Variant report

Variant	rs2933550
Chromosome Location	chr3:158329943-158329944
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs1038886	0.84[ASN][1000 genomes]
rs1047366	0.86[ASN][1000 genomes]
rs1075551	0.92[ASN][1000 genomes]
rs10936158	0.86[ASN][1000 genomes]
rs12107643	0.94[ASN][1000 genomes]
rs12496174	0.86[ASN][1000 genomes]
rs13074694	0.84[ASN][1000 genomes]
rs13324770	0.82[ASN][1000 genomes]
rs13325932	0.86[ASN][1000 genomes]
rs1369563	0.90[ASN][1000 genomes]
rs1435642	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1602760	0.84[ASN][1000 genomes]
rs1620229	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1714516	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17629360	0.89[ASN][1000 genomes]
rs17629390	0.89[ASN][1000 genomes]
rs17629414	0.89[ASN][1000 genomes]
rs1836688	0.94[ASN][1000 genomes]
rs1864503	0.91[ASN][1000 genomes]
rs1864507	0.93[ASN][1000 genomes]
rs2115943	0.91[ASN][1000 genomes]
rs2248924	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2276773	0.88[ASN][1000 genomes]
rs2303909	0.91[ASN][1000 genomes]
rs2364274	0.94[ASN][1000 genomes]
rs2566344	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2573179	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2731112	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2731118	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2731120	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2731122	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28481597	0.87[ASN][1000 genomes]
rs3765025	0.94[ASN][1000 genomes]
rs3845272	0.91[ASN][1000 genomes]
rs3851361	0.95[ASN][1000 genomes]
rs3851363	0.91[ASN][1000 genomes]
rs4680445	0.89[ASN][1000 genomes]
rs4680449	0.96[ASN][1000 genomes]
rs4680450	0.84[ASN][1000 genomes]
rs4680451	0.88[ASN][1000 genomes]
rs4680452	0.91[ASN][1000 genomes]
rs4680453	0.88[ASN][1000 genomes]
rs4680457	0.84[ASN][1000 genomes]
rs4875	0.96[ASN][1000 genomes]
rs62287933	0.89[ASN][1000 genomes]
rs6441212	0.96[ASN][1000 genomes]
rs6441220	0.85[ASN][1000 genomes]
rs6763812	0.86[ASN][1000 genomes]
rs6771248	0.94[ASN][1000 genomes]
rs6772483	0.84[ASN][1000 genomes]
rs6777711	0.91[ASN][1000 genomes]
rs6781342	0.92[ASN][1000 genomes]
rs6800914	0.96[ASN][1000 genomes]
rs6802317	0.86[ASN][1000 genomes]
rs6803047	0.94[ASN][1000 genomes]
rs6803608	0.94[ASN][1000 genomes]
rs6804259	0.96[ASN][1000 genomes]
rs7613814	0.88[ASN][1000 genomes]
rs7621897	0.84[ASN][1000 genomes]
rs7631310	0.91[ASN][1000 genomes]
rs7653826	0.96[ASN][1000 genomes]
rs8455	0.88[ASN][1000 genomes]
rs891464	0.88[ASN][1000 genomes]
rs9819567	0.91[ASN][1000 genomes]
rs9819631	0.88[ASN][1000 genomes]
rs9824985	0.86[ASN][1000 genomes]
rs9844502	0.91[ASN][1000 genomes]
rs9848908	0.91[ASN][1000 genomes]
rs9864508	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002378	chr3:157715428-158673414	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv1014381	chr3:158070451-158350118	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1004124	chr3:158146715-158808638	Genic enhancers Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2763312	chr3:158193512-158420588	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv877691	chr3:158245883-158359667	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv869644	chr3:158308783-158426343	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2933550	GFM1	Cis_1M	lymphoblastoid	RTeQTL
rs2933550	MLF1	cis	Esophagus Mucosa	GTEx
rs2933550	RP11-538P18.2	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158305600-158330200	Weak transcription	Brain Anterior Caudate	brain

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