Variant report
Variant | rs72756164 |
---|---|
Chromosome Location | chr5:50157862-50157863 |
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] |
---|---|
rs10461602 | 0.89[EUR][1000 genomes] |
rs12654246 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12656298 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16877040 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16884855 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16884926 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs16884937 | 1.00[AFR][1000 genomes] |
rs16885251 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4590146 | 0.84[EUR][1000 genomes] |
rs58225490 | 0.93[EUR][1000 genomes] |
rs72753758 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs72753773 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs72756138 | 0.89[EUR][1000 genomes] |
rs72756139 | 1.00[AFR][1000 genomes] |
rs72756140 | 1.00[AFR][1000 genomes] |
rs72756146 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs72756180 | 1.00[AFR][1000 genomes] |
rs72756185 | 1.00[AFR][1000 genomes] |
rs7705385 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7708414 | 0.89[EUR][1000 genomes] |
rs965913 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv462159 | chr5:49960673-50229851 | Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv598108 | chr5:49960673-50229851 | Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv1034445 | chr5:49986171-50492609 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
4 | nsv598116 | chr5:50064292-50318550 | Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:50155800-50160800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |