Variant report

Variant	rs16923870
Chromosome Location	chr8:59695946-59695947
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10957067	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11775629	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16923831	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16923865	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56784704	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57188954	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62505088	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62505090	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6982735	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6983982	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6999409	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6999741	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7000903	0.81[ASN][1000 genomes]
rs7004446	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7006685	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7815285	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7820121	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7830469	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs955103	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv890938	chr8:59355053-59809785	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59694000-59696800	Enhancers	Dnd41	blood
2	chr8:59694000-59697000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:59694000-59697400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:59694800-59696200	Enhancers	Primary T cells from cord blood	blood
5	chr8:59695000-59696000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:59695000-59697000	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:59695000-59697200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:59695600-59696000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr8:59695600-59696000	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr8:59695800-59696200	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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