Variant report

Variant	rs6893486
Chromosome Location	chr5:75657165-75657166
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs57064503	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6859353	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6859902	0.89[ASN][1000 genomes]
rs6860083	0.89[ASN][1000 genomes]
rs6860113	0.89[ASN][1000 genomes]
rs6860973	0.89[ASN][1000 genomes]
rs6872965	0.89[ASN][1000 genomes]
rs6881881	0.89[ASN][1000 genomes]
rs6882055	0.89[ASN][1000 genomes]
rs6886369	0.89[ASN][1000 genomes]
rs6890217	0.84[ASN][1000 genomes]
rs7704494	0.89[ASN][1000 genomes]
rs7704498	0.89[ASN][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	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv870415	chr5:75526088-75738412	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75649800-75662600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:75654800-75659400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:75655800-75659400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:75656600-75657200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr5:75656600-75657600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr5:75656800-75658000	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:75657000-75661600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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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