Variant report

Variant	rs11050870
Chromosome Location	chr12:30537820-30537821
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10771705	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10771706	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10771707	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10771708	0.82[EUR][1000 genomes]
rs10843735	0.82[EUR][1000 genomes]
rs10843736	0.80[ASN][1000 genomes]
rs10843737	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10843738	0.80[ASN][1000 genomes]
rs10843739	0.80[ASN][1000 genomes]
rs11050871	0.80[ASN][1000 genomes]
rs11050872	0.80[ASN][1000 genomes]
rs11050873	0.80[ASN][1000 genomes]
rs1114354	0.80[ASN][1000 genomes]
rs1354714	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1366942	0.80[ASN][1000 genomes]
rs1366943	0.80[ASN][1000 genomes]
rs1429634	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1500107	0.80[ASN][1000 genomes]
rs1506378	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1506379	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1506380	0.80[ASN][1000 genomes]
rs1506382	0.80[ASN][1000 genomes]
rs2062997	0.81[ASN][1000 genomes]
rs2062998	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2115687	0.80[ASN][1000 genomes]
rs2163113	0.80[ASN][1000 genomes]
rs2351474	0.80[ASN][1000 genomes]
rs3843051	0.80[ASN][1000 genomes]
rs3853384	0.80[ASN][1000 genomes]
rs3853385	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4280081	0.80[ASN][1000 genomes]
rs4930922	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4931325	0.80[ASN][1000 genomes]
rs7298853	0.80[ASN][1000 genomes]
rs7306941	0.97[EUR][1000 genomes]
rs7315137	0.80[ASN][1000 genomes]
rs7968941	0.80[ASN][1000 genomes]
rs7977669	0.80[ASN][1000 genomes]
rs7978039	0.80[ASN][1000 genomes]
rs7979416	0.80[ASN][1000 genomes]
rs7979650	0.80[ASN][1000 genomes]
rs978711	1.00[AFR][1000 genomes];0.99[EUR][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	nsv832360	chr12:30393329-30555693	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	esv2754065	chr12:30499833-30560733	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 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	chr12:30537600-30539200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr12:30537800-30538600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:30537800-30538600	Enhancers	Brain Germinal Matrix	brain

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