Variant report

Variant	rs737571
Chromosome Location	chr14:63743564-63743565
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:62629450..62630592-chr14:63743010..63744110,4	MCF-7	breast:
2	chr14:62645559..62646722-chr14:63742925..63743992,7	MCF-7	breast:
3	chr14:63641230..63642038-chr14:63743168..63743785,3	MCF-7	breast:
4	chr14:63640738..63642463-chr14:63742531..63744543,12	MCF-7	breast:
5	chr14:62629343..62630368-chr14:63743191..63744136,3	MCF-7	breast:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

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[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11845913	1.00[EUR][1000 genomes]
rs1467424	1.00[EUR][1000 genomes]
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];0.85[YRI][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]
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[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6573502	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];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]
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]
rs8007258	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8010073	1.00[EUR][1000 genomes]
rs8012345	1.00[CEU][hapmap];1.00[AMR][1000 genomes];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:9 , 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

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	chr14:63734400-63749800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr14:63736600-63750800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:63737200-63755400	Weak transcription	Fetal Intestine Large	intestine
7	chr14:63737400-63751200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:63738000-63757800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:63739400-63759400	Weak transcription	Fetal Intestine Small	intestine
10	chr14:63740600-63747400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:63740800-63747600	Weak transcription	Lung	lung
12	chr14:63740800-63749400	Weak transcription	Brain Angular Gyrus	brain
13	chr14:63740800-63749600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr14:63740800-63750400	Weak transcription	Left Ventricle	heart
15	chr14:63740800-63755400	Weak transcription	Psoas Muscle	Psoas
16	chr14:63740800-63762800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr14:63740800-63768000	Weak transcription	Right Ventricle	heart
18	chr14:63741000-63744800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:63741000-63747000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr14:63741000-63751000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr14:63741000-63757600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr14:63741200-63747600	Weak transcription	Adipose Nuclei	Adipose
23	chr14:63741400-63751200	Weak transcription	Ovary	ovary
24	chr14:63741600-63745800	Weak transcription	Fetal Lung	lung
25	chr14:63741600-63746800	Weak transcription	Fetal Stomach	stomach
26	chr14:63741800-63746800	Weak transcription	Fetal Muscle Trunk	muscle
27	chr14:63742200-63743600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:63742200-63743600	Genic enhancers	HUVEC	blood vessel
29	chr14:63742400-63743600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr14:63742400-63744600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
31	chr14:63742600-63744000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:63742800-63743600	Enhancers	Stomach Smooth Muscle	stomach
33	chr14:63742800-63746800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:63743000-63743600	Enhancers	Fetal Brain Male	brain
35	chr14:63743000-63744000	Weak transcription	Fetal Muscle Leg	muscle
36	chr14:63743200-63744200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:63743200-63744200	Enhancers	NH-A	brain
38	chr14:63743400-63743600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr14:63743400-63744000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:63743400-63744000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr14:63743400-63744000	Enhancers	HMEC	breast
42	chr14:63743400-63744200	Enhancers	Colon Smooth Muscle	Colon
43	chr14:63743400-63750000	Weak transcription	Fetal Heart	heart

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