Variant report

Variant	rs17092514
Chromosome Location	chr8:20322808-20322809
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	chr8:20315158..20318143-chr8:20322413..20324006,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10100458	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10100567	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11204116	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11204117	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11779595	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12543622	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12675436	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13249119	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13255104	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13261825	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13272433	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13281858	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13282673	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1383250	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1480347	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1480349	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1480350	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17092620	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17092624	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28368993	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2898509	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35114366	0.93[EUR][1000 genomes]
rs35145241	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4406408	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4921720	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6986569	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6989163	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7001402	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7014186	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71512703	0.80[EUR][1000 genomes]
rs7812583	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9644569	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9785133	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2758152	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759603	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv469890	chr8:20239114-20445136	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv482881	chr8:20239114-20445136	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17092514	PEBP4	cis	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20317200-20324800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr8:20317400-20324800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr8:20317400-20324800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr8:20317400-20334000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:20317800-20324400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:20318000-20324600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr8:20320400-20324800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr8:20320600-20324800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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