Variant report

Variant	rs7564810
Chromosome Location	chr2:20613801-20613802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:20605173..20606990-chr2:20613727..20616076,2	MCF-7	breast:
2	chr2:20613534..20615570-chr2:20645531..20648306,3	MCF-7	breast:
3	chr2:20611214..20614002-chr2:20617108..20620081,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143878	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10209568	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11901184	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464277	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12466143	0.87[EUR][1000 genomes]
rs12471220	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs12471293	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12477228	0.87[EUR][1000 genomes]
rs1476941	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1985318	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1985319	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2348705	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs343138	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs343140	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs343142	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs343144	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs343147	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs343152	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4666306	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4666386	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4666387	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4666389	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4666390	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6531236	0.87[ASN][1000 genomes]
rs6705947	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6734065	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67464308	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs67511352	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7563890	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7564799	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7576439	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7576806	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7603518	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7604195	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs953927	0.82[AMR][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	nsv873716	chr2:20572094-20621404	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv581165	chr2:20581058-20616990	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20601400-20614800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:20610400-20621000	Weak transcription	Left Ventricle	heart
3	chr2:20611000-20614600	Weak transcription	Esophagus	oesophagus
4	chr2:20611200-20618200	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:20611200-20618400	Weak transcription	HSMM	muscle
6	chr2:20611400-20615200	Weak transcription	HSMMtube	muscle
7	chr2:20611600-20614600	Weak transcription	Placenta	Placenta
8	chr2:20611600-20615200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:20611600-20615400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:20611600-20618000	Weak transcription	Adipose Nuclei	Adipose
11	chr2:20611600-20618400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr2:20611800-20615400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr2:20612000-20615200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:20613000-20614600	Weak transcription	HepG2	liver

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