Variant report

Variant	rs10099614
Chromosome Location	chr8:69686624-69686625
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:69489517..69490141-chr8:69685805..69686684,3	MCF-7	breast:
2	chr8:69684482..69688368-chr8:69762278..69766064,4	MCF-7	breast:
3	chr8:69684731..69687775-chr8:69763630..69766534,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254337	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10957447	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11993861	0.94[ASN][1000 genomes]
rs11994264	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11995110	0.99[ASN][1000 genomes]
rs12675214	0.98[ASN][1000 genomes]
rs12675220	0.98[ASN][1000 genomes]
rs2953945	0.83[CHB][hapmap];0.82[CHD][hapmap];0.83[ASN][1000 genomes]
rs2953947	0.83[ASN][1000 genomes]
rs2953948	0.83[CHB][hapmap];0.83[ASN][1000 genomes]
rs2953949	0.83[ASN][1000 genomes]
rs2953950	0.83[CHB][hapmap];0.82[CHD][hapmap];0.83[ASN][1000 genomes]
rs2953951	0.83[CHB][hapmap];0.83[ASN][1000 genomes]
rs2953952	0.83[ASN][1000 genomes]
rs2953954	0.82[ASN][1000 genomes]
rs2953955	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs2958333	0.82[ASN][1000 genomes]
rs2958334	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs2978237	0.82[ASN][1000 genomes]
rs2978238	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs2978239	0.82[ASN][1000 genomes]
rs2978240	0.82[ASN][1000 genomes]
rs2978241	0.83[ASN][1000 genomes]
rs2978242	0.83[ASN][1000 genomes]
rs34283177	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4374973	1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[ASN][1000 genomes]
rs4401840	1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[ASN][1000 genomes]
rs5022152	0.98[ASN][1000 genomes]
rs62520981	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6983604	0.93[ASN][1000 genomes]
rs6984482	0.98[ASN][1000 genomes]
rs6998182	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7016624	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73270234	0.95[ASN][1000 genomes]
rs7461173	0.98[ASN][1000 genomes]
rs7464182	0.98[ASN][1000 genomes]
rs7464209	0.98[ASN][1000 genomes]
rs7813466	0.83[ASN][1000 genomes]
rs7817788	1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[ASN][1000 genomes]
rs7833828	1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[ASN][1000 genomes]
rs7834286	0.95[ASN][1000 genomes]
rs7843991	0.98[ASN][1000 genomes]
rs7844031	0.83[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	nsv831349	chr8:69555461-69733515	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv465703	chr8:69641287-69814578	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv611462	chr8:69641287-69814578	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv890986	chr8:69647914-69704366	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1017131	chr8:69676989-69792515	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv519549	chr8:69682388-69687852	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 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	chr8:69683000-69688000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:69686200-69687000	Enhancers	Fetal Lung	lung

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