Variant report

Variant	rs7536907
Chromosome Location	chr1:78736793-78736794
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1004435	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10489948	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10873970	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10873971	0.81[EUR][1000 genomes]
rs11162444	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11162445	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11162447	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11162448	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11162449	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11162450	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11162452	0.81[EUR][1000 genomes]
rs11804180	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11804577	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12032466	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12036413	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12036778	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12072800	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12076370	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12082822	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1328443	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1328444	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1328445	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1417102	0.83[EUR][1000 genomes]
rs1927779	0.82[EUR][1000 genomes]
rs1952363	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1953956	0.80[AFR][1000 genomes]
rs35271660	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4650394	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56729185	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6674660	0.81[EUR][1000 genomes]
rs67402345	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7529466	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7539904	0.84[EUR][1000 genomes]
rs7545766	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7553079	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7553618	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[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	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	esv2763564	chr1:78727900-78747540	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2762158	chr1:78734241-78747540	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78734800-78749400	Weak transcription	Liver	Liver
2	chr1:78735000-78740400	Weak transcription	HMEC	breast
3	chr1:78736400-78737400	Enhancers	NHDF-Ad	bronchial

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