Variant report

Variant	rs66500830
Chromosome Location	chr4:78283329-78283330
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10010842	0.81[EUR][1000 genomes]
rs10013386	0.81[EUR][1000 genomes]
rs10015193	0.83[AMR][1000 genomes]
rs10018010	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10031809	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11724731	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12504998	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12505793	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1962026	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1962605	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2216629	0.82[EUR][1000 genomes]
rs2866281	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2866282	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2866284	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2866285	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28827478	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28858493	0.81[EUR][1000 genomes]
rs36076516	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4359931	0.81[EUR][1000 genomes]
rs4859492	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859493	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859827	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859829	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859831	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859832	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859833	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859834	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6817200	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6825194	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6831412	0.83[EUR][1000 genomes]
rs6843922	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6856470	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7679224	0.83[AMR][1000 genomes]
rs7699246	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][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	nsv1006017	chr4:78139780-78312974	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1010450	chr4:78182037-78317840	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1004824	chr4:78188691-78312974	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1000447	chr4:78191608-78291173	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv1845782	chr4:78237955-78321598	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv829974	chr4:78240718-78415642	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1000392	chr4:78273146-78301467	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1011607	chr4:78273146-78302096	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3388448	chr4:78275408-78288612	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv822623	chr4:78275840-78287983	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv964256	chr4:78275995-78288301	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv822624	chr4:78276050-78287983	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv3442840	chr4:78277532-78309591	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78277400-78287800	Weak transcription	Fetal Thymus	thymus
2	chr4:78282800-78283400	Enhancers	H9 Cell Line	embryonic stem cell
3	chr4:78282800-78283400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:78283000-78283600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:78283200-78283400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:78283200-78283600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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