Variant report
Variant | rs73267491 |
---|---|
Chromosome Location | chr10:61699620-61699621 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10994098 | 1.00[ASN][1000 genomes] |
rs10994101 | 1.00[ASN][1000 genomes] |
rs10994103 | 1.00[ASN][1000 genomes] |
rs10994207 | 1.00[ASN][1000 genomes] |
rs11592958 | 1.00[ASN][1000 genomes] |
rs11593303 | 1.00[ASN][1000 genomes] |
rs11597608 | 1.00[ASN][1000 genomes] |
rs11599447 | 1.00[ASN][1000 genomes] |
rs1171838 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1171839 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1171840 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1171842 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1171852 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1177707 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1183348 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1183349 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1185329 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12247565 | 1.00[ASN][1000 genomes] |
rs1631669 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1664264 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1664266 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1664267 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1664271 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1684909 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1684910 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1684911 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1684912 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1684915 | 1.00[ASN][1000 genomes] |
rs1684923 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1684924 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2440915 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2450451 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2450452 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34568290 | 1.00[ASN][1000 genomes] |
rs3862858 | 1.00[ASN][1000 genomes] |
rs41347048 | 1.00[ASN][1000 genomes] |
rs55668813 | 1.00[ASN][1000 genomes] |
rs56783612 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61101067 | 1.00[ASN][1000 genomes] |
rs61154079 | 1.00[ASN][1000 genomes] |
rs7068392 | 1.00[ASN][1000 genomes] |
rs7077069 | 1.00[ASN][1000 genomes] |
rs7078037 | 1.00[ASN][1000 genomes] |
rs7090532 | 1.00[ASN][1000 genomes] |
rs7095688 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7097761 | 1.00[ASN][1000 genomes] |
rs7098890 | 1.00[ASN][1000 genomes] |
rs72816442 | 1.00[ASN][1000 genomes] |
rs72816445 | 1.00[ASN][1000 genomes] |
rs72816451 | 1.00[ASN][1000 genomes] |
rs72816455 | 1.00[ASN][1000 genomes] |
rs72816463 | 1.00[ASN][1000 genomes] |
rs72816467 | 1.00[ASN][1000 genomes] |
rs72816468 | 1.00[ASN][1000 genomes] |
rs72816473 | 1.00[ASN][1000 genomes] |
rs72816475 | 1.00[ASN][1000 genomes] |
rs72816476 | 1.00[ASN][1000 genomes] |
rs72816478 | 1.00[ASN][1000 genomes] |
rs72816480 | 1.00[ASN][1000 genomes] |
rs72816484 | 1.00[ASN][1000 genomes] |
rs72818468 | 1.00[ASN][1000 genomes] |
rs73267493 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73269307 | 1.00[ASN][1000 genomes] |
rs73269313 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73269315 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs74155206 | 1.00[ASN][1000 genomes] |
rs74155209 | 1.00[ASN][1000 genomes] |
rs74155210 | 1.00[ASN][1000 genomes] |
rs7894317 | 1.00[ASN][1000 genomes] |
rs7894427 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7917800 | 1.00[ASN][1000 genomes] |
rs8677 | 1.00[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1800316 | chr10:61639599-61700473 | Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:61699400-61699800 | Enhancers | Fetal Intestine Small | intestine |
2 | chr10:61699600-61700000 | Flanking Active TSS | HepG2 | liver |