Variant report

Variant	rs12877337
Chromosome Location	chr13:93053745-93053746
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1023012	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1536620	0.81[AMR][1000 genomes]
rs17434593	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs2209834	0.90[CEU][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2225157	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4773681	0.86[CEU][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7317334	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7334105	0.95[CEU][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7336824	0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7985054	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs8000039	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs9516073	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9516076	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs9523670	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs9523671	0.81[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]

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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93049600-93060200	Weak transcription	Fetal Intestine Small	intestine
2	chr13:93053200-93058200	Weak transcription	Right Atrium	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