Variant report

Variant	rs11646831
Chromosome Location	chr16:80211981-80211982
allele	A/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	GATA3	chr16:80211817-80212127	T-47D	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000261376	TF binding region

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11150250	0.99[ASN][1000 genomes]
rs11640831	0.89[EUR][1000 genomes]
rs11642380	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11642712	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11647537	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11648337	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11649346	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11859592	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12597962	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12927541	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12927726	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12927869	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12928708	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12930060	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13380610	0.80[AMR][1000 genomes]
rs1478504	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16944269	0.95[ASN][1000 genomes]
rs17734652	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17796688	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1904184	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1904186	0.85[EUR][1000 genomes]
rs2008481	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2061792	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34149818	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34758462	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4300652	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4405565	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62049508	0.92[AFR][1000 genomes]
rs7191912	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7193739	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7201276	0.89[EUR][1000 genomes]
rs8046518	0.88[EUR][1000 genomes]
rs8060188	0.95[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs8060663	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9673176	0.88[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9935498	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9935652	0.89[EUR][1000 genomes]
rs9939067	0.89[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	nsv833298	chr16:80122337-80314603	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1055228	chr16:80207546-80378842	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1061068	chr16:80207546-80537052	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1064093	chr16:80208443-80333301	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv542985	chr16:80208443-80333301	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1059997	chr16:80209367-80247050	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80207600-80212200	Enhancers	Osteobl	bone
2	chr16:80207800-80212200	Enhancers	A549	lung
3	chr16:80210000-80216000	Weak transcription	HSMM	muscle
4	chr16:80210400-80231400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr16:80211200-80212000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr16:80211200-80212200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr16:80211400-80212000	Enhancers	HSMMtube	muscle
8	chr16:80211600-80212000	Enhancers	NHDF-Ad	bronchial

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