Variant report

Variant	rs7626999
Chromosome Location	chr3:102180556-102180557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10511195	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs10511196	0.88[CEU][hapmap]
rs10937019	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10937024	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap]
rs11714669	1.00[CHB][hapmap]
rs11720144	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs12054046	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12233481	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs1435204	1.00[CHB][hapmap]
rs1473269	1.00[CHD][hapmap]
rs16844993	0.82[MEX][hapmap];0.86[TSI][hapmap]
rs16845024	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16845027	1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16845049	0.88[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2013942	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2164264	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs3891857	1.00[CHD][hapmap]
rs55925410	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272479	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62272480	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272481	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272482	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272483	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272484	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272486	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62272490	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272491	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272492	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272493	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62274720	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274721	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274723	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274724	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62274726	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274728	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274729	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62274730	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274731	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62274734	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6784362	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs6784389	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap]
rs6784826	1.00[CHD][hapmap]
rs6807210	1.00[CHB][hapmap]
rs73146520	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7624802	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7646053	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap]
rs7653110	0.82[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9290704	1.00[CHD][hapmap]
rs9811444	1.00[CHD][hapmap]
rs9870734	1.00[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877227	chr3:102067254-102184308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1007340	chr3:102108954-102725099	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv536676	chr3:102108954-102725099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr3:102179800-102184600	Weak transcription	Hela-S3	cervix
2	chr3:102180400-102180800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr3:102180400-102182000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links