Variant report

Variant	rs357456
Chromosome Location	chr7:138014416-138014417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11983566	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1643164	0.89[ASN][1000 genomes]
rs357371	0.86[ASN][1000 genomes]
rs357372	0.89[ASN][1000 genomes]
rs357381	0.92[ASN][1000 genomes]
rs357382	0.91[ASN][1000 genomes]
rs357383	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs357386	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs357404	0.82[AMR][1000 genomes]
rs357411	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs357412	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs357414	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357421	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357427	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357428	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357435	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs357437	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs357445	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs357451	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs357454	0.95[ASN][1000 genomes]
rs357457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs367783	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs370275	0.87[ASN][1000 genomes]
rs373613	0.93[ASN][1000 genomes]
rs375018	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs380650	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs382122	0.89[ASN][1000 genomes]
rs385127	0.89[ASN][1000 genomes]
rs392162	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs396918	0.88[ASN][1000 genomes]
rs397203	0.89[ASN][1000 genomes]
rs398970	0.89[ASN][1000 genomes]
rs399486	0.89[ASN][1000 genomes]
rs402228	0.89[ASN][1000 genomes]
rs402358	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs402486	0.91[ASN][1000 genomes]
rs407687	0.88[ASN][1000 genomes]
rs409813	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs424605	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs427954	0.94[ASN][1000 genomes]
rs428488	0.94[ASN][1000 genomes]
rs429103	0.94[ASN][1000 genomes]
rs431358	0.90[ASN][1000 genomes]
rs432187	0.90[ASN][1000 genomes]
rs446384	0.90[ASN][1000 genomes]
rs447273	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs449239	0.92[ASN][1000 genomes]
rs60969	0.90[ASN][1000 genomes]
rs689683	0.89[ASN][1000 genomes]
rs690193	0.91[ASN][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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv5967	chr7:137988239-138015844	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138012400-138014600	Enhancers	Fetal Heart	heart
2	chr7:138014400-138015200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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