Variant report

Variant	rs641792
Chromosome Location	chr10:27747061-27747062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11015796	0.94[EUR][1000 genomes]
rs2478251	0.89[ASN][1000 genomes]
rs2484203	0.89[ASN][1000 genomes]
rs2484204	0.89[ASN][1000 genomes]
rs2505321	0.90[ASN][1000 genomes]
rs72810095	0.85[ASN][1000 genomes]
rs9418630	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8614	chr10:27504487-27828406	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv1045257	chr10:27572440-27926946	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv1053952	chr10:27659365-27915029	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	esv2750890	chr10:27669479-27774501	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27740000-27750000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:27742600-27752600	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr10:27743600-27749000	Weak transcription	Primary B cells from cord blood	blood
4	chr10:27746000-27748400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr10:27746600-27747600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:27746600-27747600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:27746600-27747600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr10:27746600-27747800	Enhancers	Primary hematopoietic stem cells	blood
9	chr10:27746600-27747800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:27746800-27747400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr10:27746800-27747600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr10:27746800-27747600	Enhancers	Fetal Thymus	thymus
13	chr10:27746800-27747800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr10:27746800-27748000	Enhancers	Primary T cells from cord blood	blood
15	chr10:27747000-27747600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr10:27747000-27747600	Enhancers	Thymus	Thymus

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

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