Variant report

Variant	rs4938741
Chromosome Location	chr11:119827163-119827164
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10790357	0.90[ASN][1000 genomes]
rs10790359	0.82[ASN][1000 genomes]
rs10790360	0.82[ASN][1000 genomes]
rs10892504	0.90[ASN][1000 genomes]
rs11217601	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1787024	0.88[ASN][1000 genomes]
rs1944504	0.82[ASN][1000 genomes]
rs1944505	0.90[ASN][1000 genomes]
rs4245210	0.86[ASN][1000 genomes]
rs626466	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs636518	0.85[ASN][1000 genomes]
rs651055	0.84[ASN][1000 genomes]
rs6589784	0.82[ASN][1000 genomes]
rs731392	0.90[ASN][1000 genomes]
rs731393	0.90[ASN][1000 genomes]
rs7944850	0.82[ASN][1000 genomes]
rs7951479	0.90[ASN][1000 genomes]
rs7951593	0.82[ASN][1000 genomes]
rs949096	0.90[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	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv832285	chr11:119789595-119957724	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119817200-119835600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:119826600-119827400	Weak transcription	iPS DF 19.11 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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