Variant report

Variant	rs11156991
Chromosome Location	chr14:38690637-38690638
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12437095	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12589603	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12887290	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6571847	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7152719	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][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	nsv916985	chr14:38052347-38838551	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
2	nsv533235	chr14:38558180-39117391	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv832773	chr14:38612778-38785003	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38688800-38691000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr14:38690200-38690800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr14:38690200-38690800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:38690200-38691600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:38690400-38691600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:38690400-38691800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr14:38690600-38690800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:38690600-38690800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr14:38690600-38690800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr14:38690600-38691000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr14:38690600-38693600	Weak transcription	H9 Cell Line	embryonic stem cell

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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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