Variant report

Variant	rs13293668
Chromosome Location	chr9:104203482-104203483
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1047968	1.00[CHD][hapmap]
rs10989500	1.00[CHD][hapmap];1.00[LWK][hapmap]
rs10989507	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10989508	0.87[EUR][1000 genomes]
rs10989509	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs10989510	0.81[EUR][1000 genomes]
rs13283255	0.81[EUR][1000 genomes]
rs13284199	0.81[EUR][1000 genomes]
rs13297805	0.81[EUR][1000 genomes]
rs1534828	1.00[CHD][hapmap]
rs17185855	1.00[CHD][hapmap]
rs17772514	1.00[CHD][hapmap]
rs17772845	1.00[CHD][hapmap]
rs17772869	1.00[CHD][hapmap];1.00[LWK][hapmap]
rs17773076	1.00[CHD][hapmap];1.00[LWK][hapmap]
rs34160569	0.81[EUR][1000 genomes]
rs34664558	0.81[EUR][1000 genomes]
rs71491792	0.81[EUR][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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv893626	chr9:104172936-104324545	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104195600-104207200	Enhancers	HepG2	liver
2	chr9:104197000-104211400	Weak transcription	Right Atrium	heart
3	chr9:104197200-104204600	Weak transcription	Left Ventricle	heart
4	chr9:104197400-104209600	Enhancers	Fetal Intestine Large	intestine
5	chr9:104198200-104204600	Enhancers	Fetal Intestine Small	intestine
6	chr9:104200000-104204600	Weak transcription	Colon Smooth Muscle	Colon
7	chr9:104200800-104204600	Weak transcription	Fetal Heart	heart
8	chr9:104200800-104206200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr9:104201600-104205200	Weak transcription	Stomach Mucosa	stomach
10	chr9:104202600-104204800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr9:104202800-104205200	Active TSS	Duodenum Mucosa	Duodenum
12	chr9:104203200-104205200	Active TSS	Liver	Liver
13	chr9:104203200-104206400	Enhancers	Pancreas	Pancrea

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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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