Variant report
Variant | rs1252433 |
---|---|
Chromosome Location | chr12:67632347-67632348 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000111530 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1066392 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes] |
rs1082703 | 1.00[AFR][1000 genomes] |
rs1082704 | 1.00[AFR][1000 genomes] |
rs1082705 | 1.00[AFR][1000 genomes] |
rs1082706 | 1.00[AFR][1000 genomes] |
rs1082707 | 1.00[AFR][1000 genomes] |
rs1082712 | 1.00[AFR][1000 genomes] |
rs1082713 | 1.00[AMR][1000 genomes] |
rs1082718 | 1.00[AMR][1000 genomes] |
rs1082719 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1143757 | 1.00[AFR][1000 genomes] |
rs1143946 | 1.00[AFR][1000 genomes] |
rs1143955 | 1.00[AFR][1000 genomes] |
rs1152891 | 1.00[AFR][1000 genomes] |
rs1152899 | 1.00[AFR][1000 genomes] |
rs1152903 | 1.00[AFR][1000 genomes] |
rs1186260 | 1.00[AFR][1000 genomes] |
rs1252363 | 1.00[AFR][1000 genomes] |
rs1252409 | 1.00[AFR][1000 genomes] |
rs1252420 | 1.00[AFR][1000 genomes] |
rs1252437 | 1.00[AMR][1000 genomes] |
rs1252438 | 1.00[AMR][1000 genomes] |
rs1392588 | 1.00[AFR][1000 genomes] |
rs1392589 | 1.00[AFR][1000 genomes] |
rs1658782 | 1.00[AFR][1000 genomes] |
rs1697242 | 1.00[AMR][1000 genomes] |
rs1697249 | 1.00[AFR][1000 genomes] |
rs1732535 | 1.00[AMR][1000 genomes] |
rs1732541 | 1.00[AFR][1000 genomes] |
rs710621 | 1.00[AFR][1000 genomes] |
rs710799 | 1.00[AFR][1000 genomes] |
rs775311 | 1.00[AFR][1000 genomes] |
rs775625 | 1.00[AFR][1000 genomes] |
rs775627 | 1.00[AFR][1000 genomes] |
rs775642 | 1.00[AFR][1000 genomes] |
rs775643 | 1.00[AFR][1000 genomes] |
rs775649 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes] |
rs775664 | 1.00[AFR][1000 genomes] |
rs812882 | 1.00[AFR][1000 genomes] |
rs812883 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv541524 | chr12:67311057-67700349 | Strong transcription Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv559212 | chr12:67373549-67850925 | Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
3 | nsv1054111 | chr12:67556780-67865542 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
4 | nsv899218 | chr12:67612129-67643840 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |