Variant report

Variant	rs1351791
Chromosome Location	chr3:69333428-69333429
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10049245	1.00[ASW][hapmap];0.97[LWK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10049350	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10779991	1.00[AMR][1000 genomes]
rs1351792	1.00[AMR][1000 genomes]
rs2170801	1.00[AMR][1000 genomes]
rs2872809	1.00[AMR][1000 genomes]
rs4615082	0.82[AFR][1000 genomes]
rs4855378	1.00[AMR][1000 genomes]
rs4855379	1.00[AMR][1000 genomes]
rs7619331	1.00[AMR][1000 genomes]
rs9310145	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9841198	1.00[AMR][1000 genomes]
rs9858273	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876935	chr3:69307942-69401248	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1012483	chr3:69321191-69340525	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69293000-69343400	Weak transcription	HSMM	muscle
2	chr3:69293400-69339200	Weak transcription	Aorta	Aorta
3	chr3:69310000-69337600	Weak transcription	Placenta	Placenta
4	chr3:69310200-69337200	Weak transcription	Lung	lung
5	chr3:69323000-69339200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:69326200-69337800	Weak transcription	Right Atrium	heart
7	chr3:69326400-69336400	Weak transcription	HMEC	breast
8	chr3:69327400-69337200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:69327600-69343200	Weak transcription	Fetal Stomach	stomach
10	chr3:69328200-69337400	Weak transcription	Thymus	Thymus
11	chr3:69328600-69339200	Weak transcription	Esophagus	oesophagus
12	chr3:69329000-69337400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:69329400-69337400	Weak transcription	Spleen	Spleen
14	chr3:69330400-69343200	Weak transcription	Fetal Thymus	thymus
15	chr3:69331000-69333600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr3:69331400-69334000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr3:69331400-69337400	Weak transcription	Fetal Brain Female	brain
18	chr3:69331400-69342200	Weak transcription	HSMMtube	muscle
19	chr3:69331600-69336800	Weak transcription	GM12878-XiMat	blood
20	chr3:69331600-69339400	Weak transcription	Left Ventricle	heart
21	chr3:69331600-69355400	Weak transcription	Adipose Nuclei	Adipose
22	chr3:69331800-69334600	Weak transcription	Dnd41	blood
23	chr3:69331800-69334800	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr3:69331800-69335400	Weak transcription	Fetal Lung	lung
25	chr3:69331800-69335600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:69331800-69338200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr3:69332000-69337200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr3:69332400-69337200	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr3:69332600-69333600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:69332600-69333600	Enhancers	Brain Anterior Caudate	brain
31	chr3:69332600-69333800	Enhancers	Brain Cingulate Gyrus	brain
32	chr3:69332600-69333800	Enhancers	Brain Hippocampus Middle	brain
33	chr3:69332600-69333800	Enhancers	Brain Substantia Nigra	brain
34	chr3:69332600-69335000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:69332600-69336400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr3:69332600-69337200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr3:69332600-69337200	Strong transcription	NHEK	skin
38	chr3:69332800-69333600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:69332800-69333600	Enhancers	Brain Angular Gyrus	brain
40	chr3:69332800-69336400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr3:69333000-69335400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr3:69333200-69333600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:69333200-69333600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:69333400-69334200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr3:69333400-69334400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:69333400-69335400	Weak transcription	HUVEC	blood vessel
47	chr3:69333400-69336800	Weak transcription	Fetal Heart	heart

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