Variant report

Variant	rs3905107
Chromosome Location	chr14:25003937-25003938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10144882	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11158781	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11158791	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11520369	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11849539	0.96[ASN][1000 genomes]
rs1304909	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1951125	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1951127	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1951128	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1956908	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1956909	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1956912	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1956913	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2093256	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2332399	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34079088	0.95[ASN][1000 genomes]
rs3861507	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60196546	0.91[ASN][1000 genomes]
rs62001969	0.93[ASN][1000 genomes]
rs62001970	0.84[ASN][1000 genomes]
rs62001971	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7142675	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7143951	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7155452	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8008632	0.92[ASN][1000 genomes]
rs8012655	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs987630	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1045732	chr14:24914008-25019317	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25002800-25005200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:25002800-25005400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr14:25003000-25005200	Enhancers	Primary hematopoietic stem cells	blood
4	chr14:25003000-25005400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:25003200-25004000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr14:25003800-25005200	Enhancers	Primary monocytes fromperipheralblood	blood

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