Variant report

Variant	rs57328855
Chromosome Location	chr4:62631852-62631853
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs55895677	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59461758	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60293956	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61483832	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73823214	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73823219	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73823223	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73823225	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73823230	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73823237	0.84[AMR][1000 genomes]
rs73823238	0.84[AMR][1000 genomes]
rs73825907	1.00[EUR][1000 genomes]
rs73825913	1.00[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	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

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62623800-62632200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr4:62624000-62633000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr4:62624800-62632400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr4:62624800-62633400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr4:62625200-62632600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
6	chr4:62625200-62633000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr4:62625400-62632600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
8	chr4:62627800-62635800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:62631000-62633000	Transcr. at gene 5' and 3'	H9 Cell Line	embryonic stem cell
10	chr4:62631400-62632200	Transcr. at gene 5' and 3'	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:62631400-62632600	Transcr. at gene 5' and 3'	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:62631400-62635600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:62631600-62633000	Active TSS	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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