Variant report
Variant | rs13413216 |
---|---|
Chromosome Location | chr2:127261072-127261073 |
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] |
---|---|
rs10194561 | 0.88[ASN][1000 genomes] |
rs10203788 | 0.88[ASN][1000 genomes] |
rs13382980 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs13386710 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs13415629 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs13419397 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs13425595 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs1440050 | 0.83[EUR][1000 genomes] |
rs56896312 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62159889 | 0.82[ASN][1000 genomes] |
rs6431080 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6431081 | 0.92[EUR][1000 genomes] |
rs6431097 | 0.87[EUR][1000 genomes] |
rs6727953 | 0.86[EUR][1000 genomes] |
rs6753696 | 1.00[ASN][1000 genomes] |
rs7590145 | 0.87[EUR][1000 genomes] |
rs7591893 | 0.88[EUR][1000 genomes] |
rs7598155 | 0.94[ASN][1000 genomes] |
rs7599320 | 0.93[EUR][1000 genomes] |
rs7599552 | 0.92[EUR][1000 genomes] |
rs7606965 | 0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001995 | chr2:126506739-127314488 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv1002265 | chr2:127029745-127733458 | Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
3 | nsv535919 | chr2:127029745-127733458 | Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv834364 | chr2:127100752-127267070 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:127255800-127264600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr2:127261000-127264200 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |