Variant report

Variant	rs11176568
Chromosome Location	chr12:67479571-67479572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10878556	0.89[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11176554	1.00[AMR][1000 genomes]
rs11176570	1.00[EUR][1000 genomes]
rs11176571	1.00[EUR][1000 genomes]
rs12303485	1.00[AMR][1000 genomes]
rs1392585	1.00[EUR][1000 genomes]
rs7300852	1.00[ASW][hapmap]
rs7302001	1.00[EUR][1000 genomes]
rs7314755	1.00[ASW][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs73318948	1.00[AMR][1000 genomes]
rs73318965	1.00[AMR][1000 genomes]
rs73318996	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73320977	1.00[EUR][1000 genomes]
rs7968685	1.00[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	nsv541524	chr12:67311057-67700349	Strong transcription Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv559212	chr12:67373549-67850925	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv899217	chr12:67472631-67501987	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67476800-67482200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr12:67478000-67482200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:67479000-67480000	Enhancers	Fetal Kidney	kidney
4	chr12:67479200-67479600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:67479200-67480000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr12:67479400-67479600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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