Variant report

Variant	rs13110041
Chromosome Location	chr4:122062341-122062342
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10518383	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098605	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13106084	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13108739	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13109100	0.84[EUR][1000 genomes]
rs13116723	0.84[EUR][1000 genomes]
rs13118818	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13118913	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13138203	1.00[JPT][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1511094	0.84[EUR][1000 genomes]
rs1858291	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs2068019	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6818119	0.88[ASN][1000 genomes]
rs6828327	0.84[EUR][1000 genomes]
rs6829949	0.88[ASN][1000 genomes]
rs6833114	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6833755	0.81[ASN][1000 genomes]
rs6838000	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6839726	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6846458	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs867883	0.84[EUR][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	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1009395	chr4:121841442-122557363	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv537235	chr4:121841442-122557363	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv3386870	chr4:121867625-122208448	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv879859	chr4:121892490-122438312	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv879860	chr4:122030864-122126808	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122058600-122062800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:122058600-122063200	Enhancers	Osteobl	bone
3	chr4:122058600-122063800	Enhancers	Primary T cells from cord blood	blood
4	chr4:122058800-122063000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr4:122059400-122063000	Enhancers	NHDF-Ad	bronchial
6	chr4:122059600-122062600	Enhancers	NH-A	brain
7	chr4:122060200-122062600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:122060400-122063200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:122061800-122062600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:122061800-122066000	Weak transcription	GM12878-XiMat	blood
11	chr4:122062000-122074000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr4:122062200-122065200	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr4:122062200-122068200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr4:122062200-122071400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr4:122062200-122071800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links