Variant report

Variant	rs56985814
Chromosome Location	chr11:36346840-36346841
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11033549	1.00[EUR][1000 genomes]
rs11033553	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11033554	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11033560	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033564	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11033565	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1160014	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1160015	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12099418	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12363040	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12364237	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58248666	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73443133	1.00[EUR][1000 genomes]
rs73443135	1.00[EUR][1000 genomes]
rs73443138	1.00[EUR][1000 genomes]
rs7931498	1.00[ASN][1000 genomes]
rs7931590	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	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 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	chr11:36341200-36348400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr11:36341400-36355800	Weak transcription	Brain Substantia Nigra	brain
3	chr11:36342200-36348200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:36346400-36347000	Active TSS	K562	blood
5	chr11:36346800-36347000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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