Variant report

Variant	rs4645524
Chromosome Location	chr8:91974866-91974867
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:91971665..91973537-chr8:91974194..91975735,2	K562	blood:
2	chr8:91973738..91976660-chr8:92039107..92040823,2	K562	blood:
3	chr8:91974810..91977533-chr8:91979660..91982481,3	K562	blood:
4	chr8:91973901..91977899-chr8:91982620..91986949,4	K562	blood:
5	chr8:91961850..91965214-chr8:91972320..91975888,3	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10490979	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1060583	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11989738	0.82[EUR][1000 genomes]
rs11994240	0.82[EUR][1000 genomes]
rs16905862	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16906071	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16907242	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34503257	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55999403	0.89[EUR][1000 genomes]
rs56871170	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58183914	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58624537	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58807337	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59695689	0.86[EUR][1000 genomes]
rs60121972	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6471263	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6651175	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7006863	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73298014	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73298068	0.82[EUR][1000 genomes]
rs73299912	0.84[EUR][1000 genomes]
rs73299915	0.82[EUR][1000 genomes]
rs73299920	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73299946	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299965	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299977	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299979	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299981	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7818979	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv891185	chr8:91923776-92056288	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1028201	chr8:91968527-92009964	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases
5	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91951800-91986400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:91953400-91981400	Weak transcription	HSMM	muscle
3	chr8:91953400-91984600	Weak transcription	NH-A	brain
4	chr8:91953600-91976000	Weak transcription	Brain Substantia Nigra	brain
5	chr8:91953600-91977600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr8:91955600-91975000	Weak transcription	Adipose Nuclei	Adipose
7	chr8:91957200-91976200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:91958000-91976200	Weak transcription	K562	blood
9	chr8:91958200-91996000	Weak transcription	Fetal Stomach	stomach
10	chr8:91960600-91975200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:91960600-91976000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr8:91961200-91975400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr8:91961200-91976000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:91961600-91975000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:91963000-91975000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:91963600-91975800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:91963600-91979000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:91964600-91989800	Weak transcription	Left Ventricle	heart
19	chr8:91964800-91996600	Weak transcription	Ovary	ovary
20	chr8:91965600-91979200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr8:91966200-91976200	Weak transcription	Colon Smooth Muscle	Colon
22	chr8:91970400-91976200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:91971800-91976400	Weak transcription	Brain Hippocampus Middle	brain
24	chr8:91971800-91996600	Weak transcription	Thymus	Thymus
25	chr8:91972600-91975000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:91972600-91975200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:91972600-91976200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:91972600-91976200	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr8:91972600-91976200	Weak transcription	Fetal Lung	lung
30	chr8:91973000-91977200	Weak transcription	NHDF-Ad	bronchial
31	chr8:91974000-91979800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:91974400-91975400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
33	chr8:91974600-91975600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:91974600-91976000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:91974800-91975400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr8:91974800-91978000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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