Variant report

Variant	rs9833910
Chromosome Location	chr3:180078143-180078144
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10513775	1.00[EUR][1000 genomes]
rs13320643	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13327114	1.00[EUR][1000 genomes]
rs13327183	1.00[EUR][1000 genomes]
rs1543266	1.00[EUR][1000 genomes]
rs16831253	1.00[EUR][1000 genomes]
rs16831270	1.00[EUR][1000 genomes]
rs2090762	1.00[EUR][1000 genomes]
rs28373443	1.00[EUR][1000 genomes]
rs28545820	1.00[EUR][1000 genomes]
rs28701054	1.00[EUR][1000 genomes]
rs28726303	1.00[EUR][1000 genomes]
rs28758960	1.00[EUR][1000 genomes]
rs2879655	1.00[EUR][1000 genomes]
rs28818282	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57727445	1.00[EUR][1000 genomes]
rs60008753	1.00[EUR][1000 genomes]
rs6765080	1.00[EUR][1000 genomes]
rs6765906	1.00[EUR][1000 genomes]
rs6772673	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6776289	1.00[EUR][1000 genomes]
rs6779403	1.00[EUR][1000 genomes]
rs6784007	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6803803	1.00[EUR][1000 genomes]
rs6804532	1.00[EUR][1000 genomes]
rs6809894	1.00[EUR][1000 genomes]
rs73883804	1.00[EUR][1000 genomes]
rs73883810	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73883833	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73885453	1.00[EUR][1000 genomes]
rs73885465	1.00[EUR][1000 genomes]
rs73885473	1.00[EUR][1000 genomes]
rs73885496	1.00[EUR][1000 genomes]
rs7614651	1.00[EUR][1000 genomes]
rs7628443	1.00[EUR][1000 genomes]
rs7635460	1.00[EUR][1000 genomes]
rs7643125	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7646970	1.00[EUR][1000 genomes]
rs9290698	1.00[EUR][1000 genomes]
rs9815044	1.00[EUR][1000 genomes]
rs9819315	1.00[EUR][1000 genomes]
rs9825264	1.00[EUR][1000 genomes]
rs9825542	1.00[EUR][1000 genomes]
rs9826576	1.00[EUR][1000 genomes]
rs9827331	1.00[EUR][1000 genomes]
rs9830454	1.00[EUR][1000 genomes]
rs9832076	1.00[EUR][1000 genomes]
rs9836941	1.00[EUR][1000 genomes]
rs9841642	1.00[EUR][1000 genomes]
rs9842405	1.00[EUR][1000 genomes]
rs9844266	1.00[EUR][1000 genomes]
rs9849568	1.00[EUR][1000 genomes]
rs9861136	1.00[EUR][1000 genomes]
rs9863397	1.00[EUR][1000 genomes]
rs9866861	1.00[EUR][1000 genomes]
rs9872365	1.00[EUR][1000 genomes]
rs9873559	1.00[EUR][1000 genomes]
rs9882377	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv878040	chr3:179823887-180128288	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997388	chr3:179899279-180172349	Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv536817	chr3:179899279-180172349	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv878041	chr3:179983857-180097855	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:180075600-180078200	Enhancers	Fetal Brain Male	brain
2	chr3:180076800-180083800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:180077600-180078400	Enhancers	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links