Variant report

Variant	rs72621886
Chromosome Location	chr4:128501124-128501125
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10005550	0.87[ASN][1000 genomes]
rs10212983	0.86[ASN][1000 genomes]
rs10493145	0.95[EUR][1000 genomes]
rs10493146	1.00[EUR][1000 genomes]
rs11728212	0.86[ASN][1000 genomes]
rs11935472	0.95[EUR][1000 genomes]
rs1355927	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1380155	0.90[EUR][1000 genomes]
rs1514312	0.87[ASN][1000 genomes]
rs1514313	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1514314	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1514315	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17012525	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17012586	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17012601	1.00[EUR][1000 genomes]
rs17012634	1.00[EUR][1000 genomes]
rs17012654	1.00[EUR][1000 genomes]
rs17012683	0.90[EUR][1000 genomes]
rs17012710	0.90[EUR][1000 genomes]
rs1841156	0.86[EUR][1000 genomes]
rs1841157	0.90[EUR][1000 genomes]
rs1903106	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2007243	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2276980	1.00[EUR][1000 genomes]
rs2279071	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2391185	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28570426	0.95[EUR][1000 genomes]
rs2893227	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35147318	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35858752	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4422427	0.90[EUR][1000 genomes]
rs4456965	0.86[EUR][1000 genomes]
rs4590052	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56763029	1.00[EUR][1000 genomes]
rs58486324	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60404814	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60553863	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60666303	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60803593	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60991172	0.80[ASN][1000 genomes]
rs72616920	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616921	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616922	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616923	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616924	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616925	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616926	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616927	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616928	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616929	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616930	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616931	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616932	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616933	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616934	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616935	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616936	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616937	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616938	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616939	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616940	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616941	1.00[EUR][1000 genomes]
rs72616942	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616943	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616947	1.00[EUR][1000 genomes]
rs72616948	1.00[EUR][1000 genomes]
rs72616949	1.00[EUR][1000 genomes]
rs72616950	1.00[EUR][1000 genomes]
rs72616951	0.95[EUR][1000 genomes]
rs72616952	0.90[EUR][1000 genomes]
rs72616953	0.90[EUR][1000 genomes]
rs72616956	0.90[EUR][1000 genomes]
rs72616957	0.81[EUR][1000 genomes]
rs72621863	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72621865	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72621866	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621867	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621868	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621869	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621870	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621871	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621872	0.87[ASN][1000 genomes]
rs72621891	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72621892	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72621893	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72621894	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621895	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621896	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621897	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621898	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621899	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621900	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72621901	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72621902	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72624503	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72624504	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72624505	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7439365	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9992141	0.87[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	nsv879915	chr4:128167093-129150590	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1029214	chr4:128292215-128683123	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv537247	chr4:128292215-128683123	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers 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
4	nsv817326	chr4:128292216-128915201	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1015564	chr4:128394657-128506962	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1017325	chr4:128408370-128509276	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv595387	chr4:128410916-128523964	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv879916	chr4:128422400-128694288	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv879917	chr4:128478408-128841252	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv964280	chr4:128490982-128506981	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128500800-128501200	Enhancers	K562	blood
2	chr4:128500800-128501400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:128501000-128501200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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