Variant report

Variant	rs11903539
Chromosome Location	chr2:205461753-205461754
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10181861	1.00[EUR][1000 genomes]
rs10185786	0.88[YRI][hapmap]
rs10203606	0.91[YRI][hapmap]
rs10203725	0.86[ASN][1000 genomes]
rs10932074	0.88[YRI][hapmap]
rs10932075	0.88[YRI][hapmap]
rs10932076	1.00[ASN][1000 genomes]
rs11883548	0.91[ASN][1000 genomes]
rs11887897	0.93[ASN][1000 genomes]
rs11892599	0.86[ASN][1000 genomes]
rs11901243	0.91[ASN][1000 genomes]
rs11904034	0.92[ASN][1000 genomes]
rs11904833	0.86[ASN][1000 genomes]
rs12052242	1.00[ASN][1000 genomes]
rs13412566	0.81[ASN][1000 genomes]
rs13414039	0.86[ASN][1000 genomes]
rs13418573	0.92[YRI][hapmap]
rs16836318	1.00[EUR][1000 genomes]
rs16836406	0.95[ASN][1000 genomes]
rs16836425	0.87[ASN][1000 genomes]
rs16836499	1.00[EUR][1000 genomes]
rs28368645	1.00[EUR][1000 genomes]
rs55775811	0.93[ASN][1000 genomes]
rs56086550	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56310794	0.93[ASN][1000 genomes]
rs57533510	0.91[ASN][1000 genomes]
rs57675666	0.97[ASN][1000 genomes]
rs59978061	0.89[ASN][1000 genomes]
rs60179096	0.97[ASN][1000 genomes]
rs60317037	0.87[ASN][1000 genomes]
rs61280844	0.80[ASN][1000 genomes]
rs61427199	1.00[EUR][1000 genomes]
rs6706016	1.00[EUR][1000 genomes]
rs6731832	0.93[ASN][1000 genomes]
rs6742319	1.00[EUR][1000 genomes]
rs6743145	1.00[EUR][1000 genomes]
rs6743282	0.88[ASN][1000 genomes]
rs6749339	0.96[YRI][hapmap];0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6753180	1.00[EUR][1000 genomes]
rs6753277	1.00[EUR][1000 genomes]
rs73057231	1.00[EUR][1000 genomes]
rs73057275	0.84[ASN][1000 genomes]
rs73057279	0.86[ASN][1000 genomes]
rs73057288	1.00[EUR][1000 genomes]
rs73057289	0.84[ASN][1000 genomes]
rs73059006	0.97[ASN][1000 genomes]
rs73059007	0.97[ASN][1000 genomes]
rs73059010	0.97[ASN][1000 genomes]
rs73059013	0.87[ASN][1000 genomes]
rs73059018	0.93[ASN][1000 genomes]
rs73059031	0.91[ASN][1000 genomes]
rs73984241	0.86[ASN][1000 genomes]
rs73984246	0.97[ASN][1000 genomes]
rs73984251	0.91[ASN][1000 genomes]
rs73984252	0.94[ASN][1000 genomes]
rs73984257	0.91[ASN][1000 genomes]
rs73984258	0.91[ASN][1000 genomes]
rs7557006	0.97[ASN][1000 genomes]
rs7570984	0.88[ASN][1000 genomes]
rs7575842	0.95[ASN][1000 genomes]
rs7577949	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv964353	chr2:205303005-205473935	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205459400-205462600	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:205461400-205461800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:205461400-205461800	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr2:205461400-205468800	Weak transcription	Aorta	Aorta

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