Variant report

Variant	rs2928141
Chromosome Location	chr15:41463736-41463737
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	chr15:41456615..41459900-chr15:41462571..41464669,4	K562	blood:

Extended variants
information (count: 85 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10152855	0.83[ASN][1000 genomes]
rs11070321	0.91[ASN][1000 genomes]
rs11855102	0.87[ASN][1000 genomes]
rs11858678	0.98[ASN][1000 genomes]
rs12324159	0.98[ASN][1000 genomes]
rs1659227	0.94[ASN][1000 genomes]
rs1678750	0.82[AMR][1000 genomes]
rs16971693	0.83[ASN][1000 genomes]
rs16971700	0.80[ASN][1000 genomes]
rs1717198	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1866400	0.83[ASN][1000 genomes]
rs1971131	0.94[ASN][1000 genomes]
rs2578655	0.94[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28455998	0.81[AMR][1000 genomes]
rs28493237	0.83[ASN][1000 genomes]
rs28495204	0.83[ASN][1000 genomes]
rs28729675	0.81[AMR][1000 genomes]
rs28866311	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2899013	0.95[ASN][1000 genomes]
rs2928148	0.82[AMR][1000 genomes]
rs41442144	0.81[ASN][1000 genomes]
rs4258585	0.83[ASN][1000 genomes]
rs537244	0.98[ASN][1000 genomes]
rs551482	0.98[ASN][1000 genomes]
rs55756301	0.85[ASN][1000 genomes]
rs56082289	0.85[ASN][1000 genomes]
rs56837771	0.93[ASN][1000 genomes]
rs57393155	0.82[AMR][1000 genomes]
rs57943533	0.91[ASN][1000 genomes]
rs58083671	0.89[ASN][1000 genomes]
rs58644012	0.96[ASN][1000 genomes]
rs59389433	0.85[ASN][1000 genomes]
rs59616518	0.90[ASN][1000 genomes]
rs59691280	0.85[ASN][1000 genomes]
rs60249025	0.90[ASN][1000 genomes]
rs60422198	0.90[ASN][1000 genomes]
rs61495227	0.88[ASN][1000 genomes]
rs61586152	0.93[ASN][1000 genomes]
rs6492988	0.93[ASN][1000 genomes]
rs6492991	0.90[ASN][1000 genomes]
rs66471237	0.88[ASN][1000 genomes]
rs66510055	0.89[ASN][1000 genomes]
rs66602495	0.96[ASN][1000 genomes]
rs66818965	0.82[AMR][1000 genomes]
rs67531333	0.89[ASN][1000 genomes]
rs68133575	0.96[ASN][1000 genomes]
rs690733	0.98[ASN][1000 genomes]
rs691702	0.98[ASN][1000 genomes]
rs692335	0.84[ASN][1000 genomes]
rs7165931	0.93[ASN][1000 genomes]
rs7166205	0.86[ASN][1000 genomes]
rs7166905	0.85[ASN][1000 genomes]
rs7170049	0.95[ASN][1000 genomes]
rs7170913	0.90[ASN][1000 genomes]
rs7173086	0.87[ASN][1000 genomes]
rs7178840	0.85[ASN][1000 genomes]
rs7179231	0.85[ASN][1000 genomes]
rs7179676	0.92[ASN][1000 genomes]
rs7179969	0.85[ASN][1000 genomes]
rs72737765	0.96[ASN][1000 genomes]
rs73396329	0.96[ASN][1000 genomes]
rs73396336	0.95[ASN][1000 genomes]
rs73396340	0.92[ASN][1000 genomes]
rs8023638	0.95[ASN][1000 genomes]
rs8026858	0.90[ASN][1000 genomes]
rs8029792	0.96[ASN][1000 genomes]
rs8035252	0.85[ASN][1000 genomes]
rs8037302	0.95[ASN][1000 genomes]
rs8038834	0.90[ASN][1000 genomes]
rs8039915	0.85[ASN][1000 genomes]
rs8039934	0.90[ASN][1000 genomes]
rs909023	0.82[ASN][1000 genomes]
rs909024	0.83[ASN][1000 genomes]
rs909025	0.83[ASN][1000 genomes]
rs9972345	0.93[ASN][1000 genomes]
rs9972349	0.95[ASN][1000 genomes]
rs9972622	0.95[ASN][1000 genomes]
rs9972623	0.92[ASN][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	nsv569229	chr15:41361138-41483682	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv904107	chr15:41361138-41493013	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv569230	chr15:41384649-41483682	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv904108	chr15:41384649-41486990	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	nsv904109	chr15:41410705-41481254	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv457120	chr15:41410705-41546631	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv569231	chr15:41410705-41546631	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2928141	OIP5-AS1	cis	Artery Tibial	GTEx
rs2928141	NDUFAF1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41462600-41468000	Weak transcription	Primary monocytes fromperipheralblood	blood

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