Variant report

Variant	rs7608140
Chromosome Location	chr2:151135059-151135060
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10165225	0.92[EUR][1000 genomes]
rs10165666	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10173947	0.92[EUR][1000 genomes]
rs10209398	0.92[EUR][1000 genomes]
rs1036793	0.89[AMR][1000 genomes]
rs11693655	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11888189	0.92[EUR][1000 genomes]
rs11895581	0.92[EUR][1000 genomes]
rs11899312	0.92[EUR][1000 genomes]
rs12623971	0.80[EUR][1000 genomes]
rs12692649	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13394286	0.92[EUR][1000 genomes]
rs1372436	0.89[AMR][1000 genomes]
rs1899375	0.89[AMR][1000 genomes]
rs2334315	0.91[AMR][1000 genomes]
rs4233802	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4362583	0.92[EUR][1000 genomes]
rs4366927	0.89[EUR][1000 genomes]
rs4402789	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4404295	0.92[EUR][1000 genomes]
rs4425094	0.92[EUR][1000 genomes]
rs4425095	0.92[EUR][1000 genomes]
rs4491744	0.84[EUR][1000 genomes]
rs4508619	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4563247	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4577299	0.92[EUR][1000 genomes]
rs4585053	0.92[EUR][1000 genomes]
rs4589785	0.92[EUR][1000 genomes]
rs4606957	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62167367	0.92[EUR][1000 genomes]
rs62167369	0.92[EUR][1000 genomes]
rs6727491	0.89[AMR][1000 genomes]
rs6741918	0.89[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs6748737	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6761697	0.92[EUR][1000 genomes]
rs7560459	0.89[EUR][1000 genomes]
rs7563730	0.92[EUR][1000 genomes]
rs7564257	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7564743	0.92[EUR][1000 genomes]
rs9287819	0.92[EUR][1000 genomes]
rs9287820	0.87[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	nsv995119	chr2:150556150-151294696	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1001838	chr2:150819672-151745876	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv535980	chr2:150819672-151745876	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151113000-151138400	Weak transcription	Liver	Liver
2	chr2:151128000-151138400	Weak transcription	Psoas Muscle	Psoas
3	chr2:151129600-151136000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:151133800-151137000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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