Variant report

Variant	rs6792370
Chromosome Location	chr3:23289892-23289893
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10510536	0.95[CHB][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11926494	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11927173	0.91[ASN][1000 genomes]
rs13094957	0.89[CHB][hapmap]
rs13314285	0.81[ASN][1000 genomes]
rs1495130	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1496653	1.00[CHB][hapmap];0.87[CHD][hapmap]
rs17012800	0.95[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17012829	0.95[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1908475	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2017065	0.95[CHB][hapmap];0.87[CHD][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs2173058	1.00[CHB][hapmap]
rs2359765	0.95[CHB][hapmap];0.84[CHD][hapmap]
rs2359766	0.94[CHB][hapmap]
rs4327332	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs57131555	0.90[ASN][1000 genomes]
rs58724157	0.90[ASN][1000 genomes]
rs60782093	0.91[ASN][1000 genomes]
rs61578857	0.91[ASN][1000 genomes]
rs6765801	0.89[ASN][1000 genomes]
rs6769167	0.87[ASN][1000 genomes]
rs73823472	0.81[ASN][1000 genomes]
rs7612463	1.00[ASW][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.82[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7613185	1.00[CHB][hapmap]
rs7627380	1.00[ASW][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.80[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7627525	1.00[CHB][hapmap];0.87[CHD][hapmap]
rs7628372	1.00[CHB][hapmap]
rs9831921	0.81[ASN][1000 genomes]
rs9866739	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9867046	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834636	chr3:23138653-23301443	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1014701	chr3:23257658-23416094	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv589947	chr3:23277838-23403943	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv589948	chr3:23287141-23390221	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23274800-23298200	Weak transcription	Aorta	Aorta
2	chr3:23280200-23291400	Weak transcription	Psoas Muscle	Psoas
3	chr3:23280400-23290600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr3:23281400-23298200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr3:23282000-23290200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr3:23282200-23294600	Weak transcription	A549	lung
7	chr3:23283200-23296000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr3:23283600-23302200	Weak transcription	Left Ventricle	heart
9	chr3:23283800-23292000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:23285000-23290000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr3:23285000-23292400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:23289000-23290400	Enhancers	Adipose Nuclei	Adipose
13	chr3:23289000-23294800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr3:23289200-23292400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:23289400-23290400	Enhancers	Brain Anterior Caudate	brain
16	chr3:23289600-23290000	Enhancers	Brain Angular Gyrus	brain
17	chr3:23289600-23290400	Enhancers	Brain Hippocampus Middle	brain
18	chr3:23289600-23290600	Enhancers	Brain Substantia Nigra	brain

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