Variant report

Variant	rs7776566
Chromosome Location	chr7:80808045-80808046
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1024548	0.90[EUR][1000 genomes]
rs10264882	0.91[EUR][1000 genomes]
rs11972689	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11974102	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11975023	0.85[EUR][1000 genomes]
rs11975948	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11976314	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11977048	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12111861	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12666916	0.82[EUR][1000 genomes]
rs13242185	0.91[EUR][1000 genomes]
rs1397008	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1397009	0.93[EUR][1000 genomes]
rs1509912	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1605917	0.92[EUR][1000 genomes]
rs16887017	0.91[EUR][1000 genomes]
rs17616148	0.91[EUR][1000 genomes]
rs1859678	0.88[EUR][1000 genomes]
rs327704	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs327705	0.83[EUR][1000 genomes]
rs327710	0.80[EUR][1000 genomes]
rs34252288	0.83[EUR][1000 genomes]
rs35141375	0.87[EUR][1000 genomes]
rs56034302	0.91[EUR][1000 genomes]
rs62467422	0.92[EUR][1000 genomes]
rs6467590	0.91[EUR][1000 genomes]
rs6967382	0.93[EUR][1000 genomes]
rs6967567	0.93[EUR][1000 genomes]
rs7778696	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7779992	0.92[EUR][1000 genomes]
rs7788722	0.90[EUR][1000 genomes]
rs7794312	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7794577	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7794595	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7795202	0.92[EUR][1000 genomes]
rs7797263	0.93[EUR][1000 genomes]
rs7798421	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7802063	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7809013	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810096	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs980966	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv831044	chr7:80721773-80918591	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80803600-80810600	Weak transcription	HepG2	liver
2	chr7:80803800-80819800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:80805000-80819800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:80805200-80808600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:80807400-80809800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:80808000-80808600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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