Variant report

Variant	rs10207233
Chromosome Location	chr2:67891498-67891499
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10171129	0.85[CEU][hapmap];0.95[EUR][1000 genomes]
rs10182480	0.93[EUR][1000 genomes]
rs10191839	0.93[CEU][hapmap];0.95[EUR][1000 genomes]
rs10194664	0.93[CEU][hapmap];0.95[EUR][1000 genomes]
rs10195055	0.96[CEU][hapmap];0.95[EUR][1000 genomes]
rs10195947	0.93[CEU][hapmap];0.95[EUR][1000 genomes]
rs10196069	0.93[CEU][hapmap];0.95[EUR][1000 genomes]
rs10197255	0.82[ASN][1000 genomes]
rs10204184	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10205913	0.94[EUR][1000 genomes]
rs10210853	0.89[CEU][hapmap];0.95[EUR][1000 genomes]
rs11675524	0.95[EUR][1000 genomes]
rs11675630	0.94[EUR][1000 genomes]
rs11681312	0.94[EUR][1000 genomes]
rs11688644	0.92[CEU][hapmap]
rs12476951	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13406813	0.96[EUR][1000 genomes]
rs13429296	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1367461	0.96[CEU][hapmap]
rs1978658	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1991639	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2099214	0.82[ASN][1000 genomes]
rs2116049	0.95[EUR][1000 genomes]
rs2116054	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2163366	0.95[EUR][1000 genomes]
rs2861706	0.82[ASN][1000 genomes]
rs35307778	0.95[EUR][1000 genomes]
rs4671821	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4671825	0.95[EUR][1000 genomes]
rs4671826	0.95[EUR][1000 genomes]
rs55748027	0.94[ASN][1000 genomes]
rs56209192	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62155360	0.95[EUR][1000 genomes]
rs6718114	0.94[EUR][1000 genomes]
rs7608093	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9309403	0.92[CEU][hapmap];0.94[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	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv1007345	chr2:67870225-67980094	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67888600-67893200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:67888800-67893400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr2:67891000-67893400	Weak transcription	Fetal Stomach	stomach
4	chr2:67891200-67893200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr2:67891400-67893400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:67891400-67893600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:67891400-67894600	Weak transcription	Aorta	Aorta

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