Variant report
Variant | rs62156711 |
---|---|
Chromosome Location | chr2:98859277-98859278 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:4)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:4 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | MAFK | chr2:98859105-98859392 | HepG2 | liver: | n/a | chr2:98859276-98859291 |
2 | MAFK | chr2:98859112-98859465 | HepG2 | liver: | n/a | chr2:98859276-98859291 |
3 | MAFK | chr2:98859128-98859417 | IMR90 | lung: | n/a | chr2:98859276-98859291 |
4 | MAFF | chr2:98859107-98859421 | HepG2 | liver: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
VWA3B | TF binding region |
rs_ID | r2[population] |
---|---|
rs17427314 | 1.00[AFR][1000 genomes] |
rs17427356 | 1.00[AFR][1000 genomes] |
rs17427531 | 1.00[AFR][1000 genomes] |
rs17427573 | 1.00[AFR][1000 genomes] |
rs17427636 | 1.00[AFR][1000 genomes] |
rs17427726 | 1.00[AFR][1000 genomes] |
rs17428000 | 1.00[AFR][1000 genomes] |
rs17428212 | 1.00[AFR][1000 genomes] |
rs17428262 | 1.00[AFR][1000 genomes] |
rs17428318 | 1.00[AFR][1000 genomes] |
rs17428528 | 1.00[AFR][1000 genomes] |
rs17428626 | 1.00[AFR][1000 genomes] |
rs17428843 | 1.00[AFR][1000 genomes] |
rs17429145 | 1.00[AFR][1000 genomes] |
rs17429278 | 1.00[AFR][1000 genomes] |
rs17493076 | 1.00[AFR][1000 genomes] |
rs17493153 | 1.00[AFR][1000 genomes] |
rs17493543 | 1.00[AFR][1000 genomes] |
rs17493879 | 1.00[AFR][1000 genomes] |
rs17500449 | 1.00[AFR][1000 genomes] |
rs17500559 | 1.00[AFR][1000 genomes] |
rs17500893 | 1.00[AFR][1000 genomes] |
rs17501122 | 1.00[AFR][1000 genomes] |
rs62154934 | 1.00[AFR][1000 genomes] |
rs62155276 | 1.00[AFR][1000 genomes] |
rs62155278 | 1.00[AFR][1000 genomes] |
rs62155279 | 1.00[AFR][1000 genomes] |
rs62155280 | 1.00[AFR][1000 genomes] |
rs62155282 | 1.00[AFR][1000 genomes] |
rs62155283 | 1.00[AFR][1000 genomes] |
rs62155284 | 1.00[AFR][1000 genomes] |
rs62155285 | 1.00[AFR][1000 genomes] |
rs62155286 | 1.00[AFR][1000 genomes] |
rs62155288 | 1.00[AFR][1000 genomes] |
rs62155289 | 1.00[AFR][1000 genomes] |
rs62155290 | 1.00[AFR][1000 genomes] |
rs62155291 | 1.00[AFR][1000 genomes] |
rs62155292 | 1.00[AFR][1000 genomes] |
rs62155293 | 1.00[AFR][1000 genomes] |
rs62155294 | 1.00[AFR][1000 genomes] |
rs62155295 | 1.00[AFR][1000 genomes] |
rs62155296 | 1.00[AFR][1000 genomes] |
rs62155297 | 1.00[AFR][1000 genomes] |
rs62155300 | 1.00[AFR][1000 genomes] |
rs62155301 | 1.00[AFR][1000 genomes] |
rs62155302 | 1.00[AFR][1000 genomes] |
rs62155303 | 1.00[AFR][1000 genomes] |
rs62155305 | 1.00[AFR][1000 genomes] |
rs62155308 | 1.00[AFR][1000 genomes] |
rs62155309 | 1.00[AFR][1000 genomes] |
rs62155310 | 1.00[AFR][1000 genomes] |
rs62155311 | 1.00[AFR][1000 genomes] |
rs62155314 | 1.00[AFR][1000 genomes] |
rs62155315 | 1.00[AFR][1000 genomes] |
rs62155316 | 1.00[AFR][1000 genomes] |
rs62155318 | 1.00[AFR][1000 genomes] |
rs62155348 | 1.00[AFR][1000 genomes] |
rs62155349 | 1.00[AFR][1000 genomes] |
rs62155351 | 1.00[AFR][1000 genomes] |
rs62155352 | 1.00[AFR][1000 genomes] |
rs62155353 | 1.00[AFR][1000 genomes] |
rs62155356 | 1.00[AFR][1000 genomes] |
rs62155357 | 1.00[AFR][1000 genomes] |
rs62155359 | 1.00[AFR][1000 genomes] |
rs62156260 | 1.00[AFR][1000 genomes] |
rs62156262 | 1.00[AFR][1000 genomes] |
rs62156275 | 1.00[AFR][1000 genomes] |
rs62156684 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62156685 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62156687 | 1.00[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs62156709 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156710 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156722 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62156725 | 1.00[AFR][1000 genomes] |
rs62156726 | 1.00[AFR][1000 genomes] |
rs62156727 | 1.00[AFR][1000 genomes] |
rs62156728 | 1.00[AFR][1000 genomes] |
rs62156729 | 1.00[AFR][1000 genomes] |
rs62156730 | 1.00[AFR][1000 genomes] |
rs62156731 | 1.00[AFR][1000 genomes] |
rs62156732 | 1.00[AFR][1000 genomes] |
rs62156733 | 1.00[AFR][1000 genomes] |
rs62156738 | 1.00[AFR][1000 genomes] |
rs62156739 | 1.00[AFR][1000 genomes] |
rs62156741 | 1.00[AFR][1000 genomes] |
rs62156742 | 1.00[AFR][1000 genomes] |
rs62156743 | 1.00[AFR][1000 genomes] |
rs62157893 | 1.00[AFR][1000 genomes] |
rs62157895 | 1.00[AFR][1000 genomes] |
rs62157896 | 1.00[AFR][1000 genomes] |
rs62157897 | 1.00[AFR][1000 genomes] |
rs62157898 | 1.00[AFR][1000 genomes] |
rs62157899 | 1.00[AFR][1000 genomes] |
rs62157900 | 1.00[AFR][1000 genomes] |
rs62157902 | 1.00[AFR][1000 genomes] |
rs62157903 | 1.00[AFR][1000 genomes] |
rs62157904 | 1.00[AFR][1000 genomes] |
rs62157905 | 1.00[AFR][1000 genomes] |
rs62157906 | 1.00[AFR][1000 genomes] |
rs62157909 | 1.00[AFR][1000 genomes] |
rs62157910 | 1.00[AFR][1000 genomes] |
rs62157912 | 1.00[AFR][1000 genomes] |
rs62157913 | 1.00[AFR][1000 genomes] |
rs62157917 | 1.00[AFR][1000 genomes] |
rs62157918 | 1.00[AFR][1000 genomes] |
rs62157919 | 1.00[AFR][1000 genomes] |
rs62157920 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv518056 | chr2:98586842-99156296 | Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
2 | nsv1004082 | chr2:98792256-98967681 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv535833 | chr2:98792256-98967681 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv582513 | chr2:98829237-98869914 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv582514 | chr2:98835962-98869914 | Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1014147 | chr2:98855007-98878044 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
7 | nsv818075 | chr2:98855497-98872039 | Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
8 | nsv582515 | chr2:98855497-98885925 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
9 | nsv517669 | chr2:98855497-98889961 | Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
10 | nsv437289 | chr2:98855497-98891519 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
11 | esv3459702 | chr2:98856083-98886708 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
12 | esv3459703 | chr2:98856205-98886602 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
13 | esv19987 | chr2:98856422-98886491 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
14 | nsv1010376 | chr2:98858308-98878044 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
15 | nsv1008771 | chr2:98858308-98881340 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
16 | esv2760564 | chr2:98858308-98881352 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
17 | nsv1012433 | chr2:98858308-98888391 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
18 | nsv1012121 | chr2:98858308-98889961 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:98857400-98859400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr2:98857400-98859400 | Enhancers | Brain Germinal Matrix | brain |
3 | chr2:98857400-98859600 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr2:98859200-98859400 | Enhancers | Brain Angular Gyrus | brain |
5 | chr2:98859200-98859400 | Enhancers | Brain Cingulate Gyrus | brain |
6 | chr2:98859200-98859400 | Enhancers | Brain Hippocampus Middle | brain |
7 | chr2:98859200-98859400 | Enhancers | Brain Inferior Temporal Lobe | brain |
8 | chr2:98859200-98859400 | Enhancers | Brain Substantia Nigra | brain |