Variant report

Variant	rs1542756
Chromosome Location	chr3:46272162-46272163
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10510750	0.84[EUR][1000 genomes]
rs11919943	0.94[EUR][1000 genomes]
rs11926063	0.94[EUR][1000 genomes]
rs13060713	0.97[EUR][1000 genomes]
rs13060802	0.98[EUR][1000 genomes]
rs13067058	0.93[EUR][1000 genomes]
rs13073976	0.81[EUR][1000 genomes]
rs13080757	0.81[EUR][1000 genomes]
rs13092160	0.82[EUR][1000 genomes]
rs13095946	0.82[EUR][1000 genomes]
rs13096808	0.87[EUR][1000 genomes]
rs1542755	0.98[EUR][1000 genomes]
rs2131092	1.00[EUR][1000 genomes]
rs2373156	0.94[EUR][1000 genomes]
rs33998492	0.93[EUR][1000 genomes]
rs34005848	1.00[EUR][1000 genomes]
rs34047458	0.82[EUR][1000 genomes]
rs34194160	1.00[EUR][1000 genomes]
rs34289272	1.00[EUR][1000 genomes]
rs34406035	0.81[EUR][1000 genomes]
rs34414382	1.00[EUR][1000 genomes]
rs34531115	0.82[EUR][1000 genomes]
rs34625088	0.82[EUR][1000 genomes]
rs34677490	1.00[EUR][1000 genomes]
rs34692251	0.93[EUR][1000 genomes]
rs34745455	1.00[EUR][1000 genomes]
rs35035328	0.82[EUR][1000 genomes]
rs35335084	0.82[EUR][1000 genomes]
rs35429781	0.82[EUR][1000 genomes]
rs35431271	0.94[EUR][1000 genomes]
rs35481399	0.92[EUR][1000 genomes]
rs35587265	0.82[EUR][1000 genomes]
rs35613615	1.00[EUR][1000 genomes]
rs35614049	0.82[EUR][1000 genomes]
rs35617677	0.82[EUR][1000 genomes]
rs35678191	0.94[EUR][1000 genomes]
rs35775079	0.82[EUR][1000 genomes]
rs36000011	0.94[EUR][1000 genomes]
rs36048333	0.81[EUR][1000 genomes]
rs6775046	0.94[EUR][1000 genomes]
rs71327039	0.82[EUR][1000 genomes]
rs71327040	0.98[EUR][1000 genomes]
rs71327041	1.00[EUR][1000 genomes]
rs71327042	1.00[EUR][1000 genomes]
rs71327043	0.94[EUR][1000 genomes]
rs71327044	0.94[EUR][1000 genomes]
rs71615441	1.00[EUR][1000 genomes]
rs7620586	0.94[EUR][1000 genomes]
rs7624155	0.92[EUR][1000 genomes]
rs7628489	0.94[EUR][1000 genomes]
rs7651539	0.94[EUR][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	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46264400-46276400	Weak transcription	Fetal Thymus	thymus
2	chr3:46265600-46276400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:46270400-46273000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr3:46270600-46273800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr3:46270800-46274600	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr3:46270800-46274600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr3:46271000-46274600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr3:46271200-46277600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr3:46272000-46274400	Weak transcription	Primary hematopoietic stem cells	blood

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