Variant report

Variant	rs7814906
Chromosome Location	chr8:40007597-40007598
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11988447	1.00[EUR][1000 genomes]
rs12541392	0.82[AFR][1000 genomes]
rs12546288	0.82[AFR][1000 genomes]
rs13254133	1.00[EUR][1000 genomes]
rs28687838	0.82[AFR][1000 genomes]
rs4398898	0.94[YRI][hapmap]
rs4467925	1.00[EUR][1000 genomes]
rs59010645	1.00[EUR][1000 genomes]
rs59936756	1.00[EUR][1000 genomes]
rs60420552	1.00[EUR][1000 genomes]
rs7844209	1.00[EUR][1000 genomes]
rs9298589	0.81[AMR][1000 genomes];1.00[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	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv534582	chr8:39884590-40653224	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:40002600-40009200	Weak transcription	Pancreas	Pancrea
2	chr8:40003000-40009200	Weak transcription	Ovary	ovary
3	chr8:40003000-40009400	Weak transcription	Fetal Kidney	kidney
4	chr8:40003800-40010000	Weak transcription	Fetal Stomach	stomach
5	chr8:40005800-40008000	Enhancers	Stomach Smooth Muscle	stomach
6	chr8:40006400-40008800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr8:40006600-40007600	Weak transcription	Fetal Lung	lung
8	chr8:40006600-40009000	Weak transcription	HepG2	liver
9	chr8:40006600-40010000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr8:40006800-40009200	Weak transcription	Small Intestine	intestine
11	chr8:40007000-40009400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr8:40007400-40007600	Flanking Active TSS	Rectal Smooth Muscle	rectum
13	chr8:40007400-40007800	Flanking Active TSS	Colon Smooth Muscle	Colon
14	chr8:40007400-40008000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:40007400-40008000	Enhancers	A549	lung

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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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