Variant report
Variant | rs7811687 |
---|---|
Chromosome Location | chr7:118073863-118073864 |
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] |
---|---|
rs1548812 | 0.83[EUR][1000 genomes] |
rs1859132 | 0.80[EUR][1000 genomes] |
rs1859133 | 0.80[EUR][1000 genomes] |
rs2192234 | 0.84[EUR][1000 genomes] |
rs2402357 | 0.85[EUR][1000 genomes] |
rs41912 | 0.82[EUR][1000 genomes] |
rs41921 | 0.83[EUR][1000 genomes] |
rs41923 | 0.84[EUR][1000 genomes] |
rs41924 | 0.84[EUR][1000 genomes] |
rs41930 | 0.85[EUR][1000 genomes] |
rs41931 | 0.87[EUR][1000 genomes] |
rs41936 | 0.86[EUR][1000 genomes] |
rs41962 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs41989 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4260839 | 0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4730862 | 0.83[EUR][1000 genomes] |
rs4730866 | 0.85[EUR][1000 genomes] |
rs4730868 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6466657 | 0.84[EUR][1000 genomes] |
rs6651117 | 0.84[EUR][1000 genomes] |
rs6964858 | 0.85[EUR][1000 genomes] |
rs71314617 | 0.84[EUR][1000 genomes] |
rs7801976 | 0.84[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869971 | chr7:117420583-118274149 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
2 | esv1804964 | chr7:117960973-118188573 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv889093 | chr7:117977091-118709754 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv889094 | chr7:117981820-118186543 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | esv2829882 | chr7:118009306-118222312 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv889095 | chr7:118016847-118097679 | ZNF genes & repeats Weak transcription Enhancers | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:118073400-118077800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |