Variant report

Variant	rs3115910
Chromosome Location	chr8:94950873-94950874
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:94928189..94929861-chr8:94949400..94951121,2	MCF-7	breast:
2	chr8:94949076..94950984-chr8:94954882..94956888,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000264448	Chromatin interaction
ENSG00000164951	Chromatin interaction
ENSG00000251234	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs28758779	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3115898	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115904	0.89[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115905	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115906	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115907	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115908	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3115909	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115912	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115914	0.82[ASN][1000 genomes]
rs3133978	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3133979	1.00[EUR][1000 genomes]
rs3133980	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3133983	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3133984	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3133985	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs34468383	0.87[EUR][1000 genomes]
rs57919376	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58328810	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58550934	0.96[EUR][1000 genomes]
rs58894594	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs59390113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62525235	0.96[EUR][1000 genomes]
rs62525237	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62525238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62525240	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62525241	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs723039	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754970	chr8:94675324-94991724	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:94948200-94956600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr8:94948400-94956400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:94948600-94952200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr8:94948800-94952000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:94948800-94952200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr8:94948800-94952800	Weak transcription	HSMMtube	muscle
7	chr8:94948800-94955800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr8:94948800-94955800	Weak transcription	Ovary	ovary
9	chr8:94948800-94956200	Weak transcription	NHLF	lung
10	chr8:94949000-94954200	Weak transcription	Right Ventricle	heart
11	chr8:94949800-94951200	Enhancers	NHEK	skin
12	chr8:94950400-94951000	Enhancers	Fetal Intestine Large	intestine
13	chr8:94950400-94951400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:94950400-94951800	Enhancers	Osteobl	bone
15	chr8:94950600-94951000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr8:94950600-94951000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:94950600-94951000	Enhancers	HMEC	breast
18	chr8:94950600-94951200	Enhancers	Fetal Heart	heart
19	chr8:94950600-94951200	Enhancers	HUVEC	blood vessel
20	chr8:94950600-94951400	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr8:94950600-94951600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:94950600-94951600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr8:94950600-94951600	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr8:94950600-94951800	Enhancers	NHDF-Ad	bronchial
25	chr8:94950800-94951000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:94950800-94951000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
27	chr8:94950800-94951000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:94950800-94951000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:94950800-94951000	Enhancers	Adipose Nuclei	Adipose
30	chr8:94950800-94951000	Enhancers	Aorta	Aorta
31	chr8:94950800-94951000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:94950800-94951000	Enhancers	Fetal Muscle Leg	muscle
33	chr8:94950800-94951000	Enhancers	Placenta	Placenta
34	chr8:94950800-94951000	Enhancers	Pancreas	Pancrea
35	chr8:94950800-94951000	Enhancers	Psoas Muscle	Psoas
36	chr8:94950800-94951000	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr8:94950800-94951200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:94950800-94951200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:94950800-94951200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:94950800-94951200	Enhancers	Fetal Lung	lung
41	chr8:94950800-94951200	Enhancers	HSMM	muscle
42	chr8:94950800-94951400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:94950800-94951400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr8:94950800-94951400	Enhancers	Fetal Muscle Trunk	muscle
45	chr8:94950800-94951400	Enhancers	Left Ventricle	heart
46	chr8:94950800-94951400	Enhancers	Lung	lung
47	chr8:94950800-94951400	Enhancers	Right Atrium	heart
48	chr8:94950800-94951600	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:94950800-94951600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:94950800-94951600	Enhancers	NH-A	brain

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