Variant report

Variant	rs34584605
Chromosome Location	chr10:49963479-49963480
allele	C/G
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:14)

rs_ID	r²[population]
rs11101447	0.94[EUR][1000 genomes]
rs11101454	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11101458	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101461	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12769821	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12775006	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12784705	0.98[EUR][1000 genomes]
rs17698900	0.94[EUR][1000 genomes]
rs2199846	1.00[EUR][1000 genomes]
rs2889689	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67702314	1.00[EUR][1000 genomes]
rs7087831	0.95[EUR][1000 genomes]
rs7914884	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7919695	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49958600-49967800	Weak transcription	Lung	lung
2	chr10:49959000-49968000	Weak transcription	Spleen	Spleen
3	chr10:49959400-49966800	Strong transcription	Primary B cells from peripheral blood	blood
4	chr10:49960200-49967000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:49960200-49968400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr10:49960800-49966000	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr10:49960800-49967400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr10:49962200-49964000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr10:49962400-49964000	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr10:49962400-49980600	Strong transcription	Primary B cells from cord blood	blood
11	chr10:49962800-49964000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:49963400-49965000	Weak transcription	GM12878-XiMat	blood
13	chr10:49963400-49966600	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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