Variant report

Variant	rs7586148
Chromosome Location	chr2:31342086-31342087
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10175305	0.89[CEU][hapmap];0.81[JPT][hapmap]
rs10188244	0.94[JPT][hapmap]
rs10490519	0.80[EUR][1000 genomes]
rs11124239	0.81[EUR][1000 genomes]
rs11124240	0.88[CEU][hapmap]
rs11124241	0.80[EUR][1000 genomes]
rs11674713	0.81[CEU][hapmap]
rs11686425	0.89[CEU][hapmap]
rs11692265	0.89[CEU][hapmap]
rs11888670	0.81[TSI][hapmap]
rs12471972	0.84[EUR][1000 genomes]
rs12712310	0.82[JPT][hapmap]
rs12712311	0.82[JPT][hapmap]
rs12993947	0.81[EUR][1000 genomes]
rs12996218	0.89[CEU][hapmap];0.94[JPT][hapmap]
rs13003016	0.81[EUR][1000 genomes]
rs13029054	0.88[JPT][hapmap]
rs1862978	0.81[CEU][hapmap]
rs1862979	0.89[CEU][hapmap]
rs2098787	0.85[CEU][hapmap]
rs2194464	0.83[EUR][1000 genomes]
rs2194467	0.89[CEU][hapmap];0.82[JPT][hapmap]
rs2194469	0.89[CEU][hapmap];0.82[JPT][hapmap]
rs2365192	0.89[CEU][hapmap]
rs2365196	0.81[EUR][1000 genomes]
rs2365197	0.82[JPT][hapmap]
rs2365200	0.82[JPT][hapmap]
rs2365201	0.89[CEU][hapmap];0.82[JPT][hapmap]
rs2365206	0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4951965	0.85[CEU][hapmap]
rs6543598	0.89[CEU][hapmap]
rs6543599	0.89[CEU][hapmap]
rs6708428	0.81[CEU][hapmap]
rs6718097	0.81[EUR][1000 genomes]
rs6729079	0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.88[ASN][1000 genomes]
rs6732067	0.81[CEU][hapmap]
rs6743541	0.95[CEU][hapmap];0.84[EUR][1000 genomes]
rs6760378	0.80[EUR][1000 genomes]
rs7565689	0.89[CEU][hapmap]
rs7565904	0.80[CEU][hapmap]
rs7583033	0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7583218	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7600547	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9973425	0.84[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31310600-31346800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:31329200-31348200	Weak transcription	A549	lung
3	chr2:31332400-31347400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:31332600-31348600	Weak transcription	NHEK	skin
5	chr2:31332600-31348800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:31332600-31349000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:31332600-31349000	Weak transcription	HMEC	breast
8	chr2:31332800-31346600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:31335200-31344600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr2:31336400-31343800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr2:31336600-31345000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:31337000-31345800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr2:31337200-31347800	Weak transcription	Brain Germinal Matrix	brain

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