Variant report
Variant | rs73878303 |
---|---|
Chromosome Location | chr3:161057686-161057687 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:24)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:24 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:160990169..160990978-chr3:161057288..161058124,6 | MCF-7 | breast: | |
2 | chr3:161008738..161009836-chr3:161057294..161058188,4 | MCF-7 | breast: | |
3 | chr3:161001819..161012846-chr3:161052557..161065154,32 | MCF-7 | breast: | |
4 | chr3:150454794..150455301-chr3:161057325..161057943,2 | MCF-7 | breast: | |
5 | chr3:161031627..161035949-chr3:161055362..161059558,6 | MCF-7 | breast: | |
6 | chr22:39639549..39641167-chr3:161057655..161060479,2 | MCF-7 | breast: | |
7 | chr3:160783790..160785578-chr3:161057040..161058658,2 | MCF-7 | breast: | |
8 | chr3:160939799..160942202-chr3:161055677..161057853,2 | MCF-7 | breast: | |
9 | chr3:161022226..161023030-chr3:161057225..161057825,2 | MCF-7 | breast: | |
10 | chr3:160990337..160994329-chr3:161056046..161062548,7 | MCF-7 | breast: | |
11 | chr3:160938417..160941849-chr3:161057237..161059052,3 | MCF-7 | breast: | |
12 | chr3:160748629..160749475-chr3:161057341..161057842,2 | MCF-7 | breast: | |
13 | chr3:161057161..161057765-chr3:161129649..161130192,3 | MCF-7 | breast: | |
14 | chr3:160990342..160991092-chr3:161057089..161058207,13 | MCF-7 | breast: | |
15 | chr3:161056968..161057820-chr3:161138358..161138956,2 | MCF-7 | breast: | |
16 | chr3:161057222..161057922-chr3:161123207..161123785,2 | MCF-7 | breast: | |
17 | chr3:161057284..161057901-chr3:161140131..161140710,2 | MCF-7 | breast: | |
18 | chr3:161008888..161009457-chr3:161057192..161058188,2 | MCF-7 | breast: | |
19 | chr3:160818340..160819319-chr3:161057179..161057934,3 | MCF-7 | breast: | |
20 | chr3:161057160..161058115-chr3:161139794..161140383,2 | MCF-7 | breast: | |
21 | chr3:161057269..161057791-chr3:161129680..161130247,2 | MCF-7 | breast: | |
22 | chr3:161057209..161058115-chr3:161139794..161140683,3 | MCF-7 | breast: | |
23 | chr3:150454737..150455301-chr3:161057286..161057825,2 | MCF-7 | breast: | |
24 | chr3:160990342..160991092-chr3:161057089..161058101,14 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000100311 | Chromatin interaction |
ENSG00000271052 | Chromatin interaction |
ENSG00000169251 | Chromatin interaction |
ENSG00000169255 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11539155 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12108169 | 0.84[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs12374001 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12629152 | 0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs12629929 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12630038 | 0.84[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs12631467 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12632346 | 0.84[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs12633103 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12636434 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs12636573 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12636590 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1450530 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs16832237 | 0.85[EUR][1000 genomes] |
rs16834031 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1904204 | 0.84[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs28384383 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs28853731 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4132373 | 0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs55949838 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs56174161 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56741879 | 0.84[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs56890199 | 0.83[ASN][1000 genomes] |
rs57441646 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs59827519 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs60228180 | 0.84[AMR][1000 genomes] |
rs60277631 | 0.83[AMR][1000 genomes] |
rs60801542 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs61193379 | 0.84[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs61388164 | 0.94[AMR][1000 genomes] |
rs61578814 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs61596736 | 0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6800515 | 0.95[EUR][1000 genomes] |
rs73162584 | 0.85[EUR][1000 genomes] |
rs73162595 | 0.85[EUR][1000 genomes] |
rs73162599 | 0.85[EUR][1000 genomes] |
rs73875453 | 0.94[AMR][1000 genomes] |
rs73875455 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs73875456 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs73875458 | 0.84[AMR][1000 genomes] |
rs73875460 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs73875464 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs73875472 | 0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs73875473 | 0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs73875482 | 0.84[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs73875492 | 0.84[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs73875500 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73875502 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73878304 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs73878305 | 1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7652447 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv931072 | chr3:160669567-161159779 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 98 gene(s) | inside rSNPs | diseases |
2 | nsv829770 | chr3:160989573-161069223 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv4091 | chr3:161018540-161063875 | Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
4 | nsv533237 | chr3:161019834-161804660 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 91 gene(s) | inside rSNPs | diseases |
5 | nsv829772 | chr3:161047817-161202554 | Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 88 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:161051800-161061800 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
2 | chr3:161054000-161062600 | Enhancers | HepG2 | liver |
3 | chr3:161056800-161058200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
4 | chr3:161057200-161058400 | Enhancers | NHDF-Ad | bronchial |
5 | chr3:161057200-161059200 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
6 | chr3:161057600-161058400 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |