Variant report

Variant	rs9925138
Chromosome Location	chr16:48554249-48554250
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1001872	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1004704	1.00[CHB][hapmap]
rs11076569	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11641936	0.83[EUR][1000 genomes]
rs11643514	0.86[EUR][1000 genomes]
rs11648225	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1566466	0.83[EUR][1000 genomes]
rs1566467	0.83[EUR][1000 genomes]
rs1948713	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2062553	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2062554	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.92[EUR][1000 genomes]
rs2062555	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2088753	0.83[EUR][1000 genomes]
rs2088754	0.84[EUR][1000 genomes]
rs4028695	0.85[CEU][hapmap]
rs4785244	1.00[CHB][hapmap]
rs4785520	0.84[EUR][1000 genomes]
rs4785521	0.92[EUR][1000 genomes]
rs55745119	0.86[EUR][1000 genomes]
rs6500390	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7184700	1.00[CHB][hapmap]
rs7189631	0.88[EUR][1000 genomes]
rs7194822	0.81[EUR][1000 genomes]
rs7198420	1.00[CHB][hapmap]
rs7202422	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7202699	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7206781	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes]
rs8046716	0.85[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap]
rs8052026	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs8054389	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8056201	0.89[EUR][1000 genomes]
rs8056346	0.86[EUR][1000 genomes]
rs8057027	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8063059	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs9888862	0.80[EUR][1000 genomes]
rs9921402	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9923092	0.85[EUR][1000 genomes]
rs9925108	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9926683	0.83[EUR][1000 genomes]
rs9930644	0.85[YRI][hapmap]
rs9933892	0.92[EUR][1000 genomes]
rs9937129	0.86[EUR][1000 genomes]
rs9939368	0.86[EUR][1000 genomes]
rs9939554	0.80[EUR][1000 genomes]
rs9940599	0.86[EUR][1000 genomes]
rs9941289	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061316	chr16:48264175-48594219	Weak transcription Strong transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv1800739	chr16:48418505-48560315	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	nsv428658	chr16:48438656-48587750	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1065358	chr16:48513824-48554254	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1064323	chr16:48531171-48573066	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1060196	chr16:48531171-48578101	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	esv12376	chr16:48549888-48554334	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9925138	N4BP1	cis	multi-tissue	Pritchard
rs9925138	NOD2	cis	cerebellum	SCAN
rs9925138	NKD1	cis	cerebellum	SCAN
rs9925138	PAPD5	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48554200-48555200	Enhancers	HepG2	liver

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