Variant report

Variant	rs7614082
Chromosome Location	chr3:144213705-144213706
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs11928775	0.89[ASN][1000 genomes]
rs12490144	0.80[ASN][1000 genomes]
rs12491851	0.89[ASN][1000 genomes]
rs12493075	0.89[ASN][1000 genomes]
rs12494918	0.85[ASN][1000 genomes]
rs12495279	0.89[ASN][1000 genomes]
rs13066453	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1527238	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1529752	0.86[ASN][1000 genomes]
rs1529753	0.86[ASN][1000 genomes]
rs1726536	0.83[EUR][1000 genomes]
rs1726538	0.83[EUR][1000 genomes]
rs2117004	0.85[ASN][1000 genomes]
rs4337676	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4349542	0.84[ASN][1000 genomes]
rs4398472	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4408907	0.91[ASN][1000 genomes]
rs4479640	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4544660	0.91[ASN][1000 genomes]
rs4568182	0.91[ASN][1000 genomes]
rs4594657	0.91[ASN][1000 genomes]
rs4681125	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4681328	0.89[ASN][1000 genomes]
rs4681331	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4681342	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6440258	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6763327	0.89[ASN][1000 genomes]
rs6763662	0.89[ASN][1000 genomes]
rs6783056	0.82[ASN][1000 genomes]
rs6791653	0.85[ASN][1000 genomes]
rs6799623	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6800761	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7611785	0.89[ASN][1000 genomes]
rs7613977	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7614253	0.82[ASN][1000 genomes]
rs7615146	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7616429	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7620611	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7626294	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7628103	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7634647	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7648433	0.89[ASN][1000 genomes]
rs7650699	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7652161	0.89[ASN][1000 genomes]
rs7653820	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9829827	0.86[ASN][1000 genomes]
rs9833354	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9840395	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9857163	0.89[ASN][1000 genomes]
rs9857613	0.89[ASN][1000 genomes]
rs9866115	0.89[ASN][1000 genomes]
rs9870285	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9878902	0.92[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	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1011685	chr3:143959237-144218424	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv536751	chr3:143959237-144218424	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2756108	chr3:144177836-144301659	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv877571	chr3:144188561-144291254	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 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	chr3:144210800-144215400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:144213200-144215000	Weak transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links