Variant report

Variant	rs59751131
Chromosome Location	chr22:33504182-33504183
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2195084	1.00[EUR][1000 genomes]
rs55790278	1.00[EUR][1000 genomes]
rs56220612	1.00[EUR][1000 genomes]
rs56372607	1.00[EUR][1000 genomes]
rs58050936	1.00[EUR][1000 genomes]
rs58263493	1.00[EUR][1000 genomes]
rs73881920	1.00[EUR][1000 genomes]
rs73881927	1.00[EUR][1000 genomes]
rs73881928	1.00[EUR][1000 genomes]
rs73881929	1.00[EUR][1000 genomes]
rs73881933	1.00[EUR][1000 genomes]
rs73881934	1.00[EUR][1000 genomes]
rs73881935	1.00[EUR][1000 genomes]
rs73881957	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	nsv531587	chr22:33346710-33809338	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	nsv948523	chr22:33414164-34098417	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
3	nsv1067068	chr22:33452180-33851033	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33502000-33504200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr22:33502000-33504200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr22:33502000-33505400	Weak transcription	NHDF-Ad	bronchial
4	chr22:33502000-33505800	Weak transcription	Fetal Brain Female	brain
5	chr22:33502000-33506800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr22:33502200-33504200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr22:33502200-33504200	Weak transcription	NHEK	skin
8	chr22:33502400-33504200	Weak transcription	HMEC	breast
9	chr22:33504000-33507400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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