Variant report

Variant	rs7570657
Chromosome Location	chr2:99654281-99654282
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:99345574..99348199-chr2:99652477..99654603,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000071073	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10165534	0.81[EUR][1000 genomes]
rs10167390	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10170063	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10179910	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10181344	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs10181422	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10196680	0.82[EUR][1000 genomes]
rs1115756	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1115757	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1133977	0.81[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]
rs1133978	0.90[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11683107	0.82[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs11683188	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11688004	0.81[CHB][hapmap];0.81[JPT][hapmap];0.91[ASN][1000 genomes]
rs11692336	0.86[CHB][hapmap];0.80[JPT][hapmap];0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11692669	0.81[ASN][1000 genomes]
rs11895749	0.91[ASN][1000 genomes]
rs11903311	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12464710	0.81[EUR][1000 genomes]
rs12467679	0.83[EUR][1000 genomes]
rs12470471	0.81[CHB][hapmap];0.81[JPT][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12473029	0.87[EUR][1000 genomes]
rs12477754	0.82[EUR][1000 genomes]
rs12477978	0.87[EUR][1000 genomes]
rs12613624	0.81[CHB][hapmap];0.81[JPT][hapmap];0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12619780	0.92[ASN][1000 genomes]
rs12987548	0.92[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs13000731	0.86[ASN][1000 genomes]
rs13008171	0.81[CHB][hapmap];0.81[JPT][hapmap];0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs13023501	0.84[ASN][1000 genomes]
rs13033012	0.82[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs13035357	0.88[AFR][1000 genomes]
rs13396358	0.80[EUR][1000 genomes]
rs13407840	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13412764	0.81[AMR][1000 genomes]
rs1349778	0.81[EUR][1000 genomes]
rs1349779	0.88[EUR][1000 genomes]
rs1453563	0.82[CHB][hapmap];0.81[JPT][hapmap];0.90[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1453564	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1530996	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1563106	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1563107	0.81[CHB][hapmap];0.81[JPT][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1563108	0.81[CHB][hapmap];0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1580068	0.81[EUR][1000 genomes]
rs17708262	0.82[CHB][hapmap];0.81[JPT][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17759607	0.81[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs2084988	0.86[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2123686	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs2309524	0.81[EUR][1000 genomes]
rs2516830	0.82[CHB][hapmap];0.82[JPT][hapmap];0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2516833	0.90[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2516835	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2632283	0.82[CHB][hapmap];0.81[JPT][hapmap];0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs28575117	0.84[AMR][1000 genomes]
rs28648058	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34272114	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4346438	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4347885	0.84[ASN][1000 genomes]
rs4374423	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs4585080	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4622780	0.81[EUR][1000 genomes]
rs4850897	0.82[CHB][hapmap];0.82[JPT][hapmap];0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4851179	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4851183	0.82[CHB][hapmap];0.81[JPT][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4851185	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs4851188	0.82[CHB][hapmap];0.81[JPT][hapmap];0.91[ASN][1000 genomes]
rs62154638	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6542846	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6542852	0.81[EUR][1000 genomes]
rs6542866	0.81[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs6542868	0.81[CHB][hapmap];0.81[JPT][hapmap];0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6704766	0.82[EUR][1000 genomes]
rs6707462	0.81[JPT][hapmap];0.95[ASN][1000 genomes]
rs6708878	0.84[ASN][1000 genomes]
rs6722164	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6724476	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6727749	0.81[CHB][hapmap];0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs6735801	0.82[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6736064	0.82[EUR][1000 genomes]
rs6737257	0.82[JPT][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6740035	0.81[AMR][1000 genomes]
rs6740054	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6750876	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs6753650	0.92[ASN][1000 genomes]
rs6754843	0.83[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6756880	0.85[JPT][hapmap]
rs6759354	0.81[EUR][1000 genomes]
rs720229	0.85[CHB][hapmap];0.80[JPT][hapmap];0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs72957109	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7558239	0.81[EUR][1000 genomes]
rs7571390	0.81[CHB][hapmap];0.81[JPT][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7586608	0.85[CHB][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7588059	0.91[ASN][1000 genomes]
rs7591794	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7599427	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7605734	0.82[CHB][hapmap];0.82[JPT][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7606635	0.81[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7608938	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs896886	0.82[EUR][1000 genomes]
rs9308816	0.81[EUR][1000 genomes]
rs9710648	0.81[JPT][hapmap]
rs9808541	0.82[EUR][1000 genomes]

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	nsv834310	chr2:99533832-99709999	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
2	nsv1007718	chr2:99542281-99729107	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs7570657	TSGA10	cis	multi-tissue	Pritchard
rs7570657	TSGA10	Cis_1M	lymphoblastoid	RTeQTL
rs7570657	TSGA10	cis	Skin Sun Exposed Lower leg	GTEx
rs7570657	TSGA10	cis	Thyroid	GTEx
rs7570657	LIPT1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99627600-99658800	Weak transcription	Pancreas	Pancrea
2	chr2:99650000-99656800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:99653400-99657600	Weak transcription	Aorta	Aorta

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