Variant report

Variant	rs7914884
Chromosome Location	chr10:49956125-49956126
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11101447	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11101454	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11101458	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101461	1.00[CEU][hapmap];0.87[YRI][hapmap];0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12769821	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12775006	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12784705	0.98[EUR][1000 genomes]
rs17011160	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17698900	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2199846	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2889689	0.86[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34584605	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67702314	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7087831	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7919695	1.00[AFR][1000 genomes];1.00[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:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49923400-49960200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:49931000-49956800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr10:49939600-49956200	Weak transcription	Adipose Nuclei	Adipose
4	chr10:49948600-49957200	Weak transcription	Esophagus	oesophagus
5	chr10:49952000-49956400	Weak transcription	Spleen	Spleen
6	chr10:49952000-49960800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr10:49953400-49960200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr10:49954200-49957400	Weak transcription	Lung	lung
9	chr10:49954200-49957600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr10:49955000-49956200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr10:49955000-49958000	Strong transcription	Primary hematopoietic stem cells	blood
12	chr10:49955400-49957600	Genic enhancers	GM12878-XiMat	blood
13	chr10:49955800-49957000	Genic enhancers	Primary B cells from cord blood	blood
14	chr10:49955800-49957000	Genic enhancers	Monocytes-CD14+_RO01746	blood
15	chr10:49955800-49957200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr10:49955800-49957200	Genic enhancers	Primary B cells from peripheral blood	blood
17	chr10:49956000-49956200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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