Variant report

Variant	rs56285930
Chromosome Location	chr3:151042970-151042971
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13325434	1.00[AMR][1000 genomes]
rs56956775	1.00[AMR][1000 genomes]
rs59666614	1.00[AMR][1000 genomes]
rs61576895	1.00[AMR][1000 genomes]
rs73869062	1.00[AMR][1000 genomes]
rs73869065	1.00[AMR][1000 genomes]
rs73869136	1.00[AMR][1000 genomes]
rs73869148	1.00[AMR][1000 genomes]
rs73869172	1.00[AMR][1000 genomes]
rs73869175	1.00[AMR][1000 genomes]
rs73869184	1.00[AMR][1000 genomes]
rs73869190	1.00[AMR][1000 genomes]
rs73869191	1.00[AMR][1000 genomes]
rs73869193	1.00[AMR][1000 genomes]
rs73869195	1.00[AMR][1000 genomes]
rs73869200	1.00[AMR][1000 genomes]
rs73872011	1.00[AMR][1000 genomes]
rs9876933	1.00[ASN][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	nsv460894	chr3:150770614-151095093	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv592045	chr3:150770614-151095093	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv2754555	chr3:150968302-151054302	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151002600-151044000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:151036000-151044600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr3:151036200-151043000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:151036600-151045200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:151037200-151044000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr3:151038800-151046400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr3:151039000-151045200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr3:151039000-151045200	Weak transcription	NHEK	skin
9	chr3:151039000-151045200	Weak transcription	NHLF	lung
10	chr3:151039200-151045200	Weak transcription	Hela-S3	cervix
11	chr3:151039600-151043600	Weak transcription	Adipose Nuclei	Adipose
12	chr3:151039800-151045200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr3:151040200-151043400	Weak transcription	Primary B cells from cord blood	blood
14	chr3:151041800-151045000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:151042400-151045000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:151042400-151045200	Weak transcription	HMEC	breast
17	chr3:151042600-151043000	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr3:151042600-151044400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:151042600-151046200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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