Variant report

Variant	rs5026329
Chromosome Location	chr3:69418876-69418877
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs17005675	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17005685	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17005687	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17005689	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17005691	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17005694	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17005696	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17005699	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17005712	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17005713	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2314987	0.87[AMR][1000 genomes]
rs2872808	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs4241387	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4855394	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56653941	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56682655	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57343519	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58937767	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59683429	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60969945	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72940765	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72940769	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72940771	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72940775	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72940779	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72940783	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72940785	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs881031	0.89[AMR][1000 genomes]
rs964553	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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	nsv1007730	chr3:69355932-69730587	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv520818	chr3:69401248-69421495	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2760780	chr3:69413876-69513947	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69402200-69419000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:69413600-69419000	Weak transcription	NHDF-Ad	bronchial
3	chr3:69413800-69419000	Weak transcription	Brain Angular Gyrus	brain
4	chr3:69413800-69419400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:69414000-69419000	Weak transcription	Osteobl	bone
6	chr3:69416000-69419000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:69416000-69419200	Weak transcription	Fetal Brain Male	brain
8	chr3:69416600-69420400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr3:69416800-69419800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:69416800-69420400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:69416800-69420600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:69417000-69419000	Enhancers	HUVEC	blood vessel
13	chr3:69417000-69419200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr3:69417000-69419400	Enhancers	Primary B cells from cord blood	blood
15	chr3:69417000-69420600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr3:69417000-69420600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr3:69417200-69419000	Enhancers	HMEC	breast
18	chr3:69417200-69419000	Enhancers	NHEK	skin
19	chr3:69417200-69419400	Enhancers	Brain Cingulate Gyrus	brain
20	chr3:69417200-69419400	Enhancers	Brain Hippocampus Middle	brain
21	chr3:69417200-69419400	Enhancers	HSMM	muscle
22	chr3:69417200-69420600	Flanking Active TSS	Dnd41	blood
23	chr3:69417200-69421000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:69417400-69419200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr3:69417400-69419200	Enhancers	Brain Substantia Nigra	brain
26	chr3:69417400-69419400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr3:69417400-69420800	Enhancers	Fetal Lung	lung
28	chr3:69417600-69419200	Enhancers	Primary hematopoietic stem cells	blood
29	chr3:69417600-69419400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr3:69417800-69419000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:69417800-69419000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:69417800-69419000	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr3:69417800-69419000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr3:69417800-69419200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr3:69417800-69419200	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr3:69417800-69419200	Enhancers	Primary T cells from cord blood	blood
37	chr3:69417800-69419200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr3:69417800-69419200	Weak transcription	Brain Anterior Caudate	brain
39	chr3:69417800-69419400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr3:69417800-69419400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr3:69417800-69419400	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:69417800-69419400	Weak transcription	Fetal Muscle Leg	muscle
43	chr3:69417800-69419600	Weak transcription	Spleen	Spleen
44	chr3:69417800-69420800	Weak transcription	Aorta	Aorta
45	chr3:69418000-69419200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr3:69418000-69419200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr3:69418000-69419200	Weak transcription	Placenta	Placenta
48	chr3:69418000-69419200	Weak transcription	Right Atrium	heart
49	chr3:69418000-69419400	Weak transcription	Esophagus	oesophagus
50	chr3:69418000-69419400	Weak transcription	Left Ventricle	heart

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