Variant report

Variant	rs73619300
Chromosome Location	chr16:76342266-76342267
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	CEBPB	chr16:76342151-76342311	HepG2	liver:	n/a	chr16:76342254-76342267

Variant related genes	Relation type
CNTNAP4	TF binding region

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11861029	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11861873	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11864590	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11864760	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11864949	1.00[AMR][1000 genomes]
rs55954470	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56099821	1.00[AMR][1000 genomes]
rs56162176	1.00[AMR][1000 genomes]
rs56908627	1.00[AMR][1000 genomes]
rs57473201	1.00[AMR][1000 genomes]
rs57849035	1.00[AMR][1000 genomes]
rs58741496	1.00[AMR][1000 genomes]
rs6564316	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6564317	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6564319	1.00[AMR][1000 genomes]
rs6564321	1.00[AMR][1000 genomes]
rs73619239	1.00[AMR][1000 genomes]
rs73619250	1.00[AMR][1000 genomes]
rs73619302	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73620917	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73620934	0.83[AFR][1000 genomes]
rs73620946	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73620947	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73625321	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73625336	1.00[AMR][1000 genomes]
rs73625337	1.00[AMR][1000 genomes]
rs74024929	1.00[AMR][1000 genomes]
rs74024930	1.00[AMR][1000 genomes]
rs74024937	1.00[AMR][1000 genomes]
rs74024938	1.00[AMR][1000 genomes]
rs74024960	1.00[AMR][1000 genomes]
rs74024967	1.00[AMR][1000 genomes]
rs74024969	1.00[AMR][1000 genomes]
rs74024974	1.00[AMR][1000 genomes]
rs74024976	1.00[AMR][1000 genomes]
rs74024979	1.00[AMR][1000 genomes]
rs74024995	1.00[AMR][1000 genomes]
rs74026725	1.00[AMR][1000 genomes]
rs74026731	1.00[AMR][1000 genomes]
rs74026733	1.00[AMR][1000 genomes]
rs74026735	1.00[AMR][1000 genomes]
rs74026738	1.00[AMR][1000 genomes]
rs74026741	1.00[AMR][1000 genomes]
rs74026754	1.00[AMR][1000 genomes]
rs74026780	1.00[AMR][1000 genomes]
rs74026781	1.00[AMR][1000 genomes]
rs8058106	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8058357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532562	chr16:75614947-76371158	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1064607	chr16:75787129-76449101	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1065794	chr16:75792288-76434118	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv542961	chr16:75792288-76434118	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv1059162	chr16:75929348-76730816	Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv572995	chr16:75935025-76708417	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv572996	chr16:75935025-76735249	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv817220	chr16:75939705-76735383	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv1056021	chr16:75955522-76729765	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
10	nsv542962	chr16:75955522-76729765	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv906935	chr16:76031737-76453110	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv906936	chr16:76031737-76768178	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	nsv817549	chr16:76067068-76582099	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv833285	chr16:76136345-76345398	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv1065644	chr16:76166579-76475634	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv869200	chr16:76227867-76695732	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
17	nsv833286	chr16:76243730-76444283	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	esv2763142	chr16:76271660-76461841	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76338400-76368600	Weak transcription	Brain Hippocampus Middle	brain
2	chr16:76340400-76342600	Enhancers	Brain Substantia Nigra	brain
3	chr16:76341000-76345600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr16:76342200-76342600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain

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