Variant report

Variant	rs2354554
Chromosome Location	chr6:107131685-107131686
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs3104042	0.97[EUR][1000 genomes]
rs3104043	0.97[EUR][1000 genomes]
rs3104044	0.97[EUR][1000 genomes]
rs3104045	0.97[EUR][1000 genomes]
rs3121429	0.86[EUR][1000 genomes]
rs3121430	0.97[EUR][1000 genomes]
rs3121431	0.94[EUR][1000 genomes]
rs3121432	0.94[EUR][1000 genomes]
rs6903452	0.86[EUR][1000 genomes]
rs7759832	0.87[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	nsv532047	chr6:106591482-107143252	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 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	chr6:107130400-107133200	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:107130600-107132200	Enhancers	Primary B cells from cord blood	blood
3	chr6:107131400-107132000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:107131600-107132000	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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