Variant report

Variant	rs923547
Chromosome Location	chr1:151822003-151822004
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 12 )

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

rs_ID	r²[population]
rs1056037	0.86[CHB][hapmap];0.87[ASN][1000 genomes]
rs1129117	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12567049	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12727170	0.80[CHD][hapmap]
rs16833584	0.95[CEU][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16833599	0.89[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16833604	1.00[CEU][hapmap];0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2279503	0.86[CHB][hapmap];0.84[CHD][hapmap];0.87[ASN][1000 genomes]
rs2879130	1.00[CEU][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap];0.85[MEX][hapmap];0.95[TSI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4845624	0.86[CHB][hapmap];0.81[CHD][hapmap]
rs60166269	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61815147	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6587625	0.87[ASW][hapmap];0.95[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7524706	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7556386	0.81[CHB][hapmap];0.80[CHD][hapmap];0.86[ASN][1000 genomes]
rs923548	0.93[YRI][hapmap]
rs998500	0.83[ASN][1000 genomes]
rs998501	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1804657	chr1:151784152-151825756	Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv1008033	chr1:151785029-151843154	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs923547	PLEKHO1	cis	cerebellum	SCAN
rs923547	THEM4	cis	cerebellum	SCAN
rs923547	S100A10	cis	lymphoblastoid	seeQTL
rs923547	SELENBP1	cis	parietal	SCAN
rs923547	LCE2C	cis	cerebellum	SCAN
rs923547	NPR1	cis	parietal	SCAN
rs923547	THEM4	cis	parietal	SCAN
rs923547	THEM4	cis	lymphoblastoid	seeQTL
rs923547	OTUD7B	cis	cerebellum	SCAN
rs923547	S100A10	cis	cerebellum	SCAN
rs923547	C1orf230	cis	cerebellum	SCAN
rs923547	S100A14	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151813400-151828600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr1:151814800-151827400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr1:151818400-151824400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:151819200-151825200	Weak transcription	Gastric	stomach
5	chr1:151819200-151827200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:151819200-151847600	Weak transcription	Thymus	Thymus
7	chr1:151820000-151825800	Weak transcription	Hela-S3	cervix
8	chr1:151820400-151822400	Enhancers	Primary hematopoietic stem cells	blood
9	chr1:151820400-151822400	Enhancers	Fetal Lung	lung
10	chr1:151820600-151827200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:151820800-151822200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:151820800-151822200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:151821000-151823600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:151821000-151830600	Weak transcription	Right Atrium	heart
15	chr1:151821400-151832400	Weak transcription	Spleen	Spleen
16	chr1:151821600-151824800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:151821600-151845600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr1:151821800-151825000	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr1:151822000-151822800	Enhancers	Lung	lung

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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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