Variant report

Variant	rs11843073
Chromosome Location	chr13:95319843-95319844
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11840596	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11840695	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11841629	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11841977	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11841993	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11843396	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16950001	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16950006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16950115	1.00[ASN][1000 genomes]
rs28376374	1.00[ASN][1000 genomes]
rs35629935	1.00[ASN][1000 genomes]
rs35973409	1.00[ASN][1000 genomes]
rs41389945	1.00[ASN][1000 genomes]
rs4773798	1.00[CHB][hapmap]
rs55691901	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55784615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55813732	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55944290	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56111318	1.00[ASN][1000 genomes]
rs56348714	1.00[ASN][1000 genomes]
rs56372959	1.00[ASN][1000 genomes]
rs56390739	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57648108	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58391484	1.00[ASN][1000 genomes]
rs61185933	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61965578	1.00[ASN][1000 genomes]
rs6492745	1.00[ASN][1000 genomes]
rs72638373	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72638377	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72638380	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72638383	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72638386	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72638401	1.00[ASN][1000 genomes]
rs7317507	1.00[ASN][1000 genomes]
rs73557817	1.00[ASN][1000 genomes]
rs7997429	1.00[CHB][hapmap]
rs9301994	1.00[ASN][1000 genomes]
rs9584248	1.00[ASN][1000 genomes]
rs9590059	1.00[ASN][1000 genomes]
rs9590075	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9590076	1.00[CHB][hapmap];1.00[ASN][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	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv832686	chr13:95206742-95400992	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95318000-95320200	Enhancers	K562	blood
2	chr13:95318800-95321200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:95319000-95322800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr13:95319400-95320000	Enhancers	Brain Substantia Nigra	brain
5	chr13:95319800-95321200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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