Variant report
Variant | rs5017203 |
---|---|
Chromosome Location | chr16:48239883-48239884 |
allele | A/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 | chr16:48238882..48241120-chr16:48241985..48244745,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10163354 | 0.93[ASN][1000 genomes] |
rs10163462 | 0.93[ASN][1000 genomes] |
rs10521167 | 1.00[EUR][1000 genomes] |
rs11076564 | 0.96[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs11859911 | 1.00[EUR][1000 genomes] |
rs11861031 | 0.93[ASN][1000 genomes] |
rs11861348 | 0.99[EUR][1000 genomes] |
rs11861379 | 1.00[EUR][1000 genomes] |
rs11863133 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11863233 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11863236 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11863325 | 0.93[ASN][1000 genomes] |
rs11863414 | 1.00[EUR][1000 genomes] |
rs11865596 | 1.00[EUR][1000 genomes] |
rs11866225 | 1.00[EUR][1000 genomes] |
rs11866251 | 0.93[ASN][1000 genomes] |
rs11866312 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11866529 | 1.00[ASN][1000 genomes] |
rs13331031 | 1.00[EUR][1000 genomes] |
rs13332304 | 1.00[EUR][1000 genomes] |
rs13334052 | 1.00[EUR][1000 genomes] |
rs13336264 | 0.93[ASN][1000 genomes] |
rs13336542 | 1.00[EUR][1000 genomes] |
rs13336625 | 1.00[EUR][1000 genomes] |
rs13336759 | 1.00[EUR][1000 genomes] |
rs13337955 | 1.00[EUR][1000 genomes] |
rs13338105 | 1.00[EUR][1000 genomes] |
rs16945916 | 0.93[ASN][1000 genomes] |
rs16945917 | 0.93[ASN][1000 genomes] |
rs16945919 | 0.93[ASN][1000 genomes] |
rs16945972 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs16945974 | 0.99[EUR][1000 genomes] |
rs16945988 | 1.00[EUR][1000 genomes] |
rs16945990 | 1.00[EUR][1000 genomes] |
rs16946006 | 1.00[EUR][1000 genomes] |
rs16946011 | 0.97[EUR][1000 genomes] |
rs16946014 | 0.97[EUR][1000 genomes] |
rs16946122 | 0.96[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs17743256 | 0.93[ASN][1000 genomes] |
rs2129245 | 0.93[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs28376623 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28503414 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28515165 | 0.93[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs28605399 | 1.00[EUR][1000 genomes] |
rs28626252 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28654935 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28684834 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28696036 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs28842015 | 0.97[EUR][1000 genomes] |
rs28849445 | 0.97[EUR][1000 genomes] |
rs41280939 | 0.93[ASN][1000 genomes] |
rs4325548 | 0.97[EUR][1000 genomes] |
rs4340327 | 0.97[EUR][1000 genomes] |
rs57912486 | 0.93[ASN][1000 genomes] |
rs58938063 | 0.97[EUR][1000 genomes] |
rs60431412 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs62058521 | 0.93[ASN][1000 genomes] |
rs62058522 | 0.93[ASN][1000 genomes] |
rs62058526 | 0.93[ASN][1000 genomes] |
rs62058528 | 0.93[ASN][1000 genomes] |
rs6500339 | 0.85[ASN][1000 genomes] |
rs70973926 | 0.89[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7184452 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7184831 | 0.93[ASN][1000 genomes] |
rs7186982 | 0.96[EUR][1000 genomes] |
rs7187166 | 0.97[EUR][1000 genomes] |
rs7187233 | 0.93[ASN][1000 genomes] |
rs7191181 | 0.96[EUR][1000 genomes] |
rs7191844 | 0.93[ASN][1000 genomes] |
rs7202089 | 0.97[EUR][1000 genomes] |
rs7203378 | 0.97[EUR][1000 genomes] |
rs7203432 | 0.97[EUR][1000 genomes] |
rs7203695 | 0.93[ASN][1000 genomes] |
rs7206909 | 0.93[ASN][1000 genomes] |
rs73540901 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs73542903 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs73542904 | 0.99[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs73546434 | 1.00[EUR][1000 genomes] |
rs73546437 | 1.00[EUR][1000 genomes] |
rs73546439 | 1.00[EUR][1000 genomes] |
rs73555628 | 0.97[EUR][1000 genomes] |
rs73555630 | 0.97[EUR][1000 genomes] |
rs73555643 | 0.97[EUR][1000 genomes] |
rs7359477 | 1.00[EUR][1000 genomes] |
rs74018298 | 0.85[ASN][1000 genomes] |
rs74018300 | 0.93[ASN][1000 genomes] |
rs8043685 | 0.97[EUR][1000 genomes] |
rs8043751 | 1.00[EUR][1000 genomes] |
rs8046814 | 1.00[ASN][1000 genomes] |
rs8047091 | 1.00[ASN][1000 genomes] |
rs8047397 | 1.00[EUR][1000 genomes] |
rs8049398 | 0.86[EUR][1000 genomes] |
rs8050120 | 0.93[ASN][1000 genomes] |
rs8051016 | 1.00[ASN][1000 genomes] |
rs8051205 | 1.00[ASN][1000 genomes] |
rs8051546 | 1.00[EUR][1000 genomes] |
rs8051852 | 1.00[EUR][1000 genomes] |
rs8054117 | 0.97[EUR][1000 genomes] |
rs8054444 | 0.97[EUR][1000 genomes] |
rs8055128 | 0.97[EUR][1000 genomes] |
rs8056100 | 1.00[EUR][1000 genomes] |
rs8056143 | 1.00[EUR][1000 genomes] |
rs8056692 | 0.84[EUR][1000 genomes] |
rs8057475 | 1.00[ASN][1000 genomes] |
rs8058396 | 0.97[EUR][1000 genomes] |
rs8060696 | 1.00[EUR][1000 genomes] |
rs8060722 | 0.99[EUR][1000 genomes] |
rs8062407 | 0.97[EUR][1000 genomes] |
rs957881 | 0.93[ASN][1000 genomes] |
rs9926206 | 0.87[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9932328 | 0.97[EUR][1000 genomes] |
rs9932850 | 1.00[ASN][1000 genomes] |
rs9934833 | 0.97[EUR][1000 genomes] |
rs9938414 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1059259 | chr16:48113396-48304404 | Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv542916 | chr16:48113396-48304404 | Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:48230200-48240400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr16:48237200-48240400 | Weak transcription | Adipose Nuclei | Adipose |
3 | chr16:48239400-48241200 | Enhancers | Liver | Liver |
4 | chr16:48239400-48245800 | Weak transcription | Right Atrium | heart |
5 | chr16:48239600-48240600 | Weak transcription | Stomach Mucosa | stomach |
6 | chr16:48239600-48241600 | Enhancers | HepG2 | liver |
7 | chr16:48239600-48250000 | Weak transcription | Pancreas | Pancrea |
8 | chr16:48239800-48240200 | Weak transcription | A549 | lung |
9 | chr16:48239800-48240400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |