Variant report

Variant	rs58680324
Chromosome Location	chr17:66951984-66951985
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CREB1	chr17:66951252-66951984	K562	blood:	n/a	n/a
2	CUX1	chr17:66951385-66952018	K562	blood:	n/a	n/a

Variant related genes	Relation type
ABCA8	TF binding region

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10852773	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10852774	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10852776	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11077818	0.83[EUR][1000 genomes]
rs11077819	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11077852	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1121077	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1122265	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11868372	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11869992	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12936488	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12938677	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12940203	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12940209	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12944603	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12945526	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1344055	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1860445	0.83[EUR][1000 genomes]
rs1990334	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2041321	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2159433	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2191214	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2364310	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3744498	0.82[EUR][1000 genomes]
rs3744499	0.82[EUR][1000 genomes]
rs4147944	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4147945	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4147946	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4147947	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4147948	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4147949	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4147950	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4147951	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4147953	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4147954	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4147957	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4147959	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4147963	0.82[EUR][1000 genomes]
rs4147964	0.82[EUR][1000 genomes]
rs4147968	0.82[EUR][1000 genomes]
rs4147970	0.82[EUR][1000 genomes]
rs4147971	0.81[EUR][1000 genomes]
rs4147972	0.81[EUR][1000 genomes]
rs4968827	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4968977	0.82[EUR][1000 genomes]
rs4968978	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4968980	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6501916	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6501919	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6501920	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7207730	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7210891	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7217589	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7221169	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7225239	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7225473	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7225771	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs764425	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs764426	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8065455	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8068037	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8072891	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8079972	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8082257	0.81[EUR][1000 genomes]
rs9897075	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9905330	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9916792	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1061151	chr17:66881617-66973917	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv908700	chr17:66885526-66985992	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv908701	chr17:66888346-66978319	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1066412	chr17:66897540-66954067	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	esv1846502	chr17:66899261-66966274	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv1849165	chr17:66899261-66978319	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv908703	chr17:66904001-66978319	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv908704	chr17:66925324-66959710	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66949400-66952000	Active TSS	Brain Angular Gyrus	brain
2	chr17:66949800-66952000	Active TSS	Brain Hippocampus Middle	brain
3	chr17:66949800-66952000	Active TSS	Right Atrium	heart
4	chr17:66950000-66952000	Active TSS	Ovary	ovary
5	chr17:66950600-66952200	Active TSS	K562	blood
6	chr17:66951000-66952000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr17:66951200-66952000	Flanking Active TSS	Osteobl	bone
8	chr17:66951600-66952000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr17:66951600-66952000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr17:66951600-66952000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr17:66951600-66952000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr17:66951600-66952000	Enhancers	Brain Substantia Nigra	brain
13	chr17:66951600-66952000	Flanking Active TSS	Fetal Heart	heart
14	chr17:66951600-66952000	Flanking Active TSS	Fetal Lung	lung
15	chr17:66951800-66952000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr17:66951800-66952000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr17:66951800-66952000	Enhancers	Adipose Nuclei	Adipose
18	chr17:66951800-66952000	Enhancers	Liver	Liver
19	chr17:66951800-66952000	Enhancers	Brain Anterior Caudate	brain
20	chr17:66951800-66952000	Enhancers	Brain Cingulate Gyrus	brain

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