Variant report

Variant	rs2445098
Chromosome Location	chr11:106861552-106861553
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11211991	0.81[EUR][1000 genomes]
rs1455600	0.82[EUR][1000 genomes]
rs1982496	0.89[EUR][1000 genomes]
rs2445099	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465779	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465780	0.98[ASN][1000 genomes]
rs2510595	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2510596	0.86[EUR][1000 genomes]
rs2510597	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2510598	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2510599	0.83[EUR][1000 genomes]
rs2510600	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2510601	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2513106	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2513108	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2513109	0.88[EUR][1000 genomes]
rs2513137	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2513138	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2513142	0.87[EUR][1000 genomes]
rs3133355	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66521669	0.83[EUR][1000 genomes]
rs7109634	0.80[EUR][1000 genomes]
rs7110185	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7116468	0.80[EUR][1000 genomes]
rs7127697	0.83[EUR][1000 genomes]
rs7932141	0.97[ASN][1000 genomes]
rs7938459	0.81[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531938	chr11:106760733-107156814	Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106855000-106868400	Weak transcription	Brain Angular Gyrus	brain
2	chr11:106857600-106861600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:106858200-106861600	Enhancers	Fetal Heart	heart
4	chr11:106860800-106862200	Enhancers	Fetal Muscle Leg	muscle
5	chr11:106861000-106861600	Enhancers	Fetal Brain Male	brain
6	chr11:106861000-106862000	Enhancers	Fetal Muscle Trunk	muscle
7	chr11:106861200-106861600	Enhancers	Fetal Brain Female	brain
8	chr11:106861200-106861800	Weak transcription	Placenta	Placenta
9	chr11:106861200-106869400	Weak transcription	NHLF	lung
10	chr11:106861400-106862200	Weak transcription	NHDF-Ad	bronchial
11	chr11:106861400-106862800	Enhancers	Fetal Lung	lung
12	chr11:106861400-106866400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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