Variant report

Variant	rs12088784
Chromosome Location	chr1:78952286-78952287
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11162496	1.00[AMR][1000 genomes]
rs11162497	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11485266	1.00[AMR][1000 genomes]
rs11809460	0.86[EUR][1000 genomes]
rs11809462	0.86[EUR][1000 genomes]
rs12067110	0.87[EUR][1000 genomes]
rs12073698	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12074558	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12074955	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12075295	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12076694	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12077792	0.93[EUR][1000 genomes]
rs12079105	0.93[EUR][1000 genomes]
rs12085484	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1322924	0.93[EUR][1000 genomes]
rs1927326	0.80[EUR][1000 genomes]
rs28791033	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57205467	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58034089	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58858806	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59584643	1.00[AMR][1000 genomes]
rs60047746	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61388935	0.80[EUR][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	nsv1013008	chr1:78463173-78958701	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv535012	chr1:78463173-78958701	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv870807	chr1:78867347-79032598	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78949800-78955600	Weak transcription	NHDF-Ad	bronchial
2	chr1:78950000-78956200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:78950000-78956200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:78950200-78956200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:78950400-78955600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:78950400-78956600	Weak transcription	Spleen	Spleen

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