Variant report
Variant | rs62277152 |
---|---|
Chromosome Location | chr3:156516435-156516436 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:8)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:8 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:156515560..156517669-chr3:156523840..156525586,2 | K562 | blood: | |
2 | chr3:156487668..156490241-chr3:156516348..156519090,2 | K562 | blood: | |
3 | chr3:156515946..156518416-chr3:156543029..156545847,2 | MCF-7 | breast: | |
4 | chr3:156508375..156510192-chr3:156514735..156517661,2 | MCF-7 | breast: | |
5 | chr3:156508939..156511033-chr3:156513884..156516615,2 | K562 | blood: | |
6 | chr3:156498174..156501165-chr3:156515710..156519959,5 | K562 | blood: | |
7 | chr3:156515993..156518701-chr3:156522150..156523774,2 | K562 | blood: | |
8 | chr3:156515429..156517896-chr3:156519184..156521324,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000197980 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17380639 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs17381024 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs17381930 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs17382208 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs17440227 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs17440656 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs17440944 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs17442011 | 1.00[AFR][1000 genomes] |
rs17442045 | 1.00[AFR][1000 genomes] |
rs62273860 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273861 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273862 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273892 | 1.00[AFR][1000 genomes] |
rs62273893 | 1.00[AFR][1000 genomes] |
rs62273895 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273896 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273897 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273898 | 1.00[AFR][1000 genomes] |
rs62273899 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273900 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273901 | 1.00[AFR][1000 genomes] |
rs62273902 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273904 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273905 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273906 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273907 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273908 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273909 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273910 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273912 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273913 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273914 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273915 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273916 | 0.84[EUR][1000 genomes] |
rs62273917 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273918 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273919 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273920 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62273921 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273922 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273955 | 0.82[EUR][1000 genomes] |
rs62273956 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273958 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62273959 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275160 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275163 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275164 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275165 | 1.00[AFR][1000 genomes] |
rs62275166 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275171 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275174 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275175 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275176 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275177 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275178 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275179 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275180 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275181 | 1.00[AFR][1000 genomes] |
rs62275182 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275185 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275186 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275187 | 1.00[AFR][1000 genomes] |
rs62275189 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275190 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275191 | 1.00[AFR][1000 genomes] |
rs62275238 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275241 | 1.00[AFR][1000 genomes] |
rs62275243 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275244 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275245 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275246 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275247 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275248 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275249 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275250 | 0.82[EUR][1000 genomes] |
rs62275251 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275252 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62275253 | 1.00[AFR][1000 genomes] |
rs62275255 | 1.00[AFR][1000 genomes] |
rs62275256 | 1.00[AFR][1000 genomes] |
rs62275257 | 1.00[AFR][1000 genomes] |
rs62275258 | 1.00[AFR][1000 genomes] |
rs62275259 | 1.00[AFR][1000 genomes] |
rs62275760 | 1.00[AFR][1000 genomes] |
rs62275761 | 1.00[AFR][1000 genomes] |
rs62275762 | 1.00[AFR][1000 genomes] |
rs62275764 | 1.00[AFR][1000 genomes] |
rs62275766 | 1.00[AFR][1000 genomes] |
rs62275767 | 1.00[AFR][1000 genomes] |
rs62275795 | 1.00[AFR][1000 genomes] |
rs62275796 | 1.00[AFR][1000 genomes] |
rs62275797 | 1.00[AFR][1000 genomes] |
rs62275798 | 1.00[AFR][1000 genomes] |
rs62275799 | 1.00[AFR][1000 genomes] |
rs62275800 | 1.00[AFR][1000 genomes] |
rs62275801 | 1.00[AFR][1000 genomes] |
rs62275804 | 1.00[AFR][1000 genomes] |
rs62275805 | 1.00[AFR][1000 genomes] |
rs62275806 | 1.00[AFR][1000 genomes] |
rs62275808 | 1.00[AFR][1000 genomes] |
rs62275809 | 1.00[AFR][1000 genomes] |
rs62275810 | 1.00[AFR][1000 genomes] |
rs62275811 | 1.00[AFR][1000 genomes] |
rs62275812 | 1.00[AFR][1000 genomes] |
rs62275813 | 1.00[AFR][1000 genomes] |
rs62275829 | 1.00[AFR][1000 genomes] |
rs62275830 | 1.00[AFR][1000 genomes] |
rs62275837 | 1.00[AFR][1000 genomes] |
rs62275839 | 1.00[AFR][1000 genomes] |
rs62275841 | 1.00[AFR][1000 genomes] |
rs62275842 | 1.00[AFR][1000 genomes] |
rs62275843 | 1.00[AFR][1000 genomes] |
rs62275844 | 1.00[AFR][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];0.84[EUR][1000 genomes] |
rs62277086 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277087 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277088 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277089 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277090 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277091 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277092 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277093 | 1.00[AFR][1000 genomes] |
rs62277096 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277097 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277099 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277140 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277141 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277142 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277143 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277144 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277145 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277146 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277147 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277148 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277150 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277153 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277155 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277156 | 0.84[EUR][1000 genomes] |
rs62277157 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62277158 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62278060 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62278061 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62278062 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62278064 | 1.00[AFR][1000 genomes];0.84[EUR][1000 genomes] |
rs62278065 | 1.00[AFR][1000 genomes] |
rs62278066 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428745 | chr3:156405054-156577840 | Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
2 | nsv877685 | chr3:156444383-156611676 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 48 gene(s) | inside rSNPs | diseases |
3 | nsv877686 | chr3:156489509-156557697 | Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 42 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:156502800-156528400 | Weak transcription | Esophagus | oesophagus |
2 | chr3:156502800-156529000 | Weak transcription | Liver | Liver |
3 | chr3:156511000-156519600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr3:156511200-156516600 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
5 | chr3:156511200-156529000 | Weak transcription | Primary T cells from cord blood | blood |
6 | chr3:156511400-156518800 | Weak transcription | Primary T killer memory cells from peripheral blood | blood |
7 | chr3:156511400-156530400 | Weak transcription | Primary T helper memory cells from peripheral blood 2 | blood |
8 | chr3:156511600-156519600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
9 | chr3:156514000-156519600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
10 | chr3:156514200-156517200 | Weak transcription | A549 | lung |
11 | chr3:156514200-156517600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
12 | chr3:156514400-156517400 | Weak transcription | HMEC | breast |
13 | chr3:156514400-156517800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
14 | chr3:156514400-156525400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
15 | chr3:156514400-156525800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
16 | chr3:156515800-156517600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
17 | chr3:156516400-156517600 | Weak transcription | NHEK | skin |