Variant report

Variant	rs7547015
Chromosome Location	chr1:57359729-57359730
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1360150	1.00[ASN][1000 genomes]
rs17114516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17114524	0.89[AFR][1000 genomes]
rs17114531	1.00[ASN][1000 genomes]
rs17114533	1.00[ASN][1000 genomes]
rs17114548	1.00[ASN][1000 genomes]
rs17114550	1.00[ASN][1000 genomes]
rs59755908	1.00[ASN][1000 genomes]
rs6686359	1.00[ASN][1000 genomes]
rs7417478	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7535170	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57359200-57360400	Genic enhancers	Liver	Liver
2	chr1:57359400-57360400	Enhancers	HepG2	liver
3	chr1:57359600-57362400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links