Variant report
Variant | rs73363366 |
---|---|
Chromosome Location | chr7:64406851-64406852 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | RAD21 | chr7:64406776-64408525 | SK-N-SH | brain: | n/a | chr7:64407328-64407347 chr7:64407843-64407857 chr7:64407332-64407342 chr7:64407331-64407344 chr7:64407330-64407342 |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:64314110..64316754-chr7:64405768..64408146,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000270948 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10239449 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10243927 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10253614 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10253636 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10256006 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10256702 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10258018 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10259016 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10259713 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10260579 | 0.98[AFR][1000 genomes] |
rs10265110 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10269760 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10274861 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10275331 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10499782 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12333583 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12531509 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12531631 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12533393 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12535068 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12535862 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12536001 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12537516 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12537864 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12537906 | 0.90[ASN][1000 genomes] |
rs12538078 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12539165 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12539507 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12539509 | 0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1405008 | 0.98[AFR][1000 genomes] |
rs1405009 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1534148 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17146448 | 0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1830077 | 0.92[ASN][1000 genomes] |
rs1830080 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1880658 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28398905 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28591657 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2863926 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2863985 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28664768 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3829005 | 0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4382350 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4573137 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4718164 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58472271 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59122385 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67615162 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6966781 | 0.81[AFR][1000 genomes] |
rs72504857 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73354396 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73355758 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73363367 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7783460 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7802123 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs884965 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9987044 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9987071 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2422405 | chr7:63709739-64632341 | Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 59 gene(s) | inside rSNPs | diseases |
2 | nsv427787 | chr7:63741770-64419520 | Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
3 | nsv464518 | chr7:63881238-64506904 | Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
4 | nsv607312 | chr7:63881238-64506904 | Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
5 | nsv888275 | chr7:63990100-64468590 | Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
6 | nsv888276 | chr7:63990100-64511564 | Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
7 | nsv1022042 | chr7:64226499-64566945 | Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
8 | nsv1026390 | chr7:64240323-64414364 | Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
9 | nsv888282 | chr7:64299645-64511564 | Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
10 | esv3506582 | chr7:64323055-64563984 | ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
11 | esv3506583 | chr7:64323055-64563984 | Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
12 | nsv1019180 | chr7:64329889-64512842 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
13 | nsv888283 | chr7:64343985-64511564 | Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
14 | esv2752165 | chr7:64345822-65208605 | Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
15 | nsv888284 | chr7:64406439-64562139 | ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:64397200-64407000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr7:64400600-64407600 | Weak transcription | Right Atrium | heart |
3 | chr7:64405200-64407600 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr7:64405800-64407400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr7:64405800-64407600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
6 | chr7:64405800-64407600 | Enhancers | Esophagus | oesophagus |
7 | chr7:64406000-64407200 | Enhancers | HepG2 | liver |
8 | chr7:64406200-64407400 | Bivalent Enhancer | Skeletal Muscle Female | skeletal muscle |
9 | chr7:64406400-64407200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
10 | chr7:64406400-64407400 | Enhancers | K562 | blood |
11 | chr7:64406800-64407200 | Bivalent Enhancer | Fetal Adrenal Gland | Adrenal Gland |
12 | chr7:64406800-64407600 | Weak transcription | Fetal Heart | heart |