Variant report

Variant	rs2955863
Chromosome Location	chr8:39901567-39901568
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1986745	0.82[AMR][1000 genomes]
rs2955869	0.82[ASN][1000 genomes]
rs2955870	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2955873	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2981182	0.84[AMR][1000 genomes]
rs35844645	0.82[AMR][1000 genomes]
rs62513284	0.87[ASN][1000 genomes]
rs62513286	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][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:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39897600-39903400	Enhancers	HepG2	liver
2	chr8:39899600-39901600	Enhancers	Fetal Intestine Large	intestine
3	chr8:39899600-39901600	Enhancers	Fetal Intestine Small	intestine
4	chr8:39899600-39912000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:39899800-39908800	Weak transcription	Stomach Mucosa	stomach
6	chr8:39900400-39901600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:39900400-39906800	Weak transcription	Liver	Liver
8	chr8:39900600-39903200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:39900600-39906400	Weak transcription	Pancreas	Pancrea
10	chr8:39901000-39901600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:39901200-39901600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr8:39901200-39901600	Enhancers	HSMMtube	muscle
13	chr8:39901200-39902400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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