |
rs12429137 | 0.87[CHB][hapmap];0.86[JPT][hapmap] |
rs1326135 | 0.81[ASN][1000 genomes] |
rs1326136 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs1326138 | 0.85[ASN][1000 genomes] |
rs1326139 | 0.85[ASN][1000 genomes] |
rs1326140 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.86[ASN][1000 genomes] |
rs1536301 | 0.93[CHB][hapmap];0.93[JPT][hapmap] |
rs1544078 | 0.94[ASN][1000 genomes] |
rs17071168 | 0.86[CHB][hapmap];0.93[JPT][hapmap] |
rs1853929 | 0.85[ASN][1000 genomes] |
rs1886975 | 0.90[ASN][1000 genomes] |
rs1926089 | 0.82[ASN][1000 genomes] |
rs2031590 | 0.88[ASN][1000 genomes] |
rs2094194 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2148243 | 0.82[ASN][1000 genomes] |
rs2148244 | 0.89[ASN][1000 genomes] |
rs2148245 | 0.82[ASN][1000 genomes] |
rs2182376 | 0.82[ASN][1000 genomes] |
rs2296574 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes] |
rs2406690 | 0.81[YRI][hapmap] |
rs2406693 | 0.90[ASN][1000 genomes] |
rs2406697 | 0.82[ASN][1000 genomes] |
rs4245347 | 0.89[ASN][1000 genomes] |
rs4447314 | 0.82[ASN][1000 genomes] |
rs4522322 | 0.88[ASN][1000 genomes] |
rs4941615 | 0.80[EUR][1000 genomes] |
rs4941619 | 0.87[CHB][hapmap];0.86[JPT][hapmap] |
rs4941621 | 0.88[ASN][1000 genomes] |
rs4942725 | 0.81[ASN][1000 genomes] |
rs4942726 | 0.86[ASN][1000 genomes] |
rs4942727 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs4942728 | 0.89[ASN][1000 genomes] |
rs4942729 | 0.82[ASN][1000 genomes] |
rs4942730 | 0.82[ASN][1000 genomes] |
rs4942735 | 0.81[ASN][1000 genomes] |
rs6561415 | 0.85[ASN][1000 genomes] |
rs6561417 | 0.82[ASN][1000 genomes] |
rs6561419 | 0.82[ASN][1000 genomes] |
rs6561420 | 0.82[ASN][1000 genomes] |
rs6561424 | 0.81[ASN][1000 genomes] |
rs6561427 | 0.80[ASN][1000 genomes] |
rs6561429 | 0.93[CHB][hapmap];0.85[JPT][hapmap] |
rs6561430 | 0.81[ASN][1000 genomes] |
rs6561431 | 0.80[ASN][1000 genomes] |
rs6561432 | 0.80[ASN][1000 genomes] |
rs718010 | 0.82[ASN][1000 genomes] |
rs7318770 | 1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes] |
rs7319245 | 0.88[ASN][1000 genomes] |
rs7320366 | 0.93[JPT][hapmap];0.84[ASN][1000 genomes] |
rs7320461 | 0.82[ASN][1000 genomes] |
rs7320759 | 0.82[ASN][1000 genomes] |
rs7322515 | 0.82[ASN][1000 genomes] |
rs7325189 | 0.86[ASN][1000 genomes] |
rs7325437 | 0.80[ASN][1000 genomes] |
rs7326889 | 0.90[ASN][1000 genomes] |
rs7326984 | 0.82[ASN][1000 genomes] |
rs7327730 | 0.82[ASN][1000 genomes] |
rs7328525 | 0.88[ASN][1000 genomes] |
rs7328537 | 0.88[ASN][1000 genomes] |
rs7330130 | 0.80[ASN][1000 genomes] |
rs7330913 | 0.81[ASN][1000 genomes] |
rs7331285 | 0.80[ASN][1000 genomes] |
rs7332304 | 0.80[ASN][1000 genomes] |
rs7333821 | 0.82[ASN][1000 genomes] |
rs7334207 | 0.82[ASN][1000 genomes] |
rs7335788 | 0.82[ASN][1000 genomes] |
rs7336972 | 0.96[ASN][1000 genomes] |
rs7337004 | 0.80[ASN][1000 genomes] |
rs7337744 | 0.81[ASN][1000 genomes] |
rs7338125 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs7338373 | 0.80[ASN][1000 genomes] |
rs7338894 | 0.81[ASN][1000 genomes] |
rs765809 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs7985357 | 0.88[ASN][1000 genomes] |
rs7989231 | 1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes] |
rs7990244 | 0.88[ASN][1000 genomes] |
rs7990266 | 0.88[ASN][1000 genomes] |
rs7990505 | 0.82[ASN][1000 genomes] |
rs7994359 | 0.93[ASN][1000 genomes] |
rs7996580 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes] |
rs7997802 | 1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes] |
rs7998116 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs7998260 | 0.88[ASN][1000 genomes] |
rs7998497 | 0.88[ASN][1000 genomes] |
rs7998998 | 0.82[ASN][1000 genomes] |
rs7999360 | 0.93[CHB][hapmap];0.85[JPT][hapmap] |
rs8000164 | 0.88[ASN][1000 genomes] |
rs8001432 | 0.88[ASN][1000 genomes] |
rs9316338 | 0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs9316339 | 0.86[CHB][hapmap];0.93[JPT][hapmap];0.84[ASN][1000 genomes] |
rs9316343 | 0.88[ASN][1000 genomes] |
rs9316344 | 0.82[ASN][1000 genomes] |
rs9526417 | 0.86[ASN][1000 genomes] |
rs9526422 | 0.89[ASN][1000 genomes] |
rs9526423 | 0.82[ASN][1000 genomes] |
rs9526426 | 0.82[ASN][1000 genomes] |
rs9526429 | 0.86[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes] |
rs9526430 | 0.82[ASN][1000 genomes] |
rs9526433 | 0.88[ASN][1000 genomes] |
rs9526434 | 0.80[ASN][1000 genomes] |
rs9534876 | 0.82[CHB][hapmap];0.94[ASN][1000 genomes] |
rs9534877 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9534878 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9534879 | 0.82[ASN][1000 genomes] |
rs9534880 | 0.82[ASN][1000 genomes] |
rs9534881 | 0.87[CHB][hapmap];0.92[JPT][hapmap] |
rs9534882 | 0.82[ASN][1000 genomes] |
rs9534885 | 0.82[ASN][1000 genomes] |
rs9534889 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9534892 | 0.81[ASN][1000 genomes] |
rs9534898 | 0.81[ASN][1000 genomes] |
rs9534901 | 0.81[ASN][1000 genomes] |
rs9534903 | 0.88[ASN][1000 genomes] |
rs9534904 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9534905 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9534906 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9534907 | 0.88[ASN][1000 genomes] |
rs9534908 | 0.82[ASN][1000 genomes] |
rs9534912 | 0.82[ASN][1000 genomes] |
rs9534913 | 0.88[ASN][1000 genomes] |
rs9534923 | 0.86[ASN][1000 genomes] |
rs9534926 | 0.82[ASN][1000 genomes] |
rs9534929 | 0.86[CHB][hapmap];0.93[JPT][hapmap] |
rs9562773 | 0.85[ASN][1000 genomes] |
rs9562787 | 0.82[ASN][1000 genomes] |
rs9567942 | 0.85[ASN][1000 genomes] |
rs9567954 | 0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9567955 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9567958 | 1.00[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes] |
rs9567959 | 0.82[ASN][1000 genomes] |
rs9567960 | 0.87[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9567963 | 0.82[ASN][1000 genomes] |
rs9567964 | 0.89[ASN][1000 genomes] |
rs9567972 | 0.81[ASN][1000 genomes] |
rs9567976 | 0.82[ASN][1000 genomes] |
rs9567980 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9567986 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.80[ASN][1000 genomes] |
rs9595825 | 0.93[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes] |
rs970650 | 0.85[ASN][1000 genomes] |
rs970651 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv933980 | chr13:48431000-48557419 | Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
2 | esv1803690 | chr13:48470681-48508091 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:48477000-48506400 | Weak transcription | Psoas Muscle | Psoas |
2 | chr13:48492200-48510800 | Weak transcription | Left Ventricle | heart |
3 | chr13:48495200-48506800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
4 | chr13:48496600-48506600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
5 | chr13:48501000-48531200 | Weak transcription | Spleen | Spleen |
6 | chr13:48502000-48530800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |