Variant report

Variant	rs7742886
Chromosome Location	chr6:147268342-147268343
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:147255283..147257003-chr6:147267757..147269418,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11155492	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11155493	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11155494	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12203394	0.82[AMR][1000 genomes]
rs12209913	0.80[ASN][1000 genomes]
rs12662569	0.80[ASN][1000 genomes]
rs1408577	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1529014	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1529021	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1881662	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2181942	0.89[ASW][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2328774	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4267966	0.92[EUR][1000 genomes]
rs4323329	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4431452	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4445078	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4452660	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4551178	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4605904	0.80[AMR][1000 genomes]
rs4895706	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4896897	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6913861	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7742400	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7745042	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs7774249	0.82[AMR][1000 genomes]
rs7774926	0.82[AMR][1000 genomes]
rs7775644	0.81[ASN][1000 genomes]
rs9322081	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9322082	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9373516	0.80[EUR][1000 genomes]
rs9377038	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9377040	0.91[JPT][hapmap]
rs9386176	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9399592	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403831	0.80[ASN][1000 genomes]
rs9403832	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9403834	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403836	0.86[JPT][hapmap];0.81[EUR][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	nsv830838	chr6:147090745-147274669	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv2760996	chr6:147229457-147269633	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv1846046	chr6:147258908-147271295	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7742886	STXBP5	cis	cerebellum	SCAN
rs7742886	ULBP3	cis	parietal	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147265600-147276600	Weak transcription	Pancreas	Pancrea
2	chr6:147266400-147268800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr6:147267400-147271600	Weak transcription	Small Intestine	intestine
4	chr6:147268000-147269600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:147268000-147271000	Weak transcription	HepG2	liver

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