Variant report
Variant | rs62275841 |
---|---|
Chromosome Location | chr3:156699706-156699707 |
allele | A/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 | chr3:156698217..156700249-chr3:156702856..156704415,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1482865 | 1.00[ASN][1000 genomes] |
rs17380639 | 1.00[AFR][1000 genomes] |
rs17381024 | 1.00[AFR][1000 genomes] |
rs17381930 | 1.00[AFR][1000 genomes] |
rs17382208 | 1.00[AFR][1000 genomes] |
rs17440227 | 1.00[AFR][1000 genomes] |
rs17440656 | 1.00[AFR][1000 genomes] |
rs17440944 | 1.00[AFR][1000 genomes] |
rs17442011 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs17442045 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273860 | 1.00[AFR][1000 genomes] |
rs62273861 | 1.00[AFR][1000 genomes] |
rs62273862 | 1.00[AFR][1000 genomes] |
rs62273892 | 1.00[AFR][1000 genomes] |
rs62273893 | 1.00[AFR][1000 genomes] |
rs62273895 | 1.00[AFR][1000 genomes] |
rs62273896 | 1.00[AFR][1000 genomes] |
rs62273897 | 1.00[AFR][1000 genomes] |
rs62273898 | 1.00[AFR][1000 genomes] |
rs62273899 | 1.00[AFR][1000 genomes] |
rs62273900 | 1.00[AFR][1000 genomes] |
rs62273901 | 1.00[AFR][1000 genomes] |
rs62273902 | 1.00[AFR][1000 genomes] |
rs62273904 | 1.00[AFR][1000 genomes] |
rs62273905 | 1.00[AFR][1000 genomes] |
rs62273906 | 1.00[AFR][1000 genomes] |
rs62273907 | 1.00[AFR][1000 genomes] |
rs62273908 | 1.00[AFR][1000 genomes] |
rs62273909 | 1.00[AFR][1000 genomes] |
rs62273910 | 1.00[AFR][1000 genomes] |
rs62273912 | 1.00[AFR][1000 genomes] |
rs62273913 | 1.00[AFR][1000 genomes] |
rs62273914 | 1.00[AFR][1000 genomes] |
rs62273915 | 1.00[AFR][1000 genomes] |
rs62273917 | 1.00[AFR][1000 genomes] |
rs62273918 | 1.00[AFR][1000 genomes] |
rs62273919 | 1.00[AFR][1000 genomes] |
rs62273920 | 1.00[AFR][1000 genomes] |
rs62273921 | 1.00[AFR][1000 genomes] |
rs62273922 | 1.00[AFR][1000 genomes] |
rs62273956 | 1.00[AFR][1000 genomes] |
rs62273958 | 1.00[AFR][1000 genomes] |
rs62273959 | 1.00[AFR][1000 genomes] |
rs62275160 | 1.00[AFR][1000 genomes] |
rs62275163 | 1.00[AFR][1000 genomes] |
rs62275164 | 1.00[AFR][1000 genomes] |
rs62275165 | 1.00[AFR][1000 genomes] |
rs62275166 | 1.00[AFR][1000 genomes] |
rs62275171 | 1.00[AFR][1000 genomes] |
rs62275174 | 1.00[AFR][1000 genomes] |
rs62275175 | 1.00[AFR][1000 genomes] |
rs62275176 | 1.00[AFR][1000 genomes] |
rs62275177 | 1.00[AFR][1000 genomes] |
rs62275178 | 1.00[AFR][1000 genomes] |
rs62275179 | 1.00[AFR][1000 genomes] |
rs62275180 | 1.00[AFR][1000 genomes] |
rs62275181 | 1.00[AFR][1000 genomes] |
rs62275182 | 1.00[AFR][1000 genomes] |
rs62275185 | 1.00[AFR][1000 genomes] |
rs62275186 | 1.00[AFR][1000 genomes] |
rs62275187 | 1.00[AFR][1000 genomes] |
rs62275189 | 1.00[AFR][1000 genomes] |
rs62275190 | 1.00[AFR][1000 genomes] |
rs62275191 | 1.00[AFR][1000 genomes] |
rs62275238 | 1.00[AFR][1000 genomes] |
rs62275241 | 1.00[AFR][1000 genomes] |
rs62275243 | 1.00[AFR][1000 genomes] |
rs62275244 | 1.00[AFR][1000 genomes] |
rs62275245 | 1.00[AFR][1000 genomes] |
rs62275246 | 1.00[AFR][1000 genomes] |
rs62275247 | 1.00[AFR][1000 genomes] |
rs62275248 | 1.00[AFR][1000 genomes] |
rs62275249 | 1.00[AFR][1000 genomes] |
rs62275251 | 1.00[AFR][1000 genomes] |
rs62275252 | 1.00[AFR][1000 genomes] |
rs62275253 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275255 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275256 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275257 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275258 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275259 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275760 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275761 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275762 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275764 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275766 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275767 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275795 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275796 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275797 | 1.00[AFR][1000 genomes] |
rs62275798 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275799 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275800 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275801 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275804 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275805 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275806 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275808 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275809 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275810 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275811 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275812 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275813 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275829 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs62275830 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs62275837 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs62275839 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62275840 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62275842 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62275843 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62275844 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62277076 | 1.00[AFR][1000 genomes] |
rs62277077 | 1.00[AFR][1000 genomes] |
rs62277078 | 1.00[AFR][1000 genomes] |
rs62277079 | 1.00[AFR][1000 genomes] |
rs62277080 | 1.00[AFR][1000 genomes] |
rs62277085 | 1.00[AFR][1000 genomes] |
rs62277086 | 1.00[AFR][1000 genomes] |
rs62277087 | 1.00[AFR][1000 genomes] |
rs62277088 | 1.00[AFR][1000 genomes] |
rs62277089 | 1.00[AFR][1000 genomes] |
rs62277090 | 1.00[AFR][1000 genomes] |
rs62277091 | 1.00[AFR][1000 genomes] |
rs62277092 | 1.00[AFR][1000 genomes] |
rs62277093 | 1.00[AFR][1000 genomes] |
rs62277096 | 1.00[AFR][1000 genomes] |
rs62277097 | 1.00[AFR][1000 genomes] |
rs62277099 | 1.00[AFR][1000 genomes] |
rs62277140 | 1.00[AFR][1000 genomes] |
rs62277141 | 1.00[AFR][1000 genomes] |
rs62277142 | 1.00[AFR][1000 genomes] |
rs62277143 | 1.00[AFR][1000 genomes] |
rs62277144 | 1.00[AFR][1000 genomes] |
rs62277145 | 1.00[AFR][1000 genomes] |
rs62277146 | 1.00[AFR][1000 genomes] |
rs62277147 | 1.00[AFR][1000 genomes] |
rs62277148 | 1.00[AFR][1000 genomes] |
rs62277150 | 1.00[AFR][1000 genomes] |
rs62277152 | 1.00[AFR][1000 genomes] |
rs62277153 | 1.00[AFR][1000 genomes] |
rs62277155 | 1.00[AFR][1000 genomes] |
rs62277157 | 1.00[AFR][1000 genomes] |
rs62277158 | 1.00[AFR][1000 genomes] |
rs62278060 | 1.00[AFR][1000 genomes] |
rs62278061 | 1.00[AFR][1000 genomes] |
rs62278062 | 1.00[AFR][1000 genomes] |
rs62278064 | 1.00[AFR][1000 genomes] |
rs62278065 | 1.00[AFR][1000 genomes] |
rs62278066 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv829765 | chr3:156568263-156718496 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | esv3349885 | chr3:156685409-156878910 | Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 141 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:156698200-156702200 | Weak transcription | Primary B cells from cord blood | blood |
2 | chr3:156698400-156704200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr3:156698800-156701000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |