Variant report

Variant	rs28901618
Chromosome Location	chr2:234842087-234842088
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11562956	0.85[YRI][hapmap]
rs11562977	0.93[CHB][hapmap];0.90[JPT][hapmap];0.85[YRI][hapmap];1.00[EUR][1000 genomes]
rs11563214	0.81[CHB][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs11563218	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12617866	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12620352	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1468521	1.00[EUR][1000 genomes]
rs16849914	0.83[YRI][hapmap]
rs2362291	0.93[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28900710	0.85[YRI][hapmap]
rs28900713	0.85[YRI][hapmap]
rs28901579	1.00[EUR][1000 genomes]
rs28901582	1.00[EUR][1000 genomes]
rs28901591	0.93[CHB][hapmap];0.83[JPT][hapmap];0.85[YRI][hapmap];1.00[EUR][1000 genomes]
rs28901600	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28901608	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs28901610	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28901615	1.00[EUR][1000 genomes]
rs28901629	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28901630	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs28901637	1.00[YRI][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28901868	0.81[CHB][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs28902174	0.83[EUR][1000 genomes]
rs4663342	1.00[CHB][hapmap];0.81[JPT][hapmap];0.85[YRI][hapmap];0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4663343	0.81[CHB][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs4663989	1.00[CHB][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7602303	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs9789366	0.93[CHB][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap];1.00[EUR][1000 genomes]
rs9789398	0.93[CHB][hapmap];0.90[JPT][hapmap];0.85[YRI][hapmap];1.00[EUR][1000 genomes]
rs9789675	0.93[CHB][hapmap];0.82[JPT][hapmap];0.85[YRI][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 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	chr2:234841000-234844800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:234841800-234847600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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