Variant report

Variant	rs59249377
Chromosome Location	chr9:100526068-100526069
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs56213410	1.00[AMR][1000 genomes]
rs57246563	1.00[AMR][1000 genomes]
rs60705728	1.00[AMR][1000 genomes]
rs73655166	1.00[AMR][1000 genomes]
rs73655167	1.00[AMR][1000 genomes]
rs73655168	1.00[AMR][1000 genomes]
rs73655169	1.00[AMR][1000 genomes]
rs73655171	1.00[AMR][1000 genomes]
rs73655173	1.00[AMR][1000 genomes]
rs73655174	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043753	chr9:100458109-100599265	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv614934	chr9:100482976-100550253	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr9:100522400-100526200	Weak transcription	Right Atrium	heart
2	chr9:100523600-100527800	Weak transcription	Hela-S3	cervix
3	chr9:100524000-100526600	Enhancers	Fetal Intestine Small	intestine
4	chr9:100524000-100526800	Enhancers	Fetal Intestine Large	intestine
5	chr9:100525600-100528600	Weak transcription	Esophagus	oesophagus
6	chr9:100526000-100526600	Enhancers	HSMMtube	muscle

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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