Variant report
Variant | rs2503454 |
---|---|
Chromosome Location | chr13:48089968-48089969 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10219892 | 0.92[EUR][1000 genomes] |
rs10219965 | 0.97[EUR][1000 genomes] |
rs10220186 | 0.92[EUR][1000 genomes] |
rs10220209 | 0.97[EUR][1000 genomes] |
rs10220222 | 0.97[EUR][1000 genomes] |
rs11841086 | 0.97[EUR][1000 genomes] |
rs11841823 | 0.97[EUR][1000 genomes] |
rs12385894 | 0.92[EUR][1000 genomes] |
rs1326480 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13378192 | 0.92[EUR][1000 genomes] |
rs13378386 | 0.92[EUR][1000 genomes] |
rs13378925 | 0.92[EUR][1000 genomes] |
rs13379023 | 0.95[EUR][1000 genomes] |
rs1340345 | 0.92[EUR][1000 genomes] |
rs1340346 | 0.92[EUR][1000 genomes] |
rs1359664 | 0.95[ASN][1000 genomes] |
rs1359666 | 0.95[ASN][1000 genomes] |
rs1361457 | 0.97[EUR][1000 genomes] |
rs1417197 | 0.92[EUR][1000 genomes] |
rs1538798 | 0.90[EUR][1000 genomes] |
rs1538800 | 0.92[EUR][1000 genomes] |
rs1547654 | 0.95[ASN][1000 genomes] |
rs1571064 | 0.95[ASN][1000 genomes] |
rs1575895 | 0.95[ASN][1000 genomes] |
rs17070281 | 0.90[ASN][1000 genomes] |
rs1819681 | 0.97[EUR][1000 genomes] |
rs2153448 | 0.87[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes] |
rs2478310 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2478311 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2478313 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2478317 | 0.95[ASN][1000 genomes] |
rs2478334 | 0.90[ASN][1000 genomes] |
rs2478335 | 0.95[ASN][1000 genomes] |
rs2478336 | 0.95[ASN][1000 genomes] |
rs2478338 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2478339 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2478340 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2478341 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2486999 | 0.92[EUR][1000 genomes] |
rs2487000 | 0.97[EUR][1000 genomes] |
rs2487001 | 0.86[EUR][1000 genomes] |
rs2487007 | 0.97[EUR][1000 genomes] |
rs2503428 | 0.90[ASN][1000 genomes] |
rs2503443 | 0.95[ASN][1000 genomes] |
rs2503448 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2503449 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2503450 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2503451 | 0.95[ASN][1000 genomes] |
rs2503452 | 0.95[ASN][1000 genomes] |
rs2503453 | 0.95[ASN][1000 genomes] |
rs4296164 | 0.92[EUR][1000 genomes] |
rs4366617 | 0.97[EUR][1000 genomes] |
rs4411407 | 0.92[EUR][1000 genomes] |
rs4429188 | 0.97[EUR][1000 genomes] |
rs4525393 | 0.92[EUR][1000 genomes] |
rs4525394 | 0.92[EUR][1000 genomes] |
rs4570735 | 0.97[EUR][1000 genomes] |
rs4575434 | 0.92[EUR][1000 genomes] |
rs58200007 | 0.97[EUR][1000 genomes] |
rs6561381 | 0.87[EUR][1000 genomes] |
rs73180354 | 0.92[EUR][1000 genomes] |
rs73180356 | 0.92[EUR][1000 genomes] |
rs73180359 | 0.92[EUR][1000 genomes] |
rs73180360 | 0.92[EUR][1000 genomes] |
rs73180361 | 0.92[EUR][1000 genomes] |
rs73180362 | 0.92[EUR][1000 genomes] |
rs73180363 | 0.92[EUR][1000 genomes] |
rs73180365 | 0.92[EUR][1000 genomes] |
rs73180367 | 0.92[EUR][1000 genomes] |
rs73180372 | 0.92[EUR][1000 genomes] |
rs73180373 | 0.92[EUR][1000 genomes] |
rs73180374 | 0.92[EUR][1000 genomes] |
rs73180375 | 0.92[EUR][1000 genomes] |
rs73180376 | 0.92[EUR][1000 genomes] |
rs73180378 | 0.92[EUR][1000 genomes] |
rs73180379 | 0.92[EUR][1000 genomes] |
rs73180380 | 0.92[EUR][1000 genomes] |
rs73180382 | 0.92[EUR][1000 genomes] |
rs73180383 | 0.92[EUR][1000 genomes] |
rs73180384 | 0.92[EUR][1000 genomes] |
rs73180385 | 0.92[EUR][1000 genomes] |
rs73180386 | 0.92[EUR][1000 genomes] |
rs73180387 | 0.92[EUR][1000 genomes] |
rs73180388 | 0.92[EUR][1000 genomes] |
rs73180391 | 0.92[EUR][1000 genomes] |
rs73180392 | 0.92[EUR][1000 genomes] |
rs73180393 | 0.92[EUR][1000 genomes] |
rs73180394 | 0.92[EUR][1000 genomes] |
rs73180395 | 0.92[EUR][1000 genomes] |
rs73180397 | 0.92[EUR][1000 genomes] |
rs73180398 | 0.92[EUR][1000 genomes] |
rs73180399 | 0.92[EUR][1000 genomes] |
rs73180400 | 0.92[EUR][1000 genomes] |
rs73182203 | 0.92[EUR][1000 genomes] |
rs73182204 | 0.92[EUR][1000 genomes] |
rs73182205 | 0.92[EUR][1000 genomes] |
rs73182207 | 0.92[EUR][1000 genomes] |
rs73182236 | 0.92[EUR][1000 genomes] |
rs73182238 | 0.92[EUR][1000 genomes] |
rs73182239 | 0.92[EUR][1000 genomes] |
rs73182274 | 0.92[EUR][1000 genomes] |
rs73182276 | 0.92[EUR][1000 genomes] |
rs73182277 | 0.92[EUR][1000 genomes] |
rs73182278 | 0.92[EUR][1000 genomes] |
rs73183869 | 1.00[EUR][1000 genomes] |
rs7319491 | 0.92[EUR][1000 genomes] |
rs9316297 | 0.92[EUR][1000 genomes] |
rs9316300 | 0.92[EUR][1000 genomes] |
rs9316301 | 0.92[EUR][1000 genomes] |
rs9316303 | 0.87[CEU][hapmap];0.97[EUR][1000 genomes] |
rs9316304 | 0.87[CEU][hapmap];0.97[EUR][1000 genomes] |
rs9316305 | 1.00[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes] |
rs9316306 | 0.97[EUR][1000 genomes] |
rs9534646 | 0.92[EUR][1000 genomes] |
rs9534647 | 0.92[EUR][1000 genomes] |
rs9534648 | 0.92[EUR][1000 genomes] |
rs9534649 | 0.92[EUR][1000 genomes] |
rs9567866 | 0.97[EUR][1000 genomes] |
rs9591038 | 0.90[EUR][1000 genomes] |
rs9591039 | 0.90[EUR][1000 genomes] |
rs9591041 | 0.92[EUR][1000 genomes] |
rs9591050 | 0.92[EUR][1000 genomes] |
rs9591056 | 0.92[EUR][1000 genomes] |
rs9591057 | 0.97[EUR][1000 genomes] |
rs9595659 | 0.85[EUR][1000 genomes] |
rs9595662 | 0.92[EUR][1000 genomes] |
rs9595666 | 0.92[EUR][1000 genomes] |
rs9595667 | 0.92[EUR][1000 genomes] |
rs9595668 | 0.92[EUR][1000 genomes] |
rs9595671 | 0.92[EUR][1000 genomes] |
rs9595672 | 0.92[EUR][1000 genomes] |
rs9595673 | 0.92[EUR][1000 genomes] |
rs9595674 | 0.92[EUR][1000 genomes] |
rs9595675 | 0.92[EUR][1000 genomes] |
rs9595687 | 0.92[EUR][1000 genomes] |
rs9595688 | 0.92[EUR][1000 genomes] |
rs9595691 | 0.92[EUR][1000 genomes] |
rs9595709 | 0.92[EUR][1000 genomes] |
rs9595712 | 0.87[CEU][hapmap];0.97[EUR][1000 genomes] |
rs9595713 | 0.97[EUR][1000 genomes] |
rs9595714 | 0.97[EUR][1000 genomes] |
rs9595716 | 0.97[EUR][1000 genomes] |
rs9652163 | 0.92[EUR][1000 genomes] |
rs9943957 | 0.92[EUR][1000 genomes] |
rs997708 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2763019 | chr13:47348229-48123447 | Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
2 | esv3450125 | chr13:47919050-48236684 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv455879 | chr13:47919611-48190106 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv561588 | chr13:47943829-48190106 | Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv1043543 | chr13:48079517-48104782 | Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1041047 | chr13:48081565-48104782 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv1039986 | chr13:48081565-48119960 | Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv1043240 | chr13:48082916-48119960 | Enhancers Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv1043473 | chr13:48085526-48119960 | Enhancers Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:48089800-48097000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |