Variant report
Variant | rs12078392 |
---|---|
Chromosome Location | chr1:152364383-152364384 |
allele | A/G |
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 | chr1:152358713..152362980-chr1:152363568..152366676,4 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11204983 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12057680 | 1.00[EUR][1000 genomes] |
rs12060296 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12066296 | 1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12067755 | 1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12083959 | 1.00[EUR][1000 genomes] |
rs16834174 | 1.00[EUR][1000 genomes] |
rs1858481 | 1.00[EUR][1000 genomes] |
rs28655434 | 1.00[EUR][1000 genomes] |
rs3120654 | 1.00[EUR][1000 genomes] |
rs3126087 | 1.00[EUR][1000 genomes] |
rs3126093 | 1.00[EUR][1000 genomes] |
rs3134871 | 1.00[EUR][1000 genomes] |
rs56106510 | 1.00[EUR][1000 genomes] |
rs56244386 | 1.00[EUR][1000 genomes] |
rs566973 | 1.00[EUR][1000 genomes] |
rs57272962 | 1.00[EUR][1000 genomes] |
rs57934636 | 1.00[EUR][1000 genomes] |
rs58788896 | 1.00[EUR][1000 genomes] |
rs58823849 | 1.00[EUR][1000 genomes] |
rs58935238 | 1.00[EUR][1000 genomes] |
rs60095860 | 1.00[EUR][1000 genomes] |
rs60179982 | 1.00[EUR][1000 genomes] |
rs60709044 | 1.00[EUR][1000 genomes] |
rs60963018 | 1.00[EUR][1000 genomes] |
rs61230786 | 1.00[EUR][1000 genomes] |
rs73003080 | 1.00[EUR][1000 genomes] |
rs73003789 | 1.00[EUR][1000 genomes] |
rs73004841 | 1.00[EUR][1000 genomes] |
rs73004845 | 1.00[EUR][1000 genomes] |
rs73004848 | 1.00[EUR][1000 genomes] |
rs73004856 | 1.00[EUR][1000 genomes] |
rs73004882 | 1.00[EUR][1000 genomes] |
rs73004888 | 1.00[EUR][1000 genomes] |
rs73006958 | 1.00[EUR][1000 genomes] |
rs73006962 | 1.00[EUR][1000 genomes] |
rs733439 | 1.00[EUR][1000 genomes] |
rs74127885 | 1.00[EUR][1000 genomes] |
rs74127887 | 1.00[EUR][1000 genomes] |
rs74127894 | 1.00[EUR][1000 genomes] |
rs74127895 | 1.00[EUR][1000 genomes] |
rs74127917 | 1.00[EUR][1000 genomes] |
rs74127918 | 1.00[EUR][1000 genomes] |
rs74128280 | 1.00[EUR][1000 genomes] |
rs74129414 | 1.00[EUR][1000 genomes] |
rs74129429 | 1.00[EUR][1000 genomes] |
rs74129447 | 1.00[EUR][1000 genomes] |
rs74129458 | 1.00[EUR][1000 genomes] |
rs74129459 | 1.00[EUR][1000 genomes] |
rs74129463 | 1.00[EUR][1000 genomes] |
rs74129464 | 1.00[EUR][1000 genomes] |
rs74129466 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014095 | chr1:152104486-152454591 | Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
2 | nsv1005472 | chr1:152247763-152443448 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
3 | nsv535161 | chr1:152247763-152443448 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
4 | nsv916016 | chr1:152337775-152590520 | Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:152363800-152368000 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
2 | chr1:152363800-152368200 | Enhancers | Primary T helper memory cells from peripheral blood 1 | blood |
3 | chr1:152363800-152368200 | Enhancers | Primary T helper 17 cells PMA-I stimulated | -- |
4 | chr1:152364000-152365000 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
5 | chr1:152364000-152366600 | Enhancers | NHEK | skin |
6 | chr1:152364200-152364600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |