Variant report
Variant | rs4924509 |
---|---|
Chromosome Location | chr15:41174767-41174768 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
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(count:3 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000104142 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1049598 | 0.86[CHB][hapmap] |
rs11070298 | 0.90[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11070299 | 0.89[EUR][1000 genomes] |
rs11070302 | 0.81[ASN][1000 genomes] |
rs11070303 | 0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11070304 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs11070305 | 0.81[EUR][1000 genomes] |
rs11856227 | 1.00[CEU][hapmap];0.89[EUR][1000 genomes] |
rs12101494 | 0.87[EUR][1000 genomes] |
rs12148515 | 0.82[EUR][1000 genomes] |
rs12148523 | 0.92[EUR][1000 genomes] |
rs12903603 | 0.84[EUR][1000 genomes] |
rs12916961 | 1.00[CEU][hapmap];0.81[EUR][1000 genomes] |
rs16971157 | 1.00[CEU][hapmap];0.82[EUR][1000 genomes] |
rs17649 | 0.88[CHB][hapmap] |
rs1814692 | 0.91[EUR][1000 genomes] |
rs2279578 | 1.00[CEU][hapmap];0.90[EUR][1000 genomes] |
rs2412571 | 0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs28444382 | 0.81[EUR][1000 genomes] |
rs3100809 | 0.89[ASN][1000 genomes] |
rs4244581 | 0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4384588 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4923885 | 0.89[EUR][1000 genomes] |
rs4923886 | 1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4923887 | 0.84[EUR][1000 genomes] |
rs601436 | 1.00[CEU][hapmap];0.94[EUR][1000 genomes] |
rs616606 | 0.94[EUR][1000 genomes] |
rs617377 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs618892 | 0.92[CEU][hapmap];0.96[EUR][1000 genomes] |
rs618916 | 0.96[EUR][1000 genomes] |
rs625058 | 1.00[CEU][hapmap] |
rs658752 | 0.86[CHB][hapmap] |
rs676180 | 0.86[CHB][hapmap] |
rs682130 | 0.80[EUR][1000 genomes] |
rs690136 | 0.86[CHB][hapmap] |
rs7172280 | 1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7175294 | 0.91[AFR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7403641 | 0.86[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs8024861 | 1.00[CEU][hapmap];0.96[EUR][1000 genomes] |
rs8024961 | 1.00[CEU][hapmap];0.96[EUR][1000 genomes] |
rs8028660 | 0.88[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs8042095 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv904101 | chr15:40979651-41275014 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 98 gene(s) | inside rSNPs | diseases |
2 | esv1819092 | chr15:41017682-41255750 | Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 83 gene(s) | inside rSNPs | diseases |
3 | nsv904102 | chr15:41046883-41201699 | Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 61 gene(s) | inside rSNPs | diseases |
4 | nsv1054764 | chr15:41068625-41196410 | Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
5 | nsv569228 | chr15:41106485-41194151 | Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
6 | nsv904103 | chr15:41123172-41275014 | Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 60 gene(s) | inside rSNPs | diseases |
7 | nsv904104 | chr15:41149824-41234932 | Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 50 gene(s) | inside rSNPs | diseases |
8 | nsv904105 | chr15:41149824-41275014 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 57 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:41172000-41184000 | Weak transcription | Duodenum Mucosa | Duodenum |
2 | chr15:41172600-41175200 | Weak transcription | Stomach Mucosa | stomach |
3 | chr15:41174600-41176800 | Weak transcription | Skeletal Muscle Male | skeletal muscle |