Variant report

Variant	rs11955266
Chromosome Location	chr5:100761407-100761408
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11950545	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11950589	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11953880	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs17135627	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs17135637	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs17135652	0.81[AMR][1000 genomes]
rs1874171	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56224357	0.86[AMR][1000 genomes]
rs57173603	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs58107650	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs59761964	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs60091140	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165903	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165909	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165913	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165919	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165921	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165923	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165924	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73165925	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7444022	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462320	chr5:100247554-100775607	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv599176	chr5:100247554-100775607	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv528811	chr5:100424081-101218087	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1032191	chr5:100455166-100852106	Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv516292	chr5:100490972-100925684	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv882479	chr5:100587626-100941372	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv599179	chr5:100609923-100826324	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2755981	chr5:100633738-100830395	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv882490	chr5:100640721-100826324	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1026979	chr5:100714105-100761775	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1026990	chr5:100718781-100761775	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1035047	chr5:100719864-100761775	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1023977	chr5:100719864-100766804	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1033577	chr5:100722701-100761775	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1017670	chr5:100722701-100766804	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv1026104	chr5:100723151-100761775	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1024075	chr5:100756024-100822258	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv432792	chr5:100756024-100867529	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:100759400-100762800	Enhancers	NHDF-Ad	bronchial
2	chr5:100759600-100761600	Enhancers	HSMMtube	muscle
3	chr5:100759600-100762600	Enhancers	Osteobl	bone
4	chr5:100759800-100761600	Enhancers	NH-A	brain
5	chr5:100760000-100762000	Enhancers	HSMM	muscle
6	chr5:100760200-100762400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:100760400-100761600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:100761000-100761600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:100761000-100762600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:100761000-100762600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr5:100761200-100761600	Enhancers	Fetal Lung	lung
12	chr5:100761200-100763000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:100761400-100761600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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