Variant report

Variant	rs10063478
Chromosome Location	chr5:57078397-57078398
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:57076424..57079221-chr5:57153690..57156496,2	MCF-7	breast:
2	chr5:57076851..57079934-chr5:57754416..57757350,4	MCF-7	breast:
3	chr5:57077792..57079742-chr5:57748468..57750917,2	MCF-7	breast:
4	chr5:57077135..57082051-chr5:57753020..57756988,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000145632	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10077188	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs1101571	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12652479	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs12654850	0.83[ASN][1000 genomes]
rs12657521	0.84[EUR][1000 genomes]
rs12657522	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs1821209	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2053012	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs28440142	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28489989	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58404507	0.84[EUR][1000 genomes]
rs73089900	0.83[ASN][1000 genomes]
rs7702309	1.00[CHB][hapmap]
rs7713500	1.00[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs7729312	1.00[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs7731160	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs7734787	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs854040	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs854041	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs854043	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs854044	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs854047	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs854051	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs854055	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9885075	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2756302	chr5:56978143-57180143	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830310	chr5:56989346-57176006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2763454	chr5:57006531-57161140	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57072600-57079600	Weak transcription	Ovary	ovary
2	chr5:57075400-57080400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:57076400-57078800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:57076400-57078800	Weak transcription	Brain Anterior Caudate	brain
5	chr5:57076400-57078800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr5:57076400-57078800	Weak transcription	Osteobl	bone
7	chr5:57076400-57079200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr5:57076400-57079400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:57076400-57079400	Weak transcription	Aorta	Aorta
10	chr5:57076400-57080200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:57076400-57081800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:57076600-57078600	Weak transcription	NHDF-Ad	bronchial
13	chr5:57076600-57078800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr5:57076600-57078800	Weak transcription	HSMMtube	muscle
15	chr5:57076600-57079000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:57076600-57079000	Weak transcription	Fetal Lung	lung
17	chr5:57076600-57079600	Weak transcription	Right Atrium	heart
18	chr5:57076600-57079600	Weak transcription	HMEC	breast
19	chr5:57077000-57078400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:57077000-57079400	Weak transcription	HUVEC	blood vessel
21	chr5:57077000-57080000	Weak transcription	Stomach Mucosa	stomach
22	chr5:57077200-57079400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:57077400-57079000	Weak transcription	Fetal Muscle Leg	muscle
24	chr5:57077800-57079000	Enhancers	Adipose Nuclei	Adipose
25	chr5:57078200-57079000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:57078200-57079200	Enhancers	Placenta	Placenta
27	chr5:57078200-57079200	Enhancers	HSMM	muscle

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