Variant report
Variant | rs7738592 |
---|---|
Chromosome Location | chr6:133413940-133413941 |
allele | A/G |
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] |
---|---|
rs10457002 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10457600 | 0.86[EUR][1000 genomes] |
rs10457602 | 1.00[CEU][hapmap] |
rs10457603 | 1.00[CEU][hapmap] |
rs11154715 | 0.84[EUR][1000 genomes] |
rs12154207 | 0.84[EUR][1000 genomes] |
rs12190728 | 0.83[EUR][1000 genomes] |
rs12191026 | 0.84[EUR][1000 genomes] |
rs12192002 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12192605 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12193118 | 0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12196069 | 0.83[EUR][1000 genomes] |
rs12196492 | 0.84[EUR][1000 genomes] |
rs12198619 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12199138 | 0.86[EUR][1000 genomes] |
rs12199555 | 0.84[EUR][1000 genomes] |
rs12199958 | 0.84[EUR][1000 genomes] |
rs12199972 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12200393 | 0.84[EUR][1000 genomes] |
rs12201315 | 1.00[CEU][hapmap] |
rs12205139 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12206291 | 0.81[EUR][1000 genomes] |
rs12206438 | 0.81[CEU][hapmap] |
rs12210093 | 0.81[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs12210216 | 0.84[EUR][1000 genomes] |
rs12211999 | 0.84[EUR][1000 genomes] |
rs12212715 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12213350 | 0.86[EUR][1000 genomes] |
rs12213452 | 0.86[EUR][1000 genomes] |
rs12213690 | 0.84[EUR][1000 genomes] |
rs12215217 | 0.86[EUR][1000 genomes] |
rs17062051 | 0.82[CHB][hapmap];0.82[YRI][hapmap] |
rs28538690 | 0.93[EUR][1000 genomes] |
rs4077767 | 0.90[EUR][1000 genomes] |
rs4077768 | 0.86[EUR][1000 genomes] |
rs4257872 | 0.83[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4273707 | 0.95[EUR][1000 genomes] |
rs4273708 | 0.95[EUR][1000 genomes] |
rs4895952 | 0.81[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs57161827 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58835706 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs59793266 | 0.84[EUR][1000 genomes] |
rs62428563 | 0.85[EUR][1000 genomes] |
rs62428596 | 0.84[EUR][1000 genomes] |
rs62428597 | 0.82[EUR][1000 genomes] |
rs62430562 | 0.90[EUR][1000 genomes] |
rs62430580 | 0.88[EUR][1000 genomes] |
rs62430581 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62430582 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs62430588 | 0.95[EUR][1000 genomes] |
rs62430590 | 0.95[EUR][1000 genomes] |
rs6569863 | 0.81[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap] |
rs6902225 | 0.86[EUR][1000 genomes] |
rs6902347 | 0.81[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6911954 | 0.94[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6913444 | 0.82[EUR][1000 genomes] |
rs6927627 | 0.95[EUR][1000 genomes] |
rs6933214 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6935070 | 0.95[EUR][1000 genomes] |
rs6935480 | 0.95[EUR][1000 genomes] |
rs6936410 | 0.95[EUR][1000 genomes] |
rs6937029 | 0.94[EUR][1000 genomes] |
rs6939899 | 0.90[EUR][1000 genomes] |
rs6940959 | 0.95[EUR][1000 genomes] |
rs72557636 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7738156 | 0.95[EUR][1000 genomes] |
rs7746390 | 0.84[EUR][1000 genomes] |
rs7748926 | 0.82[EUR][1000 genomes] |
rs7750218 | 0.84[EUR][1000 genomes] |
rs7750279 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs7750376 | 1.00[CEU][hapmap];0.84[EUR][1000 genomes] |
rs7754486 | 1.00[CEU][hapmap];0.82[EUR][1000 genomes] |
rs7756171 | 0.95[CEU][hapmap];0.92[CHB][hapmap];0.91[EUR][1000 genomes] |
rs7756963 | 0.83[EUR][1000 genomes] |
rs7761372 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7767651 | 0.84[EUR][1000 genomes] |
rs7770031 | 0.84[EUR][1000 genomes] |
rs9321388 | 0.90[EUR][1000 genomes] |
rs9321389 | 0.90[EUR][1000 genomes] |
rs9483529 | 0.95[EUR][1000 genomes] |
rs9483530 | 0.95[EUR][1000 genomes] |
rs9483535 | 0.91[EUR][1000 genomes] |
rs9483554 | 0.81[EUR][1000 genomes] |
rs9493513 | 0.92[EUR][1000 genomes] |
rs9493514 | 0.86[EUR][1000 genomes] |
rs9493515 | 0.95[EUR][1000 genomes] |
rs9493517 | 0.95[EUR][1000 genomes] |
rs9493518 | 0.95[EUR][1000 genomes] |
rs957183 | 0.84[EUR][1000 genomes] |
rs975225 | 0.80[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532069 | chr6:132776411-133462292 | Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 90 gene(s) | inside rSNPs | diseases |
2 | nsv428154 | chr6:133271975-133522803 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
3 | esv3445931 | chr6:133347824-133434532 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv519475 | chr6:133350936-133474673 | Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:133410800-133420200 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
2 | chr6:133413200-133414200 | Enhancers | Dnd41 | blood |
3 | chr6:133413600-133414400 | Enhancers | Fetal Thymus | thymus |
4 | chr6:133413600-133417200 | Enhancers | Brain Substantia Nigra | brain |
5 | chr6:133413800-133416200 | Enhancers | Brain Anterior Caudate | brain |