Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10955412	0.96[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs10955413	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11781331	0.90[ASN][1000 genomes]
rs11997513	0.98[ASN][1000 genomes]
rs12541635	0.98[ASN][1000 genomes]
rs12542361	0.82[EUR][1000 genomes]
rs13277300	0.89[ASN][1000 genomes]
rs1366969	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1835266	0.90[ASN][1000 genomes]
rs1896916	0.90[ASN][1000 genomes]
rs1896917	0.84[ASN][1000 genomes]
rs1896918	0.98[ASN][1000 genomes]
rs1896919	0.98[ASN][1000 genomes]
rs2881036	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2881037	0.98[ASN][1000 genomes]
rs4099936	0.90[ASN][1000 genomes]
rs4734130	0.90[ASN][1000 genomes]
rs4734131	0.90[ASN][1000 genomes]
rs4734896	1.00[ASN][1000 genomes]
rs4734897	1.00[ASN][1000 genomes]
rs6469038	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7016835	0.90[ASN][1000 genomes]
rs727419	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7459459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7464413	1.00[ASN][1000 genomes]
rs7829054	0.88[EUR][1000 genomes]
rs7836196	0.80[EUR][1000 genomes]
rs993177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021369	chr8:106493317-107243322	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv611840	chr8:106913294-107265915	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv611841	chr8:107048059-107090500	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107072400-107074800	Enhancers	NHDF-Ad	bronchial
2	chr8:107073000-107074600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:107073600-107078000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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