Variant report
Variant | rs1828126 |
---|---|
Chromosome Location | chr11:106157556-106157557 |
allele | C/T |
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] |
---|---|
rs10750750 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes] |
rs10791801 | 0.80[ASN][1000 genomes] |
rs10791802 | 1.00[CHB][hapmap];0.87[JPT][hapmap] |
rs10895935 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10895938 | 0.83[ASN][1000 genomes] |
rs11226982 | 0.82[ASN][1000 genomes] |
rs11226987 | 0.90[ASN][1000 genomes] |
rs12273190 | 0.91[EUR][1000 genomes] |
rs12283696 | 0.82[EUR][1000 genomes] |
rs12290323 | 0.91[EUR][1000 genomes] |
rs12291279 | 0.82[EUR][1000 genomes] |
rs12421469 | 0.91[EUR][1000 genomes] |
rs12421840 | 0.91[EUR][1000 genomes] |
rs1262373 | 0.93[EUR][1000 genomes] |
rs1396156 | 0.91[CHB][hapmap];0.87[JPT][hapmap] |
rs1508148 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1605565 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1605567 | 0.91[CHB][hapmap];0.87[JPT][hapmap] |
rs1806481 | 0.90[CHB][hapmap];0.87[JPT][hapmap] |
rs1893856 | 0.91[EUR][1000 genomes] |
rs1944770 | 0.91[EUR][1000 genomes] |
rs2409624 | 0.87[ASN][1000 genomes] |
rs4614415 | 0.82[EUR][1000 genomes] |
rs4755146 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes] |
rs483873 | 0.91[EUR][1000 genomes] |
rs485681 | 0.91[EUR][1000 genomes] |
rs488212 | 0.99[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs531851 | 0.93[EUR][1000 genomes] |
rs542358 | 0.99[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs565672 | 0.91[EUR][1000 genomes] |
rs594050 | 0.91[EUR][1000 genomes] |
rs602407 | 0.92[CEU][hapmap];0.93[EUR][1000 genomes] |
rs617143 | 0.96[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs633534 | 0.93[EUR][1000 genomes] |
rs657786 | 0.93[EUR][1000 genomes] |
rs660647 | 0.99[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs667501 | 0.96[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs674799 | 0.92[CEU][hapmap];0.87[CHB][hapmap] |
rs7126969 | 0.80[ASN][1000 genomes] |
rs7127780 | 0.91[EUR][1000 genomes] |
rs7131594 | 0.89[EUR][1000 genomes] |
rs726349 | 0.91[EUR][1000 genomes] |
rs72985182 | 0.82[EUR][1000 genomes] |
rs72987177 | 0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1048381 | chr11:105945117-106561574 | Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
2 | nsv898358 | chr11:105999580-106182251 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv430428 | chr11:106005901-106173046 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | esv2754854 | chr11:106092790-106245790 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:106152800-106157800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
2 | chr11:106152800-106158800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
3 | chr11:106157200-106157800 | Enhancers | NHDF-Ad | bronchial |
4 | chr11:106157200-106158000 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
5 | chr11:106157400-106158600 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |