Variant report

Variant	rs8007258
Chromosome Location	chr14:63752656-63752657
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

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]
rs12323874	0.87[ASN][1000 genomes]
rs1467424	1.00[EUR][1000 genomes]
rs15605	1.00[CHB][hapmap]
rs17100884	1.00[EUR][1000 genomes]
rs17100885	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]
rs17765428	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs1955672	1.00[EUR][1000 genomes]
rs1957780	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4902222	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	1.00[EUR][1000 genomes]
rs60078514	1.00[EUR][1000 genomes]
rs60444475	1.00[EUR][1000 genomes]
rs61302639	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]
rs74060101	1.00[EUR][1000 genomes]
rs742905	1.00[EUR][1000 genomes]
rs761550	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]
rs974700	1.00[CEU][hapmap]

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	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	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
7	nsv516899	chr14:63734499-63753078	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv521404	chr14:63741113-63758106	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv431011	chr14:63743247-63866686	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv832815	chr14:63750058-63913900	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63716000-63754600	Weak transcription	Aorta	Aorta
2	chr14:63717400-63754800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:63730800-63766000	Weak transcription	Spleen	Spleen
4	chr14:63737200-63755400	Weak transcription	Fetal Intestine Large	intestine
5	chr14:63738000-63757800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr14:63739400-63759400	Weak transcription	Fetal Intestine Small	intestine
7	chr14:63740800-63755400	Weak transcription	Psoas Muscle	Psoas
8	chr14:63740800-63762800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr14:63740800-63768000	Weak transcription	Right Ventricle	heart
10	chr14:63741000-63757600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:63744000-63755400	Weak transcription	HMEC	breast
12	chr14:63744000-63757600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:63744000-63761800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr14:63747000-63757600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr14:63747000-63761200	Strong transcription	NH-A	brain
16	chr14:63747400-63760200	Strong transcription	HUVEC	blood vessel
17	chr14:63747800-63752800	Weak transcription	Lung	lung
18	chr14:63748000-63752800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr14:63750400-63755800	Strong transcription	Left Ventricle	heart
20	chr14:63750600-63756600	Strong transcription	Fetal Muscle Trunk	muscle
21	chr14:63750600-63757600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:63750800-63753000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr14:63750800-63757400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:63751000-63753600	Strong transcription	Fetal Muscle Leg	muscle
25	chr14:63751400-63752800	Weak transcription	Fetal Lung	lung
26	chr14:63751400-63754800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr14:63751400-63762200	Weak transcription	Right Atrium	heart
28	chr14:63751600-63762400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:63752000-63753200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr14:63752000-63753800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr14:63752000-63757600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr14:63752000-63761600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:63752000-63762000	Weak transcription	Colon Smooth Muscle	Colon
34	chr14:63752200-63753400	Strong transcription	Fetal Stomach	stomach
35	chr14:63752200-63755800	Weak transcription	GM12878-XiMat	blood
36	chr14:63752200-63756400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr14:63752200-63760600	Weak transcription	Rectal Smooth Muscle	rectum
38	chr14:63752200-63762000	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr14:63752400-63755200	Strong transcription	Ovary	ovary
40	chr14:63752400-63760400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:63752400-63760800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:63752600-63753000	Enhancers	Pancreas	Pancrea
43	chr14:63752600-63753200	Enhancers	H9 Cell Line	embryonic stem cell

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