Variant report

Variant	rs4866845
Chromosome Location	chr5:43972024-43972025
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10461751	0.86[ASN][1000 genomes]
rs13155063	0.94[ASN][1000 genomes]
rs13157839	0.84[ASN][1000 genomes]
rs13159468	0.85[ASN][1000 genomes]
rs13162787	0.86[ASN][1000 genomes]
rs13163941	0.85[ASN][1000 genomes]
rs13171334	0.86[ASN][1000 genomes]
rs13175096	0.85[ASN][1000 genomes]
rs13182333	0.86[ASN][1000 genomes]
rs13184580	0.86[ASN][1000 genomes]
rs13186056	0.86[ASN][1000 genomes]
rs13189575	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34048286	0.86[ASN][1000 genomes]
rs34053815	0.87[ASN][1000 genomes]
rs34085387	0.86[ASN][1000 genomes]
rs34136561	0.86[ASN][1000 genomes]
rs34157568	0.85[ASN][1000 genomes]
rs34338792	0.86[ASN][1000 genomes]
rs34371282	0.86[ASN][1000 genomes]
rs34464981	0.89[ASN][1000 genomes]
rs34518294	0.86[ASN][1000 genomes]
rs34528370	0.85[ASN][1000 genomes]
rs34579696	0.85[ASN][1000 genomes]
rs34601610	0.85[ASN][1000 genomes]
rs34602870	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34632546	0.92[ASN][1000 genomes]
rs34685647	0.91[ASN][1000 genomes]
rs34758083	0.86[ASN][1000 genomes]
rs34782313	0.86[ASN][1000 genomes]
rs34843393	0.85[ASN][1000 genomes]
rs35013918	0.86[ASN][1000 genomes]
rs35029702	0.85[ASN][1000 genomes]
rs35092969	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35140592	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35162434	0.86[ASN][1000 genomes]
rs35182890	0.86[ASN][1000 genomes]
rs35208539	0.86[ASN][1000 genomes]
rs35289692	0.84[ASN][1000 genomes]
rs35374202	0.86[ASN][1000 genomes]
rs35430857	0.86[ASN][1000 genomes]
rs35529195	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35696398	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35697247	0.86[ASN][1000 genomes]
rs35730404	0.86[ASN][1000 genomes]
rs35789639	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35792109	0.86[ASN][1000 genomes]
rs35798472	0.85[ASN][1000 genomes]
rs35939121	0.82[ASN][1000 genomes]
rs35970538	0.81[ASN][1000 genomes]
rs36030354	0.86[ASN][1000 genomes]
rs36030928	0.83[ASN][1000 genomes]
rs36062010	0.84[ASN][1000 genomes]
rs4354051	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4543275	0.85[ASN][1000 genomes]
rs4563636	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4597977	0.86[ASN][1000 genomes]
rs4615307	0.85[ASN][1000 genomes]
rs4866756	0.87[ASN][1000 genomes]
rs4866757	0.86[ASN][1000 genomes]
rs4866760	0.99[ASN][1000 genomes]
rs4866852	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4866853	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56337432	0.86[ASN][1000 genomes]
rs58731744	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59751856	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6451737	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6451741	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs67443644	0.86[ASN][1000 genomes]
rs67991400	0.87[ASN][1000 genomes]
rs6859597	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6860696	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6864990	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6870141	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6882508	0.86[ASN][1000 genomes]
rs6887519	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6888119	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71631110	0.86[ASN][1000 genomes]
rs71631119	0.86[ASN][1000 genomes]
rs71631120	0.87[ASN][1000 genomes]
rs71631121	0.86[ASN][1000 genomes]
rs71631187	0.85[ASN][1000 genomes]
rs71631189	0.89[ASN][1000 genomes]
rs71633107	0.85[ASN][1000 genomes]
rs71633109	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71633110	0.85[ASN][1000 genomes]
rs73753694	0.91[ASN][1000 genomes]
rs7714254	0.86[ASN][1000 genomes]
rs7721923	0.86[ASN][1000 genomes]
rs7730331	0.86[ASN][1000 genomes]
rs7731350	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9800184	0.86[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	esv2830374	chr5:43785548-44341631	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1019047	chr5:43939693-44301657	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv830276	chr5:43951430-44150855	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43971600-43973400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:43972000-43974600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links