Variant report

Variant	rs36046846
Chromosome Location	chr2:37709079-37709080
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11124584	0.85[EUR][1000 genomes]
rs11124585	0.86[EUR][1000 genomes]
rs11124586	0.80[ASN][1000 genomes]
rs12616113	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12992054	0.87[EUR][1000 genomes]
rs12992431	0.84[EUR][1000 genomes]
rs12992720	0.87[EUR][1000 genomes]
rs12993204	0.87[EUR][1000 genomes]
rs13000102	0.84[ASN][1000 genomes]
rs13009200	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13016394	0.87[EUR][1000 genomes]
rs13016831	0.87[EUR][1000 genomes]
rs13387905	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13412538	0.83[ASN][1000 genomes]
rs17020823	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17020835	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2080387	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2192942	0.80[ASN][1000 genomes]
rs2192943	0.81[ASN][1000 genomes]
rs2192944	0.81[ASN][1000 genomes]
rs2216117	0.84[ASN][1000 genomes]
rs2373109	0.82[ASN][1000 genomes]
rs2373110	0.82[ASN][1000 genomes]
rs34130356	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58367831	0.87[EUR][1000 genomes]
rs58694726	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60691585	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62135566	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62135567	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62135568	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6708411	0.82[ASN][1000 genomes]
rs6724538	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6746868	0.81[ASN][1000 genomes]
rs6757678	0.84[ASN][1000 genomes]
rs7562026	0.86[EUR][1000 genomes]
rs7562161	0.87[EUR][1000 genomes]
rs7574012	0.80[ASN][1000 genomes]
rs7582204	0.81[ASN][1000 genomes]
rs7592144	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7593333	0.82[ASN][1000 genomes]
rs7595792	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs960902	0.80[ASN][1000 genomes]
rs9941697	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833814	chr2:37643132-37840247	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv456374	chr2:37669487-37868214	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv470453	chr2:37669487-37868214	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv581473	chr2:37669487-37868214	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37700600-37710000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:37705400-37711800	Weak transcription	Fetal Heart	heart
3	chr2:37708200-37709600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:37708200-37709600	Strong transcription	Liver	Liver
5	chr2:37708200-37710600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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