Variant report

Variant	rs7952071
Chromosome Location	chr11:59226225-59226226
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1026320	0.84[EUR][1000 genomes]
rs10736699	0.89[EUR][1000 genomes]
rs10750922	0.85[EUR][1000 genomes]
rs10896974	0.89[EUR][1000 genomes]
rs11229957	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11229958	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11602856	0.84[EUR][1000 genomes]
rs11604216	0.85[EUR][1000 genomes]
rs11605288	0.84[EUR][1000 genomes]
rs11605552	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11606927	0.84[EUR][1000 genomes]
rs11606980	0.83[EUR][1000 genomes]
rs12420159	0.85[EUR][1000 genomes]
rs12785234	0.85[EUR][1000 genomes]
rs1349777	0.84[EUR][1000 genomes]
rs1453541	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1453542	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1453544	0.86[EUR][1000 genomes]
rs1453547	0.83[EUR][1000 genomes]
rs1453549	0.84[EUR][1000 genomes]
rs1453550	0.84[EUR][1000 genomes]
rs1453551	0.84[EUR][1000 genomes]
rs1453552	0.85[EUR][1000 genomes]
rs17500478	0.86[EUR][1000 genomes]
rs17591107	0.86[EUR][1000 genomes]
rs1879929	0.85[EUR][1000 genomes]
rs1901855	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1901856	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2167923	0.82[EUR][1000 genomes]
rs2867731	0.88[EUR][1000 genomes]
rs2867748	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35630700	0.85[EUR][1000 genomes]
rs4939291	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61901576	0.85[EUR][1000 genomes]
rs61901620	0.86[EUR][1000 genomes]
rs61902559	0.85[EUR][1000 genomes]
rs6591536	0.89[EUR][1000 genomes]
rs7119928	0.87[EUR][1000 genomes]
rs7120797	0.87[EUR][1000 genomes]
rs7935959	0.84[EUR][1000 genomes]
rs7941591	0.88[EUR][1000 genomes]
rs7943953	0.89[EUR][1000 genomes]
rs7947471	0.88[EUR][1000 genomes]
rs896877	0.88[EUR][1000 genomes]
rs896878	0.88[EUR][1000 genomes]
rs9665874	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9787928	0.85[EUR][1000 genomes]
rs9988851	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046084	chr11:59034871-59314519	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv975342	chr11:59203908-59237268	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59224000-59226600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:59224200-59229800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:59224400-59230600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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