Variant report
Variant | rs73772970 |
---|---|
Chromosome Location | chr5:97871103-97871104 |
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] |
---|---|
rs10043870 | 1.00[EUR][1000 genomes] |
rs1421635 | 1.00[EUR][1000 genomes] |
rs17166187 | 1.00[EUR][1000 genomes] |
rs17166195 | 1.00[EUR][1000 genomes] |
rs17166198 | 1.00[EUR][1000 genomes] |
rs17166210 | 1.00[EUR][1000 genomes] |
rs17166218 | 1.00[EUR][1000 genomes] |
rs17166224 | 1.00[EUR][1000 genomes] |
rs60190260 | 1.00[EUR][1000 genomes] |
rs60740011 | 1.00[EUR][1000 genomes] |
rs60839554 | 1.00[EUR][1000 genomes] |
rs6859395 | 1.00[EUR][1000 genomes] |
rs6870416 | 1.00[EUR][1000 genomes] |
rs6871563 | 1.00[EUR][1000 genomes] |
rs6875233 | 1.00[EUR][1000 genomes] |
rs6891520 | 1.00[EUR][1000 genomes] |
rs73159254 | 1.00[EUR][1000 genomes] |
rs73772968 | 0.93[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73773002 | 1.00[EUR][1000 genomes] |
rs73777006 | 1.00[EUR][1000 genomes] |
rs73777023 | 1.00[EUR][1000 genomes] |
rs9764305 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1018555 | chr5:97719032-97873906 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
2 | nsv882412 | chr5:97796120-97953719 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:97870800-97871600 | Strong transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |