Variant report
Variant | rs73368266 |
---|---|
Chromosome Location | chr12:60753016-60753017 |
allele | C/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 | chr12:60752778..60755096-chr12:60757481..60759676,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000251822 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs57822720 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60891596 | 1.00[EUR][1000 genomes] |
rs7132956 | 1.00[EUR][1000 genomes] |
rs73355386 | 1.00[EUR][1000 genomes] |
rs73355390 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73355396 | 1.00[EUR][1000 genomes] |
rs73357118 | 1.00[EUR][1000 genomes] |
rs73357123 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73357124 | 1.00[EUR][1000 genomes] |
rs73357126 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73357128 | 1.00[EUR][1000 genomes] |
rs73357132 | 0.80[AFR][1000 genomes] |
rs73357137 | 1.00[EUR][1000 genomes] |
rs73357141 | 1.00[EUR][1000 genomes] |
rs73357774 | 1.00[EUR][1000 genomes] |
rs73365604 | 1.00[EUR][1000 genomes] |
rs73365607 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365610 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365614 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365615 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365622 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365630 | 1.00[EUR][1000 genomes] |
rs73365639 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365644 | 1.00[EUR][1000 genomes] |
rs73365647 | 1.00[EUR][1000 genomes] |
rs73365653 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73365654 | 1.00[EUR][1000 genomes] |
rs73366675 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73366682 | 1.00[EUR][1000 genomes] |
rs73368260 | 1.00[EUR][1000 genomes] |
rs73368992 | 1.00[EUR][1000 genomes] |
rs73368998 | 1.00[EUR][1000 genomes] |
rs73369000 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73370709 | 1.00[EUR][1000 genomes] |
rs73370724 | 1.00[EUR][1000 genomes] |
rs73370735 | 0.80[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73370758 | 1.00[EUR][1000 genomes] |
rs73370766 | 1.00[EUR][1000 genomes] |
rs73370770 | 1.00[EUR][1000 genomes] |
rs73370779 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv899137 | chr12:60568891-60797083 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1054287 | chr12:60601870-60861866 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv832431 | chr12:60626292-60809233 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1047466 | chr12:60702221-61521156 | Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
5 | esv2762983 | chr12:60735475-60767081 | Enhancers Active TSS Weak transcription | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | esv3500240 | chr12:60752085-60759033 | Enhancers | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | esv3500239 | chr12:60752535-60758933 | Enhancers | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | nsv8977 | chr12:60752953-60758579 | Enhancers | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |