Variant report

Variant	rs467337
Chromosome Location	chr9:98504175-98504176
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1093398	1.00[CEU][hapmap];0.97[GIH][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10982065	0.92[GIH][hapmap]
rs700967	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs467337	FBP1	cis	parietal	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98499800-98504400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr9:98502200-98505000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:98503400-98504400	Weak transcription	Fetal Stomach	stomach
4	chr9:98503800-98504200	Weak transcription	Fetal Lung	lung
5	chr9:98503800-98504600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:98504000-98504600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:98504000-98504600	Enhancers	Gastric	stomach
8	chr9:98504000-98505400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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