Variant report

Variant	rs4925088
Chromosome Location	chr17:20049344-20049345
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	chr17:20044456..20046022-chr17:20048432..20050400,2	K562	blood:
2	chr17:20044857..20047131-chr17:20049325..20051781,3	MCF-7	breast:

Extended variants
information (count: 140 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:127)

rs_ID	r²[population]
rs11204422	0.85[CHD][hapmap];0.81[GIH][hapmap];0.81[JPT][hapmap];0.84[TSI][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11654025	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.84[ASN][1000 genomes]
rs11869931	0.84[ASN][1000 genomes]
rs11870147	0.92[GIH][hapmap];0.96[MEX][hapmap]
rs11870381	0.82[JPT][hapmap]
rs11871827	0.92[GIH][hapmap];0.92[MEX][hapmap]
rs12451216	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12451841	0.86[CHB][hapmap];0.85[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12453332	0.81[ASN][1000 genomes]
rs12937827	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12942179	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12947713	0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs12949710	0.84[ASN][1000 genomes]
rs12952398	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1468953	0.84[ASN][1000 genomes]
rs1544421	0.86[AMR][1000 genomes]
rs17685923	0.84[ASN][1000 genomes]
rs17686622	0.88[MEX][hapmap]
rs17686798	0.86[CHB][hapmap];0.92[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.96[MEX][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17686839	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17759923	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17759959	1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1812934	0.91[GIH][hapmap];0.96[MEX][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1985810	0.81[AMR][1000 genomes]
rs1992562	0.92[GIH][hapmap];0.96[MEX][hapmap]
rs2013441	0.91[GIH][hapmap];1.00[MEX][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2013576	0.81[AMR][1000 genomes]
rs2034109	0.84[CEU][hapmap]
rs2034110	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs2080673	0.86[AMR][1000 genomes]
rs2107566	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2158473	0.86[AMR][1000 genomes]
rs2189710	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2243732	0.86[AMR][1000 genomes]
rs2263175	0.86[AMR][1000 genomes]
rs2386485	0.86[AMR][1000 genomes]
rs2526458	0.86[AMR][1000 genomes]
rs2526460	0.86[AMR][1000 genomes]
rs2526462	0.86[AMR][1000 genomes]
rs2526464	0.86[AMR][1000 genomes]
rs2526467	0.81[AMR][1000 genomes]
rs2526469	0.87[MEX][hapmap]
rs2526472	0.86[AMR][1000 genomes]
rs2526474	0.86[AMR][1000 genomes]
rs2526475	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2526480	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2526483	0.86[AMR][1000 genomes]
rs2526484	0.86[AMR][1000 genomes]
rs2526488	0.86[AMR][1000 genomes]
rs2526490	0.86[AMR][1000 genomes]
rs2526491	0.88[MEX][hapmap]
rs2703772	0.86[AMR][1000 genomes]
rs2703774	0.92[GIH][hapmap];0.96[MEX][hapmap];0.84[AMR][1000 genomes]
rs2703778	0.86[AMR][1000 genomes]
rs2703780	0.86[AMR][1000 genomes]
rs2703782	0.86[AMR][1000 genomes]
rs2703785	0.81[AMR][1000 genomes]
rs2703787	0.81[AMR][1000 genomes]
rs2703789	0.81[AMR][1000 genomes]
rs2703790	0.81[AMR][1000 genomes]
rs2703791	0.81[AMR][1000 genomes]
rs2703792	0.80[AMR][1000 genomes]
rs2703794	0.86[AMR][1000 genomes]
rs2703799	0.86[AMR][1000 genomes]
rs2703801	0.86[AMR][1000 genomes]
rs2703802	0.86[AMR][1000 genomes]
rs2703804	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2703806	0.86[AMR][1000 genomes]
rs2703808	0.86[AMR][1000 genomes]
rs2703810	0.86[AMR][1000 genomes]
rs2703813	0.88[MEX][hapmap]
rs2703815	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2703816	0.86[AMR][1000 genomes]
rs2703817	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs2703818	0.86[AMR][1000 genomes]
rs2703820	0.86[AMR][1000 genomes]
rs2703821	0.86[AMR][1000 genomes]
rs34089239	0.92[GIH][hapmap];0.96[MEX][hapmap];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34370440	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34644796	0.84[AMR][1000 genomes]
rs34712254	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34756775	0.84[ASN][1000 genomes]
rs35041742	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35124809	0.84[ASN][1000 genomes]
rs35156798	0.81[ASN][1000 genomes]
rs35191778	0.84[ASN][1000 genomes]
rs35244101	0.84[ASN][1000 genomes]
rs35493088	0.84[ASN][1000 genomes]
rs35770292	0.81[ASN][1000 genomes]
rs36051592	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3850783	0.92[GIH][hapmap];0.96[MEX][hapmap]
rs4341795	0.84[ASN][1000 genomes]
rs4346259	0.84[ASN][1000 genomes]
rs4350625	0.84[ASN][1000 genomes]
rs4471741	0.84[ASN][1000 genomes]
rs4588033	0.85[GIH][hapmap];0.96[MEX][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4924808	0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.96[MEX][hapmap];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4924809	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4924810	0.92[GIH][hapmap];0.96[MEX][hapmap];0.86[AMR][1000 genomes]
rs4925075	0.85[CHD][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs4925076	0.84[ASN][1000 genomes]
rs4925078	0.84[ASN][1000 genomes]
rs4925082	0.85[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4925089	0.86[AMR][1000 genomes]
rs57146223	0.87[ASN][1000 genomes]
rs62067488	0.84[ASN][1000 genomes]
rs6587207	0.82[JPT][hapmap]
rs7207459	0.82[JPT][hapmap]
rs7207611	0.92[GIH][hapmap];0.96[MEX][hapmap]
rs7207817	0.88[MEX][hapmap]
rs7215803	0.85[CHD][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7223363	0.81[JPT][hapmap]
rs7224875	0.82[JPT][hapmap]
rs7225249	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs7503407	0.84[ASN][1000 genomes]
rs8068484	0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs8074047	0.82[AMR][1000 genomes]
rs8075343	0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs8080190	0.82[JPT][hapmap]
rs8081817	0.84[ASN][1000 genomes]
rs888424	0.83[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];0.88[MEX][hapmap];0.86[TSI][hapmap];0.84[ASN][1000 genomes]
rs972966	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9897328	0.92[GIH][hapmap];0.96[MEX][hapmap];0.81[AMR][1000 genomes]
rs9901125	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9904928	0.87[MEX][hapmap]
rs9915039	0.82[JPT][hapmap]
rs9915059	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062853	chr17:19547912-20206601	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv907868	chr17:19768924-20217122	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer 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	25 gene(s)	inside rSNPs	diseases
3	nsv1060337	chr17:19828636-20204872	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv543257	chr17:19828636-20204872	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv907871	chr17:19927699-20088492	Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv482438	chr17:19934376-20089005	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv833395	chr17:19969959-20124084	Genic enhancers Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1067100	chr17:20007480-20464520	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
9	nsv543260	chr17:20007480-20464520	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
10	nsv482830	chr17:20012748-20169153	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv833396	chr17:20029183-20150808	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv2003	chr17:20046306-20090653	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv962233	chr17:20048121-20054253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs4925088	AKAP10	cis	lymphoblastoid	seeQTL
rs4925088	AKAP10	cis	multi-tissue	Pritchard
rs4925088	CYTSB	cis	multi-tissue	Pritchard
rs4925088	MYO15A	cis	parietal	SCAN
rs4925088	CYTSB	cis	cerebellum	SCAN
rs4925088	SPECC1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20026200-20049800	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr17:20029600-20058800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr17:20031600-20052400	Weak transcription	Brain Anterior Caudate	brain
4	chr17:20031800-20052600	Weak transcription	Brain Hippocampus Middle	brain
5	chr17:20031800-20056400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr17:20032000-20058600	Weak transcription	A549	lung
7	chr17:20034800-20049400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr17:20034800-20054400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr17:20040600-20052400	Weak transcription	Aorta	Aorta
10	chr17:20042400-20049800	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr17:20042800-20058400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:20045400-20058400	Weak transcription	K562	blood
13	chr17:20047400-20058400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr17:20048400-20052400	Weak transcription	Brain Substantia Nigra	brain
15	chr17:20048600-20049800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr17:20048600-20049800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:20048800-20052600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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