Variant report

Variant	rs7711625
Chromosome Location	chr5:74218494-74218495
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11738903	0.89[EUR][1000 genomes]
rs11740706	0.93[EUR][1000 genomes]
rs11740809	0.81[EUR][1000 genomes]
rs11746561	0.95[EUR][1000 genomes]
rs58010984	0.90[EUR][1000 genomes]
rs60270014	0.81[EUR][1000 genomes]
rs60430653	0.94[EUR][1000 genomes]
rs62367770	0.81[EUR][1000 genomes]
rs62367771	0.89[EUR][1000 genomes]
rs62367773	0.89[EUR][1000 genomes]
rs62367774	0.91[EUR][1000 genomes]
rs62367819	0.89[EUR][1000 genomes]
rs62367823	0.91[EUR][1000 genomes]
rs62367824	0.91[EUR][1000 genomes]
rs62367825	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62367828	0.94[EUR][1000 genomes]
rs68151843	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][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	nsv518286	chr5:74169045-74243120	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830352	chr5:74189495-74337944	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74213200-74221400	Weak transcription	Pancreas	Pancrea
2	chr5:74214000-74221400	Weak transcription	Stomach Mucosa	stomach
3	chr5:74215400-74220600	Weak transcription	HepG2	liver
4	chr5:74215400-74221600	Weak transcription	Fetal Intestine Small	intestine

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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

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