Variant report

Variant	rs34743464
Chromosome Location	chr4:56026914-56026915
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11722486	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11725581	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12331869	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13126206	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35389572	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55916282	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6818203	0.85[AMR][1000 genomes];0.91[EUR][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	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56025400-56027400	Enhancers	HUVEC	blood vessel
2	chr4:56025600-56027000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:56025800-56028600	Weak transcription	Esophagus	oesophagus
4	chr4:56026200-56028400	Weak transcription	HMEC	breast
5	chr4:56026800-56027000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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