Variant report

Variant	rs62279616
Chromosome Location	chr3:161338350-161338351
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs62278296	0.90[EUR][1000 genomes]
rs62278346	0.97[EUR][1000 genomes]
rs62279582	0.97[EUR][1000 genomes]
rs62279583	0.97[EUR][1000 genomes]
rs62279584	0.97[EUR][1000 genomes]
rs62279589	0.90[EUR][1000 genomes]
rs62279591	0.97[EUR][1000 genomes]
rs62279623	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279624	1.00[EUR][1000 genomes]
rs62279626	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279627	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279628	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279629	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279631	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279632	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62279656	1.00[AMR][1000 genomes]
rs62279657	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62281362	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281364	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281365	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62281366	1.00[EUR][1000 genomes]
rs62281466	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
2	nsv829774	chr3:161229405-161386919	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2422309	chr3:161242389-161425932	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv877711	chr3:161275848-161486665	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 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	chr3:161338200-161338600	Enhancers	Dnd41	blood

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