Variant report
Variant | rs61852497 |
---|---|
Chromosome Location | chr10:90320588-90320589 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:89620441..89622522-chr10:90319312..90321016,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10509549 | 1.00[ASN][1000 genomes] |
rs10509550 | 1.00[ASN][1000 genomes] |
rs10509554 | 1.00[ASN][1000 genomes] |
rs1169042 | 1.00[ASN][1000 genomes] |
rs11816967 | 1.00[ASN][1000 genomes] |
rs1237989 | 1.00[ASN][1000 genomes] |
rs1325901 | 1.00[ASN][1000 genomes] |
rs1573074 | 1.00[ASN][1000 genomes] |
rs1653842 | 1.00[ASN][1000 genomes] |
rs1653843 | 1.00[ASN][1000 genomes] |
rs167333 | 1.00[ASN][1000 genomes] |
rs170004 | 1.00[ASN][1000 genomes] |
rs17334741 | 1.00[ASN][1000 genomes] |
rs17336288 | 1.00[ASN][1000 genomes] |
rs17426488 | 1.00[ASN][1000 genomes] |
rs1769690 | 1.00[ASN][1000 genomes] |
rs1769691 | 1.00[ASN][1000 genomes] |
rs1769692 | 1.00[ASN][1000 genomes] |
rs1769697 | 1.00[ASN][1000 genomes] |
rs1769700 | 1.00[ASN][1000 genomes] |
rs1774977 | 1.00[ASN][1000 genomes] |
rs182493 | 1.00[ASN][1000 genomes] |
rs186226 | 1.00[ASN][1000 genomes] |
rs2765451 | 1.00[ASN][1000 genomes] |
rs303453 | 1.00[ASN][1000 genomes] |
rs303454 | 1.00[ASN][1000 genomes] |
rs303456 | 1.00[ASN][1000 genomes] |
rs303457 | 1.00[ASN][1000 genomes] |
rs303464 | 1.00[ASN][1000 genomes] |
rs303467 | 1.00[ASN][1000 genomes] |
rs303468 | 1.00[ASN][1000 genomes] |
rs303474 | 1.00[ASN][1000 genomes] |
rs303478 | 1.00[ASN][1000 genomes] |
rs303479 | 1.00[ASN][1000 genomes] |
rs303482 | 1.00[ASN][1000 genomes] |
rs303483 | 1.00[ASN][1000 genomes] |
rs303488 | 1.00[ASN][1000 genomes] |
rs303489 | 1.00[ASN][1000 genomes] |
rs303505 | 1.00[ASN][1000 genomes] |
rs303506 | 1.00[ASN][1000 genomes] |
rs303507 | 1.00[ASN][1000 genomes] |
rs303508 | 1.00[ASN][1000 genomes] |
rs303510 | 1.00[ASN][1000 genomes] |
rs303516 | 1.00[ASN][1000 genomes] |
rs303517 | 1.00[ASN][1000 genomes] |
rs365847 | 1.00[ASN][1000 genomes] |
rs367605 | 1.00[ASN][1000 genomes] |
rs372589 | 1.00[ASN][1000 genomes] |
rs376045 | 1.00[ASN][1000 genomes] |
rs377257 | 1.00[ASN][1000 genomes] |
rs378308 | 1.00[ASN][1000 genomes] |
rs378425 | 1.00[ASN][1000 genomes] |
rs385397 | 1.00[ASN][1000 genomes] |
rs387970 | 1.00[ASN][1000 genomes] |
rs388265 | 1.00[ASN][1000 genomes] |
rs390414 | 1.00[ASN][1000 genomes] |
rs391683 | 1.00[ASN][1000 genomes] |
rs399496 | 1.00[ASN][1000 genomes] |
rs406102 | 1.00[ASN][1000 genomes] |
rs407433 | 1.00[ASN][1000 genomes] |
rs407922 | 1.00[ASN][1000 genomes] |
rs408387 | 1.00[ASN][1000 genomes] |
rs410033 | 1.00[ASN][1000 genomes] |
rs41284088 | 1.00[ASN][1000 genomes] |
rs412927 | 1.00[ASN][1000 genomes] |
rs415996 | 1.00[ASN][1000 genomes] |
rs416957 | 1.00[ASN][1000 genomes] |
rs424371 | 1.00[ASN][1000 genomes] |
rs426118 | 1.00[ASN][1000 genomes] |
rs427687 | 1.00[ASN][1000 genomes] |
rs432950 | 1.00[ASN][1000 genomes] |
rs434401 | 1.00[ASN][1000 genomes] |
rs435742 | 1.00[ASN][1000 genomes] |
rs437261 | 1.00[ASN][1000 genomes] |
rs441719 | 1.00[ASN][1000 genomes] |
rs442607 | 1.00[ASN][1000 genomes] |
rs450130 | 1.00[ASN][1000 genomes] |
rs454439 | 1.00[ASN][1000 genomes] |
rs516083 | 1.00[ASN][1000 genomes] |
rs55713122 | 1.00[ASN][1000 genomes] |
rs56390975 | 1.00[ASN][1000 genomes] |
rs57260181 | 1.00[ASN][1000 genomes] |
rs61852496 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61852500 | 1.00[AFR][1000 genomes] |
rs792201 | 1.00[ASN][1000 genomes] |
rs792202 | 1.00[ASN][1000 genomes] |
rs792231 | 1.00[ASN][1000 genomes] |
rs814617 | 1.00[ASN][1000 genomes] |
rs814619 | 1.00[ASN][1000 genomes] |
rs814630 | 1.00[ASN][1000 genomes] |
rs814642 | 1.00[ASN][1000 genomes] |
rs866514 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948664 | chr10:90076715-90517150 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv529324 | chr10:90198865-90738588 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
3 | nsv533167 | chr10:90236197-90341481 | Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv430254 | chr10:90265420-90500520 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv1044680 | chr10:90316066-90466092 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
6 | nsv540740 | chr10:90316066-90466092 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:90312200-90342400 | Weak transcription | Ovary | ovary |
2 | chr10:90315400-90322200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
3 | chr10:90315400-90342400 | Weak transcription | Aorta | Aorta |
4 | chr10:90317800-90341800 | Weak transcription | Adipose Nuclei | Adipose |
5 | chr10:90319000-90321200 | Enhancers | Hela-S3 | cervix |
6 | chr10:90319200-90342000 | Weak transcription | Pancreas | Pancrea |
7 | chr10:90319400-90320600 | Enhancers | Primary T helper 17 cells PMA-I stimulated | -- |
8 | chr10:90320000-90321000 | Enhancers | Primary T helper memory cells from peripheral blood 1 | blood |
9 | chr10:90320000-90321200 | Enhancers | NHLF | lung |
10 | chr10:90320200-90320600 | Enhancers | Primary T cells fromperipheralblood | blood |
11 | chr10:90320200-90320600 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |
12 | chr10:90320200-90320600 | Enhancers | Osteobl | bone |