Variant report

Variant	rs72940786
Chromosome Location	chr3:69415697-69415698
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12107294	1.00[EUR][1000 genomes]
rs13323929	1.00[EUR][1000 genomes]
rs1384932	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17005573	1.00[EUR][1000 genomes]
rs17005591	1.00[EUR][1000 genomes]
rs59851645	1.00[EUR][1000 genomes]
rs6549210	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6549212	1.00[EUR][1000 genomes]
rs72934847	1.00[EUR][1000 genomes]
rs72934854	1.00[EUR][1000 genomes]
rs72934855	1.00[EUR][1000 genomes]
rs72934857	1.00[EUR][1000 genomes]
rs7633864	1.00[EUR][1000 genomes]
rs7639924	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs922947	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs964552	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9830380	1.00[EUR][1000 genomes]
rs9849228	1.00[EUR][1000 genomes]
rs9861534	1.00[EUR][1000 genomes]
rs9868554	1.00[EUR][1000 genomes]
rs9878971	1.00[EUR][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:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69402200-69419000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:69410200-69417400	Weak transcription	Fetal Lung	lung
3	chr3:69413600-69417200	Weak transcription	Aorta	Aorta
4	chr3:69413600-69417200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr3:69413600-69417200	Weak transcription	Brain Hippocampus Middle	brain
6	chr3:69413600-69417200	Weak transcription	Fetal Thymus	thymus
7	chr3:69413600-69417400	Weak transcription	Brain Anterior Caudate	brain
8	chr3:69413600-69417400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr3:69413600-69417400	Weak transcription	Brain Substantia Nigra	brain
10	chr3:69413600-69417600	Weak transcription	Esophagus	oesophagus
11	chr3:69413600-69418000	Weak transcription	HSMMtube	muscle
12	chr3:69413600-69419000	Weak transcription	NHDF-Ad	bronchial
13	chr3:69413800-69417000	Weak transcription	HUVEC	blood vessel
14	chr3:69413800-69417400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr3:69413800-69417600	Weak transcription	Placenta	Placenta
16	chr3:69413800-69417600	Weak transcription	Right Atrium	heart
17	chr3:69413800-69419000	Weak transcription	Brain Angular Gyrus	brain
18	chr3:69413800-69419400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:69414000-69415800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:69414000-69417200	Weak transcription	Thymus	Thymus
21	chr3:69414000-69417400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr3:69414000-69417400	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr3:69414000-69418400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:69414000-69419000	Weak transcription	Osteobl	bone
25	chr3:69414200-69418000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr3:69414400-69416400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr3:69414600-69416800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:69414600-69417000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr3:69414600-69417400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr3:69414800-69416800	Weak transcription	GM12878-XiMat	blood
31	chr3:69414800-69417200	Weak transcription	HMEC	breast
32	chr3:69414800-69417200	Weak transcription	NHEK	skin
33	chr3:69415000-69416000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr3:69415000-69417200	Weak transcription	HSMM	muscle
35	chr3:69415000-69417400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:69415000-69417400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr3:69415000-69418800	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr3:69415200-69417200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr3:69415400-69415800	Weak transcription	Dnd41	blood
40	chr3:69415400-69417200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr3:69415400-69417400	Weak transcription	Lung	lung

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