Variant report
Variant | rs11212117 |
---|---|
Chromosome Location | chr11:107147483-107147484 |
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 | chr11:107146912..107148719-chr11:107151854..107154613,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10454489 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1046094 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap] |
rs1046095 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs10502087 | 0.95[CEU][hapmap];0.93[JPT][hapmap] |
rs10749890 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10749891 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10749896 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs10749903 | 0.84[CEU][hapmap] |
rs10789592 | 0.86[ASN][1000 genomes] |
rs10789593 | 0.85[ASN][1000 genomes] |
rs10789615 | 0.81[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap] |
rs10789616 | 0.91[CEU][hapmap];0.85[CHB][hapmap];0.85[JPT][hapmap] |
rs10789617 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs10789618 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap] |
rs10789620 | 0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs10789621 | 0.91[CEU][hapmap];0.89[GIH][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap] |
rs10890676 | 0.81[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs10890680 | 0.85[EUR][1000 genomes] |
rs10890684 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10890688 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10890689 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10890690 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10890691 | 0.91[AFR][1000 genomes] |
rs10890692 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10890708 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs10890712 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs10890719 | 0.86[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap] |
rs10890720 | 0.86[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.93[JPT][hapmap];0.83[MEX][hapmap] |
rs10890721 | 0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap] |
rs11212111 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11212112 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11212113 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11212114 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11212116 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11212118 | 0.91[AFR][1000 genomes] |
rs11212166 | 0.87[CHB][hapmap];0.93[JPT][hapmap] |
rs11212182 | 0.95[CEU][hapmap];0.89[GIH][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap] |
rs11212197 | 0.90[CEU][hapmap];0.93[JPT][hapmap] |
rs11212206 | 0.91[CEU][hapmap];0.89[GIH][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap] |
rs11212207 | 0.93[JPT][hapmap];0.83[MEX][hapmap] |
rs11602033 | 0.85[CEU][hapmap];0.93[JPT][hapmap] |
rs11602214 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12286915 | 0.93[JPT][hapmap];0.83[MEX][hapmap] |
rs12287772 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1388170 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1388171 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17106875 | 0.91[CEU][hapmap];0.87[JPT][hapmap] |
rs1963372 | 0.89[AFR][1000 genomes] |
rs1963373 | 0.88[AFR][1000 genomes] |
rs2216998 | 0.83[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs2355840 | 0.82[ASN][1000 genomes] |
rs3758911 | 0.84[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.94[MEX][hapmap] |
rs4387327 | 0.82[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap] |
rs588921 | 0.82[CEU][hapmap];0.93[JPT][hapmap] |
rs590699 | 0.91[CEU][hapmap];0.93[JPT][hapmap] |
rs6588965 | 0.83[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs7131522 | 0.81[ASN][1000 genomes] |
rs7358308 | 0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs7929345 | 0.82[ASN][1000 genomes] |
rs968453 | 0.91[AFR][1000 genomes] |
rs999984 | 0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531938 | chr11:106760733-107156814 | Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv898364 | chr11:106944975-107285636 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv898365 | chr11:106944975-107430300 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv898366 | chr11:106944975-107433835 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
5 | nsv898367 | chr11:106944975-107443420 | Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
6 | nsv898369 | chr11:106958304-107443420 | Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
7 | nsv832260 | chr11:106975094-107181795 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | nsv556279 | chr11:107006900-107186896 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | nsv1035911 | chr11:107020991-107198181 | Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv898370 | chr11:107027991-107430300 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
11 | nsv1040190 | chr11:107045534-107175661 | Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
12 | nsv898372 | chr11:107049968-107433835 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
13 | nsv1038368 | chr11:107116577-107664181 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
14 | nsv541163 | chr11:107116577-107664181 | Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
15 | nsv898373 | chr11:107124903-107433835 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
16 | nsv832261 | chr11:107145901-107321562 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:107146600-107147600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
2 | chr11:107146800-107147600 | Enhancers | Fetal Muscle Leg | muscle |
3 | chr11:107147000-107147600 | Flanking Active TSS | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
4 | chr11:107147200-107149000 | Weak transcription | Psoas Muscle | Psoas |