Variant report

Variant	rs61919465
Chromosome Location	chr12:59328575-59328576
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10877188	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10877198	0.88[EUR][1000 genomes]
rs10877200	0.83[EUR][1000 genomes]
rs11172823	0.92[EUR][1000 genomes]
rs11172824	0.92[EUR][1000 genomes]
rs11172825	0.92[EUR][1000 genomes]
rs11172827	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11172831	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11172833	1.00[EUR][1000 genomes]
rs11172837	0.89[EUR][1000 genomes]
rs11172839	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172840	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172846	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11172857	0.89[EUR][1000 genomes]
rs11172858	0.88[EUR][1000 genomes]
rs11172860	0.88[EUR][1000 genomes]
rs11172861	0.88[EUR][1000 genomes]
rs11172862	0.88[EUR][1000 genomes]
rs11172866	0.83[EUR][1000 genomes]
rs11172867	0.83[EUR][1000 genomes]
rs11172868	0.85[EUR][1000 genomes]
rs12368752	0.89[EUR][1000 genomes]
rs12370522	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12423502	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12424788	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12426212	0.92[EUR][1000 genomes]
rs12426969	0.92[EUR][1000 genomes]
rs17121828	0.83[EUR][1000 genomes]
rs55888651	0.83[EUR][1000 genomes]
rs58692617	0.87[EUR][1000 genomes]
rs60522760	0.89[EUR][1000 genomes]
rs60984323	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61754220	0.92[EUR][1000 genomes]
rs61919461	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61919462	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61919464	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61919466	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61919469	0.89[EUR][1000 genomes]
rs61919471	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61919513	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61919518	0.89[EUR][1000 genomes]
rs61919519	0.89[EUR][1000 genomes]
rs61919520	0.88[EUR][1000 genomes]
rs61919521	0.89[EUR][1000 genomes]
rs61919523	0.89[EUR][1000 genomes]
rs61919524	0.88[EUR][1000 genomes]
rs61919525	0.88[EUR][1000 genomes]
rs61919531	0.87[EUR][1000 genomes]
rs61919532	0.87[EUR][1000 genomes]
rs6581224	0.88[EUR][1000 genomes]
rs7136193	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7138401	0.89[EUR][1000 genomes]
rs7294684	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7297094	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7301299	0.89[EUR][1000 genomes]
rs7302365	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7303773	0.88[EUR][1000 genomes]
rs7309872	0.89[EUR][1000 genomes]
rs7963207	0.89[EUR][1000 genomes]
rs7968111	0.88[EUR][1000 genomes]
rs7969722	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7970054	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7980136	1.00[EUR][1000 genomes]
rs7980483	0.92[EUR][1000 genomes]
rs9645802	0.88[AMR][1000 genomes];1.00[EUR][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

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59321000-59329600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:59327200-59328600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:59327600-59328600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:59328200-59328600	Enhancers	Stomach Mucosa	stomach
5	chr12:59328400-59328600	Enhancers	Gastric	stomach
6	chr12:59328400-59328600	Enhancers	Pancreas	Pancrea
7	chr12:59328400-59328600	Enhancers	Small Intestine	intestine
8	chr12:59328400-59328600	Enhancers	Spleen	Spleen
9	chr12:59328400-59328800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr12:59328400-59328800	Enhancers	Fetal Lung	lung

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