Variant report
Variant | rs36400 |
---|---|
Chromosome Location | chr14:72359993-72359994 |
allele | A/C |
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] |
---|---|
rs1009018 | 1.00[ASN][1000 genomes] |
rs17768054 | 1.00[ASN][1000 genomes] |
rs2190874 | 1.00[ASN][1000 genomes] |
rs2215133 | 1.00[ASN][1000 genomes] |
rs2877773 | 1.00[ASN][1000 genomes] |
rs36319 | 1.00[ASN][1000 genomes] |
rs36320 | 1.00[ASN][1000 genomes] |
rs36322 | 1.00[ASN][1000 genomes] |
rs36323 | 1.00[ASN][1000 genomes] |
rs36324 | 1.00[ASN][1000 genomes] |
rs36325 | 1.00[ASN][1000 genomes] |
rs36328 | 1.00[ASN][1000 genomes] |
rs36329 | 1.00[ASN][1000 genomes] |
rs36330 | 1.00[ASN][1000 genomes] |
rs36331 | 1.00[ASN][1000 genomes] |
rs36333 | 1.00[ASN][1000 genomes] |
rs36334 | 1.00[ASN][1000 genomes] |
rs36337 | 1.00[ASN][1000 genomes] |
rs36338 | 1.00[ASN][1000 genomes] |
rs36339 | 1.00[ASN][1000 genomes] |
rs36342 | 1.00[ASN][1000 genomes] |
rs36346 | 1.00[ASN][1000 genomes] |
rs36347 | 1.00[ASN][1000 genomes] |
rs36348 | 1.00[ASN][1000 genomes] |
rs36349 | 1.00[ASN][1000 genomes] |
rs36352 | 1.00[ASN][1000 genomes] |
rs36353 | 1.00[ASN][1000 genomes] |
rs36354 | 1.00[ASN][1000 genomes] |
rs36355 | 1.00[ASN][1000 genomes] |
rs36359 | 1.00[ASN][1000 genomes] |
rs36362 | 1.00[ASN][1000 genomes] |
rs36364 | 1.00[ASN][1000 genomes] |
rs36365 | 1.00[ASN][1000 genomes] |
rs36367 | 1.00[ASN][1000 genomes] |
rs36371 | 1.00[ASN][1000 genomes] |
rs36374 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36379 | 1.00[AFR][1000 genomes] |
rs36402 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36407 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36413 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36414 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36417 | 1.00[AFR][1000 genomes] |
rs36419 | 1.00[AFR][1000 genomes] |
rs36421 | 1.00[AFR][1000 genomes] |
rs4243639 | 1.00[ASN][1000 genomes] |
rs4598834 | 1.00[ASN][1000 genomes] |
rs4899406 | 1.00[ASN][1000 genomes] |
rs4899408 | 1.00[ASN][1000 genomes] |
rs4902959 | 1.00[ASN][1000 genomes] |
rs4902962 | 1.00[ASN][1000 genomes] |
rs61996396 | 1.00[ASN][1000 genomes] |
rs6574036 | 1.00[ASN][1000 genomes] |
rs722975 | 1.00[ASN][1000 genomes] |
rs728494 | 1.00[ASN][1000 genomes] |
rs728495 | 1.00[ASN][1000 genomes] |
rs728498 | 1.00[ASN][1000 genomes] |
rs758236 | 1.00[ASN][1000 genomes] |
rs8011972 | 1.00[ASN][1000 genomes] |
rs8014500 | 1.00[ASN][1000 genomes] |
rs917392 | 1.00[ASN][1000 genomes] |
rs991890 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3398985 | chr14:71927884-72404676 | Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv530794 | chr14:72113818-73034008 | Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv1035695 | chr14:72323819-72383610 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1345 | chr14:72349589-72395819 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:72357800-72360600 | Enhancers | H9 Cell Line | embryonic stem cell |
2 | chr14:72358000-72360200 | Enhancers | H1 Cell Line | embryonic stem cell |
3 | chr14:72358000-72360200 | Enhancers | HUES64 Cell Line | embryonic stem cell |
4 | chr14:72358000-72360200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
5 | chr14:72359200-72360400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
6 | chr14:72359400-72360400 | Enhancers | HUES48 Cell Line | embryonic stem cell |
7 | chr14:72359400-72360600 | Enhancers | ES-I3 Cell Line | embryonic stem cell |