Variant report
Variant | rs73663191 |
---|---|
Chromosome Location | chr8:11515819-11515820 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
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rs_ID | r2[population] |
---|---|
rs10088181 | 1.00[EUR][1000 genomes] |
rs10091294 | 1.00[EUR][1000 genomes] |
rs10094355 | 1.00[EUR][1000 genomes] |
rs10094630 | 1.00[EUR][1000 genomes] |
rs10096015 | 1.00[EUR][1000 genomes] |
rs10096526 | 1.00[EUR][1000 genomes] |
rs10097076 | 1.00[EUR][1000 genomes] |
rs10100742 | 1.00[EUR][1000 genomes] |
rs10101788 | 1.00[EUR][1000 genomes] |
rs10101900 | 1.00[EUR][1000 genomes] |
rs10102714 | 1.00[EUR][1000 genomes] |
rs10103483 | 1.00[EUR][1000 genomes] |
rs10105409 | 1.00[EUR][1000 genomes] |
rs10106250 | 1.00[EUR][1000 genomes] |
rs10108287 | 1.00[EUR][1000 genomes] |
rs10109678 | 1.00[EUR][1000 genomes] |
rs10109971 | 1.00[EUR][1000 genomes] |
rs10111542 | 1.00[EUR][1000 genomes] |
rs10112464 | 1.00[EUR][1000 genomes] |
rs10113255 | 1.00[EUR][1000 genomes] |
rs10216815 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2127130 | 1.00[EUR][1000 genomes] |
rs2127131 | 1.00[EUR][1000 genomes] |
rs2244775 | 1.00[EUR][1000 genomes] |
rs2252818 | 1.00[EUR][1000 genomes] |
rs2252906 | 1.00[EUR][1000 genomes] |
rs2252908 | 1.00[EUR][1000 genomes] |
rs2252914 | 1.00[EUR][1000 genomes] |
rs2264307 | 1.00[EUR][1000 genomes] |
rs2409812 | 1.00[EUR][1000 genomes] |
rs28394863 | 1.00[EUR][1000 genomes] |
rs28472428 | 1.00[EUR][1000 genomes] |
rs28505660 | 1.00[EUR][1000 genomes] |
rs28665608 | 1.00[EUR][1000 genomes] |
rs4841582 | 1.00[EUR][1000 genomes] |
rs5027656 | 1.00[EUR][1000 genomes] |
rs55951800 | 1.00[EUR][1000 genomes] |
rs57782848 | 1.00[EUR][1000 genomes] |
rs58467083 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59035560 | 1.00[EUR][1000 genomes] |
rs60419043 | 1.00[EUR][1000 genomes] |
rs61265429 | 1.00[EUR][1000 genomes] |
rs73207234 | 1.00[AMR][1000 genomes] |
rs73207238 | 1.00[AMR][1000 genomes] |
rs73207250 | 1.00[AMR][1000 genomes] |
rs73533953 | 1.00[EUR][1000 genomes] |
rs73545766 | 1.00[EUR][1000 genomes] |
rs73545784 | 1.00[EUR][1000 genomes] |
rs73663183 | 1.00[EUR][1000 genomes] |
rs73663184 | 1.00[EUR][1000 genomes] |
rs73663185 | 1.00[EUR][1000 genomes] |
rs73663187 | 1.00[EUR][1000 genomes] |
rs73663190 | 1.00[EUR][1000 genomes] |
rs73663201 | 1.00[EUR][1000 genomes] |
rs7831152 | 1.00[EUR][1000 genomes] |
rs7841968 | 1.00[EUR][1000 genomes] |
rs8191510 | 1.00[EUR][1000 genomes] |
rs8191543 | 1.00[EUR][1000 genomes] |
rs8191573 | 1.00[EUR][1000 genomes] |
rs8191669 | 1.00[EUR][1000 genomes] |
rs8191682 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529399 | chr8:10970091-11805960 | Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 54 gene(s) | inside rSNPs | diseases |
2 | nsv1017865 | chr8:11377795-11579954 | Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv1018978 | chr8:11438267-11858466 | Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:11514800-11516000 | Enhancers | Liver | Liver |
2 | chr8:11515200-11516000 | Enhancers | Pancreas | Pancrea |
3 | chr8:11515400-11516200 | Enhancers | Duodenum Mucosa | Duodenum |
4 | chr8:11515600-11516400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |