Variant report

Variant	rs4030102
Chromosome Location	chr8:113339106-113339107
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10447984	0.89[ASN][1000 genomes]
rs11777694	0.88[ASN][1000 genomes]
rs11778806	0.87[ASN][1000 genomes]
rs11778874	0.89[ASN][1000 genomes]
rs11780719	0.89[ASN][1000 genomes]
rs12680158	0.90[ASN][1000 genomes]
rs1388963	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1388965	0.82[ASN][1000 genomes]
rs1420859	0.82[EUR][1000 genomes]
rs1492677	0.87[ASN][1000 genomes]
rs1492678	0.85[ASN][1000 genomes]
rs1602703	0.84[ASN][1000 genomes]
rs1602704	0.84[ASN][1000 genomes]
rs1907803	0.89[ASN][1000 genomes]
rs1907804	0.89[ASN][1000 genomes]
rs2131298	0.90[ASN][1000 genomes]
rs2201204	0.88[ASN][1000 genomes]
rs28453001	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35282651	0.89[ASN][1000 genomes]
rs3950676	0.86[ASN][1000 genomes]
rs41340951	0.83[ASN][1000 genomes]
rs41467949	0.84[ASN][1000 genomes]
rs4577984	0.89[ASN][1000 genomes]
rs4876281	0.84[ASN][1000 genomes]
rs4876462	0.82[ASN][1000 genomes]
rs56064440	0.87[ASN][1000 genomes]
rs56156694	0.84[ASN][1000 genomes]
rs56276823	0.88[ASN][1000 genomes]
rs56288817	0.88[ASN][1000 genomes]
rs56403239	0.90[ASN][1000 genomes]
rs58364548	0.84[ASN][1000 genomes]
rs59156725	0.90[ASN][1000 genomes]
rs59265979	0.84[ASN][1000 genomes]
rs60340602	0.90[ASN][1000 genomes]
rs61187653	0.90[ASN][1000 genomes]
rs62514412	0.90[ASN][1000 genomes]
rs62514414	0.90[ASN][1000 genomes]
rs62514418	0.90[ASN][1000 genomes]
rs62514434	0.84[ASN][1000 genomes]
rs6469413	0.90[ASN][1000 genomes]
rs67822558	0.85[ASN][1000 genomes]
rs7003500	0.90[ASN][1000 genomes]
rs7012257	0.90[ASN][1000 genomes]
rs7012300	0.90[ASN][1000 genomes]
rs7819634	0.83[ASN][1000 genomes]
rs7826278	0.82[EUR][1000 genomes]
rs7838254	0.88[ASN][1000 genomes]
rs7838616	0.89[ASN][1000 genomes]
rs7838852	0.89[ASN][1000 genomes]
rs7845628	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7845794	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs929685	0.82[EUR][1000 genomes]
rs929687	0.81[EUR][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	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
5	esv2754232	chr8:113294967-113634842	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113338800-113339200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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