Variant report
Variant | rs73738796 |
---|---|
Chromosome Location | chr6:27375682-27375683 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:5)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:5 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | MAFF | chr6:27375268-27375795 | HepG2 | liver: | n/a | chr6:27375425-27375443 |
2 | MAFK | chr6:27375264-27375861 | HepG2 | liver: | n/a | chr6:27375427-27375442 |
3 | MAFK | chr6:27375265-27375825 | HepG2 | liver: | n/a | chr6:27375427-27375442 |
4 | NFIC | chr6:27375092-27375717 | ECC-1 | luminal epithelium: | n/a | n/a |
5 | MAFF | chr6:27375255-27375784 | K562 | blood: | n/a | chr6:27375425-27375443 |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:27374845..27377266-chr6:27859975..27862570,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000271755 | TF binding region |
ENSG00000233224 | Chromatin interaction |
ENSG00000197153 | Chromatin interaction |
ENSG00000196331 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs16895205 | 1.00[EUR][1000 genomes] |
rs16899633 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16899664 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16899742 | 0.88[AFR][1000 genomes] |
rs16899778 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16899794 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16899861 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4616979 | 1.00[EUR][1000 genomes] |
rs5030966 | 1.00[EUR][1000 genomes] |
rs56141585 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56773753 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56980568 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56982870 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57123722 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57349601 | 1.00[EUR][1000 genomes] |
rs57509377 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57655939 | 1.00[AMR][1000 genomes] |
rs58016420 | 0.88[AFR][1000 genomes] |
rs58458505 | 1.00[EUR][1000 genomes] |
rs58669069 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58685987 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58942357 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59659183 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59813908 | 1.00[EUR][1000 genomes] |
rs59886985 | 1.00[EUR][1000 genomes] |
rs61137579 | 1.00[EUR][1000 genomes] |
rs61206558 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61482673 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61483696 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs61740349 | 1.00[EUR][1000 genomes] |
rs73738714 | 1.00[EUR][1000 genomes] |
rs73738743 | 1.00[EUR][1000 genomes] |
rs73738764 | 1.00[EUR][1000 genomes] |
rs73738772 | 1.00[EUR][1000 genomes] |
rs73738775 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73738795 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73738798 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73738799 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73738802 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73739106 | 1.00[EUR][1000 genomes] |
rs73741704 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73741705 | 1.00[EUR][1000 genomes] |
rs73741706 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73741708 | 0.88[AFR][1000 genomes] |
rs73741716 | 1.00[EUR][1000 genomes] |
rs766093 | 0.91[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7744655 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7750919 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7751102 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7758568 | 1.00[EUR][1000 genomes] |
rs7765353 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7768826 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7773166 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7775305 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948921 | chr6:26556890-27443957 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 472 gene(s) | inside rSNPs | diseases |
2 | nsv1031803 | chr6:27355881-27423655 | Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
3 | nsv538166 | chr6:27355881-27423655 | Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
4 | nsv5235 | chr6:27358498-27404074 | ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:27369000-27376600 | Weak transcription | Brain Cingulate Gyrus | brain |
2 | chr6:27369200-27382000 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
3 | chr6:27370600-27379800 | Weak transcription | Ovary | ovary |
4 | chr6:27373800-27376400 | Enhancers | Breast Myoepithelial Primary Cells | Breast |