Variant report
Variant | rs509058 |
---|---|
Chromosome Location | chr11:121077211-121077212 |
allele | C/T |
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 | chr11:121073176..121075427-chr11:121076496..121078905,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10892676 | 1.00[CHB][hapmap] |
rs10892692 | 0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11218148 | 1.00[CHB][hapmap] |
rs11218158 | 1.00[CHB][hapmap] |
rs11218160 | 1.00[CHB][hapmap] |
rs11826847 | 1.00[CHB][hapmap] |
rs12275038 | 1.00[CHB][hapmap] |
rs12279811 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12288505 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17245810 | 1.00[CHB][hapmap] |
rs1939934 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1941299 | 0.89[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1943656 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4427574 | 1.00[CHB][hapmap] |
rs4499012 | 0.82[EUR][1000 genomes] |
rs4539330 | 1.00[CHB][hapmap] |
rs4623911 | 1.00[CHB][hapmap] |
rs4641485 | 1.00[CHB][hapmap] |
rs489985 | 0.81[EUR][1000 genomes] |
rs4935760 | 1.00[CHB][hapmap] |
rs4936576 | 1.00[CHB][hapmap] |
rs4936578 | 1.00[CHB][hapmap] |
rs4936579 | 1.00[CHB][hapmap] |
rs4936583 | 1.00[CHB][hapmap] |
rs4936584 | 1.00[CHB][hapmap] |
rs4936585 | 1.00[CHB][hapmap] |
rs4936586 | 1.00[CHB][hapmap] |
rs4936587 | 1.00[CHB][hapmap] |
rs4936590 | 0.81[EUR][1000 genomes] |
rs4936591 | 0.82[EUR][1000 genomes] |
rs513182 | 1.00[CHB][hapmap] |
rs524392 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs528958 | 1.00[CHB][hapmap] |
rs541623 | 1.00[CHB][hapmap] |
rs580683 | 0.81[EUR][1000 genomes] |
rs581786 | 1.00[CHB][hapmap] |
rs606674 | 1.00[CHB][hapmap] |
rs607014 | 1.00[CHB][hapmap] |
rs614634 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs615697 | 1.00[CHB][hapmap];0.81[EUR][1000 genomes] |
rs616184 | 1.00[CHB][hapmap];0.81[EUR][1000 genomes] |
rs620164 | 1.00[CHB][hapmap] |
rs620778 | 1.00[CHB][hapmap] |
rs624428 | 1.00[CHB][hapmap] |
rs639891 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6589862 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs665743 | 1.00[CHB][hapmap] |
rs688106 | 1.00[CHB][hapmap] |
rs7105356 | 1.00[CHB][hapmap] |
rs7108587 | 1.00[CHB][hapmap] |
rs7108594 | 1.00[CHB][hapmap] |
rs7108741 | 1.00[CHB][hapmap] |
rs7108971 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7110565 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7114879 | 1.00[CHB][hapmap] |
rs7114915 | 1.00[CHB][hapmap] |
rs7120647 | 1.00[CHB][hapmap] |
rs7122110 | 1.00[CHB][hapmap] |
rs7125224 | 1.00[CHB][hapmap] |
rs7128792 | 1.00[CHB][hapmap] |
rs7130952 | 1.00[CHB][hapmap] |
rs877538 | 1.00[CHB][hapmap] |
rs9736671 | 0.81[EUR][1000 genomes] |
rs9943635 | 0.88[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 | nsv1042295 | chr11:121072853-121177079 | Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | n/a |
2 | esv2761715 | chr11:121073605-121083183 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:121076800-121077800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr11:121077000-121077600 | Enhancers | Muscle Satellite Cultured Cells | -- |
3 | chr11:121077000-121077600 | Enhancers | Fetal Kidney | kidney |
4 | chr11:121077000-121077800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
5 | chr11:121077000-121078600 | Enhancers | HSMMtube | muscle |