Variant report

Variant	rs11713185
Chromosome Location	chr3:161111357-161111358
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11710086	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11710916	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1349352	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1450522	0.82[CHB][hapmap]
rs16832246	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16832279	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1811483	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1839491	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2054710	0.82[CHB][hapmap]
rs2061804	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2404341	0.91[CHB][hapmap]
rs2404342	0.85[CHB][hapmap]
rs34727114	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs404725	0.96[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs456882	0.86[ASN][1000 genomes]
rs458175	0.85[ASN][1000 genomes]
rs460950	0.86[ASN][1000 genomes]
rs463630	0.86[ASN][1000 genomes]
rs463890	0.85[ASN][1000 genomes]
rs466971	0.85[ASN][1000 genomes]
rs467458	0.86[ASN][1000 genomes]
rs67077657	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73021449	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7627320	0.91[JPT][hapmap]
rs9816665	0.90[JPT][hapmap]
rs9836881	0.91[JPT][hapmap]
rs9836887	0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv877710	chr3:161087857-161245414	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11713185	SPTSSB	cis	Thyroid	GTEx

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161107800-161112800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:161108000-161111400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr3:161108200-161111800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr3:161108600-161111600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:161108800-161114400	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr3:161110000-161112400	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr3:161110000-161112600	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr3:161110000-161114600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr3:161110200-161112600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr3:161110200-161113200	Enhancers	Stomach Mucosa	stomach
11	chr3:161110200-161114400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr3:161110200-161114600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr3:161110600-161111800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr3:161110600-161112000	Enhancers	HepG2	liver
15	chr3:161110600-161112400	Enhancers	Fetal Lung	lung
16	chr3:161110600-161112600	Enhancers	Primary T cells from cord blood	blood
17	chr3:161110800-161111600	Enhancers	Liver	Liver
18	chr3:161110800-161112000	Weak transcription	Gastric	stomach
19	chr3:161110800-161113600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr3:161111200-161113400	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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