Variant report

Variant	rs6776474
Chromosome Location	chr3:69381588-69381589
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10865649	1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11128126	0.85[AMR][1000 genomes]
rs11707515	0.80[JPT][hapmap]
rs11707811	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12492029	0.81[EUR][1000 genomes]
rs1483895	0.81[JPT][hapmap]
rs1564757	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17005615	0.81[EUR][1000 genomes]
rs17005647	0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1843046	0.80[CHB][hapmap]
rs1872152	0.86[JPT][hapmap]
rs2007584	0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2170800	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35331889	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4290808	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4428187	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4855308	1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4855389	0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56119799	0.81[EUR][1000 genomes]
rs56336456	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs56741529	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59563257	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6419766	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6549198	0.80[JPT][hapmap]
rs6549203	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6771772	0.96[CEU][hapmap];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6774274	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs67846536	0.80[EUR][1000 genomes]
rs67940491	0.80[EUR][1000 genomes]
rs68061967	0.88[ASN][1000 genomes]
rs7611647	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7612526	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7617464	0.93[ASN][1000 genomes]
rs9310148	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9310149	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9861135	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9868217	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9868990	0.86[CHB][hapmap];0.87[JPT][hapmap];0.80[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	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	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
3	esv1800315	chr3:69374729-69414587	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69360600-69382200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:69370200-69384000	Weak transcription	Left Ventricle	heart
3	chr3:69372200-69403800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:69374600-69383200	Weak transcription	Right Atrium	heart
5	chr3:69374800-69388400	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr3:69375000-69384000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr3:69376400-69388600	Weak transcription	Aorta	Aorta
8	chr3:69376600-69383200	Weak transcription	Adipose Nuclei	Adipose
9	chr3:69376800-69388400	Weak transcription	HSMMtube	muscle
10	chr3:69377400-69383800	Weak transcription	Brain Angular Gyrus	brain
11	chr3:69377800-69382400	Weak transcription	Brain Anterior Caudate	brain
12	chr3:69377800-69382600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:69378200-69383800	Weak transcription	Right Ventricle	heart
14	chr3:69378400-69381600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:69378400-69390600	Weak transcription	Thymus	Thymus
16	chr3:69378400-69400600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:69380000-69381600	Strong transcription	NHEK	skin
18	chr3:69380000-69383600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:69380400-69381800	Enhancers	Lung	lung
20	chr3:69380400-69387600	Weak transcription	Dnd41	blood
21	chr3:69380600-69383800	Weak transcription	Fetal Heart	heart
22	chr3:69380600-69387400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr3:69380600-69393200	Weak transcription	HSMM	muscle
24	chr3:69380800-69382400	Weak transcription	Brain Substantia Nigra	brain
25	chr3:69380800-69388000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr3:69380800-69390600	Weak transcription	Fetal Lung	lung
27	chr3:69381200-69388000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr3:69381200-69388400	Weak transcription	Placenta	Placenta
29	chr3:69381400-69381600	Enhancers	Brain Cingulate Gyrus	brain
30	chr3:69381400-69381600	Weak transcription	HUVEC	blood vessel
31	chr3:69381400-69382200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:69381400-69382200	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr3:69381400-69384400	Enhancers	Brain Hippocampus Middle	brain
34	chr3:69381400-69388600	Weak transcription	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links