Variant report

Variant	rs35787059
Chromosome Location	chr3:69378072-69378073
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11714469	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11720197	0.85[AMR][1000 genomes]
rs13061745	0.87[EUR][1000 genomes]
rs13066342	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13066443	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13067464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34609588	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34841224	0.92[AMR][1000 genomes]
rs4855385	0.82[EUR][1000 genomes]
rs4855386	0.82[EUR][1000 genomes]
rs4855390	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs66514154	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7651462	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[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:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69360600-69382200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:69366800-69378200	Enhancers	Brain Hippocampus Middle	brain
3	chr3:69367200-69378400	Enhancers	Brain Substantia Nigra	brain
4	chr3:69368400-69378200	Enhancers	Brain Cingulate Gyrus	brain
5	chr3:69370200-69384000	Weak transcription	Left Ventricle	heart
6	chr3:69370400-69379200	Weak transcription	Spleen	Spleen
7	chr3:69371800-69380000	Weak transcription	Fetal Heart	heart
8	chr3:69372200-69403800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:69372400-69380000	Weak transcription	NHEK	skin
10	chr3:69373600-69378400	Enhancers	Primary B cells from peripheral blood	blood
11	chr3:69373800-69380400	Weak transcription	Placenta	Placenta
12	chr3:69374600-69380400	Weak transcription	Lung	lung
13	chr3:69374600-69383200	Weak transcription	Right Atrium	heart
14	chr3:69374800-69388400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr3:69375000-69380000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:69375000-69384000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:69375400-69378400	Flanking Active TSS	Dnd41	blood
18	chr3:69375600-69378200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr3:69375600-69378200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr3:69375600-69378400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr3:69375600-69378400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr3:69375800-69378400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr3:69375800-69378400	Enhancers	NHLF	lung
24	chr3:69375800-69378600	Enhancers	HUVEC	blood vessel
25	chr3:69376000-69380000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr3:69376400-69378200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr3:69376400-69378400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr3:69376400-69378600	Enhancers	HSMM	muscle
29	chr3:69376400-69388600	Weak transcription	Aorta	Aorta
30	chr3:69376600-69378400	Enhancers	Primary T cells from cord blood	blood
31	chr3:69376600-69378400	Enhancers	Fetal Thymus	thymus
32	chr3:69376600-69378400	Enhancers	Osteobl	bone
33	chr3:69376600-69378600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:69376600-69379600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr3:69376600-69380000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr3:69376600-69380800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr3:69376600-69383200	Weak transcription	Adipose Nuclei	Adipose
38	chr3:69376800-69378400	Enhancers	Thymus	Thymus
39	chr3:69376800-69388400	Weak transcription	HSMMtube	muscle
40	chr3:69377000-69378400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr3:69377000-69381200	Enhancers	Primary hematopoietic stem cells	blood
42	chr3:69377200-69378400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr3:69377400-69378400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr3:69377400-69378400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr3:69377400-69383800	Weak transcription	Brain Angular Gyrus	brain
46	chr3:69377600-69380000	Weak transcription	Fetal Lung	lung
47	chr3:69377800-69378800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr3:69377800-69381400	Weak transcription	Fetal Brain Female	brain
49	chr3:69377800-69382400	Weak transcription	Brain Anterior Caudate	brain
50	chr3:69377800-69382600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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