Variant report
Variant | rs57429463 |
---|---|
Chromosome Location | chr1:98424571-98424572 |
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] |
---|---|
rs10735795 | 1.00[EUR][1000 genomes] |
rs10747494 | 1.00[EUR][1000 genomes] |
rs10875119 | 1.00[EUR][1000 genomes] |
rs11165926 | 1.00[EUR][1000 genomes] |
rs1333722 | 1.00[EUR][1000 genomes] |
rs17117417 | 1.00[AMR][1000 genomes] |
rs17117438 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17117480 | 1.00[EUR][1000 genomes] |
rs17117486 | 1.00[EUR][1000 genomes] |
rs17117488 | 1.00[EUR][1000 genomes] |
rs17117490 | 1.00[EUR][1000 genomes] |
rs17117528 | 1.00[EUR][1000 genomes] |
rs4269803 | 1.00[EUR][1000 genomes] |
rs4304628 | 1.00[EUR][1000 genomes] |
rs4351683 | 1.00[EUR][1000 genomes] |
rs4592283 | 1.00[EUR][1000 genomes] |
rs55989986 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57957567 | 1.00[EUR][1000 genomes] |
rs58211735 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58260707 | 1.00[EUR][1000 genomes] |
rs58615096 | 1.00[EUR][1000 genomes] |
rs59429666 | 1.00[EUR][1000 genomes] |
rs60366086 | 1.00[EUR][1000 genomes] |
rs60945684 | 1.00[EUR][1000 genomes] |
rs6604092 | 1.00[EUR][1000 genomes] |
rs6604119 | 1.00[EUR][1000 genomes] |
rs74105297 | 1.00[EUR][1000 genomes] |
rs74105460 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74106015 | 1.00[EUR][1000 genomes] |
rs74106050 | 1.00[EUR][1000 genomes] |
rs74106053 | 1.00[EUR][1000 genomes] |
rs74106056 | 1.00[EUR][1000 genomes] |
rs74106140 | 1.00[EUR][1000 genomes] |
rs74107135 | 1.00[EUR][1000 genomes] |
rs74107712 | 1.00[EUR][1000 genomes] |
rs74108221 | 1.00[EUR][1000 genomes] |
rs74108309 | 1.00[AMR][1000 genomes] |
rs74108405 | 1.00[EUR][1000 genomes] |
rs74108407 | 1.00[EUR][1000 genomes] |
rs7511709 | 1.00[EUR][1000 genomes] |
rs7511752 | 1.00[EUR][1000 genomes] |
rs7520550 | 1.00[EUR][1000 genomes] |
rs7546038 | 1.00[EUR][1000 genomes] |
rs7553943 | 1.00[EUR][1000 genomes] |
rs9324376 | 1.00[EUR][1000 genomes] |
rs9324377 | 1.00[EUR][1000 genomes] |
rs9661407 | 1.00[EUR][1000 genomes] |
rs9727974 | 1.00[EUR][1000 genomes] |
rs9729900 | 1.00[EUR][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 | nsv871625 | chr1:98165091-98564736 | Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 30 gene(s) | inside rSNPs | diseases |
3 | nsv830725 | chr1:98257894-98443497 | Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv871077 | chr1:98274132-98541677 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 27 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:98409400-98437800 | Weak transcription | HSMM | muscle |
2 | chr1:98409600-98455000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr1:98413600-98431800 | Weak transcription | NHDF-Ad | bronchial |