Variant report

Variant	rs34856622
Chromosome Location	chr11:56658150-56658151
allele	C/T
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:15)

rs_ID	r²[population]
rs12786503	1.00[ASN][1000 genomes]
rs12797809	1.00[ASN][1000 genomes]
rs12799286	1.00[ASN][1000 genomes]
rs12804217	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12807639	1.00[ASN][1000 genomes]
rs1623065	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783466	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34250458	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66492572	1.00[ASN][1000 genomes]
rs66501822	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67301579	1.00[ASN][1000 genomes]
rs67858506	1.00[ASN][1000 genomes]
rs683563	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71495233	0.90[AMR][1000 genomes]
rs73466546	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468577	chr11:56503728-56704042	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv555101	chr11:56503728-56704042	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv469960	chr11:56605222-56704042	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1045889	chr11:56624365-56737435	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56655000-56658600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:56657200-56658200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:56657200-56658400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:56657400-56658200	Enhancers	NHEK	skin
5	chr11:56657400-56658800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:56657600-56658400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr11:56657800-56658200	Enhancers	HMEC	breast
8	chr11:56658000-56658200	Enhancers	A549	lung
9	chr11:56658000-56658600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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