Variant report

Variant	rs1535278
Chromosome Location	chr6:26481317-26481318
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs15580	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes]
rs1741738	0.82[CHB][hapmap]
rs1796519	1.00[CHB][hapmap]
rs1796524	1.00[CEU][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2145319	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2224379	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3736780	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3864291	1.00[JPT][hapmap]
rs4713007	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes]
rs6905163	0.83[AMR][1000 genomes]
rs6911330	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6927012	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929908	0.90[MKK][hapmap]
rs7745632	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap]
rs9366661	0.89[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	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
4	nsv482836	chr6:26352883-26520964	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv482407	chr6:26369320-26550148	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
6	nsv1031938	chr6:26467182-26501897	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs1535278	RP11-457M11.5	cis	Adipose Subcutaneous	GTEx
rs1535278	RP11-457M11.5	cis	Thyroid	GTEx
rs1535278	ABT1	cis	cerebellum	SCAN
rs1535278	HIST1H4F	cis	cerebellum	SCAN
rs1535278	RP11-457M11.5	cis	Esophagus Mucosa	GTEx
rs1535278	HIST1H2BN	cis	parietal	SCAN
rs1535278	ZSCAN23	cis	cerebellum	SCAN
rs1535278	HMGN4	cis	parietal	SCAN
rs1535278	RP11-457M11.5	cis	Artery Aorta	GTEx
rs1535278	RP11-457M11.5	cis	lung	GTEx
rs1535278	HIST1H3E	cis	parietal	SCAN

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26475200-26481800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:26475600-26481400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:26476600-26489200	Weak transcription	Stomach Mucosa	stomach
4	chr6:26478000-26482200	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr6:26478800-26485200	Weak transcription	Small Intestine	intestine
6	chr6:26479200-26483800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:26479200-26484200	Weak transcription	Fetal Intestine Large	intestine
8	chr6:26479200-26484200	Weak transcription	Fetal Intestine Small	intestine
9	chr6:26479600-26483000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:26479600-26483200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr6:26481000-26481600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr6:26481000-26481800	Enhancers	HepG2	liver
13	chr6:26481200-26481600	Enhancers	GM12878-XiMat	blood
14	chr6:26481200-26481600	ZNF genes & repeats	K562	blood
15	chr6:26481200-26481800	Enhancers	Primary B cells from peripheral blood	blood

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

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