Variant report

Variant	rs2726711
Chromosome Location	chr8:50080109-50080110
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:50079888-50080172	A549	lung:	n/a	n/a

Variant related genes	Relation type
ENSG00000253474	TF binding region

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

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10092709	0.86[ASN][1000 genomes]
rs10097641	0.86[ASN][1000 genomes]
rs1021036	0.86[ASN][1000 genomes]
rs10808750	0.83[ASN][1000 genomes]
rs10957383	0.86[ASN][1000 genomes]
rs10957385	0.83[ASN][1000 genomes]
rs11777050	0.86[ASN][1000 genomes]
rs11986211	0.86[ASN][1000 genomes]
rs11998708	0.85[ASN][1000 genomes]
rs13263230	0.81[ASN][1000 genomes]
rs1613684	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1617791	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1842400	0.86[ASN][1000 genomes]
rs1876720	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2175033	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2219896	0.84[ASN][1000 genomes]
rs2385328	0.86[ASN][1000 genomes]
rs2385330	0.86[ASN][1000 genomes]
rs2385331	0.86[ASN][1000 genomes]
rs2726705	0.81[ASN][1000 genomes]
rs2726710	0.80[ASN][1000 genomes]
rs2726714	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35655170	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4256605	0.83[ASN][1000 genomes]
rs4873325	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4873348	0.81[ASN][1000 genomes]
rs4873349	0.84[ASN][1000 genomes]
rs55987135	0.83[ASN][1000 genomes]
rs6472291	0.86[ASN][1000 genomes]
rs6982179	0.86[ASN][1000 genomes]
rs6988643	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6999524	0.80[ASN][1000 genomes]
rs7006071	0.84[ASN][1000 genomes]
rs7012516	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7818564	0.86[ASN][1000 genomes]
rs7824009	0.84[ASN][1000 genomes]
rs7828104	0.86[ASN][1000 genomes]
rs7833419	0.86[ASN][1000 genomes]
rs7836969	0.86[ASN][1000 genomes]
rs7840704	0.84[ASN][1000 genomes]
rs7841358	0.84[ASN][1000 genomes]
rs7844505	0.81[ASN][1000 genomes]
rs7845374	0.86[ASN][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	nsv1025068	chr8:49953397-50370208	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	esv1793350	chr8:50013702-50102628	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1034908	chr8:50023423-50416049	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv539601	chr8:50023423-50416049	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1024410	chr8:50037085-50511501	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr8:50079200-50080800	Enhancers	Stomach Mucosa	stomach
2	chr8:50079400-50080600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:50080000-50081000	Enhancers	NHEK	skin

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