Variant report

Variant	rs11944659
Chromosome Location	chr4:110316961-110316962
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 131 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:128)

rs_ID	r²[population]
rs10000545	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10002595	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10005355	0.86[ASN][1000 genomes]
rs10028250	0.81[ASN][1000 genomes]
rs10155127	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10516557	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs10516558	0.86[ASN][1000 genomes]
rs11098033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11098035	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11929713	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11930655	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11933971	0.90[ASN][1000 genomes]
rs11934486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11935440	0.96[ASN][1000 genomes]
rs11935629	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[ASN][1000 genomes]
rs11937053	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs11938593	0.96[ASN][1000 genomes]
rs11941344	0.90[ASN][1000 genomes]
rs11941636	0.93[EUR][1000 genomes]
rs11942140	1.00[ASN][1000 genomes]
rs11942291	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11942858	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11942928	0.96[ASN][1000 genomes]
rs11943384	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11943430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11944375	0.96[ASN][1000 genomes]
rs11944427	0.96[ASN][1000 genomes]
rs12639832	1.00[ASN][1000 genomes]
rs12639835	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12640049	1.00[ASN][1000 genomes]
rs12640161	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12642304	0.86[ASN][1000 genomes]
rs12643055	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12643844	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12643881	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12644055	0.96[ASN][1000 genomes]
rs12647695	0.96[ASN][1000 genomes]
rs12648138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12648965	1.00[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs12650654	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12650873	0.96[ASN][1000 genomes]
rs13103034	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13123618	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13125368	0.82[ASN][1000 genomes]
rs13128124	0.86[ASN][1000 genomes]
rs13134239	0.86[ASN][1000 genomes]
rs13141701	0.86[ASN][1000 genomes]
rs13142698	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs13143825	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs13145066	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1509314	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1509315	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17040410	0.96[ASN][1000 genomes]
rs17040436	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17040439	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17040446	1.00[CEU][hapmap];0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs17040454	1.00[CEU][hapmap];0.90[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17040461	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17040488	0.86[ASN][1000 genomes]
rs17040510	0.82[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs17040519	0.86[EUR][1000 genomes]
rs17585970	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17619262	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28521972	0.83[ASN][1000 genomes]
rs28527792	0.86[EUR][1000 genomes]
rs28611124	0.86[EUR][1000 genomes]
rs28681408	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs34153531	0.86[ASN][1000 genomes]
rs34224638	0.86[ASN][1000 genomes]
rs34274964	0.86[ASN][1000 genomes]
rs34441811	0.90[ASN][1000 genomes]
rs34482781	0.90[ASN][1000 genomes]
rs34836476	0.90[ASN][1000 genomes]
rs35110951	0.86[ASN][1000 genomes]
rs35359830	0.90[ASN][1000 genomes]
rs35473144	0.82[ASN][1000 genomes]
rs35594044	0.86[ASN][1000 genomes]
rs35762958	0.86[ASN][1000 genomes]
rs35791246	0.90[ASN][1000 genomes]
rs35940980	0.86[ASN][1000 genomes]
rs36009064	0.82[ASN][1000 genomes]
rs36115572	0.86[ASN][1000 genomes]
rs3775962	0.86[ASN][1000 genomes]
rs60957336	0.90[ASN][1000 genomes]
rs61004219	0.90[ASN][1000 genomes]
rs61242473	0.84[ASN][1000 genomes]
rs61439452	0.94[ASN][1000 genomes]
rs61553525	0.96[ASN][1000 genomes]
rs6533428	0.94[ASN][1000 genomes]
rs6533429	0.96[ASN][1000 genomes]
rs66642182	0.90[ASN][1000 genomes]
rs66667140	0.86[ASN][1000 genomes]
rs67473696	0.84[ASN][1000 genomes]
rs68041341	0.86[ASN][1000 genomes]
rs6812469	0.86[ASN][1000 genomes]
rs6815455	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6817954	0.86[ASN][1000 genomes]
rs6818911	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6823032	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6827006	0.86[ASN][1000 genomes]
rs6833753	0.84[ASN][1000 genomes]
rs6835683	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6837199	0.94[ASN][1000 genomes]
rs6841198	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6845371	0.86[ASN][1000 genomes]
rs6848452	0.94[ASN][1000 genomes]
rs6851517	0.96[ASN][1000 genomes]
rs6852037	0.86[ASN][1000 genomes]
rs6856291	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6856446	0.86[ASN][1000 genomes]
rs72896619	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72896622	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72896625	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72896629	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72896632	0.84[ASN][1000 genomes]
rs73838809	0.86[ASN][1000 genomes]
rs7436583	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7436745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7440371	0.96[ASN][1000 genomes]
rs7440570	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7675602	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7679836	0.86[ASN][1000 genomes]
rs7687245	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9985632	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9985964	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9994676	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9994985	0.86[ASN][1000 genomes]
rs9999570	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv1799708	chr4:110309234-110333106	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110310800-110317000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:110310800-110318800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:110311200-110317000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:110311200-110327800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:110311600-110331400	Weak transcription	HSMMtube	muscle
6	chr4:110315600-110317000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:110316400-110317200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:110316800-110317200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:110316800-110317200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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