Variant report

Variant	rs73596902
Chromosome Location	chr14:24301216-24301217
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10130987	1.00[EUR][1000 genomes]
rs10131931	1.00[EUR][1000 genomes]
rs10132842	1.00[EUR][1000 genomes]
rs10132966	1.00[EUR][1000 genomes]
rs10137220	1.00[EUR][1000 genomes]
rs10139119	1.00[EUR][1000 genomes]
rs10145403	1.00[EUR][1000 genomes]
rs10145429	1.00[EUR][1000 genomes]
rs10149177	1.00[EUR][1000 genomes]
rs10149300	1.00[EUR][1000 genomes]
rs10149833	1.00[EUR][1000 genomes]
rs10438148	1.00[EUR][1000 genomes]
rs10467814	1.00[EUR][1000 genomes]
rs12898165	1.00[EUR][1000 genomes]
rs28386964	1.00[EUR][1000 genomes]
rs28395171	1.00[EUR][1000 genomes]
rs28570572	1.00[EUR][1000 genomes]
rs55679614	1.00[EUR][1000 genomes]
rs57963483	1.00[EUR][1000 genomes]
rs61750885	1.00[EUR][1000 genomes]
rs7145419	1.00[EUR][1000 genomes]
rs73600731	1.00[EUR][1000 genomes]
rs8003140	1.00[EUR][1000 genomes]
rs9323414	1.00[EUR][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	nsv1043299	chr14:23766696-24351724	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	esv3405661	chr14:24189883-24670942	Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription 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	131 gene(s)	inside rSNPs	diseases
3	nsv564045	chr14:24224245-24348343	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv901494	chr14:24243637-24386159	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr14:24295800-24302000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:24296400-24302000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr14:24296400-24302000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr14:24296600-24301800	Enhancers	HSMM	muscle
5	chr14:24297400-24301600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr14:24299200-24302000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:24300200-24302000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:24300400-24301400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
9	chr14:24300400-24301600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr14:24300400-24302000	Enhancers	Primary hematopoietic stem cells	blood
11	chr14:24300600-24301400	Enhancers	Primary T cells from cord blood	blood
12	chr14:24300600-24301400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr14:24301000-24301400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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Input of quick search could be:

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

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