Variant report

Variant	rs1579262
Chromosome Location	chr8:113289033-113289034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10447984	0.89[EUR][1000 genomes]
rs11776765	0.84[EUR][1000 genomes]
rs11777694	0.89[EUR][1000 genomes]
rs11778806	0.89[EUR][1000 genomes]
rs11778874	0.89[EUR][1000 genomes]
rs11780719	0.89[EUR][1000 genomes]
rs12676507	0.85[EUR][1000 genomes]
rs12678407	0.84[EUR][1000 genomes]
rs12680158	0.90[EUR][1000 genomes]
rs1388963	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1388965	0.89[EUR][1000 genomes]
rs1472166	0.85[EUR][1000 genomes]
rs1492677	0.89[EUR][1000 genomes]
rs1492678	0.89[EUR][1000 genomes]
rs1602703	0.88[EUR][1000 genomes]
rs1602704	0.89[EUR][1000 genomes]
rs1873746	0.85[EUR][1000 genomes]
rs1907803	0.89[EUR][1000 genomes]
rs1907804	0.89[EUR][1000 genomes]
rs2131298	0.89[EUR][1000 genomes]
rs2201204	0.82[EUR][1000 genomes]
rs28453001	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35282651	0.89[EUR][1000 genomes]
rs3950676	0.89[EUR][1000 genomes]
rs41340951	0.89[EUR][1000 genomes]
rs41467949	0.89[EUR][1000 genomes]
rs4469486	0.83[EUR][1000 genomes]
rs4563913	0.85[EUR][1000 genomes]
rs4577984	0.89[EUR][1000 genomes]
rs4876281	0.89[EUR][1000 genomes]
rs4876462	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56064440	0.89[EUR][1000 genomes]
rs56156694	0.89[EUR][1000 genomes]
rs56276823	0.89[EUR][1000 genomes]
rs56288817	0.89[EUR][1000 genomes]
rs56403239	0.90[EUR][1000 genomes]
rs58364548	0.89[EUR][1000 genomes]
rs59156725	0.87[EUR][1000 genomes]
rs59265979	0.89[EUR][1000 genomes]
rs60340602	0.89[EUR][1000 genomes]
rs61187653	0.89[EUR][1000 genomes]
rs62514412	0.90[EUR][1000 genomes]
rs62514414	0.89[EUR][1000 genomes]
rs62514418	0.89[EUR][1000 genomes]
rs62514434	0.89[EUR][1000 genomes]
rs6469413	0.91[EUR][1000 genomes]
rs67822558	0.89[EUR][1000 genomes]
rs7003500	0.89[EUR][1000 genomes]
rs7012192	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7012257	0.89[EUR][1000 genomes]
rs7012300	0.90[EUR][1000 genomes]
rs7819634	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7838254	0.89[EUR][1000 genomes]
rs7838616	0.89[EUR][1000 genomes]
rs7838852	0.86[EUR][1000 genomes]
rs7845628	0.81[EUR][1000 genomes]
rs963086	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[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	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2755868	chr8:113282795-113634842	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113288800-113289200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:113288800-113331400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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