Variant report

Variant	rs34094604
Chromosome Location	chr4:81930884-81930885
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10019046	0.87[EUR][1000 genomes]
rs10516738	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11099459	0.87[EUR][1000 genomes]
rs13122304	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13133972	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13138361	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13141362	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1495634	0.84[EUR][1000 genomes]
rs17005034	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34042179	0.93[EUR][1000 genomes]
rs3733549	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6831641	0.89[EUR][1000 genomes]
rs71596047	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7659948	0.89[EUR][1000 genomes]
rs7661611	0.89[EUR][1000 genomes]
rs7697151	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs924048	0.80[AMR][1000 genomes];0.93[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	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3412549	chr4:81834479-81951850	Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1006466	chr4:81888983-82009675	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr4:81930800-81933400	Weak transcription	Fetal Intestine Large	intestine

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