Variant report

Variant	rs6850445
Chromosome Location	chr4:78288636-78288637
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:78287359..78291622-chr4:78351702..78357008,5	MCF-7	breast:
2	chr4:78236163..78238480-chr4:78287943..78289669,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10021013	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12502190	0.80[EUR][1000 genomes]
rs17002614	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17002672	0.83[EUR][1000 genomes]
rs1962027	0.87[EUR][1000 genomes]
rs28408985	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28659994	0.88[EUR][1000 genomes]
rs2866283	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2866286	0.80[EUR][1000 genomes]
rs28697219	0.83[ASN][1000 genomes]
rs28715173	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28771770	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28821633	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28822468	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28844066	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28886989	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4146559	0.80[EUR][1000 genomes]
rs4586976	0.88[EUR][1000 genomes]
rs4643843	0.91[AFR][1000 genomes]
rs4859826	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57255185	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57851138	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58763343	0.91[AFR][1000 genomes]
rs61389038	0.85[AFR][1000 genomes]
rs6832224	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6843981	0.81[ASN][1000 genomes]
rs72859810	0.80[AFR][1000 genomes]
rs72859841	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72859843	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72859844	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7684946	0.85[AFR][1000 genomes]
rs9307270	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78287200-78289200	Enhancers	Fetal Muscle Leg	muscle
2	chr4:78287800-78289600	Enhancers	Fetal Thymus	thymus
3	chr4:78288400-78289400	Enhancers	Primary B cells from peripheral blood	blood

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