Variant report

Variant	rs28625045
Chromosome Location	chr4:102772190-102772191
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10016018	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11097760	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11097761	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11736568	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11930376	0.84[EUR][1000 genomes]
rs11931658	0.83[EUR][1000 genomes]
rs11932972	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11933157	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11934097	0.85[EUR][1000 genomes]
rs11939568	0.84[EUR][1000 genomes]
rs11940934	0.87[EUR][1000 genomes]
rs11942437	0.84[EUR][1000 genomes]
rs13101528	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13103438	0.85[EUR][1000 genomes]
rs13108400	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13116542	0.85[EUR][1000 genomes]
rs13126550	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13142517	0.85[EUR][1000 genomes]
rs13434472	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2216546	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28396651	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34208976	0.81[EUR][1000 genomes]
rs34321727	0.83[EUR][1000 genomes]
rs34814827	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35201947	0.85[EUR][1000 genomes]
rs35476121	0.85[EUR][1000 genomes]
rs35860418	0.85[EUR][1000 genomes]
rs3974649	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3974650	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4345184	0.85[EUR][1000 genomes]
rs4463068	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4572884	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4639076	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698839	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698971	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4698975	0.84[EUR][1000 genomes]
rs4698977	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4698978	0.84[EUR][1000 genomes]
rs4698979	0.84[EUR][1000 genomes]
rs60448423	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6816787	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6830565	0.85[EUR][1000 genomes]
rs7662572	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7679882	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9790475	0.84[EUR][1000 genomes]
rs9999440	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][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	nsv869164	chr4:102483189-103213842	Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv999861	chr4:102576115-102930562	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2757945	chr4:102662699-103008940	Genic enhancers Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2759269	chr4:102662699-103008940	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1011180	chr4:102685236-102985945	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv537202	chr4:102685236-102985945	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28625045	BANK1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102757400-102784600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:102771200-102772600	Genic enhancers	Primary B cells from cord blood	blood
3	chr4:102772000-102773200	Genic enhancers	Primary B cells from peripheral blood	blood
4	chr4:102772000-102773200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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