Variant report

Variant	rs10063167
Chromosome Location	chr5:108176242-108176243
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10038669	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10044305	0.85[EUR][1000 genomes]
rs10045220	0.95[ASN][1000 genomes]
rs10060694	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10062204	0.81[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap];0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10073668	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.97[ASN][1000 genomes]
rs10079165	0.81[CEU][hapmap]
rs1022045	0.92[JPT][hapmap]
rs10477431	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1109617	0.92[JPT][hapmap]
rs11240982	0.92[JPT][hapmap]
rs11739006	0.92[JPT][hapmap]
rs12153703	0.92[JPT][hapmap]
rs13173714	0.92[JPT][hapmap]
rs13180513	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1423457	0.92[JPT][hapmap]
rs17161476	0.92[JPT][hapmap]
rs2081126	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2081129	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2081130	0.86[EUR][1000 genomes]
rs28637651	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2900035	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34125469	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4604227	0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs4957789	0.92[JPT][hapmap]
rs6594333	0.92[JPT][hapmap]
rs6594334	0.92[JPT][hapmap]
rs6594336	0.92[JPT][hapmap]
rs6594338	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6594340	0.81[ASN][1000 genomes]
rs6871143	0.92[JPT][hapmap]
rs6871239	0.92[JPT][hapmap]
rs6874229	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6875320	0.85[EUR][1000 genomes]
rs6880284	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6889550	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6889967	0.92[JPT][hapmap]
rs6891194	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6895027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7709267	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7710482	0.81[EUR][1000 genomes]
rs7712834	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7712956	0.83[EUR][1000 genomes]
rs7716320	0.92[JPT][hapmap]
rs7716498	0.92[JPT][hapmap]
rs7725391	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7726708	0.83[EUR][1000 genomes]
rs7735235	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9285863	0.92[JPT][hapmap]
rs9326747	0.84[EUR][1000 genomes]
rs9326748	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9885082	0.87[ASN][1000 genomes]
rs9885168	0.86[EUR][1000 genomes];0.95[ASN][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	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv471039	chr5:108133967-108245089	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv1801555	chr5:108166720-108203055	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3403143	chr5:108175973-108176292	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108146800-108183600	Weak transcription	Ovary	ovary
2	chr5:108147000-108198800	Weak transcription	Aorta	Aorta
3	chr5:108147000-108208800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:108153400-108176400	Weak transcription	NHLF	lung
5	chr5:108154800-108176400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:108156400-108178200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr5:108164800-108182400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr5:108165800-108181000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:108165800-108194200	Weak transcription	NHEK	skin
10	chr5:108166400-108193600	Weak transcription	Primary B cells from cord blood	blood
11	chr5:108166400-108203200	Weak transcription	HSMM	muscle
12	chr5:108166600-108194600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr5:108166600-108217000	Weak transcription	Left Ventricle	heart
14	chr5:108166800-108176600	Weak transcription	Colon Smooth Muscle	Colon
15	chr5:108166800-108178400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:108167200-108178000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:108167200-108220400	Weak transcription	Fetal Lung	lung
18	chr5:108167600-108186400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:108167600-108187000	Weak transcription	Fetal Intestine Small	intestine
20	chr5:108167800-108186200	Weak transcription	Fetal Muscle Leg	muscle
21	chr5:108168000-108182200	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr5:108168200-108185200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr5:108168200-108186800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr5:108168200-108194400	Weak transcription	Fetal Heart	heart
25	chr5:108168200-108195000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr5:108168200-108203800	Weak transcription	Adipose Nuclei	Adipose
27	chr5:108168400-108181800	Weak transcription	Osteobl	bone
28	chr5:108168800-108180200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:108169400-108229200	Weak transcription	Fetal Stomach	stomach
30	chr5:108169800-108184800	Weak transcription	Fetal Brain Male	brain
31	chr5:108170200-108181600	Weak transcription	HMEC	breast
32	chr5:108172000-108176600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:108172000-108194000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:108172400-108179800	Weak transcription	Brain Substantia Nigra	brain
35	chr5:108173000-108199800	Weak transcription	Brain Angular Gyrus	brain
36	chr5:108173400-108239800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr5:108173600-108176400	Weak transcription	Liver	Liver
38	chr5:108174000-108180800	Weak transcription	Lung	lung
39	chr5:108174200-108177000	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr5:108174600-108178200	Weak transcription	Hela-S3	cervix
41	chr5:108174600-108186600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:108175200-108185400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr5:108175400-108179400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:108175400-108194200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr5:108175600-108178000	Weak transcription	Primary T cells from cord blood	blood
46	chr5:108176000-108177600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:108176200-108176800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:108176200-108179000	Weak transcription	Brain Cingulate Gyrus	brain

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