Variant report

Variant	rs56337432
Chromosome Location	chr5:43894300-43894301
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10461751	0.98[ASN][1000 genomes]
rs13155063	0.90[ASN][1000 genomes]
rs13157839	0.82[ASN][1000 genomes]
rs13159468	0.85[ASN][1000 genomes]
rs13162787	1.00[ASN][1000 genomes]
rs13163941	0.85[ASN][1000 genomes]
rs13171334	1.00[ASN][1000 genomes]
rs13175096	0.85[ASN][1000 genomes]
rs13182333	0.98[ASN][1000 genomes]
rs13184580	0.98[ASN][1000 genomes]
rs13186056	0.98[ASN][1000 genomes]
rs13189575	0.81[ASN][1000 genomes]
rs34048286	0.98[ASN][1000 genomes]
rs34053815	0.99[ASN][1000 genomes]
rs34085387	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34136561	1.00[ASN][1000 genomes]
rs34157568	0.81[ASN][1000 genomes]
rs34338792	0.98[ASN][1000 genomes]
rs34371282	0.98[ASN][1000 genomes]
rs34464981	0.95[ASN][1000 genomes]
rs34518294	1.00[ASN][1000 genomes]
rs34528370	0.85[ASN][1000 genomes]
rs34579696	0.85[ASN][1000 genomes]
rs34601610	0.83[ASN][1000 genomes]
rs34602870	0.81[ASN][1000 genomes]
rs34632546	0.92[ASN][1000 genomes]
rs34685647	0.93[ASN][1000 genomes]
rs34758083	0.98[ASN][1000 genomes]
rs34782313	1.00[ASN][1000 genomes]
rs34843393	0.85[ASN][1000 genomes]
rs35013918	0.98[ASN][1000 genomes]
rs35029702	0.99[ASN][1000 genomes]
rs35092969	0.85[ASN][1000 genomes]
rs35140592	0.86[ASN][1000 genomes]
rs35162434	1.00[ASN][1000 genomes]
rs35182890	0.98[ASN][1000 genomes]
rs35208539	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35289692	0.98[ASN][1000 genomes]
rs35374202	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35430857	0.98[ASN][1000 genomes]
rs35529195	0.85[ASN][1000 genomes]
rs35696398	0.92[ASN][1000 genomes]
rs35697247	1.00[ASN][1000 genomes]
rs35730404	0.98[ASN][1000 genomes]
rs35789639	0.83[ASN][1000 genomes]
rs35792109	1.00[ASN][1000 genomes]
rs35798472	0.81[ASN][1000 genomes]
rs35970538	0.81[ASN][1000 genomes]
rs36030354	1.00[ASN][1000 genomes]
rs36030928	0.83[ASN][1000 genomes]
rs36062010	0.98[ASN][1000 genomes]
rs4354051	0.85[ASN][1000 genomes]
rs4543275	0.85[ASN][1000 genomes]
rs4563636	0.81[ASN][1000 genomes]
rs4597977	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4615307	0.83[ASN][1000 genomes]
rs4866756	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4866757	1.00[ASN][1000 genomes]
rs4866760	0.85[ASN][1000 genomes]
rs4866845	0.86[ASN][1000 genomes]
rs4866852	0.83[ASN][1000 genomes]
rs4866853	0.83[ASN][1000 genomes]
rs58731744	0.98[ASN][1000 genomes]
rs59751856	0.81[ASN][1000 genomes]
rs6451737	0.85[ASN][1000 genomes]
rs6451741	0.81[ASN][1000 genomes]
rs67443644	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67991400	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6859597	0.97[ASN][1000 genomes]
rs6860696	0.85[ASN][1000 genomes]
rs6864990	0.85[ASN][1000 genomes]
rs6870141	0.98[ASN][1000 genomes]
rs6882508	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6887519	0.81[ASN][1000 genomes]
rs6888119	0.92[ASN][1000 genomes]
rs71631110	1.00[ASN][1000 genomes]
rs71631119	0.98[ASN][1000 genomes]
rs71631120	0.99[ASN][1000 genomes]
rs71631121	1.00[ASN][1000 genomes]
rs71631187	0.97[ASN][1000 genomes]
rs71631189	0.95[ASN][1000 genomes]
rs71633107	0.85[ASN][1000 genomes]
rs71633109	0.85[ASN][1000 genomes]
rs71633110	0.83[ASN][1000 genomes]
rs73753694	0.95[ASN][1000 genomes]
rs7714254	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7721923	0.86[ASN][1000 genomes]
rs7730331	0.98[ASN][1000 genomes]
rs7731350	0.85[ASN][1000 genomes]
rs9800184	0.98[ASN][1000 genomes]
rs9800296	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43893800-43895400	Enhancers	Fetal Stomach	stomach
2	chr5:43894000-43894600	Enhancers	Fetal Heart	heart
3	chr5:43894000-43894800	Weak transcription	Stomach Mucosa	stomach

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