Variant report

Variant	rs682503
Chromosome Location	chr11:57640994-57640995
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr11:57640651-57641031	MCF10A-Er-Src	breast:	n/a	n/a
2	STAT3	chr11:57640459-57641001	MCF10A-Er-Src	breast:	n/a	chr11:57640808-57640816
3	FOS	chr11:57640554-57641067	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr11:57640574-57641052	MCF10A-Er-Src	breast:	n/a	n/a
5	STAT3	chr11:57640342-57641027	MCF10A-Er-Src	breast:	n/a	chr11:57640808-57640816
6	FOS	chr11:57640545-57641052	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr11:57640687-57641008	MCF10A-Er-Src	breast:	n/a	n/a
8	STAT3	chr11:57640463-57641052	MCF10A-Er-Src	breast:	n/a	chr11:57640808-57640816

Variant related genes	Relation type
ENSG00000255266	TF binding region

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10792112	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10896633	0.81[ASN][1000 genomes]
rs10896636	0.95[CEU][hapmap]
rs10896647	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10896656	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10896661	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10896662	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11229116	0.87[EUR][1000 genomes]
rs11229130	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11229131	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11229148	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11229160	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11570190	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11601320	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11601449	0.86[EUR][1000 genomes]
rs11602109	0.85[ASN][1000 genomes]
rs11604333	0.83[ASN][1000 genomes]
rs11605731	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs11606396	0.85[ASN][1000 genomes]
rs11607056	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12146541	0.81[EUR][1000 genomes]
rs12360939	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12362166	0.83[ASN][1000 genomes]
rs12785533	0.80[EUR][1000 genomes]
rs12790660	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12798206	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12804972	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12805841	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12807250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12807357	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1647405	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs17455520	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2509808	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2847308	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs2926656	0.81[ASN][1000 genomes]
rs35808061	0.87[EUR][1000 genomes]
rs3781885	0.86[EUR][1000 genomes]
rs4827	0.81[EUR][1000 genomes]
rs488769	0.95[CEU][hapmap];0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs499188	0.83[ASN][1000 genomes]
rs547891	0.81[EUR][1000 genomes]
rs576859	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs589914	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs631791	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs644883	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6591434	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs674094	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs685149	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs708228	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7116341	0.80[EUR][1000 genomes]
rs7117205	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121169	0.83[ASN][1000 genomes]
rs71484468	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7932091	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7936998	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7949841	0.86[EUR][1000 genomes]
rs9420	0.90[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs9645687	0.88[AMR][1000 genomes];0.88[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
rs682503	MED19	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57637400-57642600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:57640200-57641800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr11:57640400-57641400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:57640400-57642800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:57640600-57641000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr11:57640600-57641400	Enhancers	HMEC	breast
7	chr11:57640600-57641600	Enhancers	Dnd41	blood
8	chr11:57640800-57641400	Enhancers	Primary T cells from cord blood	blood
9	chr11:57640800-57641800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr11:57640800-57641800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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