Variant report

Variant	rs692024
Chromosome Location	chr19:39600881-39600882
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:39600198..39604538-chr19:39898809..39902716,7	MCF-7	breast:
2	chr19:39599295..39601915-chr19:39625074..39628012,2	MCF-7	breast:
3	chr19:39542686..39543478-chr19:39600712..39601594,2	MCF-7	breast:
4	chr19:39599349..39603430-chr19:39902751..39905281,3	MCF-7	breast:
5	chr11:71157965..71160318-chr19:39600785..39602620,2	MCF-7	breast:
6	chr19:39600818..39603608-chr19:39896434..39898280,2	MCF-7	breast:
7	chr19:39595170..39597829-chr19:39598452..39601203,2	MCF-7	breast:
8	chr19:39543748..39546255-chr19:39599767..39602313,2	MCF-7	breast:
9	chr19:39600694..39601279-chr19:39688408..39689109,2	MCF-7	breast:
10	chr19:39600064..39604229-chr19:39615105..39621950,11	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000172893	Chromatin interaction
ENSG00000090924	Chromatin interaction
ENSG00000266559	Chromatin interaction
ENSG00000128016	Chromatin interaction
ENSG00000269172	Chromatin interaction
ENSG00000254682	Chromatin interaction
ENSG00000130669	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2247813	0.83[AFR][1000 genomes]
rs691662	1.00[AMR][1000 genomes]
rs691765	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs692059	0.89[AFR][1000 genomes]
rs7253778	0.85[AFR][1000 genomes]
rs774914	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv458571	chr19:39533754-39628050	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv579508	chr19:39533754-39628050	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1067028	chr19:39567228-39622846	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1060469	chr19:39567228-39624790	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv833829	chr19:39569681-39730777	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv432048	chr19:39572060-39850060	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39575800-39601200	Weak transcription	HMEC	breast
2	chr19:39590400-39602800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr19:39597400-39601000	Weak transcription	Brain Angular Gyrus	brain
4	chr19:39597400-39601000	Weak transcription	Brain Hippocampus Middle	brain
5	chr19:39597600-39602600	Weak transcription	Brain Anterior Caudate	brain
6	chr19:39597800-39601000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr19:39597800-39601200	Weak transcription	Brain Substantia Nigra	brain
8	chr19:39597800-39603000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr19:39600400-39603200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr19:39600600-39601400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr19:39600600-39601600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr19:39600800-39601000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr19:39600800-39601600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr19:39600800-39601800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr19:39600800-39602600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr19:39600800-39602600	Enhancers	A549	lung
17	chr19:39600800-39606800	Enhancers	Placenta	Placenta

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

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