Variant report

Variant	rs6591434
Chromosome Location	chr11:57644334-57644335
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10792112	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10896647	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10896656	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10896661	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10896662	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11229116	0.83[EUR][1000 genomes]
rs11229130	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11229131	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11229148	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11229160	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11570190	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11601320	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11601449	0.83[EUR][1000 genomes]
rs11602109	0.83[ASN][1000 genomes]
rs11604333	0.81[ASN][1000 genomes]
rs11605731	0.83[EUR][1000 genomes]
rs11606396	0.83[ASN][1000 genomes]
rs12360939	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12362166	0.81[ASN][1000 genomes]
rs12790660	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12798206	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12804972	0.81[ASN][1000 genomes]
rs12805841	0.85[ASN][1000 genomes]
rs12807250	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12807357	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1647405	0.80[ASN][1000 genomes]
rs17455520	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2509808	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2847308	0.80[ASN][1000 genomes]
rs2926656	0.83[ASN][1000 genomes]
rs35808061	0.83[EUR][1000 genomes]
rs3781885	0.83[EUR][1000 genomes]
rs488769	0.85[ASN][1000 genomes]
rs499188	0.85[ASN][1000 genomes]
rs547891	0.80[ASN][1000 genomes]
rs576859	0.80[ASN][1000 genomes]
rs589914	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs631791	0.86[EUR][1000 genomes]
rs644883	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs674094	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs682503	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs685149	0.87[ASN][1000 genomes]
rs708228	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7117205	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7121169	0.81[ASN][1000 genomes]
rs71484468	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7932091	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7936998	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7949841	0.82[EUR][1000 genomes]
rs9420	0.80[ASN][1000 genomes]
rs9645687	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv530621	chr11:57139699-57703639	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	nsv1040913	chr11:57315006-57696122	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
5	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
6	nsv897589	chr11:57623815-58052357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6591434	MED19	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57641200-57646200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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