Variant report
Variant | rs4387548 |
---|---|
Chromosome Location | chr15:53672556-53672557 |
allele | A/G |
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] |
---|---|
rs10083669 | 0.84[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs1021746 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1021747 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs10851539 | 0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11630701 | 0.87[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs11635444 | 0.87[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs11635520 | 0.87[AFR][1000 genomes] |
rs11635540 | 0.87[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs11636382 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1356242 | 0.80[ASN][1000 genomes] |
rs1356243 | 0.80[ASN][1000 genomes] |
rs1400217 | 0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1473565 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1473566 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1516406 | 0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1516408 | 0.88[AFR][1000 genomes];0.98[ASN][1000 genomes] |
rs1516409 | 0.85[AFR][1000 genomes];0.98[ASN][1000 genomes] |
rs2055404 | 0.87[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs2055405 | 0.87[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs4776139 | 0.80[ASN][1000 genomes] |
rs4776141 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4776144 | 0.91[EUR][1000 genomes] |
rs7167273 | 0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7167279 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7167286 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7167448 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7169159 | 0.98[ASN][1000 genomes] |
rs905034 | 0.91[EUR][1000 genomes] |
rs972893 | 0.87[AFR][1000 genomes];0.82[ASN][1000 genomes] |
rs974730 | 0.91[AFR][1000 genomes];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1037630 | chr15:53324645-53708925 | Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv833008 | chr15:53630471-53780618 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv904223 | chr15:53665247-54340070 | Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv904224 | chr15:53668018-54210677 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | esv1826996 | chr15:53671945-53679305 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
6 | nsv1049319 | chr15:53671945-53785267 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:53669200-53672600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |