Variant report

Variant	rs11590933
Chromosome Location	chr1:47929878-47929879
allele	G/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:16)

rs_ID	r²[population]
rs12239450	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17103227	0.85[ASN][1000 genomes]
rs17103249	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17103260	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2279277	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3738316	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55806846	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55834028	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56011601	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56235005	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59586402	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61412699	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6695969	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72686267	0.80[ASN][1000 genomes]
rs72686279	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72686288	0.98[EUR][1000 genomes];1.00[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	nsv1001779	chr1:47884229-48111485	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv871299	chr1:47889417-48057890	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv2755190	chr1:47907580-48048680	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr1:47925800-47934200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:47929600-47930000	Enhancers	Fetal Intestine Small	intestine

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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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