Variant report

Variant	rs4289096
Chromosome Location	chr19:52056539-52056540
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17660319	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73067342	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066308	chr19:51680133-52103974	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv544049	chr19:51680133-52103974	Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
3	nsv544051	chr19:51944903-52147459	Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers 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	26 gene(s)	inside rSNPs	diseases
4	esv2758504	chr19:51991896-52266700	Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	542 gene(s)	inside rSNPs	diseases
5	esv2758767	chr19:51991896-52604625	Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	578 gene(s)	inside rSNPs	diseases
6	nsv469584	chr19:52001381-52151821	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv482654	chr19:52001381-52151821	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52048800-52058000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr19:52054000-52057000	Flanking Active TSS	Primary B cells from cord blood	blood
3	chr19:52054600-52056800	Flanking Active TSS	Primary B cells from peripheral blood	blood
4	chr19:52055600-52056600	Active TSS	K562	blood
5	chr19:52056200-52056600	Active TSS	H9 Cell Line	embryonic stem cell
6	chr19:52056400-52056600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr19:52056400-52056600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
8	chr19:52056400-52056600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr19:52056400-52056600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:52056400-52056600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:52056400-52056600	Enhancers	Placenta	Placenta
12	chr19:52056400-52056600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
13	chr19:52056400-52056800	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr19:52056400-52056800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
15	chr19:52056400-52056800	Bivalent/Poised TSS	Fetal Brain Female	brain
16	chr19:52056400-52056800	Enhancers	Spleen	Spleen
17	chr19:52056400-52057000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
18	chr19:52056400-52057000	Bivalent/Poised TSS	Brain Germinal Matrix	brain

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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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