Variant report
Variant | rs11895552 |
---|---|
Chromosome Location | chr2:133781957-133781958 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10194766 | 1.00[EUR][1000 genomes] |
rs11887257 | 1.00[TSI][hapmap] |
rs11889166 | 1.00[EUR][1000 genomes] |
rs12475072 | 1.00[TSI][hapmap] |
rs13388152 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs16842407 | 1.00[TSI][hapmap] |
rs16842532 | 1.00[TSI][hapmap] |
rs16842747 | 1.00[TSI][hapmap] |
rs16857190 | 1.00[EUR][1000 genomes] |
rs16857197 | 1.00[EUR][1000 genomes] |
rs16857260 | 1.00[EUR][1000 genomes] |
rs16857605 | 1.00[EUR][1000 genomes] |
rs16858020 | 1.00[EUR][1000 genomes] |
rs1836220 | 1.00[EUR][1000 genomes] |
rs2069257 | 1.00[EUR][1000 genomes] |
rs2320320 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs56836351 | 1.00[EUR][1000 genomes] |
rs59741799 | 1.00[EUR][1000 genomes] |
rs61257975 | 1.00[EUR][1000 genomes] |
rs6430379 | 1.00[EUR][1000 genomes] |
rs6430393 | 1.00[EUR][1000 genomes] |
rs6713080 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs6718899 | 1.00[EUR][1000 genomes] |
rs6719786 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs6725275 | 1.00[EUR][1000 genomes] |
rs6732204 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs6733114 | 1.00[EUR][1000 genomes] |
rs6738269 | 1.00[EUR][1000 genomes] |
rs6760236 | 1.00[TSI][hapmap] |
rs6761371 | 1.00[EUR][1000 genomes] |
rs72994884 | 1.00[EUR][1000 genomes] |
rs7563261 | 1.00[EUR][1000 genomes] |
rs7568126 | 1.00[EUR][1000 genomes] |
rs7568144 | 1.00[EUR][1000 genomes] |
rs7578857 | 1.00[EUR][1000 genomes] |
rs7579940 | 1.00[EUR][1000 genomes] |
rs7584749 | 1.00[EUR][1000 genomes] |
rs7585734 | 1.00[EUR][1000 genomes] |
rs7608610 | 1.00[TSI][hapmap] |
rs997377 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv583158 | chr2:133316092-133862100 | Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
2 | nsv916805 | chr2:133664765-133924973 | Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv834381 | chr2:133722671-133897994 | Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv834382 | chr2:133728399-133891418 | Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv999703 | chr2:133734955-133817962 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv535926 | chr2:133734955-133817962 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv875139 | chr2:133777866-133929225 | Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:133759800-133784400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr2:133762600-133797200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
3 | chr2:133780200-133783800 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |