Variant report

Variant	rs73823232
Chromosome Location	chr4:62640879-62640880
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs55895677	0.84[AMR][1000 genomes]
rs57569125	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823230	0.89[AMR][1000 genomes]
rs73823231	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823233	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823236	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73823237	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73823238	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv829949	chr4:62615637-62761629	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv980206	chr4:62639183-62641506	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62637000-62641000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr4:62637600-62641200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:62637600-62656000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:62640000-62641200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:62640400-62641000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:62640400-62641600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:62640600-62641000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:62640600-62641200	Enhancers	Fetal Brain Male	brain
9	chr4:62640800-62641000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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