Variant report

Variant	rs9489589
Chromosome Location	chr6:119417210-119417211
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1334927	0.93[EUR][1000 genomes]
rs58340913	0.93[EUR][1000 genomes]
rs59123354	0.81[AFR][1000 genomes]
rs73531378	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73531393	1.00[EUR][1000 genomes]
rs73531398	1.00[EUR][1000 genomes]
rs73533310	1.00[AFR][1000 genomes]
rs73533328	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9489586	0.93[EUR][1000 genomes]
rs9489587	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9885701	0.93[EUR][1000 genomes]
rs9885891	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9885892	0.81[AFR][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	nsv1030400	chr6:119320153-119433830	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	30 gene(s)	inside rSNPs	diseases
2	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv3443997	chr6:119416803-119418801	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119415600-119418000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:119416800-119418000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:119417000-119417800	Enhancers	Adipose Nuclei	Adipose
4	chr6:119417000-119417800	Enhancers	Fetal Lung	lung
5	chr6:119417000-119417800	Enhancers	Rectal Smooth Muscle	rectum
6	chr6:119417000-119418200	Weak transcription	Placenta	Placenta
7	chr6:119417000-119419000	Enhancers	Primary T cells from cord blood	blood
8	chr6:119417000-119419200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:119417200-119417600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:119417200-119417600	Enhancers	Fetal Intestine Small	intestine
11	chr6:119417200-119418000	Enhancers	Colon Smooth Muscle	Colon
12	chr6:119417200-119418400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr6:119417200-119418600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:119417200-119418600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr6:119417200-119418600	Enhancers	NHEK	skin
16	chr6:119417200-119419000	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:119417200-119419000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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