Variant report

Variant	rs11172831
Chromosome Location	chr12:59332532-59332533
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10877188	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10877198	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10877200	0.83[EUR][1000 genomes]
rs11172823	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[MEX][hapmap];0.91[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11172824	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[GIH][hapmap];0.93[MEX][hapmap];0.91[TSI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11172825	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11172827	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11172833	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11172837	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172839	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172840	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172846	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172857	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172858	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11172860	0.88[EUR][1000 genomes]
rs11172861	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11172862	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11172866	0.83[EUR][1000 genomes]
rs11172867	0.83[EUR][1000 genomes]
rs11172868	0.85[EUR][1000 genomes]
rs12368752	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12370522	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12423502	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12424788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12426212	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12426969	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17121828	0.83[EUR][1000 genomes]
rs55888651	0.83[EUR][1000 genomes]
rs58692617	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59773498	0.80[ASN][1000 genomes]
rs60522760	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60984323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61754220	0.92[EUR][1000 genomes]
rs61919461	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61919462	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61919464	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61919465	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61919466	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61919469	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919471	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61919513	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919518	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919519	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919520	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61919521	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919523	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919524	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61919525	0.88[EUR][1000 genomes]
rs61919531	0.87[EUR][1000 genomes]
rs61919532	0.87[EUR][1000 genomes]
rs6581224	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7136193	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7138401	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7294684	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7297094	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7301299	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7302365	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7303773	0.88[EUR][1000 genomes]
rs7309872	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7963207	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7968111	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7969722	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7970054	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7980136	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7980483	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9645802	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[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	nsv1043385	chr12:59149582-59758952	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1067596	chr12:59167152-59764208	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv492251	chr12:59167152-59764208	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs11172831	INHBC	cis	parietal	SCAN
rs11172831	INHBE	cis	parietal	SCAN
rs11172831	COQ10A	cis	cerebellum	SCAN
rs11172831	MBD6	cis	cerebellum	SCAN
rs11172831	PIP4K2C	cis	cerebellum	SCAN
rs11172831	ESPL1	cis	cerebellum	SCAN
rs11172831	RAB5B	cis	cerebellum	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59328600-59333200	Weak transcription	Stomach Mucosa	stomach
2	chr12:59328600-59337000	Weak transcription	Gastric	stomach
3	chr12:59330200-59335200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:59332200-59335200	Enhancers	HUVEC	blood vessel

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