Variant report

Variant	rs7810017
Chromosome Location	chr7:25968712-25968713
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:25966171..25969818-chr7:25984590..25987095,3	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10258485	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10951118	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10951119	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10951120	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10951121	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11760762	1.00[ASN][1000 genomes]
rs11983649	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12700679	1.00[ASN][1000 genomes]
rs12700680	1.00[ASN][1000 genomes]
rs12700681	1.00[ASN][1000 genomes]
rs12700682	1.00[ASN][1000 genomes]
rs13226851	1.00[ASN][1000 genomes]
rs13231897	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17729097	1.00[ASN][1000 genomes]
rs1966841	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2391172	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2391175	1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[ASN][1000 genomes]
rs2893222	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35336240	1.00[ASN][1000 genomes]
rs4000713	0.82[ASN][1000 genomes]
rs4236321	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.87[LWK][hapmap];0.87[MKK][hapmap];0.98[TSI][hapmap];0.83[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4412274	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4422683	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4640955	1.00[CHB][hapmap];0.85[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722543	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4722545	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722546	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722547	0.95[CEU][hapmap];0.83[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722548	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722550	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4722551	1.00[CHB][hapmap];0.83[CHD][hapmap];0.93[ASN][1000 genomes]
rs6461895	0.85[AFR][1000 genomes]
rs6461896	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6461897	0.84[AFR][1000 genomes]
rs66700050	1.00[ASN][1000 genomes]
rs67494041	1.00[ASN][1000 genomes]
rs6954557	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6963094	1.00[CHB][hapmap]
rs6977848	0.85[CEU][hapmap];1.00[CHB][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs735316	1.00[ASN][1000 genomes]
rs7803374	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7805035	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7810027	0.84[AFR][1000 genomes]
rs997988	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs998357	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
2	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25967200-25979000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:25967400-25970200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links