Variant report

Variant	rs1957780
Chromosome Location	chr14:63669442-63669443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10131665	1.00[EUR][1000 genomes]
rs11845716	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11845811	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11845913	1.00[EUR][1000 genomes]
rs1467424	1.00[EUR][1000 genomes]
rs17100884	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17100885	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17100924	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17100980	1.00[EUR][1000 genomes]
rs17100987	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17100988	1.00[EUR][1000 genomes]
rs17100990	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17100992	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17100995	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17101002	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17101144	1.00[CEU][hapmap]
rs1955672	1.00[EUR][1000 genomes]
rs4902222	1.00[EUR][1000 genomes]
rs56677467	1.00[EUR][1000 genomes]
rs56713551	1.00[EUR][1000 genomes]
rs57714062	1.00[EUR][1000 genomes]
rs57768197	1.00[EUR][1000 genomes]
rs58737358	1.00[EUR][1000 genomes]
rs59466499	1.00[EUR][1000 genomes]
rs60068448	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60078514	1.00[EUR][1000 genomes]
rs60444475	1.00[EUR][1000 genomes]
rs61664340	1.00[EUR][1000 genomes]
rs6573502	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7156973	1.00[EUR][1000 genomes]
rs7157776	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs73268396	1.00[EUR][1000 genomes]
rs7342496	1.00[EUR][1000 genomes]
rs7342500	1.00[EUR][1000 genomes]
rs737571	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs74060034	1.00[EUR][1000 genomes]
rs74060038	1.00[EUR][1000 genomes]
rs74060041	1.00[EUR][1000 genomes]
rs74060043	1.00[EUR][1000 genomes]
rs742905	1.00[EUR][1000 genomes]
rs761550	1.00[EUR][1000 genomes]
rs8007258	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8010073	1.00[EUR][1000 genomes]
rs8012345	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8014212	1.00[EUR][1000 genomes]
rs8022150	1.00[CEU][hapmap]

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	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription 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 miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv564893	chr14:63526931-63796122	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1045599	chr14:63540073-63765152	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv530774	chr14:63591348-64029881	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv902017	chr14:63604188-63674832	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63662000-63670800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:63667200-63669800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr14:63667200-63670200	Weak transcription	NHDF-Ad	bronchial
4	chr14:63667800-63670000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:63668000-63670200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr14:63668000-63670200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr14:63668000-63670800	Weak transcription	Left Ventricle	heart
8	chr14:63668000-63671000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:63668200-63670200	Weak transcription	NHEK	skin
10	chr14:63668200-63670600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:63668400-63669800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr14:63668400-63670000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr14:63668400-63670200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:63668400-63670200	Weak transcription	HMEC	breast
15	chr14:63668400-63670400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr14:63668800-63671200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:63669200-63670200	Enhancers	HUVEC	blood vessel

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