Variant report

Variant	rs2125307
Chromosome Location	chr4:69869192-69869193
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10000598	0.82[EUR][1000 genomes]
rs10006282	0.82[EUR][1000 genomes]
rs10010699	0.82[EUR][1000 genomes]
rs10025070	0.93[ASN][1000 genomes]
rs10033045	0.93[ASN][1000 genomes]
rs10518057	0.82[EUR][1000 genomes]
rs10903224	0.82[EUR][1000 genomes]
rs11249529	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11931604	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11932983	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11933432	0.90[ASN][1000 genomes]
rs11936412	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11937195	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11945620	1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11945705	0.93[ASN][1000 genomes]
rs11946857	0.81[EUR][1000 genomes]
rs11946976	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12499093	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12499192	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12503622	0.82[ASN][1000 genomes]
rs12506592	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12507173	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12507556	0.93[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12508596	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12508920	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12509040	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12509066	0.81[EUR][1000 genomes]
rs13132528	0.82[EUR][1000 genomes]
rs13136922	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13148179	0.80[EUR][1000 genomes]
rs13148603	0.82[EUR][1000 genomes]
rs1379813	0.82[EUR][1000 genomes]
rs1379816	0.82[EUR][1000 genomes]
rs1458243	0.81[EUR][1000 genomes]
rs1458245	0.82[EUR][1000 genomes]
rs1458246	0.82[EUR][1000 genomes]
rs1598904	0.82[EUR][1000 genomes]
rs17605102	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1841052	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1993546	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2168840	0.81[EUR][1000 genomes]
rs28365062	0.93[ASN][1000 genomes]
rs34545777	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34561399	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4259121	0.93[ASN][1000 genomes]
rs4343788	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4348159	0.87[ASN][1000 genomes]
rs4403109	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4418041	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4434329	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4454001	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4554146	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4694152	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4694181	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs4694550	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4694606	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55647928	0.81[EUR][1000 genomes]
rs55676022	0.82[ASN][1000 genomes]
rs55795005	0.81[EUR][1000 genomes]
rs55831171	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55905314	0.93[ASN][1000 genomes]
rs56943005	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57468707	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58965335	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59314351	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59732068	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60276248	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62296919	0.93[ASN][1000 genomes]
rs62296941	0.93[ASN][1000 genomes]
rs62298861	0.90[ASN][1000 genomes]
rs62298872	0.97[ASN][1000 genomes]
rs66698711	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6843550	0.81[EUR][1000 genomes]
rs6850028	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs72642933	0.86[EUR][1000 genomes]
rs72642938	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72642947	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72642961	0.93[ASN][1000 genomes]
rs7435335	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7441753	0.82[EUR][1000 genomes]
rs7680341	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7692753	0.83[EUR][1000 genomes]
rs9329037	0.81[EUR][1000 genomes]
rs9991142	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3420586	chr4:69680878-70322918	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv1067773	chr4:69718248-70715727	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription 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	49 gene(s)	inside rSNPs	diseases
5	esv3468151	chr4:69718675-70322776	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	esv3468153	chr4:69718675-70322776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	nsv967758	chr4:69780530-69870183	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv829962	chr4:69786869-69910283	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv594582	chr4:69827340-69988378	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	esv2757064	chr4:69863174-69901607	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69868400-69869200	Weak transcription	Liver	Liver
2	chr4:69868800-69882000	Weak transcription	HepG2	liver

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