Variant report

Variant	rs7005736
Chromosome Location	chr8:69141722-69141723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1058194	0.85[CHB][hapmap];0.84[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10957423	0.83[EUR][1000 genomes]
rs10957425	0.84[EUR][1000 genomes]
rs12541905	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12544661	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12546271	0.90[CHB][hapmap];0.84[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12547567	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12547594	0.85[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12548558	0.90[CHB][hapmap];0.84[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12549883	0.95[CHB][hapmap];0.84[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12549887	0.91[ASN][1000 genomes]
rs12549980	0.90[CHB][hapmap];0.89[JPT][hapmap];0.90[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12549988	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12681348	0.83[EUR][1000 genomes]
rs13257592	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13258486	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13262547	0.90[CHB][hapmap];0.84[JPT][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13271545	0.83[EUR][1000 genomes]
rs13271692	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13272579	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13281136	0.95[CHB][hapmap];0.84[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13282050	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1404600	0.85[CHB][hapmap];0.84[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1404601	0.85[CHB][hapmap];0.84[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1525054	0.85[CHB][hapmap];0.84[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1525055	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1525056	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16934405	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1880538	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1917544	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2280636	0.90[CHB][hapmap];0.84[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2280637	0.90[CHB][hapmap];0.84[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2280638	0.89[CHB][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2280639	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2280640	0.85[CHB][hapmap];0.84[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2280641	0.90[CHB][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35741702	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6472391	0.84[EUR][1000 genomes]
rs6472392	0.83[EUR][1000 genomes]
rs6984731	0.85[CHB][hapmap];0.84[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7001824	0.90[CHB][hapmap];0.84[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7004629	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7819467	0.83[EUR][1000 genomes]
rs7821308	0.90[CHB][hapmap];0.84[JPT][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7824298	0.84[EUR][1000 genomes]
rs940664	0.90[CHB][hapmap];0.84[JPT][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs940665	0.95[CHB][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[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	esv3331644	chr8:68806705-69189171	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1028889	chr8:69026806-69308725	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv890976	chr8:69100070-69155563	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69103200-69141800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr8:69130000-69151800	Weak transcription	Lung	lung
3	chr8:69130800-69143600	Weak transcription	HUVEC	blood vessel
4	chr8:69131000-69151200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:69131200-69145000	Weak transcription	Fetal Stomach	stomach
6	chr8:69131400-69141800	Weak transcription	Brain Angular Gyrus	brain
7	chr8:69133000-69151800	Weak transcription	Left Ventricle	heart
8	chr8:69135400-69141800	Weak transcription	Right Atrium	heart
9	chr8:69138200-69141800	Weak transcription	Psoas Muscle	Psoas
10	chr8:69140000-69143000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:69140000-69143800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:69141200-69142000	Enhancers	Colon Smooth Muscle	Colon
13	chr8:69141200-69142200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr8:69141200-69142600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:69141200-69142800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:69141200-69142800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr8:69141200-69143000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:69141200-69143000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr8:69141200-69143000	Enhancers	NHDF-Ad	bronchial
20	chr8:69141200-69143200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr8:69141200-69143200	Enhancers	Adipose Nuclei	Adipose
22	chr8:69141200-69143400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:69141200-69143400	Enhancers	Brain Substantia Nigra	brain
24	chr8:69141200-69144000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:69141400-69142000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:69141400-69142000	Enhancers	Aorta	Aorta
27	chr8:69141400-69142000	Enhancers	Brain Hippocampus Middle	brain
28	chr8:69141400-69142000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr8:69141400-69142000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr8:69141400-69142000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr8:69141400-69142200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:69141400-69142200	Enhancers	Brain Germinal Matrix	brain
33	chr8:69141400-69142200	Enhancers	Ovary	ovary
34	chr8:69141400-69142400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr8:69141400-69142800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr8:69141400-69143000	Enhancers	H9 Cell Line	embryonic stem cell
37	chr8:69141400-69143200	Enhancers	Brain Anterior Caudate	brain
38	chr8:69141400-69143800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:69141400-69143800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:69141600-69141800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:69141600-69141800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:69141600-69141800	Enhancers	Fetal Brain Male	brain
43	chr8:69141600-69142000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr8:69141600-69142000	Enhancers	Fetal Muscle Leg	muscle
45	chr8:69141600-69142400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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