Variant report
Variant | rs17385037 |
---|---|
Chromosome Location | chr1:98585180-98585181 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10158436 | 1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1198585 | 1.00[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs1198591 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs1198592 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs1198593 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs1198594 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs12067700 | 0.82[JPT][hapmap] |
rs12567432 | 0.82[ASN][1000 genomes] |
rs17372140 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs17381509 | 1.00[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs17381657 | 1.00[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs17385603 | 1.00[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs2391907 | 1.00[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs2660303 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs2660304 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs4133804 | 0.86[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs4423049 | 0.82[JPT][hapmap] |
rs4456128 | 0.82[JPT][hapmap] |
rs4506495 | 1.00[CHB][hapmap];0.82[JPT][hapmap] |
rs4598523 | 0.82[JPT][hapmap] |
rs61787263 | 0.86[ASN][1000 genomes] |
rs61787319 | 1.00[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs61787320 | 1.00[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs61787321 | 1.00[AFR][1000 genomes];0.81[ASN][1000 genomes] |
rs61787322 | 0.88[ASN][1000 genomes] |
rs61787323 | 1.00[AFR][1000 genomes];0.88[ASN][1000 genomes] |
rs6703588 | 0.82[JPT][hapmap] |
rs963852 | 1.00[AFR][1000 genomes];0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1012958 | chr1:98081528-98864746 | Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
2 | nsv1009621 | chr1:98435638-98599284 | Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 20 gene(s) | inside rSNPs | diseases |
3 | nsv830736 | chr1:98488491-98663726 | Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
4 | nsv432531 | chr1:98524979-98604179 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv823631 | chr1:98554257-98687985 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv462583 | chr1:98554409-98645213 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv546875 | chr1:98554409-98645213 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:98583800-98585200 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
2 | chr1:98585000-98585200 | Enhancers | Fetal Brain Male | brain |
3 | chr1:98585000-98585600 | Enhancers | Adipose Nuclei | Adipose |