Variant report

Variant	rs7675750
Chromosome Location	chr4:7503703-7503704
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10032900	0.91[ASN][1000 genomes]
rs10937825	0.91[ASN][1000 genomes]
rs11942382	0.91[ASN][1000 genomes]
rs12330969	0.84[ASN][1000 genomes]
rs12331653	0.84[ASN][1000 genomes]
rs12506309	0.83[EUR][1000 genomes]
rs13122920	0.91[ASN][1000 genomes]
rs28372374	0.93[ASN][1000 genomes]
rs28397666	0.84[ASN][1000 genomes]
rs28612382	0.84[ASN][1000 genomes]
rs28718071	0.84[ASN][1000 genomes]
rs28751921	0.84[ASN][1000 genomes]
rs4096	0.91[ASN][1000 genomes]
rs4286514	0.84[ASN][1000 genomes]
rs4403049	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4406019	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4504253	0.84[ASN][1000 genomes]
rs4591606	0.93[EUR][1000 genomes]
rs4635817	0.84[ASN][1000 genomes]
rs4689766	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4689767	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4689768	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4689769	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4689771	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62280186	0.84[ASN][1000 genomes]
rs6446605	0.80[ASN][1000 genomes]
rs6840680	0.84[ASN][1000 genomes]
rs71647607	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs750136	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7670574	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7675968	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7693724	0.93[ASN][1000 genomes]
rs7693926	0.91[ASN][1000 genomes]
rs7695291	0.91[ASN][1000 genomes]
rs9997284	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv593569	chr4:7291363-7626136	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv469758	chr4:7370083-7546250	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
6	nsv878561	chr4:7402284-7544610	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
7	nsv878563	chr4:7420785-7529367	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv878564	chr4:7421007-7535214	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
9	nsv878566	chr4:7456717-7529367	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
10	nsv878567	chr4:7456717-7544610	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
11	esv34002	chr4:7481398-7508494	Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
12	nsv878568	chr4:7490246-7529367	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv878569	chr4:7496857-7544610	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7502000-7503800	Enhancers	Fetal Brain Male	brain
2	chr4:7502000-7504200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:7502200-7511000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:7502800-7504000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
5	chr4:7502800-7504400	Enhancers	Brain Germinal Matrix	brain
6	chr4:7503200-7507600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr4:7503200-7507600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr4:7503400-7507200	Weak transcription	Brain Anterior Caudate	brain
9	chr4:7503400-7507800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr4:7503600-7503800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:7503600-7503800	Bivalent Enhancer	Right Ventricle	heart

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