Variant report

Variant	rs4236757
Chromosome Location	chr8:39003845-39003846
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10089487	0.81[MEX][hapmap]
rs10958535	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10958537	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12056655	0.82[TSI][hapmap]
rs12541095	0.82[EUR][1000 genomes]
rs12541231	0.82[TSI][hapmap]
rs12542529	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12545085	0.93[AFR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12549232	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13256952	0.82[TSI][hapmap]
rs13268394	0.82[TSI][hapmap]
rs13274715	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs34002881	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34382496	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34494323	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35275553	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35335280	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35935390	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36042872	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4129095	0.82[TSI][hapmap]
rs4236755	0.87[ASW][hapmap];0.83[CEU][hapmap];0.87[CHB][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap];0.90[MEX][hapmap];0.88[TSI][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4292654	0.83[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4308699	0.83[CEU][hapmap];0.87[CHB][hapmap];0.90[GIH][hapmap];0.93[JPT][hapmap];0.86[MEX][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4324895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4531014	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4590405	0.82[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4593506	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4601278	0.83[CEU][hapmap];0.87[CHB][hapmap];0.88[GIH][hapmap];0.93[JPT][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4733905	0.82[TSI][hapmap]
rs4733979	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4733980	0.82[CEU][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4733981	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6474108	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6474109	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9650326	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021581	chr8:38934014-39043954	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv1015907	chr8:38967169-39718559	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539550	chr8:38967169-39718559	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1027443	chr8:38993423-39181079	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv539551	chr8:38993423-39181079	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs4236757	TM2D2	cis	cerebellum	SCAN
rs4236757	PLEKHA2	cis	lymphoblastoid	seeQTL
rs4236757	DDHD2	cis	cerebellum	SCAN
rs4236757	SGK196	cis	parietal	SCAN
rs4236757	GPR124	cis	cerebellum	SCAN
rs4236757	PLEKHA2	cis	cerebellum	SCAN
rs4236757	TM2D2	cis	parietal	SCAN
rs4236757	ADAM32	cis	cerebellum	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:38971200-39036400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:39001600-39015000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:39001800-39013800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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