Variant report

Variant	rs4818096
Chromosome Location	chr21:41154764-41154765
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1018350	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs1018351	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs11088495	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1118102	0.85[ASN][1000 genomes]
rs1118103	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs11701338	0.82[CEU][hapmap]
rs1571713	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs2142194	0.85[ASN][1000 genomes]
rs2178882	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs2205205	0.86[CEU][hapmap]
rs2837209	0.85[ASN][1000 genomes]
rs2837211	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs2837212	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs2837216	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs2837218	0.82[CEU][hapmap]
rs2837220	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2837223	0.81[CEU][hapmap];0.82[YRI][hapmap]
rs2837224	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2837225	0.81[CEU][hapmap]
rs2837227	0.81[CEU][hapmap]
rs2837229	0.81[CEU][hapmap]
rs455830	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs455942	0.82[ASN][1000 genomes]
rs456522	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs456818	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs457569	0.89[JPT][hapmap]
rs458406	0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs460549	0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs462163	0.84[ASN][1000 genomes]
rs462555	0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs463903	0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs464201	0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs464351	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs464574	0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs464623	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs465258	0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs466303	0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs467044	0.82[ASN][1000 genomes]
rs4816657	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs4816658	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs4818088	0.81[CEU][hapmap]
rs4818091	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs4818093	0.83[JPT][hapmap]
rs7278733	0.86[CEU][hapmap]
rs760285	0.81[CEU][hapmap]
rs9983185	0.89[JPT][hapmap];0.83[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41149400-41160400	Weak transcription	Placenta	Placenta
2	chr21:41154600-41155000	Enhancers	Fetal Heart	heart

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