Variant report

Variant	rs365976
Chromosome Location	chr21:41182733-41182734
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:41180463..41183269-chr21:41209070..41212997,3	MCF-7	breast:
2	chr21:41182267..41183782-chr21:41185681..41187493,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1018350	0.82[ASN][1000 genomes]
rs1018351	0.82[ASN][1000 genomes]
rs1118102	0.82[ASN][1000 genomes]
rs1118103	0.82[ASN][1000 genomes]
rs1571713	0.82[ASN][1000 genomes]
rs2142194	0.82[ASN][1000 genomes]
rs2178882	0.82[ASN][1000 genomes]
rs2837209	0.82[ASN][1000 genomes]
rs2837211	0.82[ASN][1000 genomes]
rs2837212	0.82[ASN][1000 genomes]
rs2837216	0.82[ASN][1000 genomes]
rs455359	0.92[ASN][1000 genomes]
rs455593	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs455830	0.84[ASN][1000 genomes]
rs455942	0.86[ASN][1000 genomes]
rs456522	0.82[ASN][1000 genomes]
rs456713	0.92[ASN][1000 genomes]
rs456818	0.84[ASN][1000 genomes]
rs457488	0.91[ASN][1000 genomes]
rs458406	0.84[ASN][1000 genomes]
rs458824	0.91[ASN][1000 genomes]
rs458922	0.92[ASN][1000 genomes]
rs460549	0.84[ASN][1000 genomes]
rs460648	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs461558	0.91[ASN][1000 genomes]
rs462163	0.84[ASN][1000 genomes]
rs462555	0.84[ASN][1000 genomes]
rs463903	0.84[ASN][1000 genomes]
rs464201	0.83[ASN][1000 genomes]
rs464351	0.84[ASN][1000 genomes]
rs464574	0.84[ASN][1000 genomes]
rs464623	0.82[ASN][1000 genomes]
rs465258	0.84[ASN][1000 genomes]
rs465679	0.92[ASN][1000 genomes]
rs466303	0.84[ASN][1000 genomes]
rs466946	0.91[ASN][1000 genomes]
rs467044	0.86[ASN][1000 genomes]
rs4816657	0.82[ASN][1000 genomes]
rs4816658	0.82[ASN][1000 genomes]
rs4818091	0.82[ASN][1000 genomes]
rs94967	0.91[ASN][1000 genomes]
rs9983185	0.81[ASN][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	nsv1061454	chr21:40757973-41265404	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1057956	chr21:40907707-41393396	Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv544444	chr21:40907707-41393396	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1065086	chr21:41034806-41429078	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv544445	chr21:41034806-41429078	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv834099	chr21:41076873-41206030	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41164200-41185600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr21:41176800-41184200	Weak transcription	Fetal Brain Male	brain
3	chr21:41182000-41182800	Enhancers	Placenta	Placenta

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