Variant report

Variant	rs1503537
Chromosome Location	chr4:120864103-120864104
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10446727	0.85[EUR][1000 genomes]
rs10446728	0.85[EUR][1000 genomes]
rs12502424	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13123289	0.84[ASN][1000 genomes]
rs13146693	0.84[ASN][1000 genomes]
rs13150506	0.85[CHB][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1420613	0.92[CEU][hapmap];0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1503542	0.84[ASN][1000 genomes]
rs1847336	0.88[CEU][hapmap];0.84[CHB][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2111141	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs2160499	0.81[ASN][1000 genomes]
rs4834826	0.82[ASN][1000 genomes]
rs924752	0.82[ASN][1000 genomes]
rs991867	0.84[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	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv879849	chr4:120823634-120922444	Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120864000-120865200	Enhancers	Fetal Heart	heart

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