Variant report
Variant | rs6850833 |
---|---|
Chromosome Location | chr4:82200371-82200372 |
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 | chr4:82191920..82194351-chr4:82199658..82201341,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10000303 | 1.00[EUR][1000 genomes] |
rs10014824 | 1.00[EUR][1000 genomes] |
rs10018984 | 1.00[EUR][1000 genomes] |
rs10022306 | 1.00[EUR][1000 genomes] |
rs10023642 | 1.00[EUR][1000 genomes] |
rs10027298 | 1.00[EUR][1000 genomes] |
rs10028912 | 1.00[EUR][1000 genomes] |
rs10029494 | 1.00[EUR][1000 genomes] |
rs10031760 | 1.00[EUR][1000 genomes] |
rs13434668 | 1.00[EUR][1000 genomes] |
rs17005064 | 1.00[EUR][1000 genomes] |
rs17005067 | 1.00[EUR][1000 genomes] |
rs17005089 | 1.00[EUR][1000 genomes] |
rs17005100 | 1.00[EUR][1000 genomes] |
rs17005101 | 1.00[EUR][1000 genomes] |
rs28377778 | 1.00[EUR][1000 genomes] |
rs28539711 | 1.00[EUR][1000 genomes] |
rs28550356 | 1.00[EUR][1000 genomes] |
rs28550971 | 1.00[EUR][1000 genomes] |
rs28625925 | 1.00[EUR][1000 genomes] |
rs28664024 | 1.00[EUR][1000 genomes] |
rs28665590 | 1.00[EUR][1000 genomes] |
rs28669336 | 1.00[EUR][1000 genomes] |
rs28727457 | 1.00[EUR][1000 genomes] |
rs28810974 | 1.00[EUR][1000 genomes] |
rs28860889 | 1.00[EUR][1000 genomes] |
rs28882451 | 1.00[EUR][1000 genomes] |
rs28888497 | 1.00[EUR][1000 genomes] |
rs4496577 | 1.00[EUR][1000 genomes] |
rs56236182 | 1.00[EUR][1000 genomes] |
rs56347774 | 1.00[EUR][1000 genomes] |
rs58295714 | 1.00[EUR][1000 genomes] |
rs60390550 | 1.00[EUR][1000 genomes] |
rs61676707 | 1.00[EUR][1000 genomes] |
rs6814849 | 1.00[EUR][1000 genomes] |
rs6828846 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6837264 | 1.00[EUR][1000 genomes] |
rs73829535 | 1.00[EUR][1000 genomes] |
rs73829539 | 1.00[EUR][1000 genomes] |
rs73829540 | 1.00[EUR][1000 genomes] |
rs73831298 | 1.00[EUR][1000 genomes] |
rs7655473 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999729 | chr4:81802554-82627820 | Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | nsv537156 | chr4:81802554-82627820 | Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
3 | nsv829985 | chr4:82199328-82353656 | Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:82193800-82203200 | Weak transcription | Fetal Intestine Small | intestine |
2 | chr4:82199600-82208200 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |