Variant report
Variant | rs72854129 |
---|---|
Chromosome Location | chr2:144822018-144822019 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs12613814 | 1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12614766 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1427310 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs16823481 | 1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs16823487 | 1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1861878 | 0.83[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs28544584 | 0.83[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs55716423 | 0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs55883773 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs56395361 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs58738282 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs59687135 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72852992 | 0.86[ASN][1000 genomes] |
rs72852993 | 1.00[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs72852998 | 0.83[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs72852999 | 0.83[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs72853001 | 0.83[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs72854106 | 0.83[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs72854165 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72854176 | 1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs72854193 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72854200 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72855507 | 0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72855511 | 1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7608953 | 0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532755 | chr2:144631279-145270874 | Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | nsv1006344 | chr2:144657716-145334899 | Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
3 | nsv535951 | chr2:144657716-145334899 | Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
4 | nsv1067624 | chr2:144657717-145425705 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
5 | nsv531413 | chr2:144657717-145425705 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 18 gene(s) | inside rSNPs | diseases |
6 | nsv532756 | chr2:144746353-145315596 | Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
7 | nsv1005376 | chr2:144803630-144968946 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv1013338 | chr2:144806920-144969818 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:144821800-144822200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |