Variant report
Variant | rs72952324 |
---|---|
Chromosome Location | chr4:106212230-106212231 |
allele | A/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] |
---|---|
rs57520418 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57729291 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58428131 | 0.95[AFR][1000 genomes] |
rs59479204 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60382101 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60786079 | 0.85[AFR][1000 genomes] |
rs60834172 | 1.00[EUR][1000 genomes] |
rs6811468 | 1.00[EUR][1000 genomes] |
rs72950501 | 0.85[AFR][1000 genomes] |
rs72952305 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72952317 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72952331 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72952343 | 1.00[EUR][1000 genomes] |
rs72955116 | 1.00[EUR][1000 genomes] |
rs72955127 | 1.00[EUR][1000 genomes] |
rs72955137 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72955180 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72955193 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72961197 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72961199 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963007 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963014 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963031 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963032 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963036 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963038 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72963046 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv461609 | chr4:105869548-106366209 | Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
2 | nsv470063 | chr4:105869548-106366209 | Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
3 | nsv595007 | chr4:105869548-106366209 | Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
4 | nsv879698 | chr4:106155751-106309224 | Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:106211200-106213000 | Weak transcription | Fetal Intestine Small | intestine |
2 | chr4:106211200-106214800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr4:106211200-106215600 | Weak transcription | Aorta | Aorta |