Variant report
Variant | rs73397831 |
---|---|
Chromosome Location | chr18:11707802-11707803 |
allele | C/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 | chr18:11707724..11709378-chr18:11741039..11743864,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10468679 | 1.00[ASN][1000 genomes] |
rs10468682 | 1.00[ASN][1000 genomes] |
rs10502413 | 1.00[ASN][1000 genomes] |
rs11872939 | 1.00[ASN][1000 genomes] |
rs12373424 | 1.00[ASN][1000 genomes] |
rs12457247 | 1.00[ASN][1000 genomes] |
rs1424913 | 1.00[ASN][1000 genomes] |
rs1559579 | 1.00[ASN][1000 genomes] |
rs16976625 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16976628 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16976639 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16976666 | 1.00[ASN][1000 genomes] |
rs16976687 | 1.00[ASN][1000 genomes] |
rs1834267 | 1.00[ASN][1000 genomes] |
rs1941225 | 1.00[ASN][1000 genomes] |
rs28666369 | 0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28688137 | 1.00[ASN][1000 genomes] |
rs28696966 | 1.00[ASN][1000 genomes] |
rs56314648 | 1.00[ASN][1000 genomes] |
rs56819096 | 1.00[ASN][1000 genomes] |
rs56861220 | 1.00[ASN][1000 genomes] |
rs57485078 | 1.00[ASN][1000 genomes] |
rs57491632 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57878458 | 1.00[ASN][1000 genomes] |
rs57958293 | 1.00[ASN][1000 genomes] |
rs58144032 | 1.00[ASN][1000 genomes] |
rs58248860 | 1.00[ASN][1000 genomes] |
rs58273499 | 1.00[ASN][1000 genomes] |
rs58296571 | 1.00[ASN][1000 genomes] |
rs58471713 | 1.00[ASN][1000 genomes] |
rs58617475 | 1.00[ASN][1000 genomes] |
rs58829911 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58991912 | 1.00[ASN][1000 genomes] |
rs59099814 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59286339 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59455765 | 1.00[ASN][1000 genomes] |
rs59549445 | 1.00[ASN][1000 genomes] |
rs59624432 | 1.00[ASN][1000 genomes] |
rs59870994 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59893403 | 1.00[ASN][1000 genomes] |
rs59920321 | 1.00[ASN][1000 genomes] |
rs60036326 | 1.00[ASN][1000 genomes] |
rs60590666 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61076914 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6505675 | 1.00[ASN][1000 genomes] |
rs7227117 | 1.00[ASN][1000 genomes] |
rs7227259 | 1.00[ASN][1000 genomes] |
rs73397852 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73397857 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73397859 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73397874 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73399817 | 1.00[ASN][1000 genomes] |
rs73399822 | 1.00[ASN][1000 genomes] |
rs73399842 | 1.00[ASN][1000 genomes] |
rs73401824 | 1.00[ASN][1000 genomes] |
rs73401826 | 1.00[ASN][1000 genomes] |
rs73401832 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73401838 | 1.00[ASN][1000 genomes] |
rs73401844 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73403525 | 1.00[ASN][1000 genomes] |
rs73403531 | 1.00[ASN][1000 genomes] |
rs73403540 | 1.00[ASN][1000 genomes] |
rs73403565 | 1.00[ASN][1000 genomes] |
rs73403569 | 1.00[ASN][1000 genomes] |
rs73403571 | 1.00[ASN][1000 genomes] |
rs73405491 | 1.00[ASN][1000 genomes] |
rs73405493 | 1.00[ASN][1000 genomes] |
rs73407408 | 1.00[ASN][1000 genomes] |
rs73407416 | 1.00[ASN][1000 genomes] |
rs73407420 | 1.00[ASN][1000 genomes] |
rs73407440 | 1.00[ASN][1000 genomes] |
rs787556 | 1.00[ASN][1000 genomes] |
rs8085783 | 1.00[ASN][1000 genomes] |
rs8089494 | 1.00[ASN][1000 genomes] |
rs8095571 | 1.00[ASN][1000 genomes] |
rs8095793 | 1.00[ASN][1000 genomes] |
rs8098587 | 1.00[ASN][1000 genomes] |
rs8099026 | 1.00[ASN][1000 genomes] |
rs8099153 | 1.00[ASN][1000 genomes] |
rs9303743 | 1.00[ASN][1000 genomes] |
rs9303752 | 1.00[ASN][1000 genomes] |
rs9646452 | 1.00[ASN][1000 genomes] |
rs9675502 | 1.00[ASN][1000 genomes] |
rs9675734 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9675736 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9675750 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9676233 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9676238 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9946157 | 1.00[ASN][1000 genomes] |
rs9946455 | 1.00[ASN][1000 genomes] |
rs9948287 | 1.00[ASN][1000 genomes] |
rs9954486 | 1.00[ASN][1000 genomes] |
rs9960175 | 1.00[ASN][1000 genomes] |
rs9962057 | 1.00[ASN][1000 genomes] |
rs9963594 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9967080 | 0.87[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 | nsv1066659 | chr18:11246502-11709409 | Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 24 gene(s) | inside rSNPs | diseases |
2 | esv3362008 | chr18:11647654-11959830 | Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
3 | nsv978602 | chr18:11699589-11729341 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr18:11690400-11713800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
2 | chr18:11696200-11713600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr18:11697400-11727000 | Weak transcription | Esophagus | oesophagus |
4 | chr18:11698000-11715000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr18:11702400-11708800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
6 | chr18:11702400-11712000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
7 | chr18:11707600-11708200 | Enhancers | Sigmoid Colon | Sigmoid Colon |
8 | chr18:11707800-11708600 | Enhancers | Adipose Nuclei | Adipose |
9 | chr18:11707800-11709000 | Enhancers | Breast Myoepithelial Primary Cells | Breast |