Variant report

Variant	rs132308
Chromosome Location	chr22:29559157-29559158
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs132311	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs132312	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs132313	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs132314	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.97[EUR][1000 genomes]
rs132315	0.97[EUR][1000 genomes]
rs132316	0.97[EUR][1000 genomes]
rs132317	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs132321	0.97[EUR][1000 genomes]
rs132323	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs132341	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs132348	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs132350	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs132351	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs132354	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs132363	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs132366	1.00[CEU][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs132367	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs132370	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs132373	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs132377	1.00[CEU][hapmap]
rs132378	0.85[EUR][1000 genomes]
rs132379	0.82[CEU][hapmap]
rs132380	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs132382	1.00[CEU][hapmap]
rs132386	1.00[CEU][hapmap]
rs469984	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs469985	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs713924	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.97[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531586	chr22:29252132-29902266	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv524483	chr22:29525126-29630337	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv817986	chr22:29540297-29568963	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	8 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	chr22:29551200-29561400	Weak transcription	Dnd41	blood
2	chr22:29554600-29563400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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