Variant report

Variant	rs1276274
Chromosome Location	chr11:102556512-102556513
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10791590	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1276257	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1276275	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1276278	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1276286	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1276287	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1276288	0.98[ASN][1000 genomes]
rs1276289	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1296594	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1298740	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1940041	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1940473	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1940478	0.98[ASN][1000 genomes]
rs1940480	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2155554	0.98[ASN][1000 genomes]
rs2155555	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2464362	0.98[ASN][1000 genomes]
rs2464363	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2509029	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2509243	0.98[ASN][1000 genomes]
rs2509245	0.98[ASN][1000 genomes]
rs2701963	0.98[ASN][1000 genomes]
rs2701991	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2701992	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2701993	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs2701995	0.81[ASN][1000 genomes]
rs2845674	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2846342	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2846365	0.95[CHB][hapmap];0.89[ASN][1000 genomes]
rs2846701	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2846704	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs2846705	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs2846711	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2846715	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2846723	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2846724	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4121366	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7113003	0.82[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	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:102555200-102557200	Enhancers	HMEC	breast
2	chr11:102555400-102556600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:102555400-102557200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:102555600-102556800	Enhancers	HSMM	muscle
5	chr11:102555600-102557600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:102555600-102558200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:102556000-102556600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:102556000-102557400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr11:102556000-102557400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr11:102556000-102558200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr11:102556000-102558400	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr11:102556200-102556800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr11:102556200-102556800	Enhancers	HSMMtube	muscle
14	chr11:102556200-102556800	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr11:102556200-102557000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr11:102556200-102557200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr11:102556200-102557200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr11:102556200-102557400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr11:102556400-102556600	Enhancers	NHEK	skin

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