Variant report
Variant | rs6658410 |
---|---|
Chromosome Location | chr1:102625456-102625457 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10157095 | 0.81[EUR][1000 genomes] |
rs11164388 | 0.81[EUR][1000 genomes] |
rs11164402 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11164412 | 0.84[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs12126317 | 0.81[EUR][1000 genomes] |
rs12131226 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12131245 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12134849 | 0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12136478 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12138355 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12402540 | 0.81[EUR][1000 genomes] |
rs17437455 | 0.81[EUR][1000 genomes] |
rs17437549 | 0.81[EUR][1000 genomes] |
rs17437590 | 0.81[EUR][1000 genomes] |
rs17437604 | 0.81[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs17490524 | 0.80[EUR][1000 genomes] |
rs61807668 | 0.81[EUR][1000 genomes] |
rs61807669 | 0.81[EUR][1000 genomes] |
rs6577305 | 0.82[EUR][1000 genomes] |
rs6669038 | 0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6675461 | 0.81[EUR][1000 genomes] |
rs6688291 | 0.81[EUR][1000 genomes] |
rs6688524 | 0.80[EUR][1000 genomes] |
rs6690604 | 0.81[EUR][1000 genomes] |
rs6693645 | 0.80[EUR][1000 genomes] |
rs6699426 | 0.80[EUR][1000 genomes] |
rs7355210 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv522921 | chr1:102170295-102876392 | Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | esv2422183 | chr1:102450736-102796819 | Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv871085 | chr1:102562640-102726399 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1007511 | chr1:102563992-102768968 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv528450 | chr1:102579307-102742475 | Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv870464 | chr1:102594884-102816541 | Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv462639 | chr1:102608577-102717010 | Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv546901 | chr1:102608577-102717010 | Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | nsv527496 | chr1:102608577-102726802 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:102622200-102626600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |