Variant report

Variant	rs1288088
Chromosome Location	chr6:119790051-119790052
allele	A/G
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:14)

rs_ID	r²[population]
rs1032689	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1288071	0.91[AFR][1000 genomes]
rs1288072	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1288075	1.00[AMR][1000 genomes]
rs1288078	1.00[AMR][1000 genomes]
rs1288079	1.00[AMR][1000 genomes]
rs1288083	1.00[AMR][1000 genomes]
rs1288086	0.85[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17081188	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17081296	1.00[AMR][1000 genomes]
rs17081364	1.00[AMR][1000 genomes]
rs3851207	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7764304	1.00[AMR][1000 genomes]
rs9481944	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1027904	chr6:119709488-120001986	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv533518	chr6:119712186-119998618	ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3442553	chr6:119742069-120076777	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119789200-119790800	Enhancers	Fetal Heart	heart
2	chr6:119789600-119792400	Weak transcription	K562	blood
3	chr6:119789600-119793800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:119789800-119790400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr6:119789800-119790400	Enhancers	Colon Smooth Muscle	Colon
6	chr6:119790000-119790600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr6:119790000-119790600	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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